GMDP Quality Auditor

i Pharm Consulting Ltd
12 Jan 2018
12 Feb 2018
Contract Type
Full Time
GMDP Quality Auditor

I am working with a mid-size pharma company with a large global presence, who specialise in: pain medicine; respiratory; oncology and biosimilars, to recruit a GDMP Auditor to work in their UK headquarters based in Cambridge. Significant auditing experience (4-5 years' minimum) is required for this position. In particular, you must be a trained and certified as a lead auditor by a recognised professional body. Other requirements include: experience of GDMP auditing and efficient report writing.

Location: Cambridge

The main objectives of this role include: undertaking GDMP audits in support of the company's global audit program, across multiple therapeutic areas. You will also be required to provide information and support across all areas of the business as is required, including maintaining good working relationships.

Specific duties and responsibilities include, but are not limited to:

*Participating in strategic projects, including new product introductions and new supplier approvals

*Writing and updating relevant SOPs and supporting documents to ensure compliance with current legislation

*Assist with generation and interpretation of quality metrics

Experience Required

*Experience of GDMP auditing of low/medium risk and less complex product tpes

*A good knowledge of all GDMP and associated guidelines (EU, ISO, ICH, WHO etc) and and appreciation of the differences between them

*Experience in assessment of third parties in compliance with GDMP guidelines across multiple dosage forms

*Report writing

*Trained and certified as a Lead Auditor by a recognised professional body


Excellent Flexible Benefits scheme that gives you the choice of benefits to fit your lifestyle. These include, but are not limited to:

-Dental cover

-Private medical care


-Car lease scheme

-Cycle to work scheme

-Childcare vouchers

About i-Pharm Consulting

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

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To Apply:

If you would like to discuss this vacancy further, please call Recruitment Consultant Olivia Smart on Phone number removed or email Email address removed. If this role is not suitable, Olivia is also available to discuss other possible positions or answer any general questions regarding your career and the current market.