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QA Specialist Fix-term CDD (m/f/d) 80%

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01/07/2024 80% - 100% Permanent position
Corden Pharma - A Full-Service CDMO
QA Specialist Fix-term CDD (m/f/d) 80%

CordenPharma is one of the leading Contract Development and Manufacturing Organizations (CDMO) and develops and produces active pharmaceutical ingredients, medicines and associated packaging services on behalf of its customers as a “full-service” service provider. The group employs around 3,000 people.

Our network in Europe and the USA offers flexible and specialized solutions across five technology platforms: peptides, lipids & carbohydrates, injectables, highly potent active ingredients & oncology and small molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the benefit of patients.

CordenPharma International (CPI) acts as the management company of the CordenPharma Group. In addition to the Executive Leadership Team, CPI has central functions such as Sales & Marketing, Legal, HR and Corporate Development, which work for the CordenPharma Group across locations and at an international level.

We are looking for one as soon as possible

QA Specialist Fix-term CDD (m/f/d) 80%
Villars-sur-Glâne, Fribourg, Suisse
  • Fribourg
  • 01.08.2024
  • Befristet
  • 12 months contract
Main activities and responsibilities
  • Give quality support to Production Department, quality expert in the shop floor
  • Ensure support, performs and approves investigations related to non-conformities
  • Draft deviation and complaint reports
  • Define, follow up, perform and approve suitable Corrective and Preventive actions and actions related to Change Control
  • Participate to received audits and inspections
  • Review and approve documents related to Production activities
  • Provide telephone hotline service for Production in accordance with current regulations (Standby service)
  • Perform GMP training for Production personnel.
Your Profile
  • Scientific education in chemistry, pharmacy or biology
  • Experience in Quality Assurance and/or Production of pharmaceutical products
  • Professional in French and English (both in oral and written communication)
  • Perfect knowledge of GMP and related guidelines
  • Skills over basic computer tools (Pack office).
What we offer
Retirement Pension Plan
Dynamic and exciting work environment
Home Office
Your contact person

Brandt, Raphael

About the company

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