Senior QA Specialist - GMP & QMS Leader (Shift)

BioTalent; Oxford; On-site; GBP 40,000 - 60,000; Full time

Job summary

A global pharmaceutical organization in the UK seeks a Senior QA Specialist responsible for maintaining compliance with GMP regulations and internal quality standards. The role involves overseeing Quality Systems, leading audits, and ensuring product quality. Candidates should have a degree in a relevant field and at least 2 years of experience in Quality Systems within the pharmaceutical industry. Strong analytical skills and attention to detail are essential for success in this challenging environment.

Qualifications

• Minimum of 2 years of experience in Quality Systems within the pharmaceutical industry.
• Strong knowledge of GMP regulations and quality management systems.
• Experience in sterile manufacturing or highly regulated production environments is an asset.

Responsibilities

• Maintain and oversee Quality Systems in compliance with GMP and regulatory requirements.
• Review and approve batch records and quality-related reports.
• Lead internal audits and support regulatory inspections.

Skills

Strong analytical skills

Attention to detail

Effective communication

Education

Degree in Pharmacy, Chemistry, Pharmaceutical Chemistry, or Biology

Job description

A global pharmaceutical organization in the UK seeks a Senior QA Specialist responsible for maintaining compliance with GMP regulations and internal quality standards. The role involves overseeing Quality Systems, leading audits, and ensuring product quality. Candidates should have a degree in a relevant field and at least 2 years of experience in Quality Systems within the pharmaceutical industry. Strong analytical skills and attention to detail are essential for success in this challenging environment.