Regulatory Affairs Head of RA CMC

1 week ago


Cambridge, United Kingdom Mundipharma International Full time £150 - £200

Apply (by clicking the relevant button) after checking through all the related job information below.**Regulatory Affairs Head of CMC****Location:** Cambridge**Department:** Regulatory Affairs**Job type**: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients.We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.**Role and Responsibilities**This role leads the RA CMC team, overseeing employees and vendors to deliver regulatory CMC product strategy and deliverables across EU and ROW markets for the full product portfolio.Engage with technical stakeholders across the organization including quality, supply chain and technical operations.* Responsible for RA CMC deliverables for products including RA CMC product strategy and oversight of vendor delivery.* Ensure that RA CMC strategies fully recognize risk, provide mitigations and ensure that these are communicated and acknowledged to product teams.* Serve as the go to contact for internal RA CMC queries from the technical and quality team, including due diligence and regulatory agency interactions, to resolve issues efficiently and support informed decision making* Ensure all regulatory processes, controlled documents, and knowledge resources are accurate, up to date, and consistently applied, supporting compliance and alignment with broader regulatory objectives* Ensure the team of employees and vendors delivers high quality regulatory outcomes by setting clear objectives, providing guidance, and monitoring performance to maintain operational efficiency and accountability**What you’ll bring*** 10 years pharmaceutical experience in regulatory or technical CMC* 2 years regulatory CMC experience* Excellent knowledge of RA CMC in relation to global initial registrations and lifecycle management.* Proven ability to drive efficient technical regulatory stewardship of products working in collaboration with internal and external partners.* Strong organization and problem-solving skills.* Self-motivated, driven with a positive attitude.* Excellent communicator and collaborator with strong customer and stakeholder focus.* Ability to effectively motivate and manage a team to deliver RA CMC objectives**What we offer in return**● Flexible benefits package● Opportunities for learning & development through our varied programme● Collaborative, inclusive work environment**Diversity and inclusion**Building an inclusive environment where people can thrive, grow and achieve their full potential is a priority.We believe this isn’t just the right thing, but also the smart thing to do.We are on a journey and will seek to move forward together through education and awareness to build a culture that welcomes and celebrates diversity and uniqueness.We will create a workplace environment where everyone can, every day, bring their authentic selves and is treated with dignity and respect.**About Mundipharma**Mundipharma is a global healthcare company focussing on customers across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East.Mundipharma is dedicated to bringing innovative treatments to patients in the areas of pain management, infectious disease as well as other severe and debilitating disease areas.Their guiding principles, centered around Integrity and Patient-Centricity, are at the heart of everything they do.For more information visit www.mundipharma.com.**Join our talent pool**If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles.**Additional Job Description:****Primary Location:**GB Cambridge**Job Posting Date:**2025-10-22**Job Type:**Permanent#J-18808-Ljbffr



  • Cambridge, Cambridgeshire, United Kingdom Mundipharma Full time

    Regulatory Affairs Head of CMC Location: CambridgeDepartment: Regulatory AffairsJob type: PermanentJoin us and make a difference when it matters mostAt Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our...


  • Cambridge, United Kingdom AstraZeneca Full time

    The Head of (Executive Director) International CMC Regulatory Affairsreports to the VP International Regulatory Affairs and is accountable for leading a team of Regulatory professionals (7-10 direct reports at Director level and 30-40 indirect reports) responsible for strategy delivery and execution of International CMC Regulatory strategy and leadership...


  • Cambridge, United Kingdom Gilead Sciences, Inc. Full time

    Regulatory Affairs Assoc II CMC United Kingdom - Cambridge Regulatory Regular Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these...


  • Cambridge, United Kingdom Parkside Full time

    My client is a global biopharma company. They are seeking a Regulatory Affairs Manager (CMC) to join our Regulatory Affairs Team based in Cambridge on a 12 month contract. Hybrid working Key Responsibilities Co-ordinate the preparation of high quality CMC documents to support regulatory submissions in International regions, (Asia, Latin America, Middle East,...


  • Cambridge, United Kingdom Gilead Sciences Full time

    At Gilead were creating a healthier world for all people. For more than 35 years weve tackled diseases such as HIV viral hepatitis COVID-19 and cancer working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the worlds biggest health challenges and our mission...


  • Cambridge, United Kingdom Bicycle Therapeutics Full time

    The Senior Manager Regulatory Affairs CMC will be responsible for the development execution and tracking of CMC regulatory activities for assigned BicycleTx programs or projects.You will be responsible for supporting the development of CMC regulatory strategy and processes for their assigned BicycleTx programs or projects working closely with...


  • Cambridge, Cambridgeshire, United Kingdom Gilead Sciences Full time £60,000 - £80,000 per year

    At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our...


  • Cambridge, United Kingdom Bicycle Therapeutics Full time

    Company Description Bicycle Therapeuticsis a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle®molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained with small molecule scaffolds to form two loops that stabilize their...


  • Blocks A & B, Portway Building, Granta Park, Cambridge, Suffolk, United Kingdom Bicycle Therapeutics Full time £60,000 - £120,000 per year

    Company Description Bicycle Therapeutics is a clinical-stage pharmaceutical company developing a novel class of medicines, referred to as Bicycle molecules, for diseases that are underserved by existing therapeutics. Bicycle molecules are fully synthetic short peptides constrained with small molecule scaffolds to form two loops that stabilize their...


  • Cambridge, United Kingdom Mundipharma Full time

    Global Head of Regulatory Strategy & Labelling Location: Cambridge, Hybrid - Open to remote working Department: Regulatory Affairs Job type: Full Time Join us and make a difference when it matters most! At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for...