Job Description
My client are a fast growing British Pharmaceutical manufacturer and are seeking quality control analysts to join their expanding team.
Responsibilities will include:
• Testing of all laboratory samples including raw materials, in-process and finished products
• Ensuring all GMP/GLP requirements are strictly adhered to and that SOP's are followed at all times
• Recording of analytical results accurately
• Operation, maintenance and calibration of laboratory instruments
• Maintaining usage of laboratory chemicals and keeping records
• Preparation and execution of instrument qualification and method validation protocols
• Ensuring that the laboratory is kept clean, tidy and safe at all times
• Report any non-conformance, instrument malfunction, accident or other abnormal occurrence to immediate superior
• Participate/Respond in investigation of the same where applicable
• Verify analytical data and carry out documentation as required
• Troubleshoot equipment and methods as required
• Participate in internal audits of GMP and Health & Safety
• Facilitate and participate in self-inspections, internal quality audits, customer audits and regulatory inspections
• Ensuring individual training record is kept up to date
• Any other related duties required by the management
• Review and approval of analytical documents for Stability, Finished product and Process validation
The ideal candidate will have 1 years minimum experience working within a pharmaceutical manufacturing environment.
If this role is of interest please apply with a copy of your most recent CV.