Job Opportunity

Reference: QS0987
Title: Pharmaceutical Product Transfer Project Manager
Location: Norfolk
Job Type: 2 years
Salary: The PAYE rate is £56.04 per hour
Contact Person: Miss Selina Thompson apply@qualitystart.co.uk

Opportunity: This is a brand new opportunity that has been created due to expansion.  Are you currently working as a Senior Project Manager dealing with drug development projects from research into manufacturing? Does your experience include equipment installation and validation, project planning from design through to construction and commissioning? Want to work for global pharmaceutical manufacturing leader? If yes then please read on.

Your role as a Pharmaceutical Product Transfer Project Manager based in Norfolk will involve managing the full project lifecycle of drug development projects from research into manufacturing.
Duties & responsibilities include:

• Project planning from design through to construction and commissioning. Tasks will include management of project risk; resources; budget control and ensuring the project is completed on time to the required standards.
• Equipment validation and installation.
• Leading the design, installation and validation of new Clean Rooms.
• Handing over new processes to the integrated supply chain and quality teams.
• Complying with all corporate policies and external regulatory requirements.
• Reviewing quality associated documentation (URSs / change controls / critical system drawings and system reference files).
• Acting as a liaison between stakeholders, designer and construction companies to ensure good communication of all activities.
• Manage EHS requirements and sub-contractors.
• Providing technical and project leadership in multi skilled teams.
• Generating accurate financial forecast spending.

Skills:  To apply for the Pharmaceutical Product Transfer Project Manager role you will be:

• An experienced project manager with a background in pharma / medical devices managing pharmaceutical or FMCG projects from cradle to grave.
• Able to work under pressure and prioritise workloads for the needs of the business whilst working on multiple projects.
• In-depth knowledge of Health & Safety, GMP and other regulatory matters.

How to Apply: In order to apply for this vacancy please ensure you have read and agree to the privacy policy found here and then email your CV to apply@qualitystart.co.uk quoting the reference number and the job title.