Pharmaceutical Head of Quality Assurance Gmp / Gdp

Pharmaceutical Head of Quality Assurance GMP / GDP – Essex

Job Opportunity:

This is a brand new opportunity that has been created due to expansion. Are you currently working in a pharmaceutical GMP and GDP management quality assurance systems role? Does your experience include quality assurance compliance to regulatory requirements such as the MHRA? Want to work for a growing company? Yes then this is the role for you.

Your role as a Pharmaceutical Head of Quality Assurance GMP / GDP based in Essex will involve implementing and managing a Pharmaceutical Quality System incorporating Good Manufacturing Practice, Quality Risk Management, Root Cause Analysis and Corrective Action and Preventive Action Management system that is compliant through the business.

This is a management role where you will manage the Quality Systems team and work directly with contract manufacturers on product development and drug products transfers.

Duties and responsibilities include:

• Management of the Document Control, Change Control and Quality Risk Management systems.
• Dealing with deviations and CAPAs.
• Scheduling, maintaining and carrying out internal and external auditing.
• Supplier development.
• Maintenance of Technical Agreements with contract manufacturers, contract packers, contract laboratories, distributors and wholesalers.
• Approval of specifications, test methods, manufacturing procedures, validation documents, stability protocols and Technical Agreements.
• Managing quality related issues and developing strategies in the Technical Transfer of products.

This is a full time permanent job opportunity with a great salary paying £60,000 – £72,000 per annum and benefits including pension, healthcare, holidays, bonus, company car or car allowance and much more.

Skills:

To apply for the role of Pharmaceutical Head of Quality Assurance GMP / GDP you will have the following:

• Degree in Chemistry, Biology or Pharmacy.
• Pharmaceutical Manufacturing/Contract Manufacturing expereince within a Quality function.
• Ideally have worked with contract manufacturers for drug technology transfer.

How to Apply:

To apply for this one off opportunity, please send a word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat.

My contact details are:

Miss Rashida Khan

If this sounds like the role for you or a colleague then please don’t hesitate to contact us. If we manage to successfully fill a permanent placement from your recommendation then we will send you a cheque of £300. We also have many incentive schemes for referring contractors/temp staff so please contact us with the referral and we can provide you with more information.

For a list of our current vacancies, please visit the Quality Start website.

If you do not hear from Quality Start within 2 weeks your CV has not been short listed for this role.

Quality Start are acting as a specialist recruitment consultancy for this role.