Quality Assurance Consultant - GMP

Proclinical is proud to represent a well-known international pharmaceutical company with sites around the globe looking to hire a Quality Assurance Consultant. The company specialises in developing and producing medicines and vaccines for a wide range of therapeutic areas including oncology, cardiology and immunology. This is a contract job paying $80-100 per hour.

Our client is partnering with a global pharmaceutical company to provide talent and assistance on the problem areas across the site. The Quality Assurance Consultant's role will be to ensure that the site is fully GMP compliant, and that Aseptic/sterile standards are met, and that deviations are investigated.

Job Responsibilities:

• Using tracking systems and tools relevant to them, such as trackwise.
• Ensuring the site adheres to sterility standards, using tools such as RCA to determine the cause of a non-conforming event.
• Running weekly meetings with staff to discuss and plan updates to the site.
• Coaching and mentoring staff on the correct GMP standards, when required.
• Maintaining Batch Record Review

Skills and Requirements:

• Expertise in aseptic and sterile manufacturing environments.
• Expertise in using systems and tools to track events.
• Previous Quality Assurance work desired.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please call Keri Marshall on +44 207 440 0679 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

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

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