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2027 Future Talent Program Global Regulatory Affairs & Compliance US Subsidiary Intern

MSD


Job Location:

Rahway, NJ - USA

Yearly Salary: USD 39108 - 39108
Posted: 29 September 2026 (Yesterday)
Application Deadline: 27 December 2026
Vacancies: 1 Vacancy

Job Summary

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 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 Companys 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 $39108 through $111111.

FTP2027

RL2027

Required Skills:

Preferred Skills:

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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 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:

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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 anothers thinking and approach problems collectively.

Learn more about your rights including under California Colorado and other US State Acts

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance

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 relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

10/23/2026

*A job posting is effective until 11:59:59PM on the day BEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.


Required Experience:

Intern


About Company

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Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicine ... View more

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