Internship Regulatory Affairs

Job Description Are you looking for an internship to learn and develop, take a peek into the professional world while bringing in your individual contribution? Would you like to experience working in one of the biggest multinationals in the pharmaceutical industry? We are looking for a graduating student or Master student; you must be searching for a challenging but fulfilling internship in our innovative company.       We work in a dynamic and collaborative team in the regulatory affairs department and will give you the opportunity to contribute to team challenges in main regulatory affairs activities: product registration, product life cycling  management, scientific translation, artwork management, regulatory compliance. What we offer Being an employee at our company means you will work together with a team on healthcare in an international environment.As a member you will get the opportunity to develop yourself. In addition, you'll experience: ·       Challenging tasks ·       Insights into the world of the pharmaceutical industry ·       Numerous networking opportunities, trainings & e-learning modules ·       Networking opportunities Your responsibilites • Supporting the local team in operational management of regulatory affairs projects • Supporting local team in product life cycling management • Scientific translations of product labeling • Supporting local team in Artwork Management • Acquire knowledge of relevant pharmaceutical industry regulations, guidelines and Good Regulatory Affairs Practices. Your competencies • Student or graduate of Bachelors/Masters degree in Pharmaceutical Sciences or other Health or Life Science degree • Well-organised, structured and independent way of working • Commitment, motivation and creativity • Proficient with MS Office (Excel, Powerpoint, Word, Outlook) • Strong written and verbal English skills Required Skills: Accountability, Accountability, Analytical Problem Solving, Business Strategies, Clinical Research, Data Analytics, Database Management, Data Entry, Data Visualization, Digital Learning, Document Management, Health Economics, Microsoft Excel, Office Applications, Pharmaceutical Management, Pharmaceutical Sciences, Pharmacy Regulation, Process Improvements, Product Registrations, Project Management, Regulatory Affairs Compliance, Regulatory Affairs Management, Regulatory Compliance, Regulatory Project Management, Reporting and Analysis {+ 2 more}Preferred Skills: 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: No relocationVISA Sponsorship: NoTravel Requirements: No Travel RequiredFlexible Work Arrangements: HybridShift: Not IndicatedValid Driving License: NoHazardous Material(s): N/AJob Posting End Date: 11/15/2025*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: R