Merck

This role is for a Maintenance Lead at Merck's biopharmaceutical facility. The lead will be responsible for managing a maintenance team, ensuring equipment uptime and compliance with GMP standards, and driving continuous improvement projects. The role requires strong people leadership, problem-solving skills, and experience in the pharmaceutical or biotechnology industry.

Operations Director for Biologics clinical and commercial manufacturing, responsible for capacity realization, operational excellence, and leading manufacturing teams and processes. The role involves technology transfer, PPQ, inspection readiness, and ensuring compliance with regulatory expectations. It emphasizes Lean principles, continuous improvement, and developing a strong technical and digital mindset within the department.

Director of Drug Substance Commercialisation & Development at Merck, responsible for the strategic and technical leadership of introducing, developing, and commercially manufacturing active pharmaceutical ingredients (APIs). This role involves end-to-end accountability for process development, scale-up, validation, and lifecycle management, ensuring safe, compliant, and robust supply while driving continuous improvement.

Associate Scientist in Microbiology at Merck, supporting laboratory operations, data analysis, and testing of biologics within a GMP-compliant environment. Requires a degree in Biological Sciences or Engineering with experience in microbiology and laboratory systems.

This role is for a Specialist, Safety & Environment within Merck's EHS team, focusing on developing, implementing, and maintaining EHS systems to ensure compliance with legal and corporate standards in a highly regulated pharmaceutical manufacturing environment. Responsibilities include providing technical guidance, conducting evaluations and audits, managing EHS queries, and ensuring site environmental compliance.

Chemical Engineer role focused on process development, scale-up, and manufacturing support for pharmaceutical products within Merck's global pharmaceutical and commercialization organization. The role involves working on Drug Product projects from Phase IIb through regulatory filings and commercial launch, with a focus on Active Pharmaceutical Ingredients (API) and Oral Solid Dose (OSD) products.

Associate Director, Regional Procurement leads strategic procurement initiatives supporting manufacturing operations and growth across multiple sites in a regulated biopharmaceutical environment. Drives value through sourcing strategies, supplier performance, risk mitigation, and stakeholder partnership.

This role is responsible for ensuring products managed by External Quality Assurance (EQA) are manufactured, packaged, analyzed, released, stored, and distributed in conformance with all applicable regulatory requirements, regulatory filings, and company policies. The Senior Specialist acts as a Qualified Person (QP) for batch release in the EU market and manages deviations, complaints, and change controls.

This role is for a QC Microbiology Analyst at Merck's biologics drug substance facility. The analyst will support routine laboratory operations, including testing, data processing, and microbiology studies, ensuring compliance with cGMP and cGLP standards. Responsibilities include performing various QC Microbiology tests, liaising with stakeholders, adhering to schedules, driving continuous improvement, and supporting audits.

Senior Specialist role in Quality Risk Management & Auditing within a GMP environment at a biologics R&D facility. Focuses on leading site governance for QRM and Auditing, ensuring inspection readiness, building quality culture through training, driving robust QRM processes, supporting audits, and enhancing Quality Systems. Requires at least 5 years of experience in a GMP pharma/biotech QA, QRM, or auditing role.

This role supports end-to-end production operations for biopharmaceutical manufacturing, operating equipment according to procedures and maintaining a strict safety and compliance culture. It requires a Level 6 qualification in science or engineering and experience in a GMP Manufacturing environment.

Senior Manufacturing Bioprocess Associate role at Merck's biopharmaceutical facility, focusing on operational support for late-stage and launch pipeline manufacturing. Requires Level 6 qualification, 3+ years GMP experience, and knowledge of bioprocess operations, automation, and single-use technology.

Associate Director, Site Sterility Lead at Merck in Dundalk, Ireland, focusing on driving excellence in sterile manufacturing, aseptic standards, contamination control, and regulatory compliance (EU GMP Annex 1, cGMP). Responsibilities include leading training programs, serving as a Subject Matter Expert for sterility assurance, managing the Environmental Monitoring Program, performing quality risk assessments, and ensuring inspection readiness.

Manager for Quality Control in a pharmaceutical manufacturing facility, focusing on leading teams, ensuring compliance with global policies and regulatory requirements, managing laboratory operations, budgets, and driving continuous improvement through lean projects. Requires a Bachelor's Degree in Engineering or Science and 5+ years of pharma industry experience.

Merck is seeking an experienced Aseptic Lead for their Dundalk facility to strengthen sterile manufacturing standards and build long-term capability. The role involves leading environmental and media simulation programs, developing aseptic qualification processes, overseeing cleanroom compliance, managing the End-to-End Media fill program, and developing the Isolator Glove Management Program. The position requires a Bachelor's Degree in a relevant field, at least 5 years of experience in drug product and sterile manufacturing, experience with media simulations, knowledge of sterile filling processes, and prior GMP audit experience.

This role focuses on process development, scale-up, and manufacturing support for drug product projects, specifically involving spray drying and oral solid dosage forms. It involves planning and conducting studies, participating in cross-functional teams for risk and quality assessments, process validation, and troubleshooting manufacturing issues. The role requires experience in chemical or process engineering and a strong understanding of pharmaceutical development principles.

Associate Director of Drug Substance Commercialisation at Merck, responsible for technical support, process development, scale-up, and production of clinical and commercial APIs. The role involves leading teams, ensuring regulatory compliance, and driving process improvements within a commercialization facility.

Lead day-to-day operations of an API production facility, ensuring safe, compliant, and efficient production that meets quality, budgetary, and scheduling targets. This role involves managing a multidisciplinary team, overseeing key quality subsystems, and handling financial and trade union matters within a regulated healthcare manufacturing environment.