157 Jobs in La Heutte
Rectifieur
Tavannes, Bern
Manpower
Gestern
Job angesehen
Arbeitsbeschreibung
Manpower
Depuis 1948, ManpowerGroup libère le potentiel des femmes et des hommes en fournissant des opportunités d'emploi, d'expérience et de formation. Fort d'un réseau mondial de 3'500 bureaux dans 80 pays du monde, ManpowerGroup vous accompagne dans votre développement professionnel. Mission:
- Rectification plane de pièces sur machines CNC et conventionnelles
- Montage d'éléments mécaniques par lecture de plans
- Contrôle des pièces avec outils métrologiques traditionnels (pied à coulisse, micromètre, projecteur de profil,?)
- Entretien des outils et maintenance de 1er niveau
- Participation aux diverses activités de l'atelier
Profil:
- Expérience de minimum en 5 ans en rectification Plane
- Lecture de plans et bon sens de la mécanique
- Calme, organisé, méthodique
Candidature :
CV, Certificats de travail, Diplômes, Permis de travail, Annexes
Nous nous réjouissions de recevoir votre candidature !
Branche: Anderes
Funktion: Ingenieurwesen/Planung
Leider ist dieser Job in Ihrer Region nicht verfügbar
0
Logisticien CFC
Tavannes, Bern
Manpower
Vor 5 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
Logisticien CFC
Rejoignez une entreprise innovante et dynamique, leader dans le secteur de la logistique et de la gestion des flux. Notre client valorise l'engagement de ses collaborateurs, favorise un environnement de travail stimulant et offre de nombreuses opportunités de développement professionnel.
En intégrant leur équipe, vous participerez à des projets passionnants dans un secteur en constante évolution, tout en bénéficiant d'un cadre de travail agréable au c?ur de la région de Tavannes.
Responsabilités principales
- Gérer les opérations logistiques quotidiennes, y compris la réception, le stockage et l'expédition des marchandises
- Assurer la conformité des stocks et leur mise à jour précise dans le système informatique
- Organiser et optimiser les flux de marchandises pour garantir une efficacité maximale
- Coordonner avec les fournisseurs, transporteurs et autres partenaires logistiques
- Veiller au respect des normes de sécurité et de qualité en vigueur
- Participer à l'amélioration continue des processus logistiques
- Gérer la documentation liée aux opérations logistiques et assurer un reporting précis
- Certificat Fédéral de Capacité (CFC) en logistique ou domaine connexe
- Expérience préalable dans la gestion logistique, idéalement en environnement industriel ou de production
- Maîtrise des systèmes informatiques de gestion des stocks (ERP, WMS)
- Excellentes compétences organisationnelles et sens du détail
- Capacité à travailler de manière autonome tout en étant un bon joueur d'équipe
- Bonne connaissance des normes de sécurité et de qualité en logistique
- Permis de conduire catégorie B
- Maîtrise du français, toute autre langue est un atout
Prêt à relever le défi ?
Si vous souhaitez évoluer dans un environnement stimulant, où votre expertise en logistique sera valorisée, n'attendez plus ! Postulez dès aujourd'hui pour rejoindre leur équipe et contribuer au succès commun.
Envoyez votre candidature complète et faites le premier pas vers une carrière enrichissante !
Branche: Uhrenherstellung und Luxusartikeln
Funktion: Logistik/Lager
Leider ist dieser Job in Ihrer Region nicht verfügbar
1
Chargé de conformité produits
Tavannes, Bern
Manpower
Vor 12 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
L'entreprise :
Spécialisée dans le domaine industriel et basée dans la région de Tavannes.
Votre mission :
Vous identifiez les normes légales et réglementaires des produits
Vous mettez en place les processus permettant la conformité des produits
Vous assurez et validez la conformité des produits
Vous soutenez les départements pour la compréhension des normes
Votre profil :
Vous êtes titulaire d'une formation supérieure dans le domaine technique
Vous avez une expérience sur un poste similaire (minimum 3 ans)
Vous avez de bonnes connaissances des normes et réglementations liées à la fabrication de machines
Vous êtes une personne impliquée et qui aime le travail en équipe
Vous êtes rigoureux, avec un excellent esprit d'analyse
Intéressé par ce poste ?
Transmettez-nous votre dossier en cliquant sur « postuler maintenant ».
Branche: Anderes
Funktion: Ingenieurwesen/Planung
Leider ist dieser Job in Ihrer Region nicht verfügbar
2
Ingénieur en développement Beckhoff (H/F)
Tavannes, Bern
Manpower
Vor 23 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
L'entreprise :
Spécialisée dans le domaine de la machine-outil et située dans la vallée de Tavannes Votre Mission:
Vous serez en charge de l'étude et du développement des systèmes automatisés pour le pilotage des machines.
Vous vous occuperez de la programmation des éléments d'automation ainsi que de la mise en service des éléments développés.
Vous assurerez le soutien aux clients dans le cadre des développements spécifiques.
Votre profil:
Vous êtes titulaire d'un diplôme d'ingénieur dans le domaine de l'automation.
Vous avez de solides connaissances des automates programmables Beckhoff (impératif) ainsi que des connaissances en vision et/ou asservissement (un plus)
Vous êtes autonome, rigoureux et structuré.
Votre profil correspond à cette annonce ?
N'hésitez pas et faites-nous parvenir votre dossier complet en cliquant sur postuler maintenant.
Seuls les dossiers correspondants à notre besoin seront étudiés.
Branche: Anderes
Funktion: Produktion
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3
Ingénieur automation
Tavannes, Bern
Manpower
Vor 23 Tagen gepostet
Job angesehen
Arbeitsbeschreibung
Manpower
L'entreprise :
Spécialisée dans le domaine industriel et basée dans le Jura Bernois.
Votre mission :
Vous serez en charge de la programmation des automates
Vous assurerez l'étude et le développement des systèmes automatisés pour le pilotage des machines
Vous effectuerez la mise en service des éléments développés
Vous serez le premier soutien client selon les besoins et développements à effectuer
Votre profil :
Vous êtes titulaire d'un diplôme d'ingénieur en automation
Vous avez de bonnes connaissances des automates Fanuc et Beckhoff
Vous êtes rigoureux et apte à travailler de manière autonome et fiable
Votre profil correspond à cette annonce ?
N'hésitez pas et faites-nous parvenir votre dossier complet en cliquant sur postuler maintenant.
Seuls les dossiers correspondants à notre besoin seront étudiés.
Branche: Anderes
Funktion: Technologie/EDV
Leider ist dieser Job in Ihrer Region nicht verfügbar
4
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
5
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.
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6
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
7
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
8
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.
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