166 Jobs in Rebévelier
Program Manager
Lengnau, Bern
ThermoFisher Scientific
Gestern
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Are you set for an outstanding opportunity in Switzerland with a top-notch team? As a Program Manager at Thermo Fisher Scientific Inc., you'll be crucial in ensuring flawless project execution while maintaining exceptional standards.
**Responsibilities:**
+ Manage programs allocated to the Lengnau site, guaranteeing that project achievements are met as per the plan/contract.
+ Raise issues to site leadership and uphold effective communication with clients and program owners.
+ Lead all aspects of Project Charters for each project, clearly defining objectives, timelines, communication channels, and meeting regimes.
+ Act as a role model and main driver of the execution of the Project Charter, encouraging effective communication with clients, ThermoFisher senior management, Subject Matter Experts, and project teams.
Budget Control
+ Maintain accurate financial records with the assistance of ThermoFisher's financial team.
+ Ensure timely invoicing to generate revenue for ThermoFisher.
+ Communicate with the finance department to offer detailed financial reporting of the program internally.
Expertise and Compliance
+ Provide extensive knowledge of the pharmaceutical industry to ensure safe product availability to patients.
+ Ensure ThermoFisher's Safety Standards are maintained throughout the project execution.
+ Document program activities to meet regulatory authorities' mentorship and expectations.
+ Maintain a strong network of Subject Matter Experts within the ThermoFisher team to bolster a range of skills.
**Position Qualifications:**
+ Master degree in science/engineering or other similar education
+ >7 years experience in the pharmaceutical industry, within CMC/technical development
+ >5 years in project management or related
+ Proficiency in project management methodologies, including managing project plans, schedules, and budgets
+ Understanding of the technical aspects relevant to the projects being managed
+ Ability to identify, assess, and mitigate risks throughout the project lifecycle
+ Leadership: Ability to inspire and motivate the team. Strong decision-making skills and confidence in leading the project
+ Communication: Excellent verbal and written communication skills. Ability to communicate effectively with stakeholders, team members, and management
+ Adaptability: Flexibility to adapt to changing project requirements and environments. Ability to handle unexpected challenges and changes effectively
Embark on our journey to improve global health, cleanliness, and safety. Your role at Thermo Fisher Scientific will significantly impact international health and safety benchmarks. We are looking forward to having you on board with our team!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Are you set for an outstanding opportunity in Switzerland with a top-notch team? As a Program Manager at Thermo Fisher Scientific Inc., you'll be crucial in ensuring flawless project execution while maintaining exceptional standards.
**Responsibilities:**
+ Manage programs allocated to the Lengnau site, guaranteeing that project achievements are met as per the plan/contract.
+ Raise issues to site leadership and uphold effective communication with clients and program owners.
+ Lead all aspects of Project Charters for each project, clearly defining objectives, timelines, communication channels, and meeting regimes.
+ Act as a role model and main driver of the execution of the Project Charter, encouraging effective communication with clients, ThermoFisher senior management, Subject Matter Experts, and project teams.
Budget Control
+ Maintain accurate financial records with the assistance of ThermoFisher's financial team.
+ Ensure timely invoicing to generate revenue for ThermoFisher.
+ Communicate with the finance department to offer detailed financial reporting of the program internally.
Expertise and Compliance
+ Provide extensive knowledge of the pharmaceutical industry to ensure safe product availability to patients.
+ Ensure ThermoFisher's Safety Standards are maintained throughout the project execution.
+ Document program activities to meet regulatory authorities' mentorship and expectations.
+ Maintain a strong network of Subject Matter Experts within the ThermoFisher team to bolster a range of skills.
**Position Qualifications:**
+ Master degree in science/engineering or other similar education
+ >7 years experience in the pharmaceutical industry, within CMC/technical development
+ >5 years in project management or related
+ Proficiency in project management methodologies, including managing project plans, schedules, and budgets
+ Understanding of the technical aspects relevant to the projects being managed
+ Ability to identify, assess, and mitigate risks throughout the project lifecycle
+ Leadership: Ability to inspire and motivate the team. Strong decision-making skills and confidence in leading the project
+ Communication: Excellent verbal and written communication skills. Ability to communicate effectively with stakeholders, team members, and management
+ Adaptability: Flexibility to adapt to changing project requirements and environments. Ability to handle unexpected challenges and changes effectively
Embark on our journey to improve global health, cleanliness, and safety. Your role at Thermo Fisher Scientific will significantly impact international health and safety benchmarks. We are looking forward to having you on board with our team!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
0
Manufacturing Planner
Lengnau, Bern
ThermoFisher Scientific
Vor 3 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Job Purpose:**
The Manufacturing Planner is responsible for the day-to-day scheduling and coordination of manufacturing activities to support continuous and efficient production. This includes planning campaign sequences, issuing daily schedules, monitoring progress on the shop floor, and adjusting plans in real time to ensure seamless operations. The role acts as the link between Production, Quality, Maintenance, and Supply Chain to maintain smooth campaign execution under GMP conditions.
