Product Regulatory Specialist Jobs in Cambridge, East of England, England | Glassdoor
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Product Regulatory Specialist Jobs in Cambridge, East of England, England

44 Jobs

  • Quality Start – Cambridge, East of England, England
    NEW
    assurance and regulatory affairs experience? Have you implemented and developed a companys quality and regulatory affairs strategy… developing the companies quality and regulatory affairs business strategy in line with regulatory and quality standards such as the…
  • 4.5
    i-Pharm Consulting Ltd – Cambridge, East of England, England
    NEW
    ABOUT i-PHARM REGULATORY i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market… designated regulatory labeling variations submissions for marketed products across the EE&ME region. Liaises with regulatory, manufacturing…
  • 4.3
    Cambridge Consultants – Cambridge, East of England, England
    NEW
    and manufacturing criteria Applying your knowledge of the regulatory landscape to ensure standards-compliant design Requirements… for product or system developments Working with multidisciplinary teams to deliver robust system solutions and products ready…
  • Marketplace Group – Cambridge, East of England, England
    6 days ago 6d
    Specialist Medical Device Manufacturer requires a Regulatory Affairs Associate to assist the regulatory team to ensure compliance… importing products. Carrying out legalisation of documents Complete paperwork and other requirements for regulatory submissions…
  • 4.5
    i-Pharm Consulting Ltd – Cambridge, East of England, England
    NEW
    i-Pharm Consulting is a specialist recruitment company focused on mid to high-level roles in Regulatory Affairs. We recruit for… expand their Regulatory Team. Their sole focus is to facilitate the translation of great science into medicinal products which benefit…
  • 3.6
    Vivid Resourcing – Cambridge, East of England, England
    NEW
    update existing SOPs to improve finished product QC testing and to comply with regulatory (EPA, DNR), compendial (FCC, USP), and/… Conduct validation studies for new methods, equipment and products. Guide multi-disciplinary teams in validation studies. Critically…
  • 3.6
    Vivid Resourcing Ltd – Cambridge, East of England, England
    7 days ago 7d
    Assurance Specialist is to perform routine quality assurance tasks and activities ensuring compliance with all regulatory and corporate… activities to ensure product is manufactured, packaged, tested, released and distributed in compliance with all regulatory and corporate…
  • Quality Start – Cambridge, East of England, England
    20 days ago 20d
    assurance and regulatory affairs experience? Have you implemented and developed a company’s quality and regulatory affairs strategy… developing the companies quality and regulatory affairs business strategy in line with regulatory and quality standards such as the…
  • 4.0
    Arm Holdings – Cambridge, East of England, England
    15 days ago 15d
    globally in respect of privacy and data protection regulatory compliance in all contexts. Provides timely and business focussed… processes, and where required the same for other areas of regulatory compliance (such as anti-bribery, competition law etc). Develop…
  • 3.8
    Amgen – Cambridge, East of England, England
    NEW
    experience in the Pharma/Biotech industry, especially within the regulatory. Ability to understand business functionality and translate… Specialist IS Business Systems Analyst The Company: Amgen is one of the world's largest independent biotechnology companies…
  • 3.7
    Zoek UK – Cambridge, East of England, England
    7 days ago 7d
    , validation, regulatory submission, stakeholder, consultancy, GMP, Good Manufacturing, remediation, new product development, design… Engineering or Sciences NPD/NPI Transfer to manufacture Regulatory submission Quality ISO 13485, ISO 14971 Strong communication…
  • 3.4
    MedImmune – Cambridge, East of England, England
    21 days ago 21d
    interactions with regulatory authorities as needed. Communicate toxicology data internally and to Research Project and Product Development… suitable for regulatory submission, in collaboration with Associate Toxicologists and Toxicologists. Contribute to regulatory documents…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    14 days ago 14d
    engagement and ensuring interface & alignment with payer, and regulatory initiatives. Will work with medical colleagues across the… scientific evidence and content on AZ products and disease areas of focus to support generation of product value messages to internal and…
  • 5.0
    Gold Group Ltd. – Cambridge, East of England, England
    21 days ago 21d
    in the generation of design validation and human factors regulatory documentation for assigned devices To provide guidance to… for assigned projects Support the generation of device regulatory submission data Provide input into risk management activities…
  • 3.2
    Mundipharma Research – Cambridge, East of England, England
    13 days ago 13d
    electronic databases. Global Safety-Regulatory knowledge of applicable pharmacovigilance regulatory requirements. Project management… Vigilance Standards and Collaborations Specialist Vigilance Standards und Collaborations Specialist Location Cambridge (UK)…
