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Qualified Person; Radiopharma

Job in Northwood, Worth County, Iowa, 50459, USA
Listing for: Siemens Mobility
Full Time position
Listed on 2026-06-28
Job specializations:
  • Healthcare
    Medical Science
  • Quality Assurance - QA/QC
Salary/Wage Range or Industry Benchmark: 61157 - 81543 USD Yearly USD 61157.00 81543.00 YEAR
Job Description & How to Apply Below
Position: Qualified Person (Radiopharma)
Location: Northwood

Qualified Person (QP) PETNET UK - Northwood, England

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

As part of Siemens Healthineers, PETNET is at the forefront of radiopharmaceuticals and molecular imaging. We work with some of the world’s leading research organisations, pioneering new biomarkers and changing nuclear medicine for physicians and patients. With nearly 50 radiopharmaceutical distribution centres across the world, we are one of the largest PET biomarker producers globally. We are committed to developing innovative PET tracer technologies, thus helping to expand and advance the science of molecular imaging.

We’re looking for a Qualified Person (QP) to join our PETNET team in Mount Vernon Hospital. In this essential role, you’ll ensure the certification and release of medicinal products produced at our Mount Vernon site, with future support for a new site in Dunstable.

Your role
  • Product Certification & Compliance
    :
    Certify and release batches according to UK and EU GMP, ensuring full compliance with regulatory standards and documentation.
  • Quality Assurance
    :
    Oversee quality control tests, manage deviations, and maintain a high standard in manufacturing, testing, and supply chain documentation.
  • Quality System Management
    :
    Lead the Quality Management System (QMS) at the site, collaborating with UK and European quality teams to uphold consistent, compliant practices.
  • Collaborative Support
    :
    Act as a back-up QP for Nottingham’s site when needed, ensuring seamless quality management and regulatory compliance.
Your expertise
  • Qualifications
    :
    Degree in Life Sciences; eligible to act as a Qualified Person in the UK/EU.
  • Core Skills
    :
    Strong problem‑solving, effective communication, and detailed knowledge of GMP regulations.
  • Experience
    :
    Familiarity with quality management across the full pharmaceutical lifecycle.
  • 26 days of holidays
  • Flexible benefits, including medical cover
  • Pension contribution (match up to 10%)
  • Company shares

As an equal opportunity employer, we welcome applications from individuals with disabilities.

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