Upstream Operations Support Intern

MSD Malaysia; Dublin; Hybrid; EUR 17,000 - 21,000; Full time

Job summary

Merck & Co., Inc. invites applications for an Upstream Operations IPT Intern based in Ireland.

The role supports the start-up of the Upstream manufacturing area within the bulk drug substance facility and contributes to continuous improvement, CAPA management, and quality systems. You will work with cross-functional teams to drive process improvements, support batch operations, and author protocols and SOPs while gaining exposure to QA/QMS in a biotech production environment.

Qualifications

• Pursuing Chemical Engineering or Biotechnology studies.
• Demonstrated analytical problem solving and ability to work in cross-functional teams.
• Experience or interest in manufacturing processes and CAPA/QMS is a plus.

Responsibilities

• Support start-up of Upstream manufacturing area.
• Monitor Batch Operations from Vial Thaw to Fill and Freezing of bulk drug substance.
• Assist CAPA management and QRAs.
• Prepare SOPs and Electronic Batch Records for start-up.
• Contribute to QMS compliance and deviation investigations.
• Collaborate with CQV, Automation/CSV teams to facilitate facility development.

Skills

Analytical problem solving

Batch Production Records

CAPA Management

Chemical Engineering

Data Analytics

Data Visualization

Document Management

Equipment Engineering

Facility Design

Freeze Drying

Manufacturing

Manufacturing Processes

Process Development

Education

Chemical Engineering or Biotechnology studies

Job description

## Upstream Operations Support InternApply: Not Applicable: IRL - Dublin - Swords (Biotech): Full time: Posted Today: End Date: September 16, 2026 (2 days left to apply): R412751Job DescriptionA 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 HERECurrent 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.**