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QA Specialist, Batch Disposition 80-100% (f/m/d)

QA Specialist, Batch Disposition 80-100% (f/m/d)

QA Specialist, Batch Disposition 80-100% (f/m/d)

QA Specialist, Batch Disposition 80-100% (f/m/d)

Lonza AG

Pharma, Medizintechnik

Visp

  • Art der Anstellung: Vollzeit
  • 77.500 CHF – 86.000 CHF (von XING geschätzt)
  • Vor Ort
  • Aktiv auf der Suche

QA Specialist, Batch Disposition 80-100% (f/m/d)

Über diesen Job

QA Specialist, Batch Disposition 80-100% (f/m/d)
Switzerland, Visp

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

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

In this role your responsibilities will be in the batch disposition group in Quality Assurance of the Large Scale Mammalian production facility.

What you’ll get:

  • Working in a diverse and highly dynamic team in a starting up facility

  • 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’ll do:

  • Being part of the creation of the batch disposition group and structure within the Large Scale Mammalian facility

  • Compile batch disposition packages and related activities to ensure timely release of product/intermediate

  • Track all pre-release activities supporting the Senior Batch Disposition Manager, escalating issues in a timely and constructive manner

  • Support in regulatory inspections and customer audits

  • Author of GMP documents and SOPs in area of expertise

What we’re looking for :

  • University degree in relevant discipline, preferably in Life Sciences

  • Experience in a pharmaceutical cGMP environment preferably in a Quality Assurance department

  • Good understanding of cGMP/cGDP guidelines, quality standards and quality management processes

  • Strong ability to organize workload and priorities accordingly

  • Willingness to acquire familiarity with regulatory requirements and international codes & standards (e.g., FDA, EMEA, and lCHQ7)

  • Good communication skills with internal and external international customers

  • Fluency in English, able to communicate in or willing to learn German

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Reference: R68975

Gehalts-Prognose

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