QA Officer: GMP Compliance & Batch Release Specialist

Nexus Life Sciences; Holt; On-site; GBP 30,000 - 35,000; Full time

Job summary

Nexus Life Sciences in Deeside, Wales, is seeking a QA Officer to join our pharmaceutical manufacturing team on-site. The role focuses on GMP compliance, documentation control, supplier management and contributing to a robust Quality Assurance function.

You will review batch records, support certification, manage non-conformances and CAPA, and assist internal audits while working with other departments to maintain compliance with the Pharmaceutical Quality System.

Qualifications

• A Degree in a Life Science discipline or equivalent industry experience.
• 2–3 years of QA experience in a pharmaceutical manufacturing environment.
• Knowledge of GMP, experience in and exposure to MHRA or customer audits.

Responsibilities

• Review executed Batch Manufacturing Records and associated documents to verify compliance with company procedures and GMP.
• Support batch certification activities and compile quality data for monthly and management review packs.
• Maintain and update logs for non-conformances, deviations, CAPA, change controls, cleaning records and document change requests.
• Issue controlled blank forms and support record management, filing and archiving.
• Liaise with suppliers to ensure documentation is current and compliant.
• Support internal audits, risk management activities, investigations and root cause analysis.
• Carry out routine QA administrative tasks to support the smooth running of the department.
• Work collaboratively with other departments to promote compliance with the Pharmaceutical Quality System.

Skills

GMP knowledge

Documentation control

Supplier management

CAPA

Change controls

Audit readiness

QA administration

MHRA audits

Education

Life Science degree

Job description

Nexus Life Sciences in Deeside, Wales, is seeking a QA Officer to join our pharmaceutical manufacturing team on-site. The role focuses on GMP compliance, documentation control, supplier management and contributing to a robust Quality Assurance function.

You will review batch records, support certification, manage non-conformances and CAPA, and assist internal audits while working with other departments to maintain compliance with the Pharmaceutical Quality System.