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Manufacturing Training Officer

OXB MAN 20-207
35 / per week - Full-Time

Do you want to feel inspired every day? We’re future-focused and our business is growing rapidly. We succeed together through passion, commitment and team work, and so can you.

Oxford Biomedica’s Manufacturing Team is responsible for the production and aseptic fill and finish of vectors, for our clients and partners, to GMP standard.

We are looking for a talented GMP Production professional to work as a Training Officer to ensure the training requirements for new and existing employees within Manufacturing teams are efficiently coordinated and fully implemented to meet the regulatory requirements.

Your responsibilities in this role would be:

  • Responsible for the induction of new employees within the manufacturing department and other specific activities regarding their inductions.
  • Ensure all operators are within their required qualification status at all times.
  • Organise and complete initial qualification and re-qualification’s required for GMP manufacturing in timely manner.
  • To assist senior members of the team / departmental managers in keeping the staff training records up to date with all relevant documentation and evidence required to prove competency of the staff.
  • To support senior members of the team with the organisation and structure of training schedule and training matrices. Ensure departmental training matrix are kept up to date at all times and the training percentages are reported to MAN teams periodically.
  • Required to review and follow up revision of documentation such as training folders or training logbooks involving the relevant people if required so deadlines are met.
  • Ensure alignment of training activities with OXB by participating in training forum’s and collaborating with Training compliance and MAN teams.

 To be successful in this role, you will have the following skills and experience:

  • Educated to degree level in a sciences related subject or possess sufficient industry experience
  • Strong knowledge of GMP manufacturing and regulatory standards
  • Comprehensive knowledge of aseptic processing and cleanroom requirements
  • Previous biological/chemical manufacturing experience in an MHRA /FDA regulated environment.
  • Competent at using data to drive decision making.
  • Proficient in use of Microsoft Office applications
  • Confident and able to delivery effective presentations
  • Excellent verbal and written communication skills.

Collaborate. Contribute. Change lives

We look forward to receiving your application.

No Agencies please

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