Reference Number: JO-1910-439326
Head of Quality Control
Rate: Negotiable
Job Type: Permanent
Location: Hatfield

Associate Director/Head of QC/QA Head of department opportunity
Salary details available on discussion + excellent benefits package

My client are a leading global pharmaceutical company based in Hertfordshire who are currently seeking an experienced Associate Director/Head of QC/QA to join their business on a permanent working basis. The company have over 10,000 employees globally and currently have a focus on two therapy areas with a number of exciting products.

If you are looking for the opportunity to develop yourself, a team and a department then this could be just the role for you. With excellent internal progression opportunities and the opportunity to step up in to a global level role with commercial and operational oversight, now really is the time to get in contact to explore further.

The role will be responsible for directly line managing the department and will take responsibility for all Quality activities related to the development and progression of said department.

Other key responsibilities will include:
To ensure that all materials that require testing in the laboratory are done so according to agreed specifications and procedures.
To manage all staff ensuring that job descriptions, objectives and appraisals are up to date.
To recruit and train staff for the QC functions and design and implement systems and procedures to support their development.
To design and implement systems and procedures for the efficient, productive, compliant and safe operation of the production operation.

Successful applicants must be able to demonstrate management experience as well as 8+ years of pharmaceutical QA/QC experience, within a manufacturing/laboratory environment.

You must also be able to show:
The ability to establish and maintain effective working relationships with internal and external stakeholders.
Extensive knowledge of Quality Control, Quality Assurance, Quality Systems, GMP, Regulatory Compliance and manufacture and packaging of pharmaceutical products.
Demonstrated knowledge, understanding and application of GMP guidelines and regulations.
Fluent English communications skills (written & spoken).
Ability to interpret complex data and present key findings.

To apply for this role, please call Bob Beevers at Clinical Professionals on +44 207 822 1710 or send an updated version of your CV via email to bob@scientificprofessionals.com

If this role is not for you, we do operate a bonus referral scheme should we go on to successfully place someone that you recommend to us so please feel free to share these details within your network.

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