**Key Responsibilities:**
**Daily Scheduling and Execution**
+ Prepare and issue daily and weekly production schedules for all manufacturing areas.
+ Ensure the availability of equipment, materials, and documentation before batch start.
+ Track progress of ongoing batches and update plans in real time based on operational status.
+ Communicate daily priorities and updates to Production Manager, Supervisors and Operators.
+ Adjust schedules promptly in response to deviations, equipment issues, or material delays.
**2. Campaign Planning**
+ Support the setup and coordination of manufacturing campaigns.
+ Define batch sequence, cleaning intervals, and equipment allocation to optimize efficiency.
+ Ensure readiness of all required tools, parts, and utilities prior to campaign start.
+ Maintain an overview of campaign progress and escalate delays or risks to the Production Manager.
**3. Cross-Functional Coordination**
+ Coordinate with Supply Chain and Warehouse to confirm raw material and component availability.
+ Work closely with Maintenance to plan interventions and avoid production interruptions.
+ Support communication between shifts to ensure continuity of production activities.
**4. Documentation and Systems**
+ Maintain up-to-date information in planning and tracking tools.
+ Record production plan changes, reasons for delays, and corrective actions in compliance with GMP documentation standards.
+ Prepare short-term capacity and utilization reports as needed.
**5. Continuous Improvement**
+ Propose and implement improvements to scheduling processes and coordination routines.
+ Participate in daily tier meetings and performance reviews to identify efficiency gains.
+ Support Production in troubleshooting and reducing downtime related to planning or coordination gaps.
**Education & Experience:**
+ Bachelor/Master/PhD in Chemistry, Biochemistry, Biotechnology, Biology, or Food Science.
+ Proficiency in English; German is a plus.
+ Minimum of 5 years in pharmaceutical operations within a GMP environment.
+ Strong experience in biotech processes, sterile processes, and production equipment handling.
+ Ability to thrive in a matrix environment with cross-functional teams.
+ Availability for remote on-call duties.
**Benefits:**
+ Competitive remuneration and comprehensive benefits package.
+ Work with an innovative, forward-thinking organization that values integrity, intensity, involvement, and innovation.
+ Outstanding career and development prospects.
+ A company culture that embraces diversity and values individual contributions.
Join us! At Thermo Fisher Scientific, you'll be part of a global team of over 100,000 colleagues dedicated to making the world healthier, cleaner, and safer. Start your story with us, where diverse experiences, backgrounds, and perspectives are valued. Together, we're accelerating research, solving complex scientific challenges, and supporting patients in need
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Job Purpose:**
The Manufacturing Planner is responsible for the day-to-day scheduling and coordination of manufacturing activities to support continuous and efficient production. This includes planning campaign sequences, issuing daily schedules, monitoring progress on the shop floor, and adjusting plans in real time to ensure seamless operations. The role acts as the link between Production, Quality, Maintenance, and Supply Chain to maintain smooth campaign execution under GMP conditions.
**Key Responsibilities:**
**Daily Scheduling and Execution**
+ Prepare and issue daily and weekly production schedules for all manufacturing areas.
+ Ensure the availability of equipment, materials, and documentation before batch start.
+ Track progress of ongoing batches and update plans in real time based on operational status.
+ Communicate daily priorities and updates to Production Manager, Supervisors and Operators.
+ Adjust schedules promptly in response to deviations, equipment issues, or material delays.
**2. Campaign Planning**
+ Support the setup and coordination of manufacturing campaigns.
+ Define batch sequence, cleaning intervals, and equipment allocation to optimize efficiency.
+ Ensure readiness of all required tools, parts, and utilities prior to campaign start.
+ Maintain an overview of campaign progress and escalate delays or risks to the Production Manager.
