global regulatory affairs associate director (cardio-metabolic) Jobs in London United Kingdom

global regulatory affairs associate director (cardio-metabolic)

associate director - cmc regulatory affairs Jobs in London United Kingdom

associate director - cmc regulatory affairs

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associate, healthcare consulting

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cdm consultant

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chief marketing officer (cmo) - b2b partner marketing agency - london

associate director cmc regulatory affairs

Perrigouk

Select how often (in days) to receive an alert: Associate Director - CMC Regulatory Affairs Location: London, GB, SW11 7BW; Dublin, IE, D02 TY74; Rotterdam, NL, 3062 CE; Ghent, BE, 9050; Chatillon, FR, 92320; Chatillon Cedex, FR, 92320At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill , Compeed , Solpadeine , NiQuitin , and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview As Associate Director, you will lead the development and execution of cutting-edge Chemistry, Manufacturing & Control (CMC) strategies, ensuring the highest standards of regulatory excellence across our diverse portfolio-from pharmaceuticals and medical devices to supplements, cosmetics, and beyond.You will contribute to the creation of robust quality dossiers and the seamless navigation and influencing of regulatory landscapes, turning challenges into opportunities for innovation and growth. By delivering timely submissions and proactively identifying risks and mitigation plans, you'll enable first-to-market approvals that enhance Perrigo's reputation as a global leader in CMC.You will inspire and empower a high-performing regulatory team, instilling a culture of agility, compliance, and continuous improvement. Scope of the Role <ul><li>Lead global CMC regulatory strategy and execution for innovation projects, post-approval changes, lifecycle management, and compliance across all product categories.</li><li>Oversee the preparation, review, and submission of high-quality CMC documentation (e.g., Module 3, Quality Overall Summary) for global health authority submissions, including new MAAs/NDAs/ANDAs, variations, renewals, and compliance updates.</li><li>Develop and implement response strategies for regulatory queries and deficiency letters related to CMC matters. Engage in technical discussions with Competent Authorities in partnership with Country Regulatory teams.</li><li>Collaborate with cross-functional teams to ensure regulatory CMC alignment with commercial strategy, manufacturing changes, and global supply continuity.</li><li>Manage CMC strategy and documentation for complex CMC projects, such as tech transfers, major reformulations and geo-expansion</li><li>Manage CMC risks associated with ingredient challenges and develop action plans to support defence, in partnership with Regulatory Product Stewardship team.</li><li>Monitor global CMC regulatory trends and new regulations and guidance. Provide product impact assessments and strategic guidance to ensure continued compliance and readiness for evolving requirements, in partnership with Regulatory Product Stewardship team.</li><li>Represent Perrigo in external regulatory forums and trade associations to advocate for CMC-related policy positions and regulatory best practices.</li><li>Build and lead a high-performing, globally distributed team with deep expertise in CMC</li><li>Foster a culture of excellence, agility, innovation, and continuous learning.</li><li>Develop talent pipelines and succession plans to ensure long-term organizational capability.</li></ul> Experience Required <ul><li>Advanced degree in Life Sciences (PhD, PharmD, MSc preferred).</li><li>15+ years of progressive experience including management roles in CMC</li><li>Proven track record of successful global submissions and approvals across diverse product categories.</li><li>Strong strategic, financial, and operational acumen.</li><li>Exceptional leadership, collaboration, and stakeholder engagement skills.</li><li>Experience with global regulatory systems and digital platforms.</li></ul> Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.Hybrid Working Approach We love our offices and the setting they provide for in-person collaboration and celebration. We also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more hereApplicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you.We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. <img src="https://www.jobg8.com/Tracking.aspx?HuNA3DPAJ8sb3AkohtyD6%2b1Ih9%2bnDZPTm" width="0" height="0" />

