QCS Staffing is seeking a Document Controller for a 12-month contract in Dublin, Ireland. The role involves client-side control of project documentation in the biopharma industry. Candidates should have proven experience in similar projects, hands-on EIDA use, and a strong understanding of GMP documentation. This is an excellent opportunity to enhance your skills in a pivotal sector of life sciences. Apply now to join a leading multinational in Ireland's thriving biopharma scene. #J-18808-Ljbffr
Document Controller - Ireland, Dublin - 12 Month Contract Are you a Document Controller looking for your next challenge in Dublin? A leading multinational in Ireland’s thriving biopharma industry is expanding their team for a major facility development. This project provides hands on experience with innovative equipment, large scale operations, and modern pharmaceutical technologies. It’s an ideal opportunity to build your skills within one of Europe’s fastest growing life science regions. What You’ll Do Client-side control of all project documentation across the full lifecycle Manage document receipt, review, approval, issue, revision control and archiving Interface with EPCM partners, vendors, contractors and internal stakeholders Ensure documentation complies with GMP, data integrity and ALCOA principles What you’ll need: Proven experience as a Document Controller on pharmaceutical or life sciences capital projects Hands‑on experience using EIDA for document management Experience working client‑side or within an owner’s project team Strong understanding of GMP documentation requirements Be part of something bigger. Start your application today. #J-18808-Ljbffr
Overview Primary Packaging Scientist - Cork, Ireland - 8 Month Contract. Our client is undergoing major expansion, supported by substantial investment aimed at increasing its overall manufacturing capacity in the medical device sector. Recent upgrades include the development of new, state‑of‑the‑art facilities, advanced automation systems, and additional infrastructure enhancements designed to strengthen operational resilience and meet growing global healthcare demands. With a long‑established presence and a highly skilled workforce, the site requires the role of Primary Packaging Scientist to join their project based in Cork. Responsibilities Responsible for the primary packaging components or systems (e.g., glass vials, prefilled syringes and plastic bottles, rubber stoppers and aluminium/plastic caps). Provide drug product packaging and container closure expertise to support R&D and Supply Chain projects in development. Leading lifecycle management activities of primary packaging materials for commercial products, e.g. productivity opportunities, evaluating new suppliers, implementing changes to components and technology improvements. Design, develop and test Container Closure Systems (CCS) for Drug Products to the required quality, safety, environmental and sustainability regulatory standards. Including design and execution of test protocols and reporting, to ensure the functionality and integrity of the chosen container closure solutions, as well as writing specifications. Qualifications Master or PhD of Science or of Engineering, or suitable equivalent Experience from similar roles working with primary packaging materials for parenteral pharmaceutical products. Experience with regulations for primary packaging materials – rubber closures, glass vials/bottles/syringes, plastic vials/bottles/syringes. Regulations including but not limited to USP, Ph.Eur, JP pharmacopeia, Chinese pharmacopeia. Experience with delamination studies, container closure integrity studies, and verification/validation and selection of primary materials for parenteral pharmaceutical products. #J-18808-Ljbffr
CQV Engineer (Solution Prep/Formulation Area) - Ireland, Cork - 12 Months Initial Contract Our client is undergoing major expansion, supported by substantial investment aimed at increasing its overall manufacturing capacity in the medical device sector. Recent upgrades include the development of new, state‑of‑the‑art facilities, advanced automation systems, and additional infrastructure enhancements designed to strengthen operational resilience and meet growing global healthcare demands. With a long‑established presence and a highly skilled workforce, the site requires the role of a CQV Engineer to join their project based in Cork. What You’ll Do Guide CQV activities for solution prep, ensuring timely execution and compliance with industry regulations. Develop, review, approve and execute the commissioning, installation and qualification protocols ensuring all issues identified during execution are managed correctly, efficiently and in accordance to site / project procedures. Generate, review and approve Validation