QC Analytical Specialist job in Reykjavík, Iceland

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Last Name*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: Iceland

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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