2027 Future Talent Program – Regulatory Chemistry, Manufacturing and Controls – Intern
About this opportunity
Job Description
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.
Join our Company's Research Laboratories for an exciting Summer 2027 internship opportunity within the Global Regulatory Chemistry, Manufacturing and Controls (CMC) organization. As a Regulatory CMC intern, you will have the opportunity to contribute to the development and lifecycle management of innovative products that impact patients worldwide.
This internship is designed for students interested in regulatory affairs and pharmaceutical development, with opportunities spanning biologics, small molecules, vaccines, and drug-device combination products. Students interested in advancing regulatory innovation through digital solutions, automation, artificial intelligence, and process improvement initiatives are also encouraged to apply.
Through meaningful project work, you will gain hands-on experience supporting Regulatory CMC strategy, global submissions, health authority interactions, and regulatory compliance activities.
As an intern, you will gain exposure to a diverse range of functions across our Company's research, development, manufacturing, and regulatory organizations while developing a strong foundation in Regulatory CMC principles and practices.
Experiences may include supporting the development of regulatory submission content, learning about the manufacture and testing of drug substances and drug products, understanding regulatory requirements for investigational and commercial products, contributing to post-approval regulatory strategies, and participating in cross-functional collaborations that support product development and supply continuity.
Required Education:
Currently pursuing a minimum of a bachelor’s degree in regulatory science, pharmaceutical science, pharmacy, chemistry, biomedical or other engineering disciplines, or other related fields in science and technology
Have completed at least (2) years of study undergraduate OR (1) year of study graduate by June 2027
Required Experience and Skills
Available to work full-time for up to (12) consecutive weeks beginning in May or June 2027
Superior communication and interpersonal skills
Excellent academic achievement and analytical thinking ability
Good organizational skills
Preferred Experience and Skills:
GPA of 3.5 and above
Proficiency in Microsoft Office applications
Experience writing, editing, and reviewing scientific publications and content
This internship promises to be a dynamic and enriching experience, providing you with the opportunity to learn and grow while contributing to our mission of improving global health outcomes. Don't miss your chance to be a part of our team and make a difference in the world.
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.
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:
10/9/2026 *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:R413279
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 240 comparable Intern/Fellow/Postdoc Manufacturing & CMC roles across 46 biopharma companies.
Salary context
59 of 240 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 240 comparable roles
+ 11 more countries
Seniority mix
240 of 240 peers have a known seniority level
Therapeutic area mix
5 of 240 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.