Quality Operations Manufacturing Science QC

Vor 2 Tagen


Sankt Gallen, Schweiz TN Switzerland Vollzeit

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Quality Operations Manufacturing Science QC, St. GallenClient:

CSL

Location:

St. Gallen

Job Category:

Other

Job Reference:

7d08dab9a66b

Job Views:

10

Posted:

21.01.2025

Expiry Date:

07.03.2025

Job Description:

Quality Operations Manufacturing Science QC Support Manager

In this role you will be responsible for ensuring product knowledge within CSL Vifor for providing best support for our CMOs and analytical service providers for external manufactured APIs and Finished Drug Products in the oral portfolio. Furthermore, you will be responsible for the following tasks:

  1. Management of Quality Control / Manufacturing Science and QA activities for CMOs/suppliers of the oral portfolio
  2. Ensure knowledge of manufacturing processes, QC-analytical methods, drug products, APIs and raw materials
  3. SME (Subject Matter Expert) for PQR/APR of external manufactured products
  4. SME for Stability Studies of external manufactured products
  5. Data collection, creating, review and approval of stability reports
  6. Support for regulatory submissions and variations in close cooperation with global and local stakeholders
  7. Creating, Review and approval of compliance records (Changes, complaints, deviation) and other documents
  8. Conduct, execute and document impact assessments and investigations
  9. Providing overview about Quality Performance of CMOs (CPV) and product related data
  10. Support analytical method transfer to external analytical service providers/CMOs
  11. Providing overview on deviations, complaints and follow-up of defined actions for improving Right First Time at CMOs
  12. Performing QC-releases for Oral Products

Qualification and experience

  1. Bachelor / Master Degree in Life Sciences or related industries or working experience in pharmaceutical Industry
  2. Minimum 5 years overall experience within the pharmaceutical, biotechnology, or medical device industry
  3. Experience in Quality Control, Pharm. Manufacturing or Stability Management
  4. Experience with software for Quality processes (e.g. Trackwise) and / or for data analysis (e.g. PowerBI, Excel, Minitab)
  5. Team player
  6. Fluent in English and German in an asset

Preferred Requirements

  1. Working experience in Pharmaceutical/Analytical Development

We are looking forward to receiving your online application. Applications must include a motivation letter and CV, as well as letters of references and copies of relevant transcripts and/or diplomas in the original language. Please include all these in one document together with the CV.

CSL Vifor is committed to provide equal employment opportunity for all.

About CSL Vifor

CSL Vifor aims to become the global leader in iron deficiency and nephrology. The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.

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