Senior QA Specialist, QA Project Management 80-100% (f/m/d)

Posted 3 Hours Ago
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Visp, Valais
In-Office
80-100 Annually
Senior level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
The Senior QA Specialist will ensure compliance with GMP in API production and support contract manufacturing by advising on GMP aspects and engaging with stakeholders.
Summary Generated by Built In

 

Location: Visp, Hybrid  Work Model applicable. Relocation assistance is available for eligible candidates and their families, if needed.

For our Quality Assurance team in Bioconjugates, Visp we are currently looking for a dedicated person who would like to work as a Senior QA Specialist (f/m/d) in a fast-growing and innovative environment. In this role you will support clinical phase manufacturing and will interact with internal and external stakeholders to represent Quality.

What you will get: 

  • An agile career and dynamic working culture

  • An inclusive and ethical workplace

  • Compensation programs that recognize high performance

  • A variety of benefits dependant on role and location

The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.

What you will do: 

  • As a member of the QA team (Bioconjugates), you will be responsible for ensuring production of API`s is in accordance with Good Manufacturing Practice (GMP).

  • Support the contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP.

  • Responsible for checking manufacturing documentation for conformity, processing change controls, and reviewing and approving deviations and OOS results.

  • In addition, you will be the quality contact for our clients, and will present during their GMP audits.

What we are looking for: 

  • University degree in Life Sciences (Microbiology / Biotechnology / Chemistry etc)

  • First experience in the GMP environment required, preferably in biopharmaceutical industry

  • Strong communication skills, and experience in working with stakeholders from different departments

  • Experience with TrackWise, SAP, LIMS, and DMS is a plus

  • Fluency in English AND German (written and verbal) is required

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

Top Skills

Dms
Lims
SAP
Trackwise
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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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