INTERNSHIP DETAILS

Upstream Operations Support Intern

CompanyMSD
LocationSwords
Work ModeOn Site
PostedSeptember 13, 2026
Internship Information
Core Responsibilities
The intern will support the Upstream Operations Integrated Process Team by assisting with manufacturing start-up activities and implementing lean process improvements. Responsibilities include monitoring batch operations, managing CAPA documentation, and collaborating with cross-functional teams on facility validation.
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

A fantastic opportunity has arisen for a Upstream Operations IPT Intern . This position will contribute to developing and implementing strategic planning in Ireland by providing medical insight and expert knowledge about the product or disease area. In addition, the role shall identify, develop and maintain credible relationships with healthcare professionals, providers and academic centres.  

 

Bring energy, knowledge, innovation to carry out the following: 

  • Based in the Upstream Operations Integrated Process Team with a focus on supporting projects. 
  • Supporting Operations teams as required to enable the smooth start-up of the Upstream manufacturing area within the bulk drug substance facility. 
  • Lean Improvements: Identify continuous improvement opportunities and lead/participates in cross-functional teams to implement identified improvements. Support activities in the areas of cost reduction, process efficiency, energy conservation, waste minimization and operational excellence. 
  • Monitor and Support Batch Operations from Vial Thaw to Fill and Freezing of bulk drug Substance. 
  • Support CAPA management and closure relating QRAs. 
  • Provide support for a wide range of projects to support start-up. 
  • Protocol/report authoring/execution/oversight as appropriate. 
  • Support Generation of SOPS/Electronic Batch Records for start-up and facilitate review workshops as deemed necessary. 
  • Participate and comply with internal Quality Management Systems (QMS) requirements, as relevant. 
  • Work with the manufacturing operations group, the CQV team, the Automation/CSV reps to facilitate development and validation of the manufacturing facility. 

 

Internship will be completed in a hybrid model of on-site and virtual.  

What skills you will need: 

In order to excel in this role, you will more than likely have: 

  • Studying Chemical Engineering or Biotechnology  
  • High personal integrity, credibility and energy. Demonstrated ability to work as part of diverse teams in an inclusive manner. 
  • Demonstrated ability to be self-driven with respect to driving results and implementing identified improvement initiatives.  

PQ20

Required Skills:

Analytical Problem Solving, Analytical Problem Solving, Batch Production Records, CAPA Management, Chemical Engineering, Clinical Research, Contract Manufacturing, Cost Reduction, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, Equipment Engineering, Facility Design, Freeze Drying, Health Economics, Manufacturing, Manufacturing Processes, Office Applications, Process Development (PD), Process Improvements, Production Management, Project Management, Quality Compliance {+ 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
Chemical EngineeringBiotechnologyStrategic PlanningLean ImprovementsProcess EfficiencyBatch OperationsCAPA ManagementQuality Management SystemsData AnalyticsProject ManagementAnalytical Problem SolvingManufacturing ProcessesFacility DesignDocument ManagementEquipment EngineeringProcess Development
Categories
ManufacturingEngineeringScience & ResearchHealthcareData & Analytics