INTERNSHIP DETAILS

QA Operations Intern

CompanyMSD
LocationSwords
Work ModeOn Site
PostedSeptember 13, 2026
Internship Information
Core Responsibilities
Provide direct quality support to production areas and ensure compliance with cGMPs and regulatory requirements. Review and approve GMP documentation, including electronic batch records and logbooks, to ensure accuracy and data integrity.
Internship Type
full time
Company Size
39714
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
About the Role

Job Description

Job Purpose:
This internship will give a great insight into different areas of Quality Assurance including Upstream & Downstream Operations, Quality Control and Supplier Management. These teams ensure adherence to Good Manufacturing and Documentation Practices and local procedures. 


The candidate will also spend time on the shop floor in a team environment to receive quality coaching and guidance, to enable documentation to be completed right the first time, and to ensure compliance with cGMPs and regulatory requirements.
 

Primary Responsibilities:

  • Provide direct Quality support to production and support areas.
  • Provides presence on the shop floor to support compliance and data integrity.
  • Review and approve GMP documentation/data for accuracy and completeness.
  • Review and approve executed production documentation such as electronic batch records and logbooks to ensure accuracy and compliance with cGMPs and company procedures and ensures completion of proper remediation of errors.
  • Collaborates with cross-functional team members in the identification and implementation of continuous improvement initiatives and action plans.


Qualification and Experience:

  • General competencies:
  • Motivation to be an inspiring member of a high performing team.
  • Desire to continuously learn, improve and develop.
  • Leadership skills coupled with good oral and written communication skills.
  • Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills and ability to work/ upskill/coach a team environment.

PQ20

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Client Coaching, Clinical Research, Coaching, Continuous Development, Data Analytics, Database Management, Data Entry, Data Integrity, Data Visualization, Documentation Preparation, Documentation Review, Document Management, Engineering Support, Government Regulation, Health Economics, Legal Compliance, Office Applications, Policy Compliance, Procedure Adherence, Process Improvements, Product Support, Project Management, Proper Documentation {+ 9 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 relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Not Applicable

Shift:

Not Indicated

Valid Driving License:

No

Hazardous Material(s):

N/A

Job Posting End Date:

09/16/2026

*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.

Key Skills
Analytical Problem SolvingClient CoachingClinical ResearchData AnalyticsDatabase ManagementData IntegrityData VisualizationDocumentation PreparationDocumentation ReviewDocument ManagementEngineering SupportGovernment RegulationHealth EconomicsLegal CompliancePolicy ComplianceProcedure Adherence
Categories
HealthcareManufacturingScience & ResearchData & AnalyticsEngineering