Pharmaceutical Project Manager
Rare opportunity for an accomplished Project Manager to uphold a pivotal role within a successful and expanding team in a modern, purpose built facility!
As Project Manager you will coordinate and manage a range of GLP, GMP and/or GCP regulated analytical studies, ensuring delivery is on time and within budget. You will be primary contact for sponsor studies and must maintain an excellent working relationship with clients, assuming ultimate responsibility for providing a high quality service. You will also act as Study Director and will be responsible for planning and scheduling the analytical programme as well as providing technical guidance to laboratory staff.
To be considered for this role you must have:
• A minimum of 2 years’ experience managing analytical projects within an industrial laboratory
• Excellent knowledge of GLP/GMP/GCP regulations
• A strong analytical background including method development & validation experience
• Excellent communication & team leadership skills
Apply to VRS today to be considered for this exciting new opportunity!
Key words: Project Manager, management, biopharmaceutical, biopharma, pharmaceutical, analytical chemistry, laboratory, HPLC, physicochemical, quality control, 5 batch analysis, LC-MS, LC-MS/MS, NMR, ICP-MS, GC-MS, Study Director, Principal Scientist, GMP, GLP, GCP, Manchester, VRS5497AF