Quality Systems Officer (QMS)

NMS Recruit Ltd t/a Russell Taylor Group; Knutsford; On-site; GBP 27,891 - 34,089; Full time

Benefits offered by this job

25 Days Holiday + BH

Company Pension

Onsite Parking

Job summary

NMS Recruit Ltd t/a Russell Taylor Group is seeking a Quality Systems Officer to join a growing pharmaceutical organisation in Cheshire on a permanent, onsite basis. The role focuses on maintaining the QMS, SOPs and document control, and supporting CAPAs, deviations, change controls and risk assessments.

You will assist with internal audits, audit readiness, and handling customer complaints and quality records, while keeping training records up to date and ensuring GMP compliance.

Qualifications

• Degree in a scientific discipline is preferred.
• GMP experience in Pharmaceutical/Biotech/Life Sciences.
• Knowledge of QMS processes (CAPAs, Deviations, Change Controls).
• Strong attention to detail and organisational skills.
• Good IT skills and confident communicator.

Responsibilities

• Maintain the Quality Management System (QMS) daily.
• Manage quality docs, SOPs and document control.
• Support CAPAs, Deviations, Change Controls and risk assessments.
• Assist internal audits and audit readiness activities.
• Support customer complaints, investigations and quality records.
• Maintain training records and GMP compliance.
• Contribute to continuous improvement initiatives.

Skills

GMP experience

Quality systems knowledge

Attention to detail

IT skills

Education

Degree in scientific discipline

Job description

Quality Systems Officer (QMS)

Location: Cheshire (Onsite) | Type: Permanent | Salary: Up to £30,990 DOE | Hours: Monday Friday (Days) | Benefits: 25 Days Holiday + BH, Company Pension, Onsite Parking

Our client, a growing pharmaceutical organisation, is seeking a Quality Systems Officer to join their Quality team. This is an excellent opportunity for someone with GMP experience looking to develop their career within Quality Assurance and Quality Systems.

Key Responsibilities

• Supporting the day-to-day maintenance of the Quality Management System (QMS)
• Managing quality documentation, SOPs and document control activities
• Supporting CAPAs, Deviations, Change Controls and Risk Assessments
• Assisting with internal audits and audit readiness activities
• Supporting customer complaints, investigations and quality records management
• Maintaining training records and ensuring compliance with GMP requirements
• Participating in continuous improvement initiatives across the business

Experience Required

• Degree qualified in a Scientific discipline (preferred)
• Previous GMP experience within Pharmaceutical, Biotechnology or Life Sciences
• Knowledge of QMS processes including CAPAs, Deviations and Change Controls
• Strong attention to detail and organisational skills
• Good IT skills and confident communicator

This is a fantastic opportunity to join a growing business where you can make a real impact while developing your career in Quality.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us.