Merck

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.

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.

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.

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.