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Do you want to join us in helping to fight the world's most threatening diseases and enabling access to care for more people around the world? At Siemens Healthineers, we pioneer breakthroughs in healthcare. For everyone. Everywhere.We offer you a dynamic environment with opportunities to go beyond your comfort zone in order to grow personally and professionally. Sound interesting?Then come and join our global team as Head of Quality ControlWithin the PETNET Nottingham site the Head of QC is responsible for managing the Quality Control department and relevant staff ensuring that the Quality Control department is fully operational and implemented within the local Quality Assurance System in compliance with local, regional and corporate requirements as well as with the national legislation.Your tasks and responsibilities:• Representing the QC department in the regular site management meetings.• Ensuring ongoing continuous development of the QC operators (PLP, training and rewards) to achieve a high performance of the QC department.• Performance of all necessary testing and environmental controls including evaluation of the associated records.• Qualification and maintenance of the QC equipment.• Performance of method validations• Performance of required investigation and Root Cause Analysis related to Out-of-Specification results, Deviations and Product Complaints• Reporting to the Facility Manager PETNET Nottingham regarding status and performance of the local QC department and related projects.• Responsible for line management of Quality Control chemists at the PETNET Nottingham site, ensuring that Quality Control activities are performed in accordance with cGMP.To find out more about the specific business, have a look at https://www.siemens-healthineers.com/en-uk/molecular-imaging/petnetYour qualifications and experience:5 years minimum within Manufacturing environment in Pharmaceutical Quality Control testing.Scientist with adequate background Analytical Chemistry.Proven experience in pharmaceutical quality control testing for product release. Strong knowledge of MHRA guidelines and GMP in the pharmaceutical sectorStrong written and verbal communication/presentation skillsHigh levels of commitment to customer serviceAnalytical chemistry experience including good knowledge of applicable techniques e.g. HPLC, GC.Experience in a site environment associated with the manufacture and/or commercial activities of PET radiopharmaceuticals is desirable.Working knowledge of the EA licensing process Experience in drafting SOPs.Have a strong knowledge of the business (portfolio, sector, competitors).Benefits:• 26 days' holiday with the option to buy or sell an additional 5• Up to 10% employer pension contribution• Share and bonus scheme• Access to our flexible benefits from private medical insurance to dental cover• Corporate Social Responsibility opportunities including 2 paid volunteering days per year and support from our 24/7 employee assistance programme.Our global team: We are a team of 66,000 highly dedicated employees across more than 70 countries passionately pushing the boundaries of what's possible in healthcare to help improve people's lives around the world. As a leader in the industry, we aspire to create better outcomes and experiences for patients no matter where they live or what health issues they are facing. Our portfolio, spanning from in-vitro and in-vivo diagnostics to image-guided therapy and innovative cancer care, is crucial for clinical decision-making and treatment pathways.Our culture:We are part of an incredible community of scientists, clinicians, developers, researchers, professionals, and skilled specialists pushing the boundaries of what's possible, to improve people's lives around the world. We embrace a culture of inclusivity in which the power and potential of every individual can be unleashed. We spark ideas that lead to positive impact and continued success.Salary: . Date posted: 04/03/2024 08:58 PM