QA Manager Cell Factory Inspection readiness (m|f|d)

Miltenyi Biotec

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profile Job Location:

Bergisch Gladbach - Germany

profile Monthly Salary: Not Disclosed
Posted on: 3 days ago
Vacancies: 1 Vacancy

Job Summary

As QA Manager Cell Factory you play a critical role in ensuring the highest standards of quality assurance and regulatory compliance within our organisation. This position demands unwavering attention to detail and a commitment to excellence in all aspects of quality management.

  • Maintain rigorous inspection readiness from a QA perspective collaborating extensively with operational departments project managers and other QA teams. Implement and oversee robust systems for continuous monitoring of commercial manufacturing processes to ensure strict GxP compliance.
  • Ensure absolute adherence to all applicable quality standards and regulations including GxP EU Guidelines and 21 CFR 820.20b.3. Vigilantly maintain RA & GMP compliance and conduct thorough assessments of new regulatory requirements to safeguard organisational integrity.
  • Prepare review and approve critical quality documents including batch records SOPs test procedures and risk assessments. Spearhead initiatives for continuous improvement of GMP compliance and quality systems within the Cell Factory with a focus on maintaining the highest standards of excellence.
  • Orchestrate the alignment of QA topics across Cell Factories within Miltenyi. Establish and maintain transparent professional communication channels and facilitate the exchange of crucial information between QA operational departments and external partners.
  • Develop and implement comprehensive measures to address gaps and audit deficiencies with stringent tracking of related actions. Provide expert support for decentralized manufacturing and point-of-care approaches for CGT ensuring compliance at every stage.
  • Serve as the primary point of contact for external support activities demonstrating authoritative decision-making in QA-related matters. Oversee and support rigorous employee qualification monitoring and participation to maintain the highest standards of competence within the organisation.

 


Qualifications :

  • A degree in Pharmacy Biology Biochemistry or Medicine is required along with several years of experience in the commercial pharmaceutical industry.
  • Extensive experience across various QA functions and comprehensive knowledge of international and national cGxP regulations and the regulatory environment are essential.
  • Familiarity with aseptic processes and Cell & Gene Therapy (CGT) is crucial. Knowledge of development requirements and GCP regulations is highly advantageous.
  • Demonstrated experience in preparing for and hosting inspections by local and international health authorities (e.g. EU FDA) is imperative.
  • Superior critical communication skills proficiency in managing multiple GMP topics simultaneously and the ability to proactively identify risks while proposing effective mitigation strategies are paramount.
  • Fluency in English and German (both spoken and written) is mandatory accompanied by exceptional presentation skills a highly structured working style and analytical mindset.

Additional Information :

This position is limited to 24 months.

What we offer

  • Flexible and remote work: Enable time management on your terms
  • Diversity: International teams and cross-border intercultural communication
  • Room for creativity: Its the most clever solution that we always strive for
  • Health & Sport: Corporate sports activities and health provision
  • Miltenyi University: A clever mind never stops learning take advantage of our inhouse Training Academy
  • Corporate benefits: Employee events 30 days of vacation (e)-bike leasing company pension plan and many other offers

Contact us 

If you are passionate about the purpose of your code and enjoy working in a supportive team culture then please do not hesitate to join us in our great vision and make a real difference to peoples lives.


Remote Work :

No


Employment Type :

Full-time

As QA Manager Cell Factory you play a critical role in ensuring the highest standards of quality assurance and regulatory compliance within our organisation. This position demands unwavering attention to detail and a commitment to excellence in all aspects of quality management.Maintain rigorous ins...
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Key Skills

  • Lean Manufacturing
  • Project Management Methodology
  • Kanban
  • Employee Relations
  • Succession Planning
  • Continuous Improvement
  • SyteLine
  • Conflict Management
  • Operations Management
  • Interpretation
  • Leadership Experience
  • Plant Management

About Company

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For over 30 years, Miltenyi Biotec has been a major provider of products and services that drive biomedical research and boost cell and gene therapy. More than 4,700 employees in 23 countries combine excellence in research with innovative products to create cutting-edge solutions that ... View more

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