QA Specialist

  • Lausanne
  • Posted: Jul 16, 2021

My client is a growing biopharmaceutical company based in the French part of Switzerland looking to expand their quality team. Due to this growth my client is looking for a QA Specialist to join their QA operations team based near Lausanne.

Responsabilities :

  • Collect, prepare documentation, and support batch disposition for Commercial Batches,
  • Review master and executed batch records,
  • Support stability studies management,
  • Support CMO management (QBR preparation, metrics compilation),
  • Support Suppliers audit preparation and follow up on action implementation,
  • Support Quality Agreement reviews,
  • Ensure correctness of regulatory filings,
  • Support issuance of Annual Product Quality reviews,
  • Support maintenance of the electronic Quality Systems and on-time completion of deviations, change controls and CAPAs.
  • Perform all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements,

Your Profile :

  • Bachelor or Master degree in Life Sciences, medical technologies or engineering,
  • Minimum of 2 years work experience in pharmaceutical industry, with at least 1 year in a QA department,
  • Good understanding of GMP requirements,
  • Good verbal and written communication skills,
  • Good English level written and spoken (the company language).

For more information, please contact: Noemie Oliva: noliva@axepta.com

Noémie OLIVA

Noémie OLIVA

Team Leader & Recruitment Management Life Sciences

Morgane CAYUELA

Morgane CAYUELA

Life Sciences Recruitment Specialist

Marine DOLLAT

Marine DOLLAT

Life Sciences Recruitment Specialist

QA Specialist

Jul 16, 2021QA SpecialistLausanne 12 months contract noliva@axepta.com Life Sciences

Apply For This AD

Maximum file size: 300 MB.

Allowed Type(s): .pdf, .doc, .docx

Maximum file size: 300 MB.

Allowed Type(s): .pdf, .doc, .docx

To revoke my consent or obtain more information, we invite you to contact Axepta SA directly.