Regulatory Compliance Specialist

6 days ago


Cambridge, Cambridgeshire, United Kingdom Regeneron Pharmaceuticals, Inc Full time

Job Summary

We are seeking a highly skilled and experienced Senior Quality Control Specialist to join our Quality Control team at Regeneron Pharmaceuticals, Inc. as a part of our new Regeneron Cell Medicines group.

Key Responsibilities

  • Oversee contract lab testing and support safety testing for novel drug products targeting oncological indications.
  • Provide oversight for the testing of release, stability, and routine environmental monitoring samples via contractors.
  • Train and oversee internal environmental monitoring once brought in-house.
  • Serve as the subject matter expert for environmental monitoring issues and provide technical expertise aligned with current GMPs.

Day-to-Day Activities

  • Manage the contract testing laboratory for microbial testing of in-process and final product.
  • Oversee sample collection, shipment, receiving, and reviewing test data, and deliver the results internally.
  • Oversee environmental monitoring contractors for manufacturing suites, including ensuring samples are collected at determined frequency, receiving results of sampling, and delivering results internally.
  • Support the establishment of rapid microbial method testing for lot release of drug product to support internal clinical manufacturing.
  • Support the set up, management, and maintenance of the Environmental Monitoring program for an internal manufacturing site.
  • Support all aspects of microbial testing, from sample receipt and chain of custody through generation of CoTs.
  • Provide expertise to support investigations, deviations, and CAPAs.
  • Implement process improvements to support operational efficiencies.
  • Promote a culture of Quality and Operational excellence.

Requirements

  • Highly collaborative team player who fosters open communication and facilitates mutual understanding and cooperation between all stakeholders (internal and external).
  • Demonstrated leadership within teams producing results.
  • Ability to communicate effectively in a way that fosters positive relationship building.
  • Passion for addressing the critical unmet medical needs of patients.
  • Self-directed individual who can work in a risk-tolerant, fast-paced, innovative environment.

Education and Experience

  • At least a Bachelor's degree.
  • 5+ years of relevant experience.
  • Biopharmaceutical/industry experience in the cell and gene therapy space is strongly preferred.
  • Experience with environmental monitoring, aseptic processing, and microbial testing.
  • Strong understanding of cGMP/ICH/FDA/EU guidance and regulations relating to safety testing of biologics or cell and gene therapies.
  • Leading activities in microbiology laboratories that support sterile manufacturing required.
  • Experience in site start-up operations is a plus.

About Regeneron Cell Medicines

Regeneron Cell Medicines (RCM) has been created to advance the next generation of cell therapies and explore combinations with Regeneron's proprietary antibodies and bispecifics. We are a group of about 160 research, development, manufacturing, and clinical employees based in Seattle, WA and Cambridge, MA.



  • Cambridge, Cambridgeshire, United Kingdom Reed Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Regulatory Compliance Specialist to join our team at Reed. As a key member of our regulatory affairs department, you will play a critical role in ensuring the smooth operation of our product compliance functions.Key ResponsibilitiesRegulatory SupportPrepare and submit regulatory documents,...


  • Cambridge, Cambridgeshire, United Kingdom Reed Full time

    Job SummaryWe are seeking a highly organized and detail-oriented Regulatory Compliance Specialist to join our team at Reed. As a key member of our regulatory affairs department, you will play a critical role in ensuring the smooth operation of our product compliance functions.Key ResponsibilitiesRegulatory SupportPrepare and submit regulatory documents,...


  • Cambridge, Cambridgeshire, United Kingdom Abcam Full time

    About AbcamAbcam is a leading provider of tools for the scientific community, enabling breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders.We believe that collaboration and innovation are key to making progress. Our team is dedicated to working together to bring about positive change in the...


  • Cambridge, Cambridgeshire, United Kingdom Abcam Full time

    About AbcamAbcam is a leading provider of tools for the scientific community, enabling breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders.We believe that collaboration and innovation are key to making progress. Our team is dedicated to working together to bring about positive change in the...


  • Cambridge, Cambridgeshire, United Kingdom Newton Colmore Consulting Ltd Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Specialist to join our team at Newton Colmore Consulting Ltd. As a Quality Engineer, you will play a critical role in ensuring the quality and safety of our Medical Devices.Key ResponsibilitiesCollaborate with cross-functional teams, including Mechanical Engineers, Physicists, Electronics...


  • Cambridge, Cambridgeshire, United Kingdom Newton Colmore Consulting Ltd Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Specialist to join our team at Newton Colmore Consulting Ltd. As a Quality Engineer, you will play a critical role in ensuring the quality and safety of our Medical Devices.Key ResponsibilitiesCollaborate with cross-functional teams, including Mechanical Engineers, Physicists, Electronics...


