Senior Production Scientist

Highly Competitive
  1. Permanent
  2. Senior/Director & VP
  3. United Kingdom
Stevenage, Hertfordshire
Posting date: 27 Jun 2019
SC.MD.24061_1561643503

A clinical-stage biopharmaceutical company is seeking to recruit a Senior Production Scientist to their office in the UK. The organisation develops next generation, programmed T cell therapies for the treatment of cancer and pride themselves on their broad suite of proprietary and modular T cell programming technologies. This position presents a fantastic opportunity for a bright, enthusiastic scientist to join an innovative company that is committed to delivering high quality products for use in clinical trial programmes.

Job Responsibilities:

  • Qualifying methods and processes to ensure their suitability for use in support of Clinical Trial manufacturing.
  • Supporting Clinical Trial manufacturing through provision of cell processing.
  • Developing assays suitable for product release.
  • Authoring development reports and regulatory documentation.
  • Assisting in technology transfers into the Manufacturing group.
  • Working with external service providers.
  • Supervising staff or students as necessary.
  • Selecting and purchasing appropriate laboratory equipment.
  • Assisting in Equipment Qualification.
  • Performing other duties as required following consultation with the post holder.
  • Adhering to all health and safety guidance, provided by the Company.

Skills and Requirements:

  • Higher degree in Biology/Biomedical Science/Immunology/Haematology/Pharmacology or related discipline, or 3 years' experience in a GMP field.
  • Familiarity with a range of biopharmaceutical and cell-based techniques.
  • Directly relevant biotechnology or pharmaceutical industry experience.
  • Understanding of and familiarity with quality and regulatory guidance governing biopharmaceutical development.
  • Familiarity with a range of biopharmaceutical and cell-based techniques.
  • Good understanding of cell biology and immunology.
  • Understanding of and familiarity with GMP regulations.
  • Good attention to detail and ability to accurately follow SOPs.
  • Experience of working in a busy laboratory environment.
  • Demonstrable multitasking, project management, and execution skills.
  • Good interpersonal skills, including communication, presentation, persuasion, and influence.
  • Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Proficiency with computer skills, such as MS Office.

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Marjolene D'Almeida-Ayeni at +44 203 854 2626 or upload your CV on our website - www.proclinical.com.

A full job description is available on request.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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