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Project qc radiochemist

Dinnington
Alliance Medical
€50,000 a year
Posted: 9 June
Offer description

Role Overview

We are seeking a Project QC Radiochemist to provide Quality Control and validation expertise across Alliance Medical Radiopharmacy’s UK network. Reporting to the Senior QC Manager, this role sits within the Quality function and works collaboratively with Validation, Quality Assurance, Operations and site‑based QC teams.

This is a cross‑site role combining strategic oversight with hands‑on technical involvement, supporting routine commercial operations, new product introductions and development programmes while ensuring regulatory compliance and inspection readiness.

The Project QC Radiochemist plays a key role in maintaining and enhancing consistent QC and validation standards across multiple radiopharmacy facilities.


Key Responsibilities

* Providing QC and validation oversight across UK Radiopharmacy sites, ensuring compliance with GMP, GDP and MHRA requirements
* Acting as a key interface between Quality Control, Quality Assurance and Project teams
* Supporting QC project activities, including method development, validation and continuous improvement initiatives
* Preparing, executing and reporting validation and qualification protocols
* Providing QC input into product development, technology transfer and new product introductions
* Supporting regulatory inspections, audits and responses, and maintaining ongoing compliance commitments
* Reviewing and approving quality and regulatory documentation, including SOPs, validation protocols and reports
* Coaching and mentoring site teams in QC method development and best practice


Qualifications

* A degree in a scientific discipline or equivalent experience within a pharmaceutical setting
* Significant Quality Control experience, ideally 5+ years, within radiopharmacy, sterile manufacturing, nuclear medicine or aseptic processing
* Proven experience in QC method validation, equipment qualification and project support
* Strong knowledge of GMP and regulatory requirements
* Experience with analytical QC equipment such as HPLC, GC, rTLC and related techniques
* Excellent communication and stakeholder‑management skills, with confidence working across multiple sites
* Strong organisational skills, attention to detail and the ability to work autonomously and proactively
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