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

Posted 10 Days Ago
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Visp, Valais, CHE
In-Office
Senior level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
Supports QA Operations project preparation, campaign execution, and closeout. Acts as the GMP contact for internal and external stakeholders, reviews and approves deviations, change controls, CAPAs, investigations, effectiveness checks, and extensions, authors and approves GMP documents and SOPs, and participates in audits and regulatory inspections.
Summary Generated by Built In

 

Location: Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

As a member of the QA Operations Team, the Senior QA Specialist (f/m/d) supports project preparation, execution and close out of campaigns. He/she will be the point of contact for both internal and external stakeholder for GMP topics.

What you will get:
  • An agile career and a dynamic work culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

Benefits in Visp: https://bit.ly/3wjkoFi

What you will do:

  • Represent the Quality Assurance department in cross-functional project teams and ensuring and managing interfaces to different internal and external stakeholder

  • Assess, review and approve quality records for assigned customer projects such as deviations, change controls, CAPAs, investigations, effectiveness checks, and extensions in line with valid SOPs

  • Author, review and approve GMP-relevant documents and SOPs in the ownership of QA

  • Support and participate in internal and customer audits and regulatory inspections

What we are looking for:
  • Academic degree in Life Sciences (e.g. Chemistry/ Biotechnology or any related field)

  • Significant work experience in QA in the GMP-regulated industry

  • Strong communication skills for effective communication with stakeholders

  • Agility, resilience and flexibility, growth mindset

  • English language skills (written and spoken) are required, German is an advantage

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.

Skills Required

  • Academic degree in Life Sciences, such as Chemistry, Biotechnology, or a related field
  • Significant QA experience in a GMP-regulated industry
  • Strong communication skills for stakeholder communication
  • English language proficiency, written and spoken
  • German language skills
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The Company
HQ: Basel
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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