  • Cambridge, Cambridgeshire, United Kingdom Cambridge University Press Full time

    Are you ready to explore your potential? We are seeking a dedicated Compliance Manager to oversee and enhance our regulatory frameworks. This role is essential in ensuring that our operations align with industry standards and legal requirements. Key Responsibilities: Develop and implement compliance policies and procedures. Conduct regular audits...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time

    Job OverviewBio Source Ltd, a leading company in the MedTech industry, is seeking a highly skilled Regulatory Manager to join their team. As a key member of the organization, you will be responsible for ensuring compliance with regulatory requirements and managing the technical file.Key Responsibilities:Conduct internal and regulatory audits to ensure...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time

    Job OverviewBio Source Ltd, a leading company in the MedTech industry, is seeking a highly skilled Regulatory Manager to join their team. As a key member of the organization, you will be responsible for ensuring compliance with regulatory requirements and managing the technical file.Key Responsibilities:Conduct internal and regulatory audits to ensure...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About Bio Source Ltd (a Logik Source company)**We are a MedTech company focused on the development of IoT medical wearable technology. Our company is committed to delivering innovative solutions that improve patient outcomes.Job SummaryWe are seeking a highly skilled Regulatory Compliance Manager to join our team. The successful candidate...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About Bio Source Ltd (a Logik Source company)**We are a MedTech company focused on the development of IoT medical wearable technology. Our company is committed to delivering innovative solutions that improve patient outcomes.Job SummaryWe are seeking a highly skilled Regulatory Compliance Manager to join our team. The successful candidate...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About Bio Source Ltd (a Logik Source company)**We are a MedTech company focused on the development of IoT medical wearable technology. Our company is committed to delivering innovative solutions that improve patient outcomes.Job SummaryWe are seeking a highly skilled Regulatory Compliance Manager to join our team. The successful candidate...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About Bio Source Ltd (a Logik Source company)**We are a MedTech company focused on the development of IoT medical wearable technology. Our company is committed to delivering innovative solutions that improve patient outcomes.Job SummaryWe are seeking a highly skilled Regulatory Compliance Manager to join our team. The successful candidate...


  • Cambridge, Cambridgeshire, United Kingdom SearchTech Full time

    **Job Summary**The Permitting Manager is a critical role at SearchTech, responsible for ensuring the company's compliance with environmental regulations. This position requires a strong understanding of regulatory requirements and the ability to manage permit applications, modifications, and reporting.**Key Responsibilities****Evaluate and Recommend...


  • Cambridge, Cambridgeshire, United Kingdom SearchTech Full time

    **Job Summary**The Permitting Manager is a critical role at SearchTech, responsible for ensuring the company's compliance with environmental regulations. This position requires a strong understanding of regulatory requirements and the ability to manage permit applications, modifications, and reporting.**Key Responsibilities****Evaluate and Recommend...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time

    Job Title: Regulatory ManagerCompany: Bio Source Ltd (a Logik Source company)Job Type: Full-time or Part-timeLocation: Remote (North Cambridgeshire)About the Role:We are seeking a highly skilled Regulatory Manager to join our team. As a Regulatory Manager, you will be responsible for ensuring that our medical devices comply with regulatory requirements.Key...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time

    Job Title: Regulatory ManagerCompany: Bio Source Ltd (a Logik Source company)Job Type: Full-time or Part-timeLocation: Remote (North Cambridgeshire)About the Role:We are seeking a highly skilled Regulatory Manager to join our team. As a Regulatory Manager, you will be responsible for ensuring that our medical devices comply with regulatory requirements.Key...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About the Role**We are seeking a highly skilled Regulatory Compliance Manager to join our team at Bio Source Ltd (a Logik Source company). As a key member of our organization, you will be responsible for ensuring our medical wearable technology products meet the highest regulatory standards.Key Responsibilities:Conduct internal and...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time £6

    Job Description**About the Role**We are seeking a highly skilled Regulatory Compliance Manager to join our team at Bio Source Ltd (a Logik Source company). As a key member of our organization, you will be responsible for ensuring our medical wearable technology products meet the highest regulatory standards.Key Responsibilities:Conduct internal and...


  • Cambridge, Cambridgeshire, United Kingdom Bio Source Ltd (a Logik Source company) Full time

    Position Overview: Join Bio Source Ltd, a Logik Source company, as a Regulatory Manager, where you will play a pivotal role in ensuring compliance within the MedTech sector, particularly focusing on IoT medical wearable technology.Key Responsibilities:Conduct internal and regulatory audits, ensuring adherence to standards such as ATEX, FDA, and CE Medical...