Candidates

Global Supply Chain Analytics Manager

Dublin Supply Chain and Logistics

Ref: JOB-14005_1742575056

ob Advertisement: Global Supply Chain Analytics Manager Are you ready to shape the future of global logistics within a leading healthcare organisation? 🚚🌍 Our client, a rapidly expanding global healthcare company, is seeking a Global Logistics Analytics Manager to join their dynamic team. Over the last decade, the organisation has experienced remarkable growth through mergers, acquisitions, and organic expansion. This growth has significantly increased their global product portfolio, market presence, and manufacturing footprint-driving demand for a robust and efficient global supply chain. The Role Reporting to the Senior Manager, Global Logistics, this pivotal role focuses on: Logistics Spend Analysis: Analysing and managing spend across global and European freight and distribution suppliers. Supplier Relationship Management: Building and maintaining strong relationships with freight suppliers across all transport modes. Process Optimisation: Consolidating and re-engineering global logistics processes to enhance efficiency and reduce costs. What You'll Bring We're looking for a proactive, data-driven professional with: Proven experience in logistics analytics or supply chain management, ideally in a global or regional role. Strong analytical skills to manage and optimise spend effectively. Expertise in working with freight suppliers across multiple modes of transport. A strategic mindset with the ability to identify and implement process improvements. The Next Step for you: Should this position be of interest to you please forward your CV to Sarah Mac Mullan from Next Generation Recruitment or alternatively call on the main line on 00 353 1 6498546 Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Quality Specialist - QMS - 22465 - 35ph - Brinny

Cork Pharmaceutical

Ref: JOB-14070_1742558082

Quality Specialist - Quality Systems Are you a quality-driven professional with a passion for compliance and continuous improvement? We are looking for a Quality Specialist - Quality Systems to provide expert oversight and support across site operations. This role is embedded in production, ensuring a strong Quality Management System that meets the highest industry standards. What You'll Do: 🔹 Quality Oversight & Compliance Act as a subject matter expert (SME) in Quality Systems, including investigations, change management, and sterility assurance. Provide quality approval and oversight for commissioning and qualification activities (IQ/OQ/PQ). Ensure compliance with regulatory requirements and contribute to regulatory inspections and audits. 🔹 Problem Solving & Continuous Improvement Apply your knowledge to enhance Quality Systems, resolve complex issues, and drive process improvements. Participate in GMP walkthroughs and champion a culture of compliance and quality excellence. Support corporate quality initiatives and ensure site-wide execution of quality actions. 🔹 Collaboration & Leadership Provide guidance and coaching to colleagues, sharing expertise in operational quality. Lead small projects and contribute to cross-functional teams. Manage relationships with key stakeholders, auditors, and regulatory bodies. What We're Looking For: ✔ Education: Degree or 3rd level qualification in Science, Quality, or related field. ✔ Experience: 5+ years in the pharmaceutical or similar regulated industry, with expertise in Quality Assurance. ✔ Technical Skills: Strong understanding of regulatory compliance, quality systems, and pharmaceutical manufacturing processes. ✔ Soft Skills: Excellent problem-solving, decision-making, and stakeholder management abilities. ✔ Bonus: Experience leading small projects and applying continuous improvement methodologies. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

MS&T Scientist

Dublin Pharmaceutical

Ref: JOB-14068_1742377645

MS&T Scientist (Specialist) - Bioprocess Laboratory Are you passionate about innovation in biologics manufacturing? We are looking for an MS&T Scientist (Specialist) to join our Manufacturing Science and Technology (MS&T) team at our state-of-the-art, single-use, multi-product facility. About the Role As an MS&T Scientist (Specialist), you will contribute to the overall operation of the MS&T Bioprocess Laboratory, working as part of a dynamic and interdisciplinary team. You will play a key role in building capability and knowledge in biologics manufacturing and supporting new product introductions. Key Responsibilities Plan and execute analytical testing to support USP-DSP scale-down model establishments, satellite runs, and improvement studies. Design and perform DSP laboratory studies, including chromatography runs and filter assessments. Support the transfer of analytical methods into the MS&T laboratory. Provide specialist analytical support for non-routine analysis and troubleshooting. Conduct experimental design, execution, data analysis, and interpretation. Author and review standard operating procedures (SOPs) and technical reports. Collaborate with multidisciplinary teams (MS&T, quality, analytics, regulatory) for process improvement and troubleshooting. Apply Lean Six Sigma and Change Management principles in the Analytical Sciences group. Lead and coach others in problem-solving and continuous improvement initiatives. Serve as an analytical specialist during internal audits and external inspections. Align and exchange knowledge with development organizations, commercial nodes, and external manufacturing partners. Conduct product robustness monitoring in partnership with global technical teams and lead investigations. Demonstrate a safety-first, quality-always mindset in all responsibilities. Qualifications & Experience Bachelor's degree in a relevant scientific discipline with 5+ years of experience, OR Master's degree with 3+ years of experience, OR PhD in biotechnology, biochemistry, pharmacy, process engineering, or equivalent. Technical expertise in biologics drug substance upstream and downstream operations, analytical testing, process development, and tech transfer. Ability to work independently and as part of a team in a fast-paced, innovative environment. Strong problem-solving, troubleshooting, and influencing skills. Excellent communication skills and deep scientific expertise. Experience in a GMP / regulated environment is desirable. Strong organizational skills with the ability to manage multiple priorities and escalate issues as needed. The Next Step for you: Should this position be of interest to you please submit your CV to Barry O'Mahony from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Senior Quality Technologist

Kildare FMCG & Food Production

Ref: JOB-13976_1741958167

We are seeking a highly skilled and detail-oriented Senior Quality Technologist on behalf of our client. This role is central to the development and maintenance of quality and food safety systems, ensuring compliance with customer, third-party, and regulatory standards. As a key member of the Quality team, the successful candidate will play an essential role in supplier and customer management, auditing, compliance, and driving continuous improvement initiatives. Key Responsibilities Supplier & Customer Management Maintain supplier management processes, including specification updates, risk assessments, and audits. Conduct supplier evaluations and provide feedback on performance. Ensure customer specifications and quality standards are developed, implemented, and maintained using relevant software. Quality Management Systems (QMS) & HACCP Participate in the HACCP team to maintain robust food safety systems. Manage document control, update processes, and assist in internal audits. Support external audits (e.g., BRC, Dept. of Agriculture) and ensure traceability compliance. Testing & Compliance Oversee raw material, process, and finished product testing, including microbiological, chemical, and organoleptic assessments. Drive root cause analysis for non-conformances and customer complaints, implementing preventive measures. Manage quarantined products, traceability, and shelf-life analyses for chilled and frozen items. Process & Quality Improvement Analyze data trends and identify opportunities for quality and system enhancements. Collaborate with cross-functional teams to implement process improvements. Support new product development, ensuring smooth integration into the QMS. Technical Administration Maintain records for due diligence and audit purposes. Manage pest control processes with external contractors and ensure compliance. Coordinate the calibration of factory and testing equipment. Qualifications & Experience Diploma or higher in a Food Science-related subject. 3-5 years of experience in a similar role within FMCG or food retail. Proficiency in food safety standards (HACCP, BRC) and legislation. Strong numerical, analytical, and communication skills. Lead Auditor certification and HACCP certification are advantageous. Proven ability to train and coach teams effectively. Proficiency in MS Office tools and relevant software applications. What We're Looking For: A proactive, adaptable professional with a passion for quality and food safety. A strong team player with the ability to work cross-functionally and build relationships. Excellent organizational and problem-solving skills, capable of managing multiple priorities. Note: This role may require occasional travel, and candidates must be eligible to work in Ireland. The Next Step for You Should this position be of interest, please apply with an up-to-date CV to Jessica from Next Generation Recruitment or call us on the main line at 016629120. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical, and Operation positions (permanent, contract, and temporary). All applications are handled in strict confidence. We never share your data outside of our organization without your prior written consent. For more information, please review our Data Protection Policy on our website

QC Associate Microbiology Specialist - 22609

Carlow Pharmaceutical

Ref: JOB-14025_1741958140

Are you an experienced Microbiology Specialist looking for an exciting opportunity in the pharmaceutical industry? We are currently hiring for a QC Associate Microbiology Specialist to join a leading pharmaceutical company based in Carlow. About the Role In this role, you will provide technical support to the QC Microbiology Laboratory and Operations, ensuring the continued manufacture and supply of high-quality pharmaceutical products. This position involves method validation, equipment validation, troubleshooting, documentation development, and microbiological support across the site. You will also play a key role in driving continuous improvement, training, and regulatory compliance within the microbiology function. Key Responsibilities Develop and execute Microbiology test methods and project validations Troubleshoot issues during validation studies and routine microbiology testing Provide microbiological support for site investigations Drive Continuous Improvement initiatives, including lean lab practices and method optimization Author and manage change controls, procedures, test methods, and deviations Authorize microbiological test results to support batch release Perform LIMS system updates and assess regulatory updates relevant to the microbiology lab Support the environmental control program, including trend analysis and CAPA implementation Ensure compliance with regulatory, compendial, and company quality standards Maintain the highest safety standards in all lab operations What We're Looking For Bachelor's degree or higher in Microbiology or a related discipline Minimum 5 years of experience in a pharmaceutical microbiology environment Strong knowledge and experience with microbiology test methods (e.g., Bioburden, Endotoxin, and Sterility testing) Demonstrated expertise in method validation and development Experience in pharmaceutical regulatory compliance and change management Excellent problem-solving, leadership, and communication skills Ability to work independently while collaborating with cross-functional teams This is an excellent opportunity to join a dynamic and innovative company where you can make a real impact in quality, compliance, and continuous improvement. If you have a passion for microbiology and pharmaceutical quality, we would love to hear from you! The Next Step for You Should this position be of interest, please forward your CV to Jessica from Next Generation Recruitment or call us on the main line at 016629120. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical, and Operation positions (permanent, contract, and temporary). All applications are handled in strict confidence. We never share your data outside of our organisation without your prior written consent. For more information, please review our Data Protection Policy on our website.

Quality Control Specialist - 22952

Carlow Pharmaceutical

Ref: JOB-14066_1741957734

My client, a leading pharmaceutical company in Carlow, is expanding and seeking an Associate Quality Control Specialist to join their Incoming Quality team on a contract basis. This role offers the opportunity to work in a fast-paced environment, supporting key quality processes and collaborating with global teams. Key Responsibilities: Support the New Material Introduction process and supplier qualification Coordinate and manage quality standards for raw materials and components Collaborate with external testing laboratories to ensure compliance Support internal/external investigations and audits Contribute to lab capability improvements and efficiency projects Ensure adherence to cGMP, cGLP, and company safety policies What You'll Need: 2-4 years' experience in a cGMP laboratory environment Strong knowledge of New Material Introduction processes Excellent problem-solving and communication skills Bachelor's degree in Chemistry, Analytical Chemistry, or a related science discipline Experience in method validation and transfer (a plus) This is an exciting opportunity to join a growing site, gain valuable industry experience, and contribute to high-quality pharmaceutical production. The Next Step for you: Should this position be of interest to you please submit your CV to Jessica Maguire from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Quality Control Technician - 22683

Carlow Pharmaceutical

Ref: JOB-14026_1741957700

Are you detail-oriented, highly organized, and looking to take the next step in your career within a cutting-edge pharmaceutical environment? We are seeking a Quality Control Technician to join a dynamic team working in a state-of-the-art facility with a strong focus on compliance and quality. What's in it for you? Gain hands-on experience in sample management and regulatory requirements. Be part of a collaborative and supportive team. Excellent career development opportunities. Key Responsibilities: Act as the point of contact for QC sample and retain management. Oversee QC external sample shipments and retain sample processes. Ensure compliance with cGMP standards and regulatory requirements. Utilize LIMS and Microsoft Office for documentation and tracking. Support audits, investigations, and continuous improvement initiatives. What We're Looking For: Strong proficiency in Microsoft Office and LIMS. Knowledge of GMP regulations and industry best practices. Excellent organizational and time management skills. Strong communication and teamwork abilities. A flexible and proactive approach to problem-solving. The Next Step for you: Should this position be of interest to you please submit your CV to Jessica Maguire from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.

Quality Control Specialist - 22952

Carlow Pharmaceutical

Ref: JOB-14066_1741790500

My client, a leading pharmaceutical company in Carlow, is expanding and seeking an Associate Quality Control Specialist to join their Incoming Quality team on a contract basis. This role offers the opportunity to work in a fast-paced environment, supporting key quality processes and collaborating with global teams. Key Responsibilities: Support the New Material Introduction process and supplier qualification Coordinate and manage quality standards for raw materials and components Collaborate with external testing laboratories to ensure compliance Support internal/external investigations and audits Contribute to lab capability improvements and efficiency projects Ensure adherence to cGMP, cGLP, and company safety policies What You'll Need: 2-4 years' experience in a cGMP laboratory environment Strong knowledge of New Material Introduction processes Excellent problem-solving and communication skills Bachelor's degree in Chemistry, Analytical Chemistry, or a related science discipline Experience in method validation and transfer (a plus) This is an exciting opportunity to join a growing site, gain valuable industry experience, and contribute