QA Manager - Freelance GCP/GVP job in Spain

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Contract

Discipline: Good Clinical Practice (GCP)

Location: Spain

This vacancy has now expired

A growing European Headquartered Global CRO is looking for an enthusiastic and experienced QA Manager - Freelance GCP/GVP. This is a brilliant opportunity to join one of the largest independent CROs who provide flexible solutions whilst providing depth and breadth in multiple therapeutic and scientific areas

Job Responsibilities:

Prepare, conduct and follow up on all types of internal and external GxP audits including
system/process audits, vendor audits, investigator site audits, and pharmacovigilance audits, TMF audits, document audits (e.g. CSRs), database audits, CSV / computerised system audits.
Provide quality management advice and support to internal and external customers.
Support and guide operational staff in preparing for customer audits and regulatory
inspections.
Support, guide and facilitate customer audits including system/process/qualification audits and regulatory inspections.
Peer review of audit reports.
Act as Quality Lead auditor when applicable.
Train other Quality & Compliance personnel as required.
Participate in internal meetings as required and liaise with other departments as necessary.
Actively and independently contribute to the development and improvement of the company's FS Quality Management System (QMS).
Actively contribute to continuous improvement of the organisation and processes/procedures
development to enhance the work at the company.
Develop new and review existing Quality & Compliance SOPs as required.
Maintain required knowledge of applicable regulations and company GxP standards and
procedures.
Assist in writing SOPs for other departments.
Assist in providing input into proposals, which include Quality & Compliance.
Assist with business development of external Quality & Compliance services.
Accompany Commercial Operations colleagues on customer visits and participate in
presentations when required.

Skills and Requirements:

Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Strong organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficient user of MS Office, Excel, Word, PowerPoint.

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 contact Steven Fuller at +44 203 854 2630 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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