  • 4.7
    Gold Group – Cambridge, East of England, England
    21 days ago 21d
    in the generation of design validation and human factors regulatory documentation for assigned devices To provide guidance to… for assigned projects Support the generation of device regulatory submission data Provide input into risk management activities…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    NEW
    in commercial, early stage development; Medical Affairs, Regulatory, Government Affairs, MCs, as well as within the Global Payer… least one global Oncology launch as pricing and market access specialist. Knowledge of the needs and expectations of national and…
  • 4.5
    JCW Search Ltd – United Kingdom
    Today 3hr
    quality, safety, best practice and adherence to cGMP and regulatory requirements Degree Level Education preferably in Chemical… pharmaceutical processes and utility systems to cGMP and regulatory requirements. If you think that this is an opportunity…
  • 3.7
    Zoek UK – Cambridge, East of England, England
    25 days ago 25d
    , validation, regulatory submission, stakeholder, consultancy, GMP, Good Manufacturing, remediation, new product development, design… Engineering or Sciences *NPD/NPI Transfer to manufacture *Regulatory submission *Quality ISO 13485, ISO 14971 *Strong communication…
  • 5.0
    The One Group – Cambridge, East of England, England
    30+ days ago 30d+
    projects and awareness of the regulatory requirements with regards to IT systems. To be a willing, productive and co-operative member… and Cambridgeshire. Our recruitment experts provide specialist consultancy staffing services to some of the leading household…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    25 days ago 25d
    the pharmaceutical industry and regulatory requirements from a global perspective and product development processes at all life… produce (or direct the production of) scientific evidence for regulatory submissions, global reimbursement dossiers and market access…
  • 3.7
    Zoek UK – Cambridge, East of England, England
    22 days ago 22d
    ) International If you are an experienced Regulatory Affairs and CMC specialist looking for a step up in your career, we have… Cambridge area, this company offers a wide range of successful products while also providing their services to a broad network of partners…
  • 4.2
    Hays Specialist Recruitment Limited – United Kingdom
    14 days ago 14d
    A good understanding of European regulatory requirements and guidelines for generic products. Previous CMC experience (or a demonstrated… Regulatory Affairs Manager EU Harlow Your new company Have you got experience in European Regulatory Affairs, with a Life…
  • 5.0
    Ceema Technology Recruitment Limited – Letchworth Garden City, England
    NEW
    working environment and delivers products OTIF to the production plan, meeting all quality, regulatory and legislative requirements… in helping candidates find quality placements. Our team of specialist consultants have significant experience within the recruitment…
  • 3.6
    AstraZeneca – Cambridge, East of England, England
    14 days ago 14d
    engagement and ensuring interface & alignment with payer, and regulatory initiatives. Will work with medical colleagues across the… scientific evidence and content on AZ products and disease areas of focus to support generation of product value messages to internal and…
  • 3.1
    Costello Medical Consulting – Cambridge, East of England, England
    22 days ago 22d
    such events. In addition, you may have the chance to work on regulatory documents, lay summaries and policy-related publications.… scientific publications, book chapters, grant applications, regulatory documents If you wish to speak directly to one our Analysts…
  • 3.0
    GW Pharmaceuticals – Cambridge, East of England, England
    15 days ago 15d
    Knowledge of medical information systems, pharmacovigilance and regulatory requirements. Ability to analyze and appraise clinical, biomedical… providing brand support for assigned therapeutic area as well as specialist Medical Information support. Responsibilities: Provide…
  • 3.6
    Barclays – United Kingdom
    NEW
    negotiator. We will expect you to attain the highest standards of regulatory compliance and customer satisfaction, and in return will give… Regulations and may require the role holder to hold mandatory regulatory qualifications or the minimum qualifications to meet internal…
  • 1.0
    Freight Personnel – Cambridge, East of England, England
    8 days ago 8d
    best-in-class industry experts in quality, cold chain and regulatory compliance amongst others. They have offices in China, Japan… Providing chain of custody details to the customer for specialist shipments Receiving feedback from the consignee and following…
  • 3.2
    Bosch Global Associates Ltd – Cambridge, East of England, England
    30+ days ago 30d+
    relevant regulatory requirements Project management: Lead projects including regularly reviews of all 'scheduled product development… Proficiency in the creation of regulatory submission reports for medical devices and combination products. Management experience of…
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