Plan, SRA, DQ, URS’s etc. Manage and coordinate Solution Prep equipment commissioning and qualification activities. What you’ll need Relevant qualification (Degree) and / or relevant experience in biotech / pharmaceutical industry qualifying GXP systems. Guide CQV activities for solution prep, ensuring timely execution and compliance with industry regulations. Develop, review, approve and execute the commissioning, installation and qualification protocols ensuring all issues identified during execution are managed correctly, efficiently and in accordance to site / project procedures. Generate, review and approve Validation Plan, SRA, DQ, URS’s etc. Manage and coordinate Solution Prep equipment commissioning and qualification activities. #J-18808-Ljbffr
QCS Staffing is seeking a CQV Engineer for a 12-month contract in County Cork, Ireland. This role involves guiding CQV activities in the solution preparation area, ensuring compliance with industry regulations, and managing equipment commissioning and qualification activities. Candidates should have a relevant degree and experience in the biotech or pharmaceutical industry related to GXP systems. This position offers a unique opportunity to contribute to significant expansion in medical device manufacturing. #J-18808-Ljbffr
C&Q Engineer (HVAC) – Ireland, Dublin – 11 Month Contract Our client, a globally recognised pioneer in Biotechnology, is recruiting for the position of C'Q Engineer. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join them on their global mission to better the lives of those affected by disease and illness. What You'll Do Execution of qualification documentation for HVAC systems Ensure that C&Q Schedule is maintained Manage Daily C&Q coordination meetings Responsible for tracking and reporting of C&Q status and risks/issues Ensure startup of relevant systems is completed in a safe and coordinated manner What You’ll Need Extensive HVAC system commissioning and qualification experience within a biologic manufacturing environment C&Q execution experience Large capital project experience beneficialExperience with C&Q schedule management Ability to drive project delivery and meet tight deadlines If this role is of interest, please apply now! #J-18808-Ljbffr
QCS Staffing is seeking a C&Q Engineer for an 11-month contract in Dublin, Ireland. The successful candidate will execute qualification documentation for HVAC systems, manage C&Q coordination meetings, and ensure the safe startup of relevant systems. Ideal candidates will possess extensive HVAC commissioning experience within biologic manufacturing. This role offers the opportunity to join a leader in Biotechnology focused on high unmet medical needs. #J-18808-Ljbffr
A global pharmaceutical organization is seeking a QC Instrument Engineer for a 6-month contract based in Denmark. The role involves conducting full qualifications of continuous particle counters and ensuring stakeholder engagement. Ideal candidates will have extensive experience in the pharmaceutical industry, particularly with cGMP and data integrity. This position offers a unique chance to advance your career within a well-known pharma environment. #J-18808-Ljbffr
QC Instrument Engineer - Denmark - 6 month contract Our client, a global organisation within the pharmaceutical industry, needs a QC Instrument Engineer to join their large-scale CAPEX project based near Copenhagen. This is a fantastic opportunity for a professional in the life sciences sector to advancing their career within a globally recognised pharmaceutical environment. What You’ll Do You will be the main responsible for running a full qualification of 11 continuous particle counters (Met One 3400 ) in laminar airflow hoods and biosafety cabinets across downstream and upstream manufacturing. You will be the expert driving the qualification and must ensure key stakeholders are involved and participate accordingly. You will be part of a bigger project (and team) that aims to improve how the client is monitoring and operating in bulk fill and inoc suites. Coordinate deliverables and ensure proper administration and adherence to all the clients policies and procedures. What You’ll Need Experience within the field, and with cGMP and Data Integrity Pharma experience is a must CMR experience is preferred #J-18808-Ljbffr
A leading staffing agency is looking for a CSV Engineer for an initial 11-month contract based in Carlow, Ireland. The role involves ensuring compliance with Global SDLC/CSV policies and contributing to high-quality pharmaceutical projects. Candidates should have a degree in Science or Engineering, GxP experience, and the ability to work effectively in dynamic teams. This is a great opportunity to engage with a Centre of Excellence in the veterinary vaccines sector. #J-18808-Ljbffr
