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Connect with headhunters to apply for similar jobsSenior QA Engineer (100% remote - UK)
Tether Operations Limited
QA Officer - Biotechnology
Job summary
A biotechnology company in Knutsford is seeking a skilled QA Officer/Specialist to strengthen their team. This role involves ensuring GMP compliance, generating SOPs, and handling customer complaints. The ideal candidate should have a degree in a relevant scientific discipline and possess strong interpersonal skills. This permanent position offers a salary between £28,000 and £33,000, along with additional benefits including 25 days holiday, private medical, and a pension scheme.
Benefits
Qualifications
- Experience in CAPA, Deviations, OOS, OOT, Internal auditing.
- Customer complaints handling is advantageous.
Responsibilities
- Generate or review SOPs and other documents.
- Support customers and answer queries.
- Coordinate and resolve customer complaints.
- Participate in internal audits for GMP compliance.
- Maintain quality documentation system.
- Execute and maintain the QMS.
Skills
Education
- Location: Cheshire (onsite)
- Type: Permanent
- Salary: £28000-£33,000 (dependant on experience)
- Hours: Days (Monday - Friday), 08:00 - 16:30
- Parking on site
- Additional benefits: 25 days holiday + Bank Holidays, private medical, share options scheme, company pension
Our Client a Biotech company is looking to strengthen their QA team and recruit an experienced QA Specialist.
- Generation or review of SOPs and other documents (where applicable)
- Providing support the customers and answering queries and product investigations
- Coordinate and resolve immediate/urgent customer complaints, ensuring prompt responses/ resolution
- Participate in the internal audit programme to ensure continued GMP compliance of all site activities
- Utilise scientific resources in order to work on improving quality of products and services
- To maintain personal training folder in an auditable state
- Maintaining quality documentation system
- Participate in quality improvement initiatives
- Supporting in the process or maintaining and archiving documentation
- Supporting and executing external audits where applicable
- Supporting management when hosting regulatory audits
- Working on executing and maintaining the QMS, including but not limited to:
- Risk Assessments
- Change Controls
- CAPAs
- Deviations
- Complaints
- Recalls
- OOS/OOT
- Will have a Degree in a relevant- Scientific discipline
- Will have good knowledge of GMP
- Experience in CAPA, Deviations, OOS, OOT, Internal auditing (preferred), Customer Complaints handling would be very advantageous
- Strong IT skills (Microsoft applications)
- Good interpersonal skills and strong written/ verbal report writing skills
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here .
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.
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