QC Analytical Specialist

Highly Competitive
  1. Contract
  2. Good Manufacturing Practice (GMP)
  3. Iceland
Reykjavík, Iceland
Posting date: 20 Oct 2023
57144

This vacancy has now expired. Please see similar roles below...

Proclinical are recruiting for a QC Analytical Specialist to join a biotech organisation. This role is on a permanent basis.

Responsibilities:

  • Conduct regular actions in assistance of qualification and validation.
  • You will qualify and optimise crucial reagents, for example: reference materials.
  • Recognise necessary document changes and update quality documentation.
  • Serve as a software expert for multiple applications such as empower and Maurice.
  • Contribute to deviations, corrective and preventive actions, change control, inspections and qualification/validation procedures.
  • Contribute to tasks which include cross-functional divisions.
  • Preserve attention to detail and accurate work habits.
  • Adhere to GMP and environmental health and safety standards.
  • Other duties may be assigned.

Key Skills and Requirements:

  • Educated to a degree level in a life science field.
  • Demonstrable experience working in the field.
  • Communication skills both verbally and in writing.
  • Computer literacy.
  • Expertise on both cGMP and GDP practices.

If you are having difficulty in applying or if you have any questions, please contact Robert Scott on r.scott@proclinical.com

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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#QACompliance

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