Senior QC Analyst / Team Leader
- Recruiter
- Confidential
- Location
- Luton
- Salary
- 20000.00 - 35000.00 GBP Annual
- Posted
- 30 Jun 2021
- Closes
- 27 Jul 2021
- Sectors
- Accountancy
- Contract Type
- Permanent
- Hours
- Full Time
Company Profile
Bristol Laboratories is a fast-growing pharmaceutical company engaged in the development, manufacture, marketing, and distribution of generic medicines in the UK and Europe. We work to offer a wide range of high-quality medicines to the health sector in the UK, which optimizes cost efficiency and ensures reliable supply.
Main Responsibilities
• Testing of all laboratory samples including raw materials, in-process, finished products, Validation, stability, environmental (as per written procedure or as per pharmacopoeia).
• Ensuring all cGMP/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.
• Verify analytical data and carryout 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
Additional
* Confident in HPLC
* Practice Health and Safety practice in the laboratory
* A team player
Bristol Laboratories is a fast-growing pharmaceutical company engaged in the development, manufacture, marketing, and distribution of generic medicines in the UK and Europe. We work to offer a wide range of high-quality medicines to the health sector in the UK, which optimizes cost efficiency and ensures reliable supply.
Main Responsibilities
• Testing of all laboratory samples including raw materials, in-process, finished products, Validation, stability, environmental (as per written procedure or as per pharmacopoeia).
• Ensuring all cGMP/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.
• Verify analytical data and carryout 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
Additional
* Confident in HPLC
* Practice Health and Safety practice in the laboratory
* A team player