Your new company

A biopharmaceutical site focused on the development and manufacturing of medicines, particularly for the neuroscience area.

Your new role

• Review of experiment write-ups, reports and production batch records, identification, and trending of data for process parameters.

• Support documentation management activities.

• Lead COSHH and Risk assessment authoring and review activities for the team.

• Support manufacturing facility activities e.g. Tier 1 planning, environmental monitoring, materials processing.

• Support for laboratory experimentation as required.

• Work in compliance with GxP/EHS requirements and report any compliance concerns to your line-manager, QA Compliance or Health and Safety Team.

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.