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Our client is a major manufacturer of biological pharmceutical products and they are looking for an experienced Down Stream Production operator to join their expanding team.
cGMP Downstream Production Operator will perform a wide range of activities associated with the Downstream manufacture of cGMP biopharmaceutical Investigational Medicinal Products (IMPs) within the Production Facility. There is also a requirement to ensure all work is in accordance with regulatory requirements, Quality and HSE Policies and Procedures.
The role involves manufacture of Downstream processes to cGMP within the cleanroom facility from Bioreactor Primary Recovery to Downstream Purification. The Downstream Production Operator will prepare manufacturing instructions and specifications and manufactures the products within the cGMP production facility to meet project timelines, ensuring all documentation is completed compliantly.
In particular, this candidate will be expected to plan and organize their workload to manufacturing schedules. In addition, the role includes more routine operations associated with maintaining the production facility such as cleaning and environmental monitoring.
This role will involve moving to an unsociable hours working pattern for periods of time in line with the working hours policy to meet the project demands.
Hands-on processing experience required within a biopharmaceutical or pharmaceutical production or development environment.
Good working knowledge of cGMP and a broad knowledge of safety.
Experience in following SOPs and completing batch records.
Downstream processing, preferably with Chromatography experience.
Experience in the following advantageous:
writing and reviewing SOPs and batch records, execution of equipment qualification.
To apply for this position, candidates must be eligible to live and work in the UK
Matchtech is acting as an Employment Business in relation to this vacancy.