2027 Future Talent Program - Global Regulatory Affairs & Compliance US Subsidiary - Intern
PharmaBiotechRegulatory AffairsQuality Assurancemedicalemafdacroraveinformaws
Job description
Job Description 2027 Future Talent Program - Global Regulatory Affairs & Compliance US Subsidiary - Intern Drug Shortages & Support Functions (DSSF) The Future Talent Program features internships that last up to 12 weeks and will include one or more projects. These opportunities in our Research and Development Division can provide you with great development and a chance to see if we are the right company for your long-term goals This intern position is part of the Global Regulatory Affairs and Clinical Safety (GRACS) US Subsidiary function within our Company's Research Laboratories. This is an exciting time to join the US Subsidiary regulatory space, as we navigate evolving expectations and drive impactful change in our industry. The US Subsidiary team serves as a trusted regulatory center of excellence leading strategic interactions with the U.S. Food and Drug Administration (FDA) related to drug shortages and other regulatory support activities. The team partners with stakeholders across Regulatory Affairs, Manufacturing, Supply Chain, Quality, Medical Affairs, Communications, and Legal to help prevent, mitigate, and minimize the impact of supply disruptions on patients, while ensuring compliance with applicable regulatory requirements. The organization also supports regulatory intelligence activities, process improvement initiatives, FDA inquiries, and industry engagement to advance supply resiliency efforts. Flexibility and agility in responding to evolving business processes are crucial, as expectations continually change. As a Summer Intern, you will have the opportunity to gain hands-on experience in pharmaceutical regulatory affairs by supporting the Drug Shortages & Support Functions team and various company and industry-wide initiatives through cross-functional collaboration with internal and external stakeholders. The intern will contribute to projects focused on regulatory intelligence, regulatory strategy, and drug shortage prevention activities while working alongside experienced regulatory professionals. Primary Activities Under the supervision of the US Subsidiary Drug Shortages & Support Functions team, the intern may: Support monitoring and analysis of U.S. drug shortage regulations, FDA communications, and emerging regulatory trends Assist with maintaining and enhancing internal resources, playbooks, procedures, and training materials Conduct research and regulatory intelligence assessments related to drug shortages, supply continuity, and shortage prevention initiatives Engage with external industry working groups to advance supply resiliency initiatives Support departmental initiatives including but not limited to digital innovation and automation projects, to support business process improvements and operational effectiveness Develop presentations, reports, and communication materials for internal stakeholders Participate in cross-functional discussions supporting regulatory strategy development for actual or potential supply disruptions Required Education Candidates must be currently pursuing: Bachelor of Science (BS) degree , or Doctor of Pharmacy (PharmD) degree Candidates must be enrolled in an accredited college or university and returning to school following completion of the internship Required Experience and Skills Demonstrated interest in pharmaceutical industry, healthcare, policy, life sciences, regulatory affairs, or related disciplines Strong analytical, problem-solving, and critical-thinking skills Excellent written and verbal communication skills Strong organizational skills and attention to detail Ability to manage multiple assignments and prioritize effectively Demonstrated leadership through academic, professional, volunteer, or extracurricular activities Proficiency in Microsoft Office applications, including Excel, PowerPoint, Word, and Teams Ability to work both independently and collaboratively in a team environment Willingness to learn and adapt in a dynamic business environment Preferred Experience and Skills Coursework or experience in pharmacy, pharmaceutical sciences, regulatory affairs, healthcare, public health, biotechnology, or life sciences Knowledge of FDA regulations, pharmaceutical manufacturing, supply chain operations, or drug development processes Experience conducting scientific, regulatory, or business research Familiarity with data analysis, visualization, or automation tools (e.g., Power BI, Power Automate, AI-enabled technologies) Please note that this position may be closed before the posted end date or may remain open longer, at the discretion of the company. Salary range: The salary range for this role is $39,108 through $111,111. FTP2027 RL2027 Required Skills: Preferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. <
Stand out for this role
NoxPharm tailors your CV to this job description by aligning your experience with the role requirements and terminology. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Manager, Software Engineer Integration - SRE
Merck & Co — IND - Telangana - Hyderabad (Hitec City Raidurg)
Stage nella funzione di Market Access
Merck & Co — ITA - Lazio - Roma
Werkstudent (m/w/d) Research Antiparasitics
Merck & Co — DEU - Rheinland-Pfalz - Schwabenheim
Maintenance Support Engineer
Merck & Co — NLD - North Brabant - Boxmeer
Material Master Data Operations Specialist
Merck & Co — NLD - North Brabant - Boxmeer
Senior Operator Media Productie
Merck & Co — NLD - North Brabant - Boxmeer