[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Merck KGaA, Darmstadt, Germany and its affiliates jobs](https://jobs.opennash.com/companies/merck-kgaa-germany/) · [Search jobs](/search/) Merck KGaA, Darmstadt, Germany and its affiliates · Billerica, MA # Director, Global Regulatory Affairs Billerica, Massachusetts, United States Full-time Director $171,600 - $230,900 Legal & Compliance Listed on Merck KGaA, Darmstadt, Germany and its affiliates’s official careers site. Posted October 2, 2026. Check that it is still open and apply there. [Apply on Merck KGaA, Darmstadt, Germany and its affiliates’s careers site →](https://careers.merckgroup.com/global/en/job/MQAMKDGLOBAL299590EXTERNALENGLOBAL/Director-Global-Regulatory-Affairs) [OpenNash Jobs](https://jobs.opennash.com/) / [Merck KGaA, Darmstadt, Germany and its affiliates](https://jobs.opennash.com/companies/merck-kgaa-germany/) / Director, Global Regulatory Affairs ## Job description Work Your Magic with us! Start your next chapter and join EMD Serono. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. ### Position Scope The Director of Global Regulatory Affairs is responsible for defining and executing the global regulatory strategy for designated oncology programs, ensuring timely and compliant approvals across geographies. This role requires strong leadership in cross-functional teams and deep expertise in regulatory interactions with major health authorities. Key accountabilities Develop and execute global regulatory strategy for oncology programs within the Oncology TA. Lead regulatory submissions and life-cycle management across multiple regions in collaboration with the global regulatory team. Manage and optimize interactions with health authorities (e.g., FDA, EMA) to facilitate approvals and label extensions. Provide strategic regulatory input to portfolio and program teams; influence decision-making with a data-driven approach. Lead a cross-functional, matrix-driven team to align on regulatory requirements, timelines, and deliverables. Ensure compliance with global/regional regulations, quality standards, and internal governance. Mentor and develop junior regulatory colleagues; foster a culture of regulatory excellence and proactive risk management. Monitor evolving regulatory landscape to anticipate impact on programs and adapt strategies accordingly. Collaborate with global patients- and science-focused teams to support program milestones and lifecycle planning. Required background and qualifications Advanced degree (e.g., PhD, PharmD, MD, or equivalent). At least 6 years of relevant regulatory experience with at least 3 years in Oncology. Demonstrated track record as an effective strategy developer and HA/EMA/FDA interaction expert. Proven ability to lead in a matrixed, cross-functional environment. Strong written and spoken English communication skills; proficiency in other languages is a plus. Excellent project management and influencing skills; able to drive programs across complex organizations. Desired skills and attributes Strategic thinker with a hands-on, execution-focused mindset. Strong stakeholder management and negotiation capabilities. Ability to manage competing priorities with a clear gaze on risk management and compliance. Experience with global regulatory submissions (eCTD/dossier delivery) and lifecycle planning. Patient-centric mindset and commitment to scientific rigor. ### Location This is an onsite role based in our Billerica, MA facility requiring and onsite presence at least 3 days per week. ### Pay Range for this position $171,600 - $230,900. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. ### For more information click here [https://careers.emdgroup.com/us/en/benefits](https://careers.emdgroup.com/us/en/benefits) What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! ## At a glance - Posted by the employer: Oct 2, 2026 - First seen by OpenNash: Oct 19, 2026 - Last checked: Oct 19, 2026 - Listed for: 17 days - Location: Billerica, Massachusetts, United States - Employment type: Full-time - Pay: $171,600 - $230,900[Apply on Merck KGaA, Darmstadt, Germany and its affiliates’s careers site →](https://careers.merckgroup.com/global/en/job/MQAMKDGLOBAL299590EXTERNALENGLOBAL/Director-Global-Regulatory-Affairs) ## More jobs at Merck KGaA, Darmstadt, Germany and its affiliates ### [Associate Director, Global Regulatory Affairs](https://jobs.opennash.com/companies/merck-kgaa-germany/jobs/8bc79877480963ae7b04/) Billerica, Massachusetts, United States ### [Director, Global Labeling - Regulatory Affairs](https://jobs.opennash.com/companies/merck-kgaa-germany/jobs/f2446bde870ed2f41eeb/) Billerica, Massachusetts, United States ### [Global Safety Lead](https://jobs.opennash.com/companies/merck-kgaa-germany/jobs/10e6cc9ef35ebfceef3c/) Billerica, Massachusetts, United States ### [Associate Director, Clinical Trial Lead](https://jobs.opennash.com/companies/merck-kgaa-germany/jobs/ba553d6e97123b814c2a/) Billerica, Massachusetts, United States ### [Associate Director, Global Labeling Strategy Lead](https://jobs.opennash.com/companies/merck-kgaa-germany/jobs/75f953e143d0e5561f95/) Billerica, Massachusetts, United States ## Similar jobs at other companies ### [Director, Global Regulatory Affairs (GRL)](https://jobs.opennash.com/companies/daiichi-sankyo/jobs/23bdbd6a298974011fee/) Daiichi Sankyo · Basking Ridge, NJ, USA ### [Global Regulatory Affairs Manager, Oncology](https://jobs.opennash.com/companies/gsk/jobs/09fdd8d7e12226e3ad65/) GSK · Rockville, Maryland, United States of America ### [Director, Regulatory Affairs, Companion Diagnostics](https://jobs.opennash.com/companies/daiichi-sankyo/jobs/fdf9cbaa775b4385105d/) Daiichi Sankyo · Basking Ridge, NJ, USA ### [Global Regulatory Affairs Director](https://jobs.opennash.com/companies/astrazeneca/jobs/ab2ff68af721f9ab4cf3/) AstraZeneca · Gaithersburg, Maryland ### [Director, Regulatory Affairs (Global Filing Lead)](https://jobs.opennash.com/companies/revolution-medicines/jobs/1106eea77796073469ed/) Revolution Medicines · Redwood City, CA OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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