Associate Director - CMC Regulatory Affairs

Novartis Farmacéutica

Choose LocationChoose Location# Global Regulatory Affairs Associate Director (Cardio-Metabolic)REQ-Oct 14, 2025United Kingdom Summary (12 days per month on-site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Associate Director We are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Regulatory Affairs team.The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle. About the Role Major accountabilities: Lead the implementation of regulatory strategies and operational activities across major global regions. Provide strategic input into global regulatory plans, identifying risks and contributing to key planning documents. Align regional regulatory approaches with global objectives through collaboration with cross-functional and regional teams. Define and manage Health Authority (HA) interaction strategies, including preparation of briefing materials. Oversee the planning, coordination, and submission of regulatory dossiers (e.g., CTAs, INDs, Risk Management Plans). Serve as a liaison with local HAs (e.g., FDA, EMA) and lead or support negotiations for regional approvals. Develop and implement strategies to minimize review delays and regulatory clock stops. Ensure timely and compliant responses to HA queries and requests. Contribute to departmental goal setting and lead initiatives to improve regulatory processes. Ensure adherence to internal policies, SOPs, and global regulatory requirements. Minimum requirements: Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field. Significant experience in regulatory affairs within the pharmaceutical industry. Proven track record in project management and regulatory operations. Experience representing the organization in cross-functional and cross-cultural settings. Strong knowledge of clinical trials, drug development, and regulatory compliance. Excellent problem-solving, negotiation, and communication skills. Detail-oriented with the ability to manage complex regulatory projects. Skilled in risk management and working with cross-functional teams. Ability to navigate and influence Health Authority interactions. Fluency in English (written and spoken) is essential. Commitment to Diversity and Inclusion/EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Why Novartis: Join our Novartis Network: Benefits and Rewards: Read our handbook to learn about all the ways we'll help you thrive personally and professionally:DevelopmentUniversal Hierarchy NodeUnited KingdomLondon (The Westworks)GB16 (FCRS = GB016) Novartis Pharmaceuticals UK Ltd.Research & DevelopmentFull timeRegularNoNovartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.REQ- Global Regulatory Affairs Associate Director (Cardio-Metabolic)<img src="https://www.jobg8.com/Tracking.aspx?n70Gs5vBCd8IWwUuLMXZlaNb9isvX8%2f5f" width="0" height="0" />

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Healthcare Businesswomens Association

Job Description Summary (12 days per month on-site) Location: London (The Westworks), United Kingdom or Dublin, Ireland Internal Job Title: Global Program Regulatory Associate Director Job Description We are looking for an experienced and proactive Senior Global Program Regulatory Manager to join our Global Regulatory Affairs team. The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals. It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle. Major Accountabilities <ul> <li>Lead the implementation of regulatory strategies and operational activities across major global regions.</li> <li>Provide strategic input into global regulatory plans, identifying risks and contributing to key planning documents.</li> <li>Align regional regulatory approaches with global objectives through collaboration with cross-functional and regional teams.</li> <li>Define and manage Health Authority (HA) interaction strategies, including preparation of briefing materials.</li> <li>Oversee the planning, coordination, and submission of regulatory dossiers (e.g., CTAs, INDs, Risk Management Plans).</li> <li>Serve as a liaison with local HAs (e.g., FDA, EMA) and lead or support negotiations for regional approvals.</li> <li>Develop and implement strategies to minimize review delays and regulatory clock stops.</li> <li>Ensure timely and compliant responses to HA queries and requests.</li> <li>Contribute to departmental goal setting and lead initiatives to improve regulatory processes.</li> <li>Ensure adherence to internal policies, SOPs, and global regulatory requirements.</li> </ul> Minimum Requirements <ul> <li>Bachelor's or Master's degree in Life Sciences, Pharmacy, or a related field.</li> <li>Significant experience in regulatory affairs within the pharmaceutical industry.</li> <li>Proven track record in project management and regulatory operations.</li> <li>Experience representing the organization in cross-functional and cross-cultural settings.</li> <li>Strong knowledge of clinical trials, drug development, and regulatory compliance.</li> <li>Excellent problem-solving, negotiation, and communication skills.</li> <li>Detail-oriented with the ability to manage complex regulatory projects.</li> <li>Skilled in risk management and working with cross-functional teams.</li> <li>Ability to navigate and influence Health Authority interactions.</li> <li>Fluency in English (written and spoken) is essential.</li> </ul> Commitment to Diversity and Inclusion/EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Skills Desired <ul> <li>Clinical Trials</li> <li>Cross-Functional Teams</li> <li>Detail-Oriented</li> <li>Drug Development</li> <li>Lifesciences</li> <li>Negotiation SkillsProblem Solving SkillsRegulatory ComplianceRisk Management</li> </ul><img src="https://www.jobg8.com/Tracking.aspx?vAeLusD9WE0pILu4uWEJNiiMBr948H6fb" width="0" height="0" />

