Current jobs related to Regulatory Affairs Specialist - Uxbridge - Park Street People


  • Uxbridge, United Kingdom Regeneron Full time

    {"title": "CMC Regulatory Affairs Specialist", "description": "Job SummaryWe are seeking a highly skilled CMC Regulatory Affairs Specialist to join our team at Regeneron. As a key member of our regulatory team, you will be responsible for ensuring the compliance of our global regulatory and CMC submissions.Key ResponsibilitiesReview and assess regulatory...


  • Uxbridge, United Kingdom Regeneron Full time

    {"title": "CMC Regulatory Affairs Specialist", "description": "Job SummaryWe are seeking a highly skilled CMC Regulatory Affairs Specialist to join our team at Regeneron. As a key member of our regulatory team, you will be responsible for ensuring the compliance of our global regulatory and CMC submissions.Key ResponsibilitiesReview and assess regulatory...


  • Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    Job DescriptionCMC Regulatory Affairs SpecialistWe are seeking a highly skilled CMC Regulatory Affairs Specialist to join our team at Regeneron Pharmaceuticals Inc.Key ResponsibilitiesRegulatory Submission ReviewReview regulatory submissions to ensure compliance with global regulations and CMC requirements.Collaboration and CommunicationCollaborate with...


  • Uxbridge, United Kingdom Lifelancer Full time

    Principal Regulatory Affairs Consultant - CMC small moleculeParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs...


  • Uxbridge, United Kingdom Park Street People Full time

    Park Street People Ltd is seeking a highly skilled Regulatory Affairs Manager to join their team on a 12-month temporary contract. The ideal candidate will have experience in CTA, EU, and early-stage development, as well as strong communication and interpersonal skills.The successful candidate will provide regulatory strategy and guidance across the region,...


  • Uxbridge, United Kingdom BTA Full time

    We are seeking a talented Regulatory Affairs Specialist to join our dynamic team at BTA. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key Responsibilities:Develop submission strategies and...


  • Uxbridge, United Kingdom BTA Full time

    Key ResponsibilitiesWe are seeking a talented Regulatory Affairs Specialist to join our dynamic team. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Develop submission strategies and plans for...


  • Uxbridge, United Kingdom Bristol-Myers Squibb Full time

    Transforming Patients' Lives through ScienceBristol Myers Squibb is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. As a Regulatory Affairs Specialist, you will play an integral role in work that goes far beyond...


  • Uxbridge, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager - CMCLifelancer is seeking a highly experienced Senior Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with regulatory requirements and guidelines.This is a challenging role that offers the opportunity to work on diverse...


  • Uxbridge, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager - CMCLifelancer is seeking a seasoned Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global...


  • Uxbridge, United Kingdom Lifelancer Full time

    Senior Regulatory Affairs Manager - CMCLifelancer is seeking a seasoned Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron is seeking a highly skilled Regulatory Affairs Senior Associate to join our team. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Regulatory Assessment and Compliance:...


  • Uxbridge, United Kingdom Regeneron Full time

    Job Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Regeneron. As a key member of our regulatory team, you will be responsible for ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Review and assess regulatory submissions to ensure compliance with global regulatory...


  • Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron Pharmaceuticals Inc. is seeking a highly skilled Regulatory Affairs Senior Associate to join our team.Job Summary:The Regulatory Affairs Senior Associate will be responsible for performing regulatory assessments of changes, interpreting the current, approved, and planned clinical regulatory landscape by...


  • Uxbridge, United Kingdom Regeneron Pharmaceuticals Inc. Full time

    Job Title: Regulatory Affairs Senior AssociateRegeneron Pharmaceuticals Inc. is seeking a highly skilled Regulatory Affairs Senior Associate to join our team.Job Summary:The Regulatory Affairs Senior Associate will be responsible for performing regulatory assessments of changes, interpreting the current, approved, and planned clinical regulatory landscape by...


  • Uxbridge, United Kingdom CK Group Full time

    CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. **Job...


  • Uxbridge, United Kingdom CK Group Full time

    CK Group is seeking a Senior Associate in Regulatory Affairs to join a global pharmaceutical company on a 12-month contract basis. **Company Overview** Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing, and delivering innovative human therapeutics. **Job...


  • Uxbridge, United Kingdom Proclinical Full time

    Proclinical are recruiting for a Regulatory Affairs Associate to join a pharmaceutical organisation. This role is on a contract basis and is either located in Uxbridge or Cambridge. **Key Skills and Requirements**: - Familiarity in an administrative field within a corporate or similar setting preferably within a healthcare sector. - Educated to a degree...


  • Uxbridge, United Kingdom Lifelancer Full time

    Job Title: Principal Regulatory Affairs ConsultantParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs experience,...

Regulatory Affairs Specialist

2 months ago


Uxbridge, United Kingdom Park Street People Full time

Regulatory Affairs Manager Opportunity

Park Street People Ltd is seeking a highly skilled Regulatory Affairs Manager to join their team on a 12-month temporary contract. The ideal candidate will have experience in CTA, EU, and early-stage development, with a proven track record of providing regulatory strategy and guidance across the region.

Key Responsibilities:

  • Develop and prepare high-quality regulatory documents to support clinical trials and medical products.
  • Contribute regulatory guidance to enhance product development and ensure alignment with the company's strategy and global regulatory requirements.
  • Act as a point of contact between the company and regulatory agencies, providing critical information and support.

Requirements:

  • Previous experience in Regulatory Affairs and Compliance, particularly in the pharmaceutical industry.
  • Proven background working on CTA and MA.
  • Strong communication and interpersonal skills.
  • Exposure to Regulatory Affairs legislation and procedures.

Park Street People Ltd is an Equal Opportunities Employer, committed to diversity and inclusion. We do not discriminate on the grounds of age, race, gender, disability, creed, or sexual orientation.