SRG - QA Officer

Bionow; Manchester; On-site; GBP 30,000 - 40,000; Full time

Job summary

An award-winning CDMO in Greater Manchester is seeking an experienced QA Officer to support day-to-day QMS activities. You will ensure ongoing compliance with quality and regulatory standards, and your role includes assessing CAPAs and managing quality documentation. Candidates should have a degree in a relevant Scientific discipline and recent QA experience in a Pharmaceutical GMP environment.

Qualifications

• Recent QA experience within a Pharmaceutical GMP environment is crucial.
• Experience with Investigational Medicinal Products (IMPs) is advantageous.

Responsibilities

• Support day-to-day QMS activities.
• Ensure ongoing compliance with quality/regulatory standards.
• Assess and implement CAPAs and change controls.

Skills

Excellent communication skills

Attention to detail

Education

Degree in relevant Scientific discipline

Job description

SRG is currently working exclusively with a highly successful & award winning, CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials, and to approval. They are now looking for an experienced QA Officer to join the quality team, and support GMP operations.

Role

Working alongside the QA Manager you will be responsible for supporting the day-to-day QMS activities, ensuring the sites ongoing compliance with quality / regulatory standards and industry best practises.

Key duties

• Assessing & implementing CAPAs & change controls.
• Creating, reviewing, approving & managing quality documentation such as specification, SOPs, & protocols.
• Supporting QP release activities.

Requirements

• A degree or higher qualification in a relevant Scientific discipline
• Recent QA experience within a Pharmaceutical GMP environment
• Experience with Investigational Medicinal Products (IMPs) would be advantageous
• Excellent communication skills and a keen eye for detail