3626 BURGWEDEL BIOTECH GMBH
Lead Technician Impfstoffproduktion(m/w/x)
Full-timeTemporary contractOn-siteManagement
Burgwedel
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MEMerck & Co., Inc.
Head of Manufacturing(m/w/x)
Burgwedel
Full-timeOn-siteManagement
Nejo AI Summary
Leading GMP-compliant biopharmaceutical manufacturing in sterile environments, managing production teams. Several years of pharmaceutical production experience in sterile environments, with leadership experience, required. Flexible work options available.
Requirements
- Degree in pharmacy, biology, biotechnology, or comparable qualification
- Several years of experience in pharmaceutical production or quality assurance, ideally in sterile environment
- Very good knowledge of relevant regulations (AMG, AMWHV, GMP)
- Experience in leading leaders
- Technical understanding of manufacturing processes and qualification/validation topics
- Communication and organizational skills, calm and solution-oriented in dynamic situations
- Enjoyment of team leadership, development, and structured coaching
- High sense of responsibility and interest in continuous improvement
- Proven experience in regulatory inspections
- Degree in pharmacy, biology, biotechnology, or comparable qualification
- Several years of leadership experience in pharmaceutical manufacturing or quality assurance, ideally in sterile environment
- Deep knowledge of applicable regulations and guidelines (AMG, AMWHV, GMP)
- Proven experience leading leaders in complex, regulated environments
- Strong technical understanding of manufacturing processes, qualification and validation activities
- Calm, structured, and solution-oriented leadership style in high-pressure situations
- Strong people leadership mindset focused on development, accountability, and performance
- High ownership mentality and continuous improvement mindset
- Proven experience supporting and leading regulatory inspections
Tasks
- Lead shift supervisors and production teams with full responsibility
- Ensure GMP-compliant manufacturing across all activities
- Own occupational health and safety standards
- Manage production planning and resource allocation
- Develop leaders and teams through coaching and feedback
- Establish strong shopfloor routines and transparent communication
- Oversee cGMP training compliance and manage budgets
- Collaborate with Engineering, QA, QC, and global stakeholders
- Ensure high equipment availability and maintenance standards
- Lead operational escalations and set priorities under pressure
- Drive continuous improvement across manufacturing processes
- Develop the organization in line with business needs and budgets
- Contribute to departmental budget planning and preparation
Work Experience
- approx. 4 - 6 years
Education
- Vocational certification
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible work arrangements
Informal Culture
- Strong team cohesion
Other Benefits
- Continuous investment in quality
Modern Equipment
- Investment in technology
Mentorship & Coaching
- Investment in people
Purpose-Driven Work
- Leadership scope to shape processes
Career Advancement
- Access to development opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Merck & Co., Inc. and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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- Sanacorp Pharmahandel GmbH
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Full-timeOn-siteSeniorHannover - WDT
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Full-timeTemporary contractOn-siteExperiencedGarbsen - RENK Group
Teamleitung der Qualitätssicherung(m/w/x)
Full-timeOn-siteSeniorHannover
MEMerck & Co., Inc.
Head of Manufacturing(m/w/x)
Burgwedel
Full-timeOn-siteManagement
Nejo AI Summary
Leading GMP-compliant biopharmaceutical manufacturing in sterile environments, managing production teams. Several years of pharmaceutical production experience in sterile environments, with leadership experience, required. Flexible work options available.
Requirements
- Degree in pharmacy, biology, biotechnology, or comparable qualification
- Several years of experience in pharmaceutical production or quality assurance, ideally in sterile environment
- Very good knowledge of relevant regulations (AMG, AMWHV, GMP)
- Experience in leading leaders
- Technical understanding of manufacturing processes and qualification/validation topics
- Communication and organizational skills, calm and solution-oriented in dynamic situations
- Enjoyment of team leadership, development, and structured coaching
- High sense of responsibility and interest in continuous improvement
- Proven experience in regulatory inspections
- Degree in pharmacy, biology, biotechnology, or comparable qualification
- Several years of leadership experience in pharmaceutical manufacturing or quality assurance, ideally in sterile environment
- Deep knowledge of applicable regulations and guidelines (AMG, AMWHV, GMP)
- Proven experience leading leaders in complex, regulated environments
- Strong technical understanding of manufacturing processes, qualification and validation activities
- Calm, structured, and solution-oriented leadership style in high-pressure situations
- Strong people leadership mindset focused on development, accountability, and performance
- High ownership mentality and continuous improvement mindset
- Proven experience supporting and leading regulatory inspections
Tasks
- Lead shift supervisors and production teams with full responsibility
- Ensure GMP-compliant manufacturing across all activities
- Own occupational health and safety standards
- Manage production planning and resource allocation
- Develop leaders and teams through coaching and feedback
- Establish strong shopfloor routines and transparent communication
- Oversee cGMP training compliance and manage budgets
- Collaborate with Engineering, QA, QC, and global stakeholders
- Ensure high equipment availability and maintenance standards
- Lead operational escalations and set priorities under pressure
- Drive continuous improvement across manufacturing processes
- Develop the organization in line with business needs and budgets
- Contribute to departmental budget planning and preparation
Work Experience
- approx. 4 - 6 years
Education
- Vocational certification
Languages
- English – Business Fluent
Benefits
Flexible Working
- Flexible work arrangements
Informal Culture
- Strong team cohesion
Other Benefits
- Continuous investment in quality
Modern Equipment
- Investment in technology
Mentorship & Coaching
- Investment in people
Purpose-Driven Work
- Leadership scope to shape processes
Career Advancement
- Access to development opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Merck & Co., Inc. and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
Merck & Co., Inc.
Industry
Pharmaceuticals
Description
Das Unternehmen agiert als weltweit zuverlässiger Hersteller und Lieferant von Biopharmazeutika und beliefert Kunden und Patienten mit qualitativ hochwertigen Produkten.
Not a perfect match?
- 3626 BURGWEDEL BIOTECH GMBH
Lead Technician Impfstoffproduktion(m/w/x)
Full-timeTemporary contractOn-siteManagementBurgwedel - Sanacorp Pharmahandel GmbH
Abteilungsleiter Lager(m/w/x)
Full-timeOn-siteSeniorHannover - RZH Rechenzentrum für Heilberufe GmbH
Teamleitung Produktion im Gesundheitswesen(m/w/x)
Full-timeOn-siteSeniorHannover - WDT
Projektmanager im pharmazeutischen Umfeld(m/w/x)
Full-timeTemporary contractOn-siteExperiencedGarbsen - RENK Group
Teamleitung der Qualitätssicherung(m/w/x)
Full-timeOn-siteSeniorHannover