Barrington James Limited

I'm currently partnering with an innovative biotech company advancing a novel immunology pipeline and preparing for their first-in-human clinical study. This is a unique opportunity to join at a pivotal stage and shape the clinical and scientific strategy from the ground up.Key Responsibilities:<ul><li>Provide strategic clinical leadership as the company progresses from preclinical into FIH studies.</li><li>Oversee the design, execution, and medical oversight of early-phase clinical trials.</li><li>Lead interactions with global regulatory authorities to support IND and trial initiation.</li><li>Build and guide a high-performing clinical and medical affairs function.</li><li>Partner with executive leadership, board members, and investors to drive long-term development strategy.</li></ul>Ideal Profile:<ul><li>MD (board-certified in immunology is strongly preferred).</li><li>Significant clinical development experience, with a proven track record in early-phase and FIH trials.</li><li>Deep scientific expertise in immunology and immune-mediated diseases.</li><li>Entrepreneurial mindset with the ability to thrive in a lean, fast-paced biotech environment.</li><li>Previous CMO or senior clinical leadership experience in biotech or pharma.</li></ul><img src="https://www.jobg8.com/Tracking.aspx?CY95c1eotcyg1FqGBiopGnG0iTh3CxGCd" width="0" height="0" />

Chief Medical Officer

Michael Page

We're seeking a highly organised and proactive Directorate Assistant to support a senior leadership team within a regulatory standards department. This is a varied and rewarding role offering close collaboration with senior stakeholders and the opportunity to contribute to impactful work.Client DetailsOur client is a respected regulatory body committed to promoting high standards, diversity, and access to justice within the legal profession. The Regulatory Standards Department plays a vital role in ensuring that professional standards evolve in response to societal needs, technological change, and consumer expectations. The organisation is driven by values of fairness, independence, and excellence, and fosters a collaborative and inclusive working culture.DescriptionAs Directorate Assistant, you will:<ul><li>Provide diary and administrative support to the Director of Regulatory Standards and senior stakeholders.</li><li>Organise internal and external meetings, including agendas, papers, and minute-taking.</li><li>Support the Supervision Team with case management, record keeping, and visit logistics.</li><li>Assist with recruitment administration and issuing contracts and cover letters.</li><li>Raise purchase orders and support financial processes within the department.</li><li>Coordinate the monthly Directorate newsletter.</li><li>Organise events such as conferences and away days.</li><li>Carry out ad hoc duties as required by the Director and senior team members.</li></ul>Profile <ul><li>A-Level education or equivalent experience.</li><li>Strong administrative and IT skills, including data management and MS Office.</li><li>Excellent communication skills, both written and verbal, with a diplomatic and professional approach.</li><li>Proven ability to manage multiple tasks, prioritise effectively, and meet deadlines.</li><li>High integrity and discretion when handling confidential information.</li><li>A collaborative mindset with the ability to build strong working relationships.</li></ul> Job Offer <ul><li>Hybrid working: minimum 8 days per month in the central London office.</li><li>A values-led culture that supports personal and professional development.</li><li>The opportunity to work closely with senior leaders in a respected regulatory environment.</li><li>A varied and impactful role within a supportive and inclusive team.</li></ul> If you're an organised, proactive professional looking to make a difference in a respected regulatory environment, we'd love to hear from you. Apply today and help shape the future of professional standards. <img src="https://www.jobg8.com/Tracking.aspx?ArXQWHzQuHjs2XljxlVa404wZWmraNzwa" width="0" height="0" />

