Company Description
- Job Title: QC Analyst
- Job Type: Permanent
- Hours: 35 per week Monday - Friday
- Job Location: Glasgow
- Salary: From £22,000
As a global leader in sustainability, quality, and integrity, our 99,600-strong workforce across 2,600 offices and labs is dedicated to fostering a safer, more connected world. Our services impact every facet of daily life, enhancing the safety of food, consumer products, transport, and healthcare, to advancing nuclear industry testing. Your role is crucial in providing safer products, superior services, and maintaining societal connectivity.
At SGS, We're committed to recognising the dedication and effort of our team. By joining us, you'll have access to a range of benefits including performance-related bonuses, private medical cover, a competitive pension scheme with life assurance, and a generous annual leave allowance that grows with your service. Enjoy extra perks like a day off for your birthday, discounted gym memberships, retail discounts, an electric vehicle leasing scheme, enhanced parental leave, service awards, Christmas vouchers, and health & wellbeing initiatives.
Job Description
We're seeking a dynamic QC Analyst to join our team and take their career to the next level!
Role Overview:
The QC Analyst is crucial in ensuring our products are up to the mark with regulatory standards and customer expectations. Collaborating with the Quality Control team, this role involves conducting various analytical tests and inspections to guarantee the quality and integrity of our products.
Responsibilities:
- Execute laboratory tasks and data analysis promptly and to an exceptional standard, adhering to all relevant procedures, Study Plans, and SOPs.
- Comply with GLP/GMP standards, ensuring all activities meet health and safety guidelines and understanding all risk assessments related to the tasks (COSHH, GMO, etc.).
- Maintain GMP compliance for all Quality Control duties.
- Keep department laboratories aligned with cleaning, housekeeping, and general procedural SOPs.
- Update Study Directors/Scientists/Department Managers on project and study statuses, including immediate reporting of any deviations or non-conformances.
- Support in investigations and CAPAs processes, providing technical laboratory assistance as needed.
Qualifications
The ideal candidate will have experience in a laboratory environment, ideally within the pharmaceutical, biological science, or a similar sector.
- A proven ability to develop high technical competence.
- Exceptional attention to detail.
- Strong communication abilities.
Join us and be a part of a team that values growth, quality, and excellence!
Additional Information
APPLY NOW for full consideration, you can be sure that your application will be treated confidentially and impartially, and you will always receive an update within 10 business days.