Quality Control Supervisor Job at Alliance Medical Ltd (Guildford)

Quality Control Supervisor

Alliance Medical Ltd

Location:
United Kingdom , Guildford

Category:
Quality Control

Contract Type:
Not provided

Salary:

Not provided

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Job Description:

We are looking for a dedicated Quality Control Supervisor to join our Radiopharmacy team. This is a senior role within the QC function, offering the opportunity to lead a team, drive high standards, and support the reliable operation of our Radiopharmaceutical Production. As the QC Supervisor, you will oversee the day‑to‑day delivery of Quality Control activities within the Radiopharmaceutical Production Unit. You will ensure full compliance with Good Manufacturing Practice (GMP), provide leadership and guidance to QC staff, and support the safe, reliable, and efficient operation of the facility. In this role, you will work closely with the QC Manager and deputise for them when required. You will also be appointed as a Radiation Protection Supervisor, supporting the safe handling and disposal of radioactive materials throughout the QC process. Flexibility is essential, as the role occasionally requires working unsociable hours, weekends, and providing short-notice support to meet operational and service needs.

Job Responsibility:

Oversee day-to-day QC activities for all radiopharmaceutical products
Maintain full competency in QC analysis and participate in routine testing
Manage raw materials including testing and release
Oversee environmental monitoring and media fills
Communicate any equipment, facility, or process issues to management
Share best practice across the UK radiopharmacy network
Undertake training to perform frontline fault diagnosis
Support QC Manager and OEM engineers during maintenance, testing, and validation
Support routine calibration of all QC equipment
Liaise with QC Managers to ensure adequate resources meet operational demands
Provide occasional out-of-hours support, including weekends, evening work, and short-notice cover
Support validation and recovery activities following maintenance
Provide cover for night shift QC when required
Support validation projects and new product introductions
Prepare, execute, and report validation protocols
Lead routine qualification of QC equipment including HPLC, GC, rTLC, and dose calibrators
Assist with validation activities following equipment upgrades
Support delivery of training plans and development of QC staff
Take part in internal and external training, including Radiation Protection Supervisor (RPS) certification
Maintain accurate records of equipment, operational, and environmental faults
Assist with fault interpretation and rectification and escalate when required
Ensure documentation is completed and submitted to the relevant manager
Follow Good Manufacturing Practice (GMP), Quality Control, and Quality Assurance procedures
Complete Deviations, CAPAs, Change Controls, OOS/OOT reports within agreed timelines
Contribute to SOP updates, QA reporting, and internal audits
Work in accordance with site safety procedures
Act as a Radiation Protection Supervisor (RPS), ensuring adherence to local rules and safe handling of radiopharmaceuticals
Manage radioactive waste safely and supervise team compliance
Follow site security plans and assist with emergency exercises
Adhere strictly to GMP, GLP, and safety protocols required by MHRA, EA, HSE, and ONR
Comply with local rules and licensing conditions

Requirements:

Educated to degree level in a relevant scientific discipline
Appropriate industrial experience in QC testing of pharmaceuticals
Experience in radiopharmacy is highly desirable
Previous experience in QC testing of radiopharmaceuticals within a GMP‑compliant environment
Experience in the operation, maintenance, and validation of QC equipment (HPLC, GC, rTLC, Gamma spectrometry, Traditional wet chemistry techniques)
Understanding of completing maintenance activities within a GMP‑regulated facility
Experience working in a radiation‑controlled environment is desirable
Proficient in Microsoft Windows, Word, Excel, PowerPoint, and Project
Excellent written and verbal communication skills
Strong interpersonal skills
Highly organised and reliable, with strong timekeeping
Exceptional attention to detail
Active listening skills
Self-motivated, proactive, and able to work independently
Leads by example, demonstrating professionalism and accountability
Strong working knowledge of regulatory requirements including GMP and safety standards

Nice to have:

Experience in radiopharmacy
Experience working in a radiation‑controlled environment

Additional Information:

Job Posted:
February 18, 2026

Employment Type:

Fulltime

Work Type:

On-site work

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