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Job Details

GMP Quality Auditor

Company: Optimus Search Limited
Location: London
Reference: BBBH8698
Closing Date: 15 Dec 17
Type: Contract
Salary (£): Negotiable
Benefits:

Job Summary:

Are you a GMP Quality Auditor interested in working for one of Englands leading names in the Pharmaceutical industry? Are you looking for something new?! Then stop what you are doing and read on!Title: GMP Quality AuditorRate: NegotiableLocation: LondonType: Contract (12 Months rolling)A Fantastic new role has just opened up at one of our leading London based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutic ...

Requirements:

Are you a GMP Quality Auditor interested in working for one of Englands leading names in the Pharmaceutical industry?
Are you looking for something new?!
Then stop what you are doing and read on!

Title: GMP Quality Auditor

Rate: Negotiable

Location: London

Type: Contract (12 Months rolling)

A Fantastic new role has just opened up at one of our leading London based clients offering the successful candidate the opportunity to join a hard-working team working on exciting projects in the pharmaceutical sector.

The proposed start date is January 2018 - We need YOU

Responsibilities include:

* You will complete audits of data, information, procedures, facilities, equipment, and systems (including computer systems) to ensure compliance with SOPs, GMPs and applicable regulations.
* Your responsibilities will include reviewing and approving production and analytical documentation accompanying the release of drug substance, drug product and packaged finished goods to ensure conformance to appropriate SOPs, GMP and regulatory requirements, including supporting QP certification.
* You will be a good communicator and collaborate with functional areas to develop a strong working relationship and understanding of roles and responsibilities. This will enable you to utilise this network to help resolve comments and issues that arise during audit and review.
* You will regularly perform and review complaints and deviation investigations, change controls and CAPA’s, following standard procedures, consulting with managers and supervisors where necessary.
* You will be expected to compile data for reports and presentations and using this to draw conclusions.
* You will be responsible for carrying out all assignments to the standards of compliance, efficiency, innovation, accuracy, and safety in accordance with Company and regulatory requirements.
* You will keep abreast of cGMP requirements as described in applicable worldwide regulations.

Requirements

* The ideal candidate will have prior experience working in pharmaceutical/Bio pharmaceutical industries.
* To be successful in this role you will also have experience in Quality auditing.
* Previous experience working to cGMP requirements.

If you are interested please do not hesitate to email or call me!

Shubert@optimussearch.com

+44 20 30969 392

Apply for this job: GMP Quality Auditor

Contact Information:

Address:  Head Office
171-177 Great Portland Street, London
W1W 5PG
England
Tel:  +44 (0) 20 3418 8033
Fax:  +44 (0) 20 7287 4908
Website:  Visit Our Web Site

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