Job Title: Quality Control (QC) Specialist – GMP Manufacturing (ATMPs & Vaccines) Location: Dublin 18 Industry: Advanced Therapeutics & Vaccines | Experience: 2+ years in GMP QC About the Company: Our client is a pioneering Irish-owned company transforming pharmaceutical manufacturing through advanced research in APC and digital-led processes. Their facility—dedicated to GMP clinical manufacturing—offers a seamless transition from process development to full-scale GMP manufacturing, focusing on Advanced Therapeutic Medicinal Products (ATMPs) and vaccines. Role Overview: This is a unique opportunity to help shape QC operations in a next-generation manufacturing site. You'll be instrumental in establishing QC systems, managing outsourced testing, and supporting regulatory compliance across vaccine and ATMP production. Key Responsibilities: Develop and implement QC systems, sampling plans, and testing strategies. Collaborate with internal/external teams to ensure GMP/GLP compliance. Review and execute documentation (SOPs, CoAs, test methods, reports, investigations). Investigate out-of-spec/limit results and lead CAPA implementation. Support analytical training programs and drive continuous improvement initiatives. Manage lab systems (e.g., LIMS, LabX, UV software) and maintain good housekeeping practices (6S). Top Skills & Qualifications: 2+ years' QC experience in a GMP pharmaceutical environment . Scientific degree required; postgraduate qualification a plus. Proficiency in QC documentation and lab investigations. Strong knowledge of analytical systems and quality standards. Excellent problem-solving , organisation , and cross-functional communication skills. Ability to work independently and in a team-focused environment. Why Join? Be part of a revolutionary company driving local supply chain solutions for life-saving medicines. This is a high-growth opportunity to develop technically and professionally within a state-of-the-art facility on a collaborative campus shared with APC. #J-18808-Ljbffr
Quality Control Specialist Our Client is seeking an experienced QAV / DDQ Specialist to join the Quality Assurance team at their facility in Co. Meath, where you'll play a key role in maintaining digital data quality and validation compliance across a state-of-the-art biopharmaceutical site. This position offers the opportunity to lead and support quality oversight for validation, computer systems, and regulatory compliance in line with cGMP, FDA, and EMEA standards. Key Responsibilities: Provide QA oversight for validation and digital data activities (CSV, equipment, and process systems) Review and approve GMP documentation (Change Controls, Deviations, CAPAs, SOPs) Support cross-functional teams and lead risk assessments Drive continuous improvement and audit readiness Interpret evolving regulatory guidance and update quality systems accordingly Ideal Candidate: 5+ years’ QA/Validation experience in pharma/biotech (CSV experience essential) Strong knowledge of GAMP, cGMP, and regulatory agency requirements Proficient in systems like Veeva Vault, SAP, Trackwise, and KNEAT Excellent communication and problem-solving skills Relevant degree in science, engineering, or a related field (postgraduate preferred) This is a fantastic opportunity to contribute to a forward-thinking, compliance-focused QA team in a globally respected organization. Apply now to be part of a world-class team shaping the future of biopharma quality, email your CV to jobs@forcerecruitment.com. #J-18808-Ljbffr
Utilities Engineer– Pharmaceutical Sector Location: Dublin Industry: Biopharmaceutical Manufacturing Type: Full-Time | On-Site Are you an experienced Utilities Engineer ready to lead critical systems in a world-class biopharma facility? We are recruiting on behalf of a leading pharmaceutical client in Dublinfor a Utilities Subject Matter Expert (SME) to own and manage Black and Clean Utility systems across the site. Key Responsibilities: Act as system owner for key utility infrastructure (Black or Clean Utilities) Ensure full compliance with GMP, EHS, and regulatory standards Develop and manage maintenance strategies, CMMS data, and spare part requirements Lead root cause analysis and implement corrective actions Support audits and change controls as system SME Drive continuous improvement, reliability, and efficiency Budget and manage capital projects related to utility systems Your Profile: Level 8 BEng in Engineering (or equivalent) 8+ years in a utilities/maintenance engineering role within pharma/biopharma Strong knowledge of utility systems design, operation, and compliance Proven ability to lead and collaborate in team-based environments Experienced in interacting with regulatory bodies This is a high-impact role ideal for an engineer passionate about system ownership, compliance, and innovation in pharmaceutical operations. Apply now to join a forward-thinking team in one of Ireland’s top biopharma sites. Send your CV to jobs@forcerecruitment.com or contact us for more information. #J-18808-Ljbffr
Qualified Person / Responsible Person – Biopharmaceutical Industry Location: Dublin Sector: Pharmaceutical / Clinical Supply Chain Type: Full-Time | Contract We are recruiting on behalf of a leading biopharmaceutical company for a Qualified Person (QP) / Responsible Person (RP) to play a pivotal role in ensuring the quality, compliance, and regulatory readiness of clinical supply chain operations. Key Responsibilities: QP certification and batch release of clinical supplies Serve as RP under a Wholesale Distribution Authorisation (WDA) for Pre-Approval Access Lead and support GMP/GDP inspections and audits Advise stakeholders on quality improvements, compliance, and risk mitigation Maintain and update the Site Master File and Manufacturer’s Authorisation Ensure timely communication of quality issues to partners and leadership Review and approve SOPs and procedural documents Contribute to global audit planning and continuous improvement programs Stay ahead of global regulatory changes and integrate them into quality systems Influence external quality standards through engagement with regulators and industry bodies Candidate Profile: Degree in science, engineering, or related discipline Eligible to act as a Qualified Person (QP) under EU regulations Experience as a Responsible Person (RP) under a WDA is preferred Minimum 10 years in the pharmaceutical/biopharma industry #J-18808-Ljbffr
