QC/QA Officer

Hyper Recruitment Solutions; North East; Sur place; GBP 38 000 - 54 000; Plein temps

Résumé du poste

Hyper Recruitment Solutions is seeking a QA/QC Officer for a leading nuclear medicine organisation in the North East. You will support quality control, environmental monitoring and QC testing to GMP guidelines, working with production and quality teams to ensure patient-focused outcomes.

The role requires a degree in a relevant science, proven QC experience, GMP knowledge and good communication. Radiopharmacy experience is desirable with flexibility for shift work where needed.

Qualifications

• Degree or higher in a relevant scientific field (Pharmaceutical Chemistry, Chemistry, Biology, Radiopharmacy).
• Proven experience in quality control with GMP knowledge and data interpretation.
• Radiopharmacy experience is desirable; willingness to undertake shift work where required.
• Excellent attention to detail, communication and organisational skills; teamwork and time management.

Responsabilités

• Support quality control and release of radiopharmaceutical products to EP and GMP standards.
• Review and maintain SOPs, QC logbooks and quality records to ensure data integrity.
• Assist with deviations, CAPA, change control and root cause investigations.
• Perform environmental and radiation monitoring, and validation activities as required.
• Train technicians in QC activities and promote compliance with safety and procedures.

Connaissances

Quality control

GMP knowledge

Radiopharmacy

Attention to detail

Teamwork

Communication

Formation

Degree in Pharmaceutical Chemistry, Chemistry, Biology, Radiopharmacy or related field

Description du poste

Role Overview

We are currently looking for a QA/QC Officer to join a leading nuclear medicine organisation based in the North East. This is an exciting opportunity to support the quality control of radiopharmaceutical products and the maintenance of a Radiopharmacy in accordance with Good Manufacturing Practice (GMP). The successful candidate will contribute to quality systems, environmental monitoring, validation activities and accurate QC testing, while working collaboratively with production and quality teams to support patient-focused outcomes.

Key Duties And Responsibilities

Your duties as the QA/QC Officer will be varied however the key duties and responsibilities are as follows:

• Support the quality control and release of manufactured radiopharmaceutical products, ensuring testing is completed accurately in line with applicable product specifications, European Pharmacopoeia (EP) requirements and GMP guidelines.
• Review and maintain SOPs, forms, QC logbooks, quality records and trackers to support compliance, data integrity and ongoing site objectives.
• Assist with quality management system activities, including deviations, incidents, Out of Specification results, CAPA, change control, complaints, recalls, risk assessments, investigations and root cause analysis.
• Perform and coordinate environmental and radiation monitoring, microbiological testing, facility and isolator cleaning, incoming goods inspections, equipment checks and relevant validation activities.
• As the QA/QC Officer you will support effective communication across production and quality teams, train Technicians in QC activities, assist with equipment maintenance and help ensure all legal, safety, health, environmental and organisational procedures are followed.

Role Requirements

To be successful in your application to this exciting role as the QA/QC Officer we are looking to identify the following on your profile and past history:

• A Degree or higher level in a relevant scientific field, such as Pharmaceutical Chemistry, Chemistry, Biology, Radiopharmacy or a related discipline.
• Proven experience in quality control, with knowledge of pharmaceutical chemistry, GMP and the accurate review and interpretation of analytical or microbiological data.
• Radiopharmacy experience and knowledge of radiation are desirable, alongside the flexibility to undertake shift work where required.
• Excellent attention to detail, communication and organisational skills, with practical ability, basic computer proficiency, strong teamwork, effective time management and the ability to manage competing priorities.

WHAT’S IN IT FOR YOU?

• The opportunity to contribute to the quality and safety of radiopharmaceutical products that support patient care.
• A varied role combining quality control, quality systems, environmental monitoring, validation and Radiopharmacy activities.
• The opportunity to develop leadership capability by supporting Technician training and contributing to GMP compliance across the site.
• The chance to work collaboratively with production and quality colleagues in a supportive, detail-focused environment.

Key Words: QA/QC Officer / Quality Control / Radiopharmacy / Radiopharmaceuticals / Good Manufacturing Practice / GMP / Quality Management System / QMS / Environmental Monitoring / Microbiology / Validation / CAPA / Deviations / Out of Specification / OOS / Data Integrity / Pharmaceutical Chemistry / Quality Assurance / Nuclear Medicine

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements.