Job Description

If you’re an experienced pharmaceutical quality professional with strong understanding of GxP auditing and QMS implementation, then perhaps this speciality drug-device combinations business could be presenting a desirable opportunity for you. Following the success of their first approved product, this business is growing significantly throughout, creating opportunities for knowledgeable and passionate people.

Your primary responsibility will be supporting the definition, implementation and maintenance of the Quality Management System in line with global regulations. You will provide oversight for the quality function, ensuring compliance and driving process improvement.

Additional responsibilities include:

• Collaborating with Project Management and Clinical Operations to resolve quality-related issues
• Supporting audits
• Performing Trial Master File Quality Control (TMF QC)
• Generating and reviewing Standard Operating Procedures
• Promoting a quality approach across the business

For more information or to apply, please contact Ryan Kennedy on 01423 813520.

Due to the volume of applications received during this time, we are finding it incredibly difficult to respond to each and every one. Should you not hear back from us within two weeks, please assume your application was unsuccessful on this occasion.

Network Scientific is an award-winning science recruitment agency specialising in the provision of temporary, permanent and contract recruitment services to the scientific and related technical industries. We’re an ethical and knowledgeable consultancy passionate about our candidate care.

Please note that all applicants for this pharmaceutical job should be able to prove that they are legally entitled to work in the UK. Network Scientific Recruitment, part of Network Scientific Ltd. is an Employment Business/Agency.

To be considered...

To be considered for this opportunity, you must possess in-depth theoretical and practical knowledge relating to QMS requirements and auditing. You will have gained rich experience in this field in a pharmaceutical, biotechnology or contract research environment. Your understanding of ICH, GCP and additional regulations will be of paramount importance. Above all you must be flexible and an excellent communicator.

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