Mundipharma International

Senior Project Manager page is loaded Senior Project Managerlocations: GB Cambridge: GB Londontime type: Full timeposted on: Posted 2 Days Agojob requisition id: JR2361 Senior Project Manager Location: Cambridge, Hybrid Department: IT 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 patients, healthcare professionals, our partners, and our employees. The Team The Senior Project Manager (IT) is responsible for leading and delivering complex technology projects within scope, budget, and schedule. This role provides strategic direction, drives cross functional collaboration,manages stakeholders at all levels, and ensures successful delivery of technical solutions that support organizational goals. The Senior PM acts as a key partner to the Mundipharma Business, the IT Business Partners and Technical Leadership, ensuring projects are well governed, well communicated, and aligned with enterprise objectives. You will have previous full project lifecycle exprrience-from issuing RFPs and vendor selection to final change management and communication with a main focus within the CRM and ERP domains. Role and Responsibilities Project Delivery & Governance: Lead multiple concurrent workstreams and vendors for projects Validation & GxP: Navigate technical change control within strictly validated environments, ensuring full compliance with regulatory standards Act as a key advisor to senior leadership, managing expectations and driving cross-functional collaboration Financial & Risk Management: Maintain rigorous control over project budgets and proactively mitigate risks, issues, and dependencies. Risk, Issue & Dependency Management Change Management - running sessions, managing communications, and ensuring business readiness for upgrades and new implementations What you'll bring Qualified Project Manager - Ideally PMP / PMI-ACP Certified Proven IT Project Manager experience delivering transformation projects in the Pharma/Life Sciences industry E2E full lifecycle transformation project delivery in Pharma / Life science (more than one £1m + project) Major project experience in at least one of these areas; SAP, Oracle, Veeva or Salesforce CRM Specialism: Specific experience with Salesforce Life Sciences CRM or Veeva products is highly preferred Validated Environments: A deep understanding of GxP and delivering IT solutions within a regulatory framework Expert at managing multiple vendors, conducting daily stand-ups, and handling complex RFP processes. 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 . 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, and be the first to hear about new roles. Additional Job Description: Primary Location: GB Cambridge Job Posting Date: 2026-03-02 Job Type: Permanent

Global Head of Regulatory Strategy & Labelling page is loaded Global Head of Regulatory Strategy & Labellinglocations: GB Cambridgetime type: Full timeposted on: Posted Yesterdayjob requisition id: JR2069 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 patients, healthcare professionals, our partners, and our employees. The Team Global Head of Regulatory Strategy & Labelling will join the Senior Leadership team in the Regulatory Affairs department at Mundipharma being accountable for global regulatory strategic leadership and CCDS and labelling updates. The Global Head will ensure efficient, effective leadership, management and delivery of regulatory strategy and labelling strategy for the full portfolio across the product lifecycle being accountable for the internal RA strategy lead team and for oversight for outsourced RA activity. Role and Responsibilities The Global Head of Regulatory Strategy & Labelling will have a clinical strategy focus on regulatory strategy on both marketed products and ongoing clinical development. Main responsibilities for the role will include: Accountable for overall Regulatory Strategy for all products including effective deployment of specific regulatory expertise to ensure portfolio regulatory deliverables are met, alignment of the strategy with RA CMC and the market clusters. Accountable for the regulatory stewardship of assets in clinical development and for labelling strategy across the product lifecycle and portfolios. Accountable for the successful execution of the regulatory strategy with nimble and proactive leadership of regulatory strategy revisions based on availability of new data or changes in company/commercial position. Responsible for generating global regulatory strategy plans for all products in the portfolio Proactive engagement with stakeholders and senior leaders in the development of regulatory strategies and delivery of regulatory expertise and results in line with Commercial goals. Engagement with external experts and consultants as needed to support regulatory strategic decision making. Ensure that regulatory and Regulatory strategies fully recognise risk, provide mitigations and ensure that these are communicated and acknowledged within the organisation for appropriate decision-making Accountable for optimal engagement with Regulatory Authorities in developing Mundipharma's assets and ensuring Regulator feedback and requirements are understood and adequately reflected in product strategic and tactical plans Accountable for regulatory contribution and oversight of promotional materials. Representing Regulatory as a core member of the Signal Evaluation and Labelling Group. Accountable for regulatory intelligence What you'll bring Proven experience in Pharma Regulatory Affairs strategy and experience in managing labelling activities A track record of developing and executing innovative regulatory strategies and leading successful interactions with key Health Authorities such as EMA, FDA, BfArM, MHRA, TGA, PMDA etc An excellent regulatory strategist with strong commercial instincts and demonstrated ability in delivering superior regulatory outcomes across a diverse product portfolio. Strong understanding and expertise in Clinical Strategy Demonstrated knowledge in labelling strategy and management of product labels across the product lifecycle. Excellent collaborator with strong customer and stakeholder focus. Able to build relationships and inspire confidence and respect at all levels, Including with senior leaders within the organisation. 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 . 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, and be the first to hear about new roles. Additional Job Description: Primary Location: GB Cambridge Job Posting Date: 2025-09-05 Job Type: Permanent

A global healthcare company based in Cambridge is seeking a Global Head of Regulatory Strategy & Labelling. The ideal candidate will lead regulatory strategy and labelling updates for a diverse products portfolio, ensuring alignment with global standards while engaging with key health authorities. Proven experience in Pharma Regulatory Affairs and strong collaboration skills are essential. This role offers a flexible benefits package in a hybrid working environment.