Description
Position Description:- Performing as part of a team the walk down, commissioning, optimisation and OQ teams.
- The review and approval of commissioning dossiers, OQ protocols and OQ reports.
- Ensuring all commissioning and validation documentation is completed in accordance with Project standards.
- Performing loop testing on automation systems.
- Ensuring all punch items have been closed out.
- Generating SOPs and providing end user input into training material for specific equipment.
Primary Tasks:
- Good knowledge of GMP and validation require good organisational skills.
- Provide Technical support and leadership for Technology Transfer Teams.
- Provide support and technical input to regulatory submissions and filings.
Experience and Education:
- Experience of working in an EU/FDA regulated environment.
- Hands on experience of Technology Transfer would be of specific interest.
- A minimum bachelors degree qualification in science or engineering.
- Knowledge and experience of all relevant Environmental, Health and Safety regulations and guidelines.
- The Candidate should have a proven ability and experience of, interacting with personnel from all levels within an organization.
This is an exciting opportunity to join a large and dynamic organisation offering competitive hourly rates. If you would like to apply please call me on or reply with a copy of your most recent CV. We also offer shopping vouchers for any successful referrals so feel free to get in touch if you know of anyone who is currently looking.