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Apply now for the position of Chemist where you will be responsible for manufacturing or testing PET Radiopharmaceuticals. The role will ensure that the requirements of radiopharmaceutical manufacturing, testing, Radiation compliance, Health & Safety, Good Manufacturing Practice and licensing commitments are met. 

The role requires shift work (night shifts starting at 9 pm or midnight, day shifts starting at 5 am, 6 am, or 7 am), Monday-Saturday.

The role will be located in Northwood initially but will be moved to Dunstable in late 2025/early 2026.

We hiring 2 different roles - production and QC chemists. Please clarify in your application which of the roles you are interested in.

1. QC Chemist

Your role: 

Perform QC testing of radiopharmaceuticals according to Marketing Authorisations and/or specials license, ensuring that QC activities are performed to the PETNET Quality System in accordance with cGMP. Carry out environmental monitoring according to schedule. Assist in the periodic review of PETNET standard operating procedures and writing of new procedures as required. Report monthly customer doses/missed doses/credits to account s for monthly billing. Assist in facility preparation for audits and inspections. Ensure adequate stock levels of consumables are maintained. Shipment of dangerous goods according to ADR regulations. Ensure ongoing continuous professional development to achieve full awareness and technical knowledge of all current legislation and scientific development associated with PET radiopharmaceuticals and their testing. Work with other PETNET staff to ensure alignment of operational processes and back up capabilities across all PETNET sites. Operation of the cyclotron particle accelerator. 

Your expertise:

Relevant science degree Radiopharmaceutical or pharmaceutical testing experience Experience in analytical chemistry methods (HPLC, GC) Knowledge of cGMP standards

2. Production Chemist

Your role:

Manufacture radiopharmaceuticals in compliance with Marketing Authorisations and/or specials licenses, ensuring production activities adhere to the PETNET Quality System and cGMP standards. Perform cleaning and maintenance of clean rooms and associated equipment. Assist in the periodic review and drafting of PETNET standard operating procedures as needed. Work according to a shift pattern that meets customer demands and business needs, occasional weekend work Assist in the preparation of the facility for audits and inspections. Maintain adequate stock levels of consumables. Handle the shipment of dangerous goods in accordance with ADR regulations. Engage in continuous professional development to stay informed of current legislation and scientific advancements in PET radiopharmaceuticals and their production. Collaborate with other PETNET staff to ensure the alignment of operational processes and backup capabilities across all PETNET sites. Operate the cyclotron particle accelerator.

Your expertise:

Relevant science Degree Radiopharmaceutical or pharmaceutical production experience Clean room experience Knowledge of cGMP standards

Benefits:

·A competitive salary

·Generous pension contributions

·26 days holiday

·Access to our flexible benefits from private medical insurance to dental cover

·Corporate Social Responsibility opportunities including 2 paid volunteering days per year

·Support from our 24/7 employee assistance programme

Who we are:
We are a team of more than 71,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision-making and treatment pathways.

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