187 Jobs in Büren an der Aare
Industrielackierer EFZ oder EBA auch Lehrabgänger
Büren an der Aare, Bern
DAS PERSONAL.
Vor 16 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Aufgaben
- Abwechslungsreiche Lackierarbeiten
- Reparatur und Ausbesserungsarbeiten
- Vorbereitungsarbeiten
Qualifikation
- Ausgebildeter Industrielackierer EFZ oder gleichwertige Ausbildung oder langjährige Berufserfahrung beim gleichen Betrieb
- Freude an Ihrem Handwerk & Teamgeist
- Motiviert und zuverlässig
Benefits
- Attraktiver Lohn (Vergütung)
- Bonuszahlungen bei erfolgreicher Vermittlung von neuen Mitarbeitern
- Karriere- und Weiterbildungschancen
- Persönliche Betreuung
Wir freuen uns auf Ihre Bewerbung!
Verwandte Berufe: Industrielackierer, Lackierer, Fahrzeuglackierer, Maler und Lackierer, Oberflächenbeschichter, Industriemaler, Pulverbeschichter, Lackiertechniker, Autolackierer, Spritzlackierer, Beschichtungstechniker, Metalllackierer, Bautenlackierer, Korrosionsschutzfachmann, Industriebeschichter, Pulverlackierer, Bautenlackierer
Branche: Bauwesen/Bauingenieurwesen
Funktion: Bauwesen/Handwerk
Anstellungsart: Try and Hire
Leider ist dieser Job in Ihrer Region nicht verfügbar
0
Sandstrahler
Dotzigen, Bern
DAS PERSONAL.
Vor 17 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Aufgaben
- Abwechslungsreiche Sandstrahlerarbeiten
- Reparatur und Ausbesserungsarbeiten
- Vorbereitungsarbeiten
Qualifikation
- Ausgebildeter Industrielackierer EFZ oder gleichwertige Ausbildung oder langjährige Berufserfahrung beim gleichen Betrieb
- Freude an Ihrem Handwerk & Teamgeist
- Motiviert und zuverlässig
Benefits
- Attraktiver Lohn (Vergütung)
- Bonuszahlungen bei erfolgreicher Vermittlung von neuen Mitarbeitern
- Karriere- und Weiterbildungschancen
- Persönliche Betreuung
Wir freuen uns auf Ihre Bewerbung!
Verwandte Berufe: Industrielackierer, Lackierer, Fahrzeuglackierer, Maler und Lackierer, Oberflächenbeschichter, Industriemaler, Pulverbeschichter, Lackiertechniker, Autolackierer, Spritzlackierer, Beschichtungstechniker, Metalllackierer, Bautenlackierer, Korrosionsschutzfachmann, Industriebeschichter, Pulverlackierer, Bautenlackierer
Branche: Automobilindustrie
Funktion: Anderes
Anstellungsart: Try and Hire
Leider ist dieser Job in Ihrer Region nicht verfügbar
1
Deckenmonteur (m/w, 100%) für Metalldeckensysteme - der Plafond macht noch lange keine Decke...
Solothurn, Solothurn
PKS Personal AG
Vor 12 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Für unsere Mandantin, eine junge und aufstrebende Unternehmung im Bereich Deckensysteme, suchen wir zur weiteren Unterstützung per sofort oder nach Vereinbarung einen qualifizierten
Das machen Sie:
- Montage der Unterkonstruktion
- Einhängen der Metalldeckenelemente
- Erstellen von Aussparungen und Spezialzuschnitten
- Erstellen der Isolierung
Anforderungen:
- Fundierte Berufskenntnisse
- Sichere und selbständige Arbeitsweise nach Plan
- Hohe Leistungbereitschaft sowie Flexibilität
- Zuverlässige und teamfähige Persönlichkeit
Wir bieten:
- Langfristige Anstellungsmöglichkei
- Interessante und vielseitige Projekte und Aufgaben
- Gute Entwicklungsmöglichkeiten
- Zeitgemässe Entlöhnung
- Angenehmes Arbeitsklima
- Übernahme der Kosten für Sicherheitskurse (PSAgA + Hebebühne)
Leider ist dieser Job in Ihrer Region nicht verfügbar
2
Kalibriertechniker / Servicetechniker (m/w 100%) - du kennst dich mit Messungen aus...
Luterbach, Solothurn
PKS Personal AG
Vor 12 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Für unsere Kundin, eines der weltweit grössten Dienstleistungsunternehmen, suchen wir per sofort oder nach Vereinbarung für den Standort Luterbach / SO eine selbständige, verantwortungsbewusste und teamfähige Persönlichkeit als
Ihre Hauptaufgaben:
- Selbstständige termingerechte Kalibrierung von elektr. Geräten, Messgeräten und Sensoren unter der Berücksichtigung von GMP/GDP unter Einhaltung aller SOP Vor-schriften und Firmenweisungen
- Verantwortung für termingerechte (interne oder externe) Kalibrierung der Prüfmittel oder Messgeräte unter Berücksichtigung von GMP/GDP mit der Einhaltung aller SOP Vorschriften und Firmenweisungen
- Verantwortung für die zeitnahe Rückmeldung der durchgeführten Kalibrierungen
- Informierung des Vorgesetzten bei Abweichungen bzgl. Qualität, Quantität, Termin und Kosten
- Störungsbehebung an Messgeräten
- Bereitschaft zu Pikettdienst gemäss Einsatzplan
Das bietet unsere Mandantin:
- Regionale und internationale Entwicklungsmöglichkeiten in einem stark wachsenden Unternehmen
- Vielfältige interne und externe Weiterbildungsmöglichkeiten
- Global Player im Dienstleistungsbereich mit namhaften Kunden aus einem multinationalen Umfeld
- Gute Rahmenbedingungen, wie z.B. min. fünf Wochen Ferien, 40 Stunden Woche, sowie eine attraktive Pensionskassenlösung.
Leider ist dieser Job in Ihrer Region nicht verfügbar
3
Program Manager
Lengnau, Bern
ThermoFisher Scientific
Heute
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
4
Manufacturing Planner
Lengnau, Bern
ThermoFisher Scientific
Vor 2 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
5
Manufacturing Specialist (USP or DSP)
Lengnau, Bern
ThermoFisher Scientific
Vor 2 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
Seien Sie der Erste, der es erfährt
Über das Neueste Alles Jobs In Büren an der Aare !
6
Ingenieur (m/w/d) für Projekte im Bereich Automatisierung - Medizintechnik
Selzach, Solothurn
Stryker
Vor 2 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
7
Manufacturing Professional (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 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
8
DSP Manufacturing Team Leader
Lengnau, Bern
ThermoFisher Scientific
Vor 2 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
9