Student Placement - Regulatory CMC (Chemistry, Manufacturing and Controls) at Merck Sharp & Dohme Corp. /Netherlands

London, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

28 Dec, 25

Salary

0.0

Posted On

29 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Regulatory Strategies, Dossier Assessment, Submission Packages, Health Authority Interactions, Operational Excellence, Regulatory Science, Regulatory Policy, Team Collaboration

Industry

Pharmaceutical Manufacturing

Description

Job Description This role will be based in our state-of-the-art co-working facilities in Moorgate, London; with fantastic amenities and support services including a gym, coffee bar and conference rooms. Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized compliance across regulatory agencies. We are an international network on the leading-edge of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world. In Regulatory CMC (Chemistry, Manufacturing and Controls) our experts maintain the scientific and technical aspects of products that ensure patients receive medicines that are manufactured and tested to a high quality and within compliance of the requirements of the world’s Health Authorities. International Regulatory Affairs CMC is a key component of our company’s strategy to build regional CMC regulatory knowledge and effective local relationships with country offices to deliver appropriate regulatory strategies and deliver right first-time regulatory submissions. As part of the EMEA team you will be one of the regional experts for CMC in Europe, Middle East and Africa. Duties The Associate Scientist Regulatory CMC will be involved in and responsible for the execution and management of the EMEA region submissions including new product registrations and life-cycle submissions to keep our products compliant and available for patients. In this role you will be working to: Generate regulatory strategies Assess changes to dossiers in the EMEA region Liaise with colleagues globally Review submission packages Work alongside our team in health authority interactions Additionally, you will: Work alongside our team to deliver on operational excellence projects Work alongside our team in developing best practises for regulatory science Learn and apply regulatory policy Work alongside our team in health authority engagements Eligibility/Education You will be looking to complete a 12-month placement in your penultimate or final year of study, returning to your course at the end of the placement Working towards a BSc in a scientific discipline such as chemistry, biological sciences, engineering, or a related field. Fields of study include (but are not limited to) Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry (or equivalent qualification) How to Apply (Please Read): Please complete the online application form by answering questions within the application and upload your CV and Cover Letter in a combined document in the ‘resume/CV’ section. Our standard Future Talent recruitment process is: An online application, a virtual conversation and then a final assessment. Next Steps: In the event of your successful progression to the next stage, one of our future talent team will contact you within two - three weeks of the application closing date. Start Date: June 2026 Equal Opportunity Employer: We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace. For more Information visit our Future Talent page! #UKFT25 Current Employees apply HERE Current Contingent Workers apply HERE Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. Employee Status: Intern/Co-op (Fixed Term) Relocation: VISA Sponsorship: Travel Requirements: Flexible Work Arrangements: Hybrid Shift: Valid Driving License: Hazardous Material(s): Required Skills: Preferred Skills: Job Posting End Date: 10/7/2025 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R365739

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Responsibilities

The Associate Scientist Regulatory CMC will be responsible for the execution and management of EMEA region submissions, including new product registrations and life-cycle submissions. This role involves generating regulatory strategies, assessing changes to dossiers, and liaising with global colleagues.