Quality Assurance officer

TieTalent; Manchester; On-site; GBP 30,000 - 35,000; Full time

Job summary

A leading quality-focused company in Greater Manchester seeks a Quality Assurance Officer to support GMP operations. The ideal candidate will have a degree in a relevant scientific discipline and recent QA experience in a Pharmaceutical GMP environment. Responsibilities include ensuring compliance with quality standards, investigating deviations, and managing quality documentation. This full-time role offers a salary of £30,000 - £35,000.

Qualifications

• Experience in a Pharmaceutical GMP environment.
• Experience with Investigational Medicinal Products (IMPs) would be advantageous.

Responsibilities

• Support day-to-day QMS activities to ensure compliance with standards.
• Investigate and address deviations.
• Assess and implement CAPAs and change controls.

Skills

Excellent communication skills

Attention to detail

Quality Management Systems (QMS)

Education

Degree in a relevant scientific discipline

Job description

Overview

Quality Assurance Officer – Greater Manchester – £30,000 - £35,000

SRG is currently working exclusively with a highly successful and award-winning CDMO based in Greater Manchester. Growing rapidly, the business specializes 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.

Responsibilities

• Working alongside the QA Manager you will be responsible for supporting the day-to-day QMS activities, ensuring the site\'s ongoing compliance with quality/regulatory standards and industry best practises.
• Investigating and addressing deviations.
• Assessing and implementing CAPAs and change controls.
• Supporting continuous improvement activities.
• Creating, reviewing, approving and managing quality documentation such as specifications, SOPs, and 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.

Note: Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

Job details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Quality Assurance
• Industries: Technology, Information and Internet