Quality Operations Specialist - GCP & SOPs, Hybrid Contract

ARM; Slough; Hybrid; GBP 50,000 - 70,000; Full time

Job summary

A leading multinational biopharmaceutical company is seeking a Quality Operations Specialist in Slough. The role involves supporting quality systems and compliance, with a focus on GCP regulations and SOP writing. The ideal candidate has over 8 years of pharmaceutical experience and will work in a hybrid setting, with at least 2 days on site. This is a contract position inside IR35, initially for 12 months.

Qualifications

• 8+ years of pharmaceutical experience, preferably in a global quality assurance or clinical development setting.
• In-depth experience of GCP audits and inspections.
• 2+ years of experience in SOP writing essential.

Responsibilities

• Support the Head with quality and compliance infrastructure development.
• Collaborate with Global Quality, Patient Safety, and Regulatory Affairs.
• Drive inspection readiness activities across functions.
• Participate in audit and inspection planning.
• Ensure representation during audits and inspections.

Skills

GCP regulations

SOP writing

Quality compliance

Audit preparation

Collaboration with stakeholders

Job description

A leading multinational biopharmaceutical company is seeking a Quality Operations Specialist in Slough. The role involves supporting quality systems and compliance, with a focus on GCP regulations and SOP writing. The ideal candidate has over 8 years of pharmaceutical experience and will work in a hybrid setting, with at least 2 days on site. This is a contract position inside IR35, initially for 12 months.