INTERNSHIP DETAILS

Manufacturing Intern, Operations

CompanyMSD
LocationDunboyne
Work ModeOn Site
PostedSeptember 13, 2026
Internship Information
Core Responsibilities
The intern will support commercial manufacturing operations and continuous improvement initiatives at a state-of-the-art facility. Responsibilities include managing GMP documentation, supporting batch production delivery, and collaborating with cross-functional teams to resolve technical issues.
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

Purpose:

  • This role will be part of our Manufacturing Technical Excellence Team in our new state of the art single use multi-product facility in Dunboyne, County Meath, Ireland.
  • The Manufacturing Technical Excellence intern role involves supporting commercial operations, continuous improvements and standard work principles at the single use multi-product facility by ensuring adherence to divisional policies and guidelines as well as regulatory requirements.
  •  The Manufacturing Tech excellence intern will work across the site self-directed work teams and hub teams to identify and resolve issues in order to allow the site to deliver on our commit culture that support Quality, EHS, Learning and Continuous improvement.

Responsibilities:

  • Responsible for the generation and approval of GMP documentation to support compliance and regulatory expectations for manufacturing operations: change control support, process improvement opportunity identification through implementation, and more.
  • Work with the Integrated Process Team (IPT) to ensure the effective and efficient on-time delivery of batch production within the IPT area.
  • Support operations team to consistently deliver on specific area Key Performance Indicators (KPIs), e.g. EHS metrics, Production Plan, OEE, compliance and team training.
  • Provide assistance and/or support maintenance, engineering, quality or other colleagues as requested.
  • Pull together cross functional teams to deliver on improvements and equipment changes that will move the production processes forward in the facility.
  • Support/Drive future updates to the batch recipe on the PAS (process automation system), the BOM (bill of materials) and the EBR (electronic batch record) for specific process steps.
  • Resolve issues and identify risks and escalate in a timely fashion.
  • Adhere to Right First-Time principles.

Education & Experience:

  • Currently pursuing a Bachelor’s or Master’s degree in a relevant field.

  • Demonstrated knowledge of continuous improvement methodologies & in-depth understanding of site level products & related processes.
  • Demonstrated collaboration, negotiation & conflict resolution skills.
  • Excellent communication skills (written and oral).
  • Exceptional analytical, problem solving & root-cause analysis skills.
  • Ability to multi-task and handle tasks with competing priorities effectively.
  • Strong technical aptitude (i.e. able to read & comprehend technical documentation & execute procedures), global regulatory experience & demonstrated experience interfacing with regulators.

PQ20

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Clinical Research, Commercialization, Conflict Resolution, Continuous Process Improvement, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, GMP Compliance, Health Economics, Manufacturing Execution Systems (MES), Multitasking, Office Applications, Problem Solving, Process Changes, Process Improvements, Project Management, Regulatory Requirements, Reporting and Analysis, Team-Building, Teamwork, Technical Support {+ 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 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 SolvingContinuous Process ImprovementGMP ComplianceManufacturing Execution SystemsData AnalyticsProject ManagementRegulatory RequirementsTechnical SupportConflict ResolutionTeamworkDocument ManagementData VisualizationDatabase ManagementClinical ResearchCommercializationMultitasking
Categories
ManufacturingEngineeringScience & ResearchHealthcareData & Analytics