Work ScheduleStandard (Mon-Fri) Environmental ConditionsLaboratory Setting Job Description Location: The role is currently based in Stevenage, with a planned move to Cambridge in 2029 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive
Jabil seeks a Director of Global Sterility Assurance to lead the strategy for sterilization, clean rooms, contamination control, and aseptic processing. You will be responsible for regulatory documentation, audits, and global remediation actions to ensure compliance and quality
Microbiology & Contamination Control Manager Permanent | Pharmaceutical / Biologics Manufacturing An exciting opportunity has arisen for an experienced Microbiology leader to take ownership of both QC Microbiology operations and site-wide Contamination Control Strategy (CCS) within
About Curia Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. We have a fantastic opportunity to come and join our Formulation team here in Glasgow. If you are looking to
Job ref: HOV Job type: Permanent Location: Newry Closing date: Tuesday 18 Aug :00 We are seeking an experienced and strategic Head of Validations to lead our global validation function across our pharmaceutical manufacturing operations. Reporting
Company Description Cell therapies have shown the ability to cure the incurable and yet we cannot get them to patients because of an inability to scale manufacturing. The Cellular Origins team is transforming patient access to
Job Description Summary As QA Manager - New Product Implementation at GE HealthCare, you will provide quality leadership for the development of innovative diagnostic radiopharmaceutical products and associated clinical manufacturing activities. You will serve as the
Job Title: UK Sales Manager Salary: £negotiable / highly competitve + commission + car + bonus + 25 days holiday + pension Location: home based with travel to UK customer sites and occasional European travel Incredible
Position Summary The Device Lead of Global MSAT Drug Delivery and Aseptic Technology will be the technical owner of the Device platform and be globally accountable for Device delivery into GSK Manufacturing sites from the Supply Base.
Job DescriptionGeneral/Position Summary The Director, Quality Assurance GMP Operations is responsible for the applicable Cell & Gene CDMO and is responsible for the end to end quality oversight of all product and activities at the CDMO. Responsibilities include day-to day operational quality oversight including assuring progression of batch record operations, resolution and on time disposition of product, quality continuous improvements, changes associated
Head of Validation An established pharmaceutical manufacturer is seeking an experienced Head of Validation to provide strategic and technical leadership across its validation function. You will lead a multidisciplinary team and oversee validation across equipment, facilities,
You will need to login before you can apply for a job. Employer Siemens Healthineers Location Northwood, United Kingdom Of Great Britain And Northern Ireland Salary Competitive Closing date 1 Oct 2026 At Siemens Healthineers (SHS)
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You will need to login before you can apply for a job. Head of Sterility Assurance, Italy (f/m/d) Employer Siemens Healthineers Location Northwood, United Kingdom Of Great Britain And Northern Ireland Salary EUR 80.00 - 90.00
Reference: PR/ _ Operational Excellence Engineer IILocation: Windsor, CO (Onsite)Schedule: Monday-Friday, 8:00 AM-5:00 PMOverviewOur client is seeking an Operational Excellence Engineer II to drive continuous improvement initiatives across pharmaceutical manufacturing and quality operations. This role will
Title:Sterility Assurance ExpertCompany:Ipsen Biopharm LtdAbout Ipsen:Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with
Mace combines construction expertise with consultancy to unlock potential in every person or project and redefine the boundaries of ambition. Our values shape the way we consult and define the people we want to join us
Reference: BBBH _ Microbiology & Contamination Control ManagerCentral Scotland | Permanent | Pharmaceutical / Biologics ManufacturingAn exciting opportunity has arisen for an experienced Microbiology leader to take ownership of both QC Microbiology operations and site-wide Contamination
Reporting to the Head of Quality UK, the QA and Validation Manager can be Located at a Choice of Company UK Locations and will have Responsibility for the Quality Assurance Projects Team ROLE Providing Quality and
Title: QC Micro & Sterility Assurance Company: Ipsen Biopharm Ltd About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by