Our employees are able to develop their careers in exciting new medical technologies, and so can you.
Oxford Biomedica’s Process R&D team consists of experienced scientists and engineers that have extensive expertise in all aspects of upstream and downstream development. PR&D take processes from the laboratory “bench” scale and apply process expertise and engineering fundamentals for delivery to Manufacturing.
We are currently recruiting for a Training Coordinator to join the team. The purpose of this role is to drive the timely coordination of training, to support the high quality work conducted within the PR&D team, ensuring that all team members are adequately trained.
Your responsibilities in this role would be:
Owner of departmental training trackers and responsible for driving the department’s training metrics
Responsible for identifying all training needs for the multi-disciplinary Process R&D department and ensuring these training needs are met
Key PR&D point of contact with training department and coordinator for the PR&D training representatives, responsible for maintaining a high level of training within the department
Identify and coordinate updates to and reviews of departmental Risk Assessments and Standard Operating Procedures
Keep abreast with all new and updated company and Process R&D SOPs and Policy’s and ensure Process R&D training is up to date
Work with OXB training Team to roll out new training initiatives to the PR&D department
Coordinate the multifaceted Process R&D On the Job Training sessions (OJT)
Lead introduction and guidance to new starters on training folders and archiving of leavers’ training folders
Coordinate and lead audits of departmental training
Where appropriate, develop and lead training delivery for department
Accountable for own performance in alignment with group objectives and deadlines.
Work in accordance with the OXB quality management system.
To be successful in this role, you will have the following skills and experience:
Maths & English GCSE as a minimum requirement
Previous training experience, ideally within the pharmaceutical industry/relevant in an MHRA/FDA regulated environment
Experience with documentation such as SOPs, Policies, Technical Protocols.
Experience of working within a GMP manufacturing or GLP environment would be beneficial
Understands training requirements for each group within the multi-disciplinary Process R&D department
Fluency in written and spoken English
Strong oral communication and interpersonal skills
Organised, self-motivated, pragmatic, and have an excellent attention to detail
Excellent organisational and time management skills
Possess a strong appreciation for the training requirements of the department
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.