Quality Control (QC) Officer
| Dyddiad hysbysebu: | 02 Hydref 2025 |
|---|---|
| Cyflog: | £28,000 i £30,000 bob blwyddyn |
| Oriau: | Llawn Amser |
| Dyddiad cau: | 01 Tachwedd 2025 |
| Lleoliad: | SM3 9BW |
| Gweithio o bell: | Ar y safle yn unig |
| Cwmni: | TriOn Pharma Limited |
| Math o swydd: | Parhaol |
| Cyfeirnod swydd: | TRI/QC2 |
Crynodeb
The QC Officer will be responsible for conducting and overseeing laboratory testing to ensure that pharmaceutical products meet required quality standards before release. The role involves working closely with the Qualified Person, Quality Assurance team, and contract laboratories to ensure compliance with MHRA, EU GMP, and company standards.
Key responsibilities will include:
Performing and supervising analytical testing of raw materials, packaging components, and finished products.
Reviewing and approving laboratory results, analytical reports, and Certificates of Analysis.
Ensuring laboratory operations are in full compliance with GMP, GLP, and company SOPs.
Conducting stability studies and validating analytical methods as required.
Investigating and documenting laboratory deviations and out-of-specification (OOS) results.
Maintaining laboratory equipment, calibration schedules, and reagent stock control.
Assisting in audits and regulatory inspections.
Supporting continual improvement initiatives within the QC department.
Skills, Experience, and Qualifications Required:
Bachelor’s degree (or equivalent) in Pharmaceutical Sciences, Chemistry, Biology, or related discipline.
Minimum 2 years’ experience in a pharmaceutical quality control laboratory.
Strong understanding of GMP, GLP, and analytical testing methodologies.
Familiarity with analytical techniques such as HPLC, GC, UV spectroscopy, and dissolution testing.
Excellent documentation and data integrity practices.
Ability to interpret analytical results and make informed quality decisions.
Key responsibilities will include:
Performing and supervising analytical testing of raw materials, packaging components, and finished products.
Reviewing and approving laboratory results, analytical reports, and Certificates of Analysis.
Ensuring laboratory operations are in full compliance with GMP, GLP, and company SOPs.
Conducting stability studies and validating analytical methods as required.
Investigating and documenting laboratory deviations and out-of-specification (OOS) results.
Maintaining laboratory equipment, calibration schedules, and reagent stock control.
Assisting in audits and regulatory inspections.
Supporting continual improvement initiatives within the QC department.
Skills, Experience, and Qualifications Required:
Bachelor’s degree (or equivalent) in Pharmaceutical Sciences, Chemistry, Biology, or related discipline.
Minimum 2 years’ experience in a pharmaceutical quality control laboratory.
Strong understanding of GMP, GLP, and analytical testing methodologies.
Familiarity with analytical techniques such as HPLC, GC, UV spectroscopy, and dissolution testing.
Excellent documentation and data integrity practices.
Ability to interpret analytical results and make informed quality decisions.