• Project management and execution of designated projects, to ensure that pharmaceutical products are bought from 'concept' to market within agreed timelines, regulatory guidelines and in a cost effective manner • Manage designated technology transfer or new product development projects by developing action plans with timelines and appropriate strategies in accordance with the product licence and GMP Guidelines. • Ensure compliance in technology transfer and process changes with EU GMP under the supervision of nominated Qualified Person (QP) • Approve with the QP the stability protocol's validation protocol's and change control for designated products and processes.
Who we're looking for
• You will preferably have significant experience in sterile and solid dosage pharmaceutical production, with proven experience in technical transfer of the aforementioned pharmaceutical products • You will also have good project management skills, supported by excellent communication skills • You will have a comprehensive understanding of the quality compliance knowledge within the EU and US environment and a good understanding of GxP systems • This role would suit a self starter with the ability to 'think outside the box' and have a high level of professional credibility with the skills required to develop strong alliances and partnerships, internally and externally. • You will also possess outstanding interpersonal, communication and influencing/negotiating skills, a strong analytical approach to problem solving along with the ability to debate issues in a constructive manner • You will hold a relevant degree in life sciences.
About our client
Our client is a Pharmaceutical organisation based in Essex
What's on offer
Competitive package
Michael Page Contact For further info, apply or phone on +44 (0) 20 7831 2000. Job Ref: 13220747 Your application will be sent to Keith Fullarton.