Qc/Qa Officer Oxford

Curium Live Forward

Oxford

On-site

GBP 28,000 - 38,000

Full time

14 days+

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Job summary

Curium Live Forward is seeking a Quality Control professional to perform QC testing on radiopharmaceuticals and support GMP compliant operations at the Oxford radiopharmacy. The role involves reviewing production methods against GMP guidelines, updating SOPs, and assisting with deviations and CAPA processes.

The successful candidate will have a related science degree and experience in radiopharmacy or QC, with strong attention to detail and good communication skills.

Qualifications

  • Knowledge of radiation (Desirable)
  • Shift work required
  • Related Science Degree
  • Quality Control Experience desirable
  • Radiopharmacy Experience desirable

Responsibilities

  • Perform quality control testing on radiopharmaceuticals in accordance with SmPC, EP and GMP guidelines
  • Review and update SOPs and forms to ensure GMP compliance
  • Assist with deviations, incidents, investigations, OOS, CAPA, Change control and release of incoming materials
  • Review QC tests and Micro results; manage Out of Specification results
  • Maintain GMP-compliant quality records and trackers; keep QMS up to date
  • Participate in root cause analysis and CAPA identification
  • Monitor aseptic suite operations including sanitation and environmental/radiation monitoring
  • Record logs for fridges, freezers, isolators and other equipment logs

Skills

Team player
Basic computer skills
Customer relations
Communication skills
Attention to detail
Stress management

Education

Related Science Degree
Radiopharmacy Experience desirable

Job description

Summary of Position

To perform quality control on radiopharmaceuticals and assist with maintenance of the Radiopharmacy in accordance with principles of Good Manufacturing Practice.

Essential Functions

  • Reviewing compliance of production and analytical methods with GMP/specials guidelines and EP, BP and/or SmPC
  • Review and update SOPs and forms
  • Assist with deviations, incidents and investigations, OOS, CAPA, Change control and release of incoming materials
  • Review QC tests and Micro results, managing Out of specification results
  • Ensure timely completion and update of all Quality records and trackers
  • Support the site to ensure it is GMP complaint by making sure SOPs are up to date
  • Assist with elements of the QMS including Deviations, Complaints, OOS, CAPA, Change Control, Recall, Micro Out of Specification, Risk Assessments and related trending
  • Sanitation and transferring of consumables in the aseptic suite and isolators
  • Cleaning the isolators and Radiopharmacy facility according to SOP’s
  • Aseptic Suite monitoring including Environmental monitoring, Radiation monitoring
  • Recording of the logs for fridge, freezers, isolator checks and all other logs
  • Raising and completing deviation reports OOS and MOOS where applicable
  • Participate in Root Cause Analysis and CAPA identification
  • Effective communication with all colleagues to facilitate efficiency in both production and quality related matters
  • Ensure all GMP guidelines and processes are followed
  • Goods in check/inspection as part of quality inspections of incoming materials
  • Adherence to legal and organizational procedures & guidelines about quality, safety, health and environmental issues
  • Training of Technicians in QC
  • Accurately perform Quality Control testing on all manufactured products at the Oxford Radiopharmacy according to SmPC and EP guidelines
  • Manage Environmental Monitoring process and ensure data are recorded and trended in the QMS
  • Reading Microbiological plates, broth and sterility samples
  • Interpretation and recording of Microbiological data and report any out of specifications ensuring appropriate action is taken in a timely manner
  • First line maintenance of equipment
  • Review and maintain QC logbooks and data to ensure the site meets all its objectives in relation to data integrity policy
  • Responsible for validation activities, and preparation and execution of protocols.
  • Setting up production orders in the system
  • Checking stock level and ordering products

Requirements

Level of professional and intellectual ability

  • Knowledge of radiation (Desirable)
  • Shift work required

Education/experience

  • Related Science Degree
  • Quality Control Experience desirable
  • Radiopharmacy Experience desirable

Skills

  • Excellent team player
  • Basic computer skills
  • Good customer relation skills
  • Communication skills
  • Practical ability
  • Excellent timekeeping competences
  • Stress handling
  • Excellent attention to detail
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