MSD
Here's everything MSD is advertising at the moment. We pick these roles up from its careers site and check them again each day.
MSD is a research-intensive biopharmaceutical company that develops medicines and vaccines. The company focuses on answering tough scientific questions to make a difference in health.
Open positions
API Maintenance Lead
MSD
This role is responsible for all maintenance activities for the API IPT and its equipment, leading a maintenance team focused on talent development and growth. The successful candidate will ensure effective maintenance planning and scheduling to achieve high asset availability, meet compliance, and manage costs.
Sr. Spclst, Business Consulting
MSD
This role provides sitewide support to achieve significant business results through the use of MPS, acting as the MPS subject matter expert for critical improvement projects. The specialist will work with the site MPS lead to maintain an active MPS strategy linked to company objectives and enable World Class Supply through Value Stream analysis.
Senior Commercialization Engineer
MSD
This role supports internal and external manufacturing operations, focusing on continuous improvement and innovation. Responsibilities include guiding new product introductions, technical transfers, and directing development plans across projects, involving API process development, optimization, and regulatory compliance.
Digital Record Design Hub Lead, Manufacturing Execution Systems Biologics Drug Substance- Ireland
MSD
This role leads the Manufacturing Execution System (MES) Digital Record Design Hub (DRDH) across multiple sites, responsible for authoring, maintaining, and optimizing manufacturing batch records. The lead will manage a regional team, collaborate with various divisions, and drive continuous improvement of electronic manufacturing batch records.
Tech, Operations
MSD
The Manufacturing Bioprocess Associate is responsible for end-to-end production operations, operating equipment according to procedures, and adhering to safety and compliance standards. This role requires working as part of a flexible and collaborative multi-disciplined process team.
Facility Operational Readiness Associate Director
MSD
The Facility Operational Readiness Associate Director will coordinate and drive readiness activities across multiple functions to prepare a new vaccines manufacturing facility for product launch and commercial operations. This role involves partnering with various departments to ensure alignment, manage risks, and execute readiness plans.
Launch Excellence Leader (Assoc. Dir.)
MSD
The Launch Excellence Leader is a cross-site, cross-functional role focused on improving business processes for New Product Introduction (NPI) and Receiving Unit (RU) Readiness execution across the biologics network. This role leads Launch Excellence workstreams, partners with stakeholders, and translates launch learnings into best practices and schedule improvements.
EURAM Commercial Lead - Dairy Milking & Automation Solutions
MSD
This role leads the commercial growth strategy for Dairy Milking & Automation Solutions across the EURAM region, focusing on business development, portfolio commercialization, and strategic partnerships to drive market adoption and sustainable growth.
Site Lead Auditor (Associate Director)
MSD
The Site Lead Auditor is responsible for leading the internal audit and inspection readiness programs at the Carlow site, ensuring cGMP compliance and patient safety. This role involves providing Quality oversight for sterile fill-finish manufacturing processes and representing the Quality Management System during inspections.
Analytical Sciences Associate Specialist
MSD
This role supports the Analytical Procedure Life Cycle through end-to-end method lifecycle management, including new method introduction, transfers, and troubleshooting. The specialist will utilize expertise in separations and biochemistry to support pipeline and commercial products.
Analytical Sciences Specialist
MSD
This role champions the end-to-end lifecycle management of site analytical procedures, leading the introduction and transfer of new analytical methods, providing expert assessments for equipment and method qualifications, and heading technical investigations. The specialist will also oversee product testing and deliver robust technical rationales to support site operations.
Associate Director, Quality Assurance (Quality Management System)
MSD
This role leads the multi-site laboratory Quality Management System, ensuring alignment with standards and corporate expectations. The position involves partnering with laboratory teams to maintain quality procedures, manage audits, and drive continuous improvement.
Senior Specialist, Manufacturing Automation
MSD
This role supports the reliable and efficient operation of automation systems used in biologics manufacturing. The Senior Automation Engineer will provide automation support across DeltaV, OEM, and digital manufacturing systems, contributing to continuous improvement and project delivery.
Associate Specialist Quality Control
MSD
The Quality Control Associate Specialist supports Quality Control operations and quality systems to ensure compliance with company Global Quality standards, regulatory requirements, and cGMP. This role provides technical expertise in QC documentation, investigations, and continuous improvement to support product quality and supply.
Lead Tech, Operations
MSD
This role provides operational support for shop floor operations in a new biotechnology facility, focusing on late-stage and launch pipeline production. The Lead Manufacturing Bioprocess Associate will operate equipment, support end-to-end production, and lead team members in unit operations.
Senior Technology Compliance Specialist
MSD
The Senior Technology Compliance Specialist will ensure IT compliance and validation support for a Biotech facility, focusing on Computer Systems Validation (CSV), Systems Development Lifecycle (SDLC), cyber security, and data integrity for pharmaceutical product manufacturing.
Technology Compliance Specialist / CSV
MSD
The Technology Compliance Specialist is responsible for ensuring that computerized systems, data management processes, and system development activities comply with global regulatory, validation, cybersecurity, and data integrity requirements. This role provides IT compliance and Computer Systems Validation (CSV) expertise to safeguard the Systems Development Lifecycle (SDLC) and maintain inspection readiness.
Oncology Marketing Manager
MSD
This role involves developing and executing annual indication-specific strategy plans for the Irish oncology market, managing brands, and focusing on customer experience. It requires cross-functional collaboration, leadership, and a deep understanding of the pharmaceutical industry and oncology market.
Senior Packaging Engineer
MSD
This role serves as an essential part of the External Manufacturing & Network Equipment team, overseeing product and technology transfers to Contract Manufacturing Organizations (CMOs). The individual will leverage their scientific, technical, and business expertise to support teams in solving complex packaging issues, optimizing processes, and ensuring compliance.
Sr. Tech, Operations
MSD
This role provides operational support for shop floor operations in a biotechnology facility, focusing on end-to-end production for Fed Batch and Continuous Manufacturing. The Senior Manufacturing Bioprocess Associate will operate equipment, solve problems, and adhere to safety and compliance standards.
Stability Coordinator
MSD
The Stability Coordinator role involves coordinating daily, weekly, and monthly stability activities for the stability program, leading daily workflows, assigning tasks, and supporting stability-related investigations. This position also entails data entry and analytics of stability test results, maintaining and reporting metrics, and ensuring compliance with company policies and regulatory requirements.
Technology Compliance Specialist
MSD
The Technology Compliance Specialist ensures that computerized systems, data management processes, and system development activities comply with regulatory, validation, cybersecurity, and data integrity requirements within a Biotech facility. This role provides IT compliance and Computer Systems Validation (CSV) expertise to support the Systems Development Lifecycle (SDLC) and maintain inspection readiness.
QC Team Lead
MSD
The QC Team Lead will report to the QC Manager and be responsible for leading and mentoring the Sample Management Team, driving CGMP/GDP compliance, and ensuring data integrity principles are adhered to for records and data.
Spclst, Operations
MSD
This role supports the development of a biotech facility by participating in cross-functional teams to deliver project milestones and commercialization activities. The Manufacturing Technical Operations Specialist drives commercial operations and continuous improvements by ensuring adherence to policies and regulatory requirements.
Specialist, Process Engineering (MS&T) - Upstream or Downstream
MSD
Job Description Our Biotech facility in Dublin began construction in 2018 and has progressed at an impressive rate since then. The site plays a pivotal role in the manufacture of our Company’s biologics-based medicines, …
Associate Director, Quality Control
MSD
The Associate Director of Quality Control will lead Bioassay and Chemistry teams responsible for testing, stability, and release samples, providing analytical support and driving compliance and continuous improvement.