QC Microbiology Internship - Dunboyne

Job Description This role will be part of our Testing Self-Directed work team in our state of the art single use multi- product biotech facility in Dunboyne, County Meath, Ireland. • The organisational structure at the site will be based on self-directed work teams where decisions will be made at the level where the data exists. • The Quality Control Analyst 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. • The Quality Control analyst intern will be responsible for supporting testing on in-process drug substance/drug product, final drug products, and stability samples at the new single use multi-product biotech facility in Dunboyne, County Meath, Ireland. • The overall responsibility for this role will be to support the Quality Control testing function related to Analytical/Microbiology/Biochemistry & Cell Biology methods, ensuring compliance with cGMP and corporate regulations. This is a critical role within the Quality organisation to help establish the Laboratories as a hub for specialised analytical testing and create value for our patients. Key Accountabilities: • Perform a variety of routine Analytical/Microbiology/Biochemistry & Cell Biology testing techniques and associated documentation in compliance with GMP requirements as required, Following all relevant Standard Operating Procedures. • Observe GLP/cGMP always • Review Analytical Testing data. • Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation. • Get actively involved by participating in inspections, GEMBA’s and Go-See’s. • Operate to the highest standards of Safety, Quality and Compliance. • Routinely talk about any safety issues you are concerned about. • Know the hazards of the tasks you are performing, actively conduct risk assessments for inclusion into operational SOPs. • Be part of a motivated and high performing team Requirements: Pursuing a degree qualification in Science/Quality/Technical (disciplines). • Good written and oral communication skills. • An understanding of cGMP requirements for manufacturing and/or systems and compliance. • Required to work on his/her own initiative in a constructive manner in addition to working as part of a team. • Excellent time management and organisational skills. • Ability to manage multiple priorities and know when to escalate issues for resolution. • Ability to think logically and be proactive under pressure. • Flexible and self-motivated. PQ20 Required Skills: Analytical Problem Solving, Analytical Problem Solving, Biochemistry, Cell-Based Assays, Clinical Research, Data Analytics, Database Management, Data Entry, Data Visualization, Document Management, GMP Compliance, Health Economics, Immunoassays, Immunochemistry, Key Performance Indicators (KPI), Microbiology, Office Applications, Pressure Management, Process Improvements, Project Management, Reporting and Analysis, Risk Assessments, Safety Standards, Safety Training Programs, 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.