{ “@context”: “http://schema.org”, “@type”: “JobPosting”, “title”: “QA Officer, Pharmaceutical”, “description”: “
Position
QA Officer, Pharmaceutical/Biotech
Location: Cheshire (onsite)
Type: Permanent
Salary: £28,000-£34,000 (dependent on experience)
Hours: Days (Monday – Friday), parking onsite
Additional: 25 days holiday + BH, private medical, share options scheme, company pension
Responsibilities
- Generation or review of SOPs and other documents (where applicable)
- Providing support to customers and answering queries and product investigations
- Coordinating and resolving immediate/urgent customer complaints, ensuring prompt responses/resolution
- Participating in the internal audit programme to ensure continued GMP compliance of all site activities
- Utilizing scientific resources to improve quality of products and services
- Maintaining personal training folder in an auditable state
- Maintaining quality documentation system
- Participating in quality improvement initiatives
- Supporting the process of maintaining and archiving documentation
- Supporting and executing external audits where applicable
- Supporting management when hosting regulatory audits
- Executing and maintaining the QMS: Risk Assessments, Change Controls, CAPAs, Deviations, Complaints, Recalls, OOS/OOT
Qualifications
- Degree in a relevant scientific discipline
- Good knowledge of GMP
- Experience in CAPA, Deviations, OOS, OOT, internal auditing (preferred), customer complaints handling advantageous
- Strong IT skills (Microsoft applications)
- Good interpersonal skills and strong written/verbal report writing skills
Company: NMS Recruit Ltd t/a Russell Taylor Group
Location:
Job Description:
Position
QA Officer, Pharmaceutical/Biotech
Location: Cheshire (onsite)
Type: Permanent
Salary: £28,000-£34,000 (dependent on experience)
Hours: Days (Monday – Friday), parking onsite
Additional: 25 days holiday + BH, private medical, share options scheme, company pension
Responsibilities
- Generation or review of SOPs and other documents (where applicable)
- Providing support to customers and answering queries and product investigations
- Coordinating and resolving immediate/urgent customer complaints, ensuring prompt responses/resolution
- Participating in the internal audit programme to ensure continued GMP compliance of all site activities
- Utilizing scientific resources to improve quality of products and services
- Maintaining personal training folder in an auditable state
- Maintaining quality documentation system
- Participating in quality improvement initiatives
- Supporting the process of maintaining and archiving documentation
- Supporting and executing external audits where applicable
- Supporting management when hosting regulatory audits
- Executing and maintaining the QMS: Risk Assessments, Change Controls, CAPAs, Deviations, Complaints, Recalls, OOS/OOT
Qualifications
- Degree in a relevant scientific discipline
- Good knowledge of GMP
- Experience in CAPA, Deviations, OOS, OOT, internal auditing (preferred), customer complaints handling advantageous
- Strong IT skills (Microsoft applications)
- Good interpersonal skills and strong written/verbal report writing skills
#J-18808-Ljbffr…
Posted: May 15th, 2026