Directorate Assistant

Jas Gujral

Overview Admin Officer - Executive PAOur client, an international company with offices in the City of London, is looking to recruit an Admin Officer. Responsibilities <ul><li>Provide professional and good secretarial support and personal assistance to Chief Representative of the Company.</li><li>Provide administrative support to Expatriate Human Resources & General Affairs Department on Entertainment and Security Management tasks.</li><li>Arranging meetings and managing the diary for senior management (SM).</li><li>Organising business and personal trips for SM both within and outside the UK.</li><li>Meeting and greeting high profile customers and guests of SM.</li><li>Managing budgets and accounts (incl. bookkeeping) and processing and recording all the expenses for SM.</li><li>Organising lunches, dinners, parties and receptions.</li><li>Responsible for booking golf club memberships, record log, bookings, fees and expenses.</li><li>Dealing with customer and client hospitality - such as booking them into hotels, arranging transportation for them, buying gifts, booking golf courses, etc. when required.</li><li>Dealing with all relevant activities (incl. Ringi preparation for the membership) needed for Nippon Club, Japanese school, JCCI, Sanyuu-Kai, Japan Society and all other Japanese societies and Japanese social activities related matters involving the Company in the UK.</li><li>Advising on, assisting in choosing and booking restaurants and other venues for functions.</li><li>Acting as an intermediary between members of staff, customers and SM.</li><li>Supporting EUAJA (HR department) on Entertainment (ROH, Arsenal, RAC etc.) and security management tasks etc.</li><li>Dealing with Car lease and Chauffeur company.</li><li>Providing support to Personal Assistant (PA) to Managing Director (MD) as and when required.</li></ul> Skills <ul><li>A bright professional, with a flexible approach</li><li>Well-organized with the ability to use their initiative</li><li>High levels of literacy and numeracy</li><li>Good communication skills in English</li><li>A good working knowledge of WORD, EXCEL, and POWERPOINT is essential along with the ability to communicate effectively using e-mail</li></ul>Open minded, respectful and team worker Details <ul><li>The Client is based in St Pauls London.</li><li>This is a 3 days in the office position.</li><li>The salary for this role is circa £40K plus overtime.</li><li>Do send your CV to us in Word format along with your salary and notice period.</li></ul><img src="https://www.jobg8.com/Tracking.aspx?IEHdHPGpx6QOWLMmtLqjXtqXcKpoyz5Ux" width="0" height="0" />

Admin Officer- Executive PA

The Planner Jobs Redactive Publishing Limited

Job Title: Principal Town Planner / Associate director Location: London or Nottingham Employment Type: Full-Time, Permanent Working Pattern: Hybrid (3 days per week in the office)An excellent opportunity has arisen for a Principal Town Planner or Associate Town Planner to join a well-regarded national Law Firm based in either their London or Nottingham offices. This is a rare chance to work within a truly multidisciplinary environment that brings together legal expertise and planning consultancy under one roof. This role offers high-level exposure to complex and high-profile projects across the UK, with a strong pipeline of work covering infrastructure, energy, residential, commercial, and mixed-use development.Key Responsibilities: Provide high-quality, commercially focused planning advice to a broad client base including developers, landowners, and public sector bodies Lead on major projects and manage a varied portfolio of planning work Draft and submit planning applications, appeals, and development plan representations Prepare planning appraisals and due diligence reports Contribute to business development and client relationship management Support and mentor junior team membersAbout You: MRTPI chartered with significant post-qualification experience (ideally 7+ years) Strong knowledge of UK planning legislation, policy, and procedure A background in either consultancy, local government, or a legal/planning interface environment Experience managing complex planning applications, appeals, and negotiations Confident communicator with strong client-facing skills Demonstrated ability to work collaboratively across teams and disciplinesWhat's on Offer: Competitive salary and benefits package Hybrid working model (3 days a week in-office) A collaborative, professional environment with access to legal and planning expertise The opportunity to work on nationally significant developments and policy matters Clear pathways for career development and progressionLooking to elevate your planning career within a unique, cross-disciplinary environment? If you are a Principal Town Planner or Associate Town Planner looking to join a team that will really value and help you progress, please do pop your CV across to or call Reference - 57129<img src="https://www.jobg8.com/Tracking.aspx?vX6ucqYYTObqcxwHGtI99SjjM9XLA7ohv" width="0" height="0" />

Principal Town Planner

Explore 72+ Associate director cmc regulatory affairs in London United Kingdom this November. Find roles across top companies and apply now to boost your career.

72 associate director cmc regulatory affairs jobs IN London United Kingdom

Associate Director - CMC Regulatory Affairs

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Global Regulatory Affairs Associate Director (Cardio-Metabolic)

Chief Medical Officer

Directorate Assistant

Admin Officer- Executive PA

Principal Town Planner