Quality Control Analyst job in Liverpool, England

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United Kingdom

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

Proclinical are recruiting for a Quality Control Analyst to join a pharmaceutical organisation. This role is on a contract basis and is located in Liverpool.

Responsibilities:

Adhere to both good manufacturing practices and good documentation practices.
Help the QC Manager with any reasonable request linking to the laboratory operation.
You will book in as well as control samples.
Collaborate with the team and QC Manager to arrange work.
Conduct assistance actions necessary for the function of the lab.
The ideal candidate will drive constant improvements and digital transformation in the QC footprint.
Cooperate with the broader teams during the business to offer aid when needed.
Other duties may be assigned to this role.

Key Skills and Requirements:

Educated to a degree level in a scientific field with familiarity working in a QC lab.
Constant improvement driven/change agent personality.
Knowledge of analytical weighing and sample dilutions.
Acquaintance with instrumental practices such as SEC-HPLC, AAS, pH, Conductivity, TOC, etc.
Capable of reacting to unexpected situations.
Able to troubleshoot as well as comprehend GMP needs and regulators expectations.
Works well in a team within a fast-paced lab setting.
Interpersonal and communication skills both verbally and in writing.
Ability to take a proactive approach to tasks.

If you are having difficulty in applying or if you have any questions, please contact Will Hitchcock at +44 203 0789 554.

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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