Part-Time QA Advisor: GMP Compliance & Audits

Pharmaron; Hoddesdon; On-site; GBP 14,000 - 22,000; Part time

Job summary

Pharmaron Hoddesdon is seeking a Part-time QA Advisor (2 days per week) to join our Quality Assurance team. You will support the day-to-day operation of the electronic Quality Management System (eQMS) and help ensure GMP compliance across API and Drug Product manufacturing activities.

Key duties include handling quality systems, supporting audits, managing deviations, CAPAs, change controls, and training administration, with a focus on continuous improvement and a strong quality culture across

Qualifications

• BSc degree in Chemistry or a related scientific discipline.
• 1–2 years of Quality Assurance experience in an API or Drug Product GMP environment.
• Strong knowledge of GMP guidelines (Eudralex Volume 4 Parts I & II, ICH).

Responsibilities

• Quality Systems & Documentation: input, propose and modify SOPs with guidance; review quality systems and generate metrics; support qualification and validation activities; review stability protocols and reports; support vendor qualifications and reviews.
• Audit & Inspection Support: assist in audit preparation and provide back-room support during client and regulatory inspections (e.g., MHRA).
• Deviation, CAPA & Change Control Management: investigate deviations and quality issues; support change controls and OOS investigations; track CAPAs to closure.
• Training & System Support: administer Training Management System; release GMP manufacturing materials as requested.
• Quality Culture & Compliance: uphold GMP principles and Pharmaron policies; promote a culture where quality is everyone’s responsibility; encourage continuous improvement.

Skills

GMP knowledge

Attention to detail

Documentation & QA

Education

BSc Chemistry

Tools

Microsoft Word

Excel

PowerPoint

Job description

Pharmaron Hoddesdon is seeking a Part-time QA Advisor (2 days per week) to join our Quality Assurance team. You will support the day-to-day operation of the electronic Quality Management System (eQMS) and help ensure GMP compliance across API and Drug Product manufacturing activities.

Key duties include handling quality systems, supporting audits, managing deviations, CAPAs, change controls, and training administration, with a focus on continuous improvement and a strong quality culture across