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MSAT Process Validation Specialist (80-100%) (f/m/d)

MSAT Process Validation Specialist (80-100%) (f/m/d)

MSAT Process Validation Specialist (80-100%) (f/m/d)

MSAT Process Validation Specialist (80-100%) (f/m/d)

Lonza AG

Bio- und Nanotechnologie

Visp

  • Art der Beschäftigung: Vollzeit
  • 88.000 CHF – 106.500 CHF (von XING geschätzt)
  • Vor Ort
  • Zu den Ersten gehören

MSAT Process Validation Specialist (80-100%) (f/m/d)

Über diesen Job

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

At our Visp site, we are growing and looking for a MSAT Process Validation Specialist to join our Biologics organization. In this role, you will support process validation for a vaccine manufacturing process and help ensure the highest standards of quality and compliance.

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 here: https://bit.ly/3wjkoFi

What you will do:

  • Define validation strategies for assigned projects in line with Lonza GMP guidelines
  • Prepare process validation protocols and reports, including supporting studies (e.g., hold time, resin lifetime, leachable/extractable studies)
  • Assess validation data against acceptance criteria and support investigations of deviations
  • Act as Subject Matter Expert for Non-Conformity Records and Change Requests
  • Assist in developing programs and SOPs to meet industry standards and regulatory requirements
  • Participate in regulatory inspections and customer audits
  • Review and approve Product Quality Reviews

What we are looking for:

  • Master’s degree in Chemistry, Biotechnology, Life Sciences, or related field
  • Experience in project management, preferably in MSAT, Quality, or Compliance
  • Strong stakeholder management skills and ability to interact with regulatory agencies (Swissmedic, FDA, etc.)
  • Fluent English communication (written and spoken); German is an advantage
  • Ability to manage multiple tasks and meet deadlines effectively

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.

Gehalts-Prognose

Unternehmens-Details

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Lonza AG

Bio- und Nanotechnologie

Köln, Deutschland

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