**3. Cross-Functional Coordination**
+ Coordinate with Supply Chain and Warehouse to confirm raw material and component availability.
+ Work closely with Maintenance to plan interventions and avoid production interruptions.
+ Support communication between shifts to ensure continuity of production activities.
**4. Documentation and Systems**
+ Maintain up-to-date information in planning and tracking tools.
+ Record production plan changes, reasons for delays, and corrective actions in compliance with GMP documentation standards.
+ Prepare short-term capacity and utilization reports as needed.
**5. Continuous Improvement**
+ Propose and implement improvements to scheduling processes and coordination routines.
+ Participate in daily tier meetings and performance reviews to identify efficiency gains.
+ Support Production in troubleshooting and reducing downtime related to planning or coordination gaps.
**Education & Experience:**
+ Bachelor/Master/PhD in Chemistry, Biochemistry, Biotechnology, Biology, or Food Science.
+ Proficiency in English; German is a plus.
+ Minimum of 5 years in pharmaceutical operations within a GMP environment.
+ Strong experience in biotech processes, sterile processes, and production equipment handling.
+ Ability to thrive in a matrix environment with cross-functional teams.
+ Availability for remote on-call duties.
**Benefits:**
+ Competitive remuneration and comprehensive benefits package.
+ Work with an innovative, forward-thinking organization that values integrity, intensity, involvement, and innovation.
+ Outstanding career and development prospects.
+ A company culture that embraces diversity and values individual contributions.
Join us! At Thermo Fisher Scientific, you'll be part of a global team of over 100,000 colleagues dedicated to making the world healthier, cleaner, and safer. Start your story with us, where diverse experiences, backgrounds, and perspectives are valued. Together, we're accelerating research, solving complex scientific challenges, and supporting patients in need
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
1
Manufacturing Specialist (USP or DSP)
Lengnau, Bern
ThermoFisher Scientific
Vor 3 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule,
+ Is responsible for the daily execution of manufacturing activities in USP or DSP
+ Owns Work Instructions and SOP in their area
+ Support Manufacturing Excellence in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards.
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives.
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Contributes to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor's degree in pharmaceutical, food or chemistry
+ Language: English or German
+ 1-3 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires a first experience in pharmaceutical industry
+ Willingness to learn
+ Can-do attitude
+ Work on a shift rotation model, this includes regular weekend, and public holiday work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule,
+ Is responsible for the daily execution of manufacturing activities in USP or DSP
+ Owns Work Instructions and SOP in their area
+ Support Manufacturing Excellence in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards.
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives.
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Contributes to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor's degree in pharmaceutical, food or chemistry
+ Language: English or German
+ 1-3 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires a first experience in pharmaceutical industry
+ Willingness to learn
+ Can-do attitude
+ Work on a shift rotation model, this includes regular weekend, and public holiday work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
2
Ingenieur (m/w/d) für Projekte im Bereich Automatisierung - Medizintechnik
Selzach, Solothurn
Stryker
Vor 3 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Für unser lokales Team von Manufacturing Engineers am Standort Selzach in der Schweiz suchen wir zum nächstmöglichen Zeitpunkt einen Ingenieur (m/w/d) für Projekte im Bereich Automatisierung. In Ihrer neuen Rolle sind Sie hauptverantwortlich für die Einführung einer Software und deren Integration in bestehende automatisierte Fertigungslinien im Bereich unserer Produktlabels _._
Bitte beachten Sie, dass die Stelle vorerst für 9 Monate zu besetzen ist.
**Das erwartet Sie**
+ Leitung der Einführung einer neuen Labeling-Software am Standort Selzach inklusive Einarbeitung in bestehende Hardware, Druck- und Inspektionssysteme
+ Erarbeitung der Softwareanbindung und Automatisierung in Zusammenarbeit mit Projektteam und Lieferanten unter Berücksichtigung von Softwarearchitektur, Schnittstellen und Systemintegration
+ Erstellung technischer Konzepte, Dokumentation, Validierung der Software und Prozesse sowie Entwicklung von Arbeitsanweisungen und Schulung der Mitarbeitenden
+ Unterstützung des Manufacturing Engineering Teams bei Prozessoptimierungen und Sicherstellung der GMP-konformen Umsetzung
+ Enge Zusammenarbeit und Kommunikation mit Schnittstellenbereichen, insbesondere an den Standorten Selzach, Kiel und im globalen Projektteam zur Koordination von Prozessfortschritten und Best Practices
**Das bringen Sie mit**
+ Abgeschlossenes Studium im ingenieurswissenschaftlichen oder technischen Bereich (Fachhochschule oder Universität)
+ Erste praktische Erfahrungen im produzierenden Umfeld, idealerweise durch Berufstätigkeit oder Praktika
+ Fähigkeit zur eigenständigen Planung und Umsetzung von Arbeitspaketen; Kenntnisse in Lean-Methoden sind von Vorteil
+ Fundierte Kenntnisse in Netzwerktechnologie, Datenanalyse und der Integration von Softwareanwendungen im Produktionsumfeld
+ Ausgeprägtes Organisations- und Planungstalent sowie hervorragende Kommunikationsfähigkeiten in Deutsch und Englisch zur sicheren Zusammenarbeit im internationalen Umfeld
**Zusätzliche Informationen**
Dank unseres flexiblen Arbeitszeitmodells haben Sie die Möglichkeit, an einem Tag der Woche aus dem Home-Office zu arbeiten. Eine regelmäßige Präsenz vor Ort an unserem Standort in Selzach sollte stets gegeben sein, um tragfähige Beziehungen aufzubauen und den persönlichen Kontakt zu Kolleg*innen sowie den Fachbereichen aufrecht zu erhalten.
Die vorgegebene Zeit von 9 Monaten bietet Ihnen und uns eine optimale Möglichkeit des Kennenlernens. Aufgrund der Vielzahl unterschiedlicher Positionen und Aufgabenbereiche bietet Stryker häufig die Optionen der Übernahme in eine unbefristete Anstellung.
**Ihre Bewerbung**
Wir freuen uns auf Ihre aussagekräftige Online-Bewerbung unter Angabe Ihrer Gehaltsvorstellungen und inklusive aller relevanten Dokumente (Anschreiben, aktueller Lebenslauf, Zeugnisse, ggf. Arbeitserlaubnis). Laden Sie bitte unter dem Punkt "Lebenslauf" alle Anhänge direkt hoch.
Falls Sie bereits in Besitz einer Arbeitsbewilligung sind, bitten wir Sie die genaue Bewilligungsart mit Ihrer Bewerbung hochzuladen.
Bitte beachten Sie, dass der Anzeigentitel vom internen Stellentitel abweichen kann.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Bitte beachten Sie, dass die Stelle vorerst für 9 Monate zu besetzen ist.
**Das erwartet Sie**
+ Leitung der Einführung einer neuen Labeling-Software am Standort Selzach inklusive Einarbeitung in bestehende Hardware, Druck- und Inspektionssysteme
+ Erarbeitung der Softwareanbindung und Automatisierung in Zusammenarbeit mit Projektteam und Lieferanten unter Berücksichtigung von Softwarearchitektur, Schnittstellen und Systemintegration
+ Erstellung technischer Konzepte, Dokumentation, Validierung der Software und Prozesse sowie Entwicklung von Arbeitsanweisungen und Schulung der Mitarbeitenden
+ Unterstützung des Manufacturing Engineering Teams bei Prozessoptimierungen und Sicherstellung der GMP-konformen Umsetzung
+ Enge Zusammenarbeit und Kommunikation mit Schnittstellenbereichen, insbesondere an den Standorten Selzach, Kiel und im globalen Projektteam zur Koordination von Prozessfortschritten und Best Practices
**Das bringen Sie mit**
+ Abgeschlossenes Studium im ingenieurswissenschaftlichen oder technischen Bereich (Fachhochschule oder Universität)
+ Erste praktische Erfahrungen im produzierenden Umfeld, idealerweise durch Berufstätigkeit oder Praktika
+ Fähigkeit zur eigenständigen Planung und Umsetzung von Arbeitspaketen; Kenntnisse in Lean-Methoden sind von Vorteil
+ Fundierte Kenntnisse in Netzwerktechnologie, Datenanalyse und der Integration von Softwareanwendungen im Produktionsumfeld
+ Ausgeprägtes Organisations- und Planungstalent sowie hervorragende Kommunikationsfähigkeiten in Deutsch und Englisch zur sicheren Zusammenarbeit im internationalen Umfeld
**Zusätzliche Informationen**
Dank unseres flexiblen Arbeitszeitmodells haben Sie die Möglichkeit, an einem Tag der Woche aus dem Home-Office zu arbeiten. Eine regelmäßige Präsenz vor Ort an unserem Standort in Selzach sollte stets gegeben sein, um tragfähige Beziehungen aufzubauen und den persönlichen Kontakt zu Kolleg*innen sowie den Fachbereichen aufrecht zu erhalten.
Die vorgegebene Zeit von 9 Monaten bietet Ihnen und uns eine optimale Möglichkeit des Kennenlernens. Aufgrund der Vielzahl unterschiedlicher Positionen und Aufgabenbereiche bietet Stryker häufig die Optionen der Übernahme in eine unbefristete Anstellung.
**Ihre Bewerbung**
Wir freuen uns auf Ihre aussagekräftige Online-Bewerbung unter Angabe Ihrer Gehaltsvorstellungen und inklusive aller relevanten Dokumente (Anschreiben, aktueller Lebenslauf, Zeugnisse, ggf. Arbeitserlaubnis). Laden Sie bitte unter dem Punkt "Lebenslauf" alle Anhänge direkt hoch.
Falls Sie bereits in Besitz einer Arbeitsbewilligung sind, bitten wir Sie die genaue Bewilligungsart mit Ihrer Bewerbung hochzuladen.
Bitte beachten Sie, dass der Anzeigentitel vom internen Stellentitel abweichen kann.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Leider ist dieser Job in Ihrer Region nicht verfügbar
3
Manufacturing Professional (USP or DSP)
Lengnau, Bern
ThermoFisher Scientific
Vor 4 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position conducts the production of recombinant products by operating automated production equipment
+ The holder supports compliance, scheduling, material management, change controls, investigation, CAPA, operational excellence, etc
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports the start-up of new production lines
**Responsibilities**
+ Is responsible for the daily execution of manufacturing activities in USP, DSP or support area (media and buffer preparation, equipment cleaning and preparation)
+ Act as first point of contact and reference within manufacturing team regarding training and troubleshooting
+ Owns Work Instructions and SOP in their area
+ Investigate Manufacturing Excellence initiatives in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility
+ Actively contributes to EHSS initiatives and issues as well as near miss reporting and follow-up
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 3-5 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Willingness to learn
+ Can-do attitude
+ Language: English and German preferred
+ Work on a shift rotation mode, this includes regular weekend and public holiday work as well as night work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position conducts the production of recombinant products by operating automated production equipment
+ The holder supports compliance, scheduling, material management, change controls, investigation, CAPA, operational excellence, etc
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports the start-up of new production lines
**Responsibilities**
+ Is responsible for the daily execution of manufacturing activities in USP, DSP or support area (media and buffer preparation, equipment cleaning and preparation)
+ Act as first point of contact and reference within manufacturing team regarding training and troubleshooting
+ Owns Work Instructions and SOP in their area
+ Investigate Manufacturing Excellence initiatives in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility
+ Actively contributes to EHSS initiatives and issues as well as near miss reporting and follow-up
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 3-5 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Willingness to learn
+ Can-do attitude
+ Language: English and German preferred
+ Work on a shift rotation mode, this includes regular weekend and public holiday work as well as night work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
4
DSP Manufacturing Team Leader
Lengnau, Bern
ThermoFisher Scientific
Vor 3 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
5
USP Manufacturing Team Leader
Lengnau, Bern
ThermoFisher Scientific
Vor 3 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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6
QA Lead, Sterility
Lengnau, Bern
ThermoFisher Scientific
Vor 12 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office
**Job Description**
At Thermo Fisher Scientific Inc., the QA Lead, Sterility role offers an outstanding opportunity to ensure robust compliance of aseptic operations and sterility assurance systems across biologics manufacturing. This position is pivotal in driving excellence and flawless performance in contamination control, validation, and continuous improvement, strictly adhering to regulatory and corporate quality standards.
**Key Responsibilities**
Sterility Assurance System:
+ Lead and uphold the Sterility Assurance Program and Contamination Control Strategy (CCS) for facility, utilities, equipment, materials, personnel, and processes.
+ Lead risk assessments for aseptic processes, single-use systems, and critical interventions.
+ Establish, assess, and authorize sterility assurance benchmarks; track, report, and intensify performance.
**Aseptic Operations Oversight:**
+ Coordinate QA for aseptic processing for drug substance and drug product (e.g., upstream bioreactors, downstream filtration, UF/DF, DS).
+ Perform routine Gemba/walkthroughs and provide on-floor QA support during aseptic operations.
**Environmental & Utilities Control:**
+ Oversees planning, execution, and monitoring of environmental monitoring programs.
+ Investigate EM excursions and drive CAPA efficiency and preventive actions.
**Sterilization & Decontamination:**
+ Provide QA oversight of sterilization methods, load configurations, biological indicators, and requalification schedules.
+ Approve sterilization cycle development, validation protocols/reports, and change controls for single-use assemblies, filters, and aseptic connectors.
+ Ensure validated cleaning and decontamination procedures for equipment and rooms (including sporicidal rotations).
**Quality Systems & Compliance:**
+ Evaluate, assess, and endorse SOPs, validation protocols, master batch records, and QA standards linked to aseptic operations.
+ Lead and respond to internal/external audits (e.g., FDA, EMA, MHRA, PIC/S); ensure readiness and remediation.
+ Lead deviations, root cause analyses, CAPA, and efficiency checks for sterility-related issues (bioburden, endotoxin, EM).
+ Lead QA for changes impacting sterility (facility, equipment, single-use components, filters, cleaning agents, disinfectants).
+ Support tech transfers for new biomolecule products/processes ensuring sterility requirements are incorporated into process development and validation.
**Training & Culture:**
+ Formulate and present aseptic behavior training, gowning certifications, and programs highlighting proficiency in sterility assurance.
+ Mentor operations and QA staff to reinforce contamination control culture and right-first-time behaviors.
**Qualifications:**
+ Bachelor's or Master's or equivalent experience in Microbiology, Biotechnology, Pharmacy, Chemical/Biomedical Engineering, or related field.
+ 5+ years in GMP biologics or sterile manufacturing with 2+ years in QA sterility/aseptic leadership.
+ Profound understanding of aseptic processing, EM, validation of sterilization, and control of contamination in biologics.
+ Strong experience with investigations (root cause analysis), CAPA, risk management, and audit interactions.
+ Excellent communication, collaborator management, and decision-making under time-sensitive operations.
+ Proficiency in maintaining sterility standards and hands-on aseptic supervision.
+ Detailed problem solving and risk-based thinking.
+ Continuous improvement approach.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office
**Job Description**
At Thermo Fisher Scientific Inc., the QA Lead, Sterility role offers an outstanding opportunity to ensure robust compliance of aseptic operations and sterility assurance systems across biologics manufacturing. This position is pivotal in driving excellence and flawless performance in contamination control, validation, and continuous improvement, strictly adhering to regulatory and corporate quality standards.
**Key Responsibilities**
Sterility Assurance System:
+ Lead and uphold the Sterility Assurance Program and Contamination Control Strategy (CCS) for facility, utilities, equipment, materials, personnel, and processes.
+ Lead risk assessments for aseptic processes, single-use systems, and critical interventions.
+ Establish, assess, and authorize sterility assurance benchmarks; track, report, and intensify performance.
**Aseptic Operations Oversight:**
+ Coordinate QA for aseptic processing for drug substance and drug product (e.g., upstream bioreactors, downstream filtration, UF/DF, DS).
+ Perform routine Gemba/walkthroughs and provide on-floor QA support during aseptic operations.
**Environmental & Utilities Control:**
+ Oversees planning, execution, and monitoring of environmental monitoring programs.
+ Investigate EM excursions and drive CAPA efficiency and preventive actions.
**Sterilization & Decontamination:**
+ Provide QA oversight of sterilization methods, load configurations, biological indicators, and requalification schedules.
+ Approve sterilization cycle development, validation protocols/reports, and change controls for single-use assemblies, filters, and aseptic connectors.
+ Ensure validated cleaning and decontamination procedures for equipment and rooms (including sporicidal rotations).
**Quality Systems & Compliance:**
+ Evaluate, assess, and endorse SOPs, validation protocols, master batch records, and QA standards linked to aseptic operations.
+ Lead and respond to internal/external audits (e.g., FDA, EMA, MHRA, PIC/S); ensure readiness and remediation.
+ Lead deviations, root cause analyses, CAPA, and efficiency checks for sterility-related issues (bioburden, endotoxin, EM).
+ Lead QA for changes impacting sterility (facility, equipment, single-use components, filters, cleaning agents, disinfectants).
+ Support tech transfers for new biomolecule products/processes ensuring sterility requirements are incorporated into process development and validation.
**Training & Culture:**
+ Formulate and present aseptic behavior training, gowning certifications, and programs highlighting proficiency in sterility assurance.
+ Mentor operations and QA staff to reinforce contamination control culture and right-first-time behaviors.
**Qualifications:**
+ Bachelor's or Master's or equivalent experience in Microbiology, Biotechnology, Pharmacy, Chemical/Biomedical Engineering, or related field.
+ 5+ years in GMP biologics or sterile manufacturing with 2+ years in QA sterility/aseptic leadership.
+ Profound understanding of aseptic processing, EM, validation of sterilization, and control of contamination in biologics.
+ Strong experience with investigations (root cause analysis), CAPA, risk management, and audit interactions.
+ Excellent communication, collaborator management, and decision-making under time-sensitive operations.
+ Proficiency in maintaining sterility standards and hands-on aseptic supervision.
+ Detailed problem solving and risk-based thinking.
+ Continuous improvement approach.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Leider ist dieser Job in Ihrer Region nicht verfügbar
7
Praktikum Administration und Human Resources / Projektmanagement (Digitalisierung) - Februar/März...
Selzach, Solothurn
Stryker
Vor 14 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**Unser Angebot an Dich**
+ Du übernimmst eigenständig Projekte zur Automatisierung und Digitalisierung administrativer Prozesse.
+ Im Rahmen von unterschiedlichen Projekten und bei der Umsetzung von diversen HR-Prozessen (Performance-, Compensation- und Talent Management) unterstützt Du die lokalen HR Business Partner.
+ Die Mitarbeit und Bearbeitung von arbeitsrechtlichen Fragestellungen gehört ebenso zu Deinen täglichen Arbeiten wie die Unterstützung beim kompletten Onboarding Programm. Darüber hinaus bist du in der Mitarbeiterbetreuung, Personalentwicklung und Mitarbeiterbindung tätig und gestaltest aktiv den Employee Life Cycle mit.
**Das zeichnet Dich aus**
+ Du hast entweder eine kaufmännische Grundausbildung (EFZ), eine Ausbildung als Mediamatiker-/in (EFZ) oder einen Abschluss an einer Handelsschule - oder du befindest dich in einem fortgeschrittenen Semester eines Studiums der Wirtschaftswissenschaften, Psychologie, Sozial- oder Geisteswissenschaften, Pädagogik oder eines vergleichbaren Fachbereichs bzw. hast dein Studium bereits erfolgreich abgeschlossen.
+ Dein grosses Interesse an moderner Personalarbeit in einem internationalen Konzern motiviert Dich, anspruchsvolle Aufgaben sowohl eigenständig als auch im Team anzugehen.
+ Du begeisterst dich für Informatiklösungen und Medienwissenschaften (Kommunikation) und verfügst über sehr gute Deutsch- und Englischkenntnisse.
Vielfalt ist uns wichtig. Wir freuen uns über Bewerbungen von Menschen ungeachtet ihrer ethnischen, nationalen oder sozialen Herkunft, des Geschlechts, einer Behinderung, des Alters oder ihrer sexuellen Identität.
**Dauer** : 6-12 Monate
**Start** : ab Februar/März 2026
**Pensum** : 60-100 %
**Ort** : Selzach, SO
Wir freuen uns auf Deine aussagekräftige Online-Bewerbung inklusive aller relevanten Dokumente (Anschreiben, aktueller Lebenslauf, Zeugnisse). Bitte beachte im Bewerbungsverfahren unter dem Punkt "Lebenslauf" direkt alle Anhänge hochzuladen.
Pay rate will not be below any applicable local minimum wage rates.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
+ Du übernimmst eigenständig Projekte zur Automatisierung und Digitalisierung administrativer Prozesse.
+ Im Rahmen von unterschiedlichen Projekten und bei der Umsetzung von diversen HR-Prozessen (Performance-, Compensation- und Talent Management) unterstützt Du die lokalen HR Business Partner.
+ Die Mitarbeit und Bearbeitung von arbeitsrechtlichen Fragestellungen gehört ebenso zu Deinen täglichen Arbeiten wie die Unterstützung beim kompletten Onboarding Programm. Darüber hinaus bist du in der Mitarbeiterbetreuung, Personalentwicklung und Mitarbeiterbindung tätig und gestaltest aktiv den Employee Life Cycle mit.
**Das zeichnet Dich aus**
+ Du hast entweder eine kaufmännische Grundausbildung (EFZ), eine Ausbildung als Mediamatiker-/in (EFZ) oder einen Abschluss an einer Handelsschule - oder du befindest dich in einem fortgeschrittenen Semester eines Studiums der Wirtschaftswissenschaften, Psychologie, Sozial- oder Geisteswissenschaften, Pädagogik oder eines vergleichbaren Fachbereichs bzw. hast dein Studium bereits erfolgreich abgeschlossen.
+ Dein grosses Interesse an moderner Personalarbeit in einem internationalen Konzern motiviert Dich, anspruchsvolle Aufgaben sowohl eigenständig als auch im Team anzugehen.
+ Du begeisterst dich für Informatiklösungen und Medienwissenschaften (Kommunikation) und verfügst über sehr gute Deutsch- und Englischkenntnisse.
Vielfalt ist uns wichtig. Wir freuen uns über Bewerbungen von Menschen ungeachtet ihrer ethnischen, nationalen oder sozialen Herkunft, des Geschlechts, einer Behinderung, des Alters oder ihrer sexuellen Identität.
**Dauer** : 6-12 Monate
**Start** : ab Februar/März 2026
**Pensum** : 60-100 %
**Ort** : Selzach, SO
Wir freuen uns auf Deine aussagekräftige Online-Bewerbung inklusive aller relevanten Dokumente (Anschreiben, aktueller Lebenslauf, Zeugnisse). Bitte beachte im Bewerbungsverfahren unter dem Punkt "Lebenslauf" direkt alle Anhänge hochzuladen.
Pay rate will not be below any applicable local minimum wage rates.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Leider ist dieser Job in Ihrer Region nicht verfügbar
8
Internship Research & Development Biomechanics Test Laboratory - from February/March 2026 for 6 m...
Selzach, Solothurn
Stryker
Vor 16 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
**What you will do**
+ As member of the biomechanics test laboratory team, you are in contact with product safety testing.
+ You effectively support the local team in biomechanical performance testing, data analysis, documentation of testing activities and results in technical reports as well as maintaining laboratory equipment.
+ Using your scientific skills, you may also work on literature search and review.
+ In addition, you coordinate and agree all your activities with highly experienced biomechanical engineers mentoring your internship.
**What you need**
+ You are studying engineering with a focus on mechanical engineering, biomechanics, medical engineering, material science or similar subjects.
+ Ideally, you have gained first experience in mechanical testing of medical devices.
+ You are a communicative and creative team player who likes an environment allowing for solution oriented, independent and precise work style.
+ The grades you have achieved thus far are above average and you enjoy working focused to achieve outstanding results.
+ You value an international working environment where you can use your very good command of English, good command of German, and ideally also basic command in French.
**Start:** Feb / March 2026
**Location** : Selzach (SO), CH
**Duration:** 6 months
We look forward to receiving your informative **online application** including all relevant documents (motivational letter, CV, examination regulations, current overview of grades, etc.). Please note to upload all attachments directly in one file under the "CV" section and the reference number .
Pay rate will not be below any applicable local minimum wage rates.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
+ As member of the biomechanics test laboratory team, you are in contact with product safety testing.
+ You effectively support the local team in biomechanical performance testing, data analysis, documentation of testing activities and results in technical reports as well as maintaining laboratory equipment.
+ Using your scientific skills, you may also work on literature search and review.
+ In addition, you coordinate and agree all your activities with highly experienced biomechanical engineers mentoring your internship.
**What you need**
+ You are studying engineering with a focus on mechanical engineering, biomechanics, medical engineering, material science or similar subjects.
+ Ideally, you have gained first experience in mechanical testing of medical devices.
+ You are a communicative and creative team player who likes an environment allowing for solution oriented, independent and precise work style.
+ The grades you have achieved thus far are above average and you enjoy working focused to achieve outstanding results.
+ You value an international working environment where you can use your very good command of English, good command of German, and ideally also basic command in French.
**Start:** Feb / March 2026
**Location** : Selzach (SO), CH
**Duration:** 6 months
We look forward to receiving your informative **online application** including all relevant documents (motivational letter, CV, examination regulations, current overview of grades, etc.). Please note to upload all attachments directly in one file under the "CV" section and the reference number .
Pay rate will not be below any applicable local minimum wage rates.
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
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