Project Manger (GLP)


Negotiable dependent on experience

REF: 0044

Are you looking for an exciting and challenging opportunity within the Biopharmaceutical industry? Do you have experience in method development and validation of cell based assays and immunochemistry? Are you experienced in a wide range of bioanalytical techniques? Do you have GMP Project Management or Study Direction experience?

Key Information

  • North West
  • 01423 813520
  • Permanent
  • 19-12-2018
  • Negotiable dependent on experience
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Job Description

Our client, a leading provider of GLP, GCP and GMP analysis for the pharmaceutical and speciality chemical industries, is looking to recruit a Regulatory Study Director / Project Manager to work within their expanding team.

This is an excellent opportunity for the right calibre of individual to enhance their career in the scientific industry.

Key responsibilities include:

  • Developing existing and new immunochemistry and cell based assays to support research, product development and registration.
  • Devising, price and carry out a programme of work containing both long and short term goals, interpret results and suggest new areas of work in order to meet agreed targets.
  • Producing and contribute to Technical Reports, and report analytical data, results and conclusions directly to the customer businesses, and ensuring that good lines of communication are maintained throughout the analytical process.
  • Ensuring that all analytical work and support activities are performed in accordance with Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing and ensure compliant recording of all experimental data.
  • Training and coach junior members of the team in analytical techniques and procedures as appropriate.
  • Managing, in conjunction with the Group Leader, the day to day activities of personnel in the Team, to ensure that the needs of the contract customer businesses are met, and that the teams’ activities are fully recorder and reported.

The ideal candidates will have previous experience of cGMP Project Manager, GCP Responsible Scientist and/or of a GLP Study Director role and responsibilities are essential. You will have a minimum of a good first degree in Science and a broad general knowledge of immunochemistry and cell based assays, including pharmacokinetics, anti-drug antibody, biomarker and cell based potency assays.

For more information or to apply, please contact Dawn Alderman on 01423 813520 or alternatively send your CV along with a cover letter, including your salary requirements to dawn.alderman@networkscientific.co.uk.

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

To be considered...

  • Previous experience of cGMP Project Manager, GCP Responsible Scientist and/or of a GLP Study Director role and responsibilities are essential.
  • You will have a minimum of a good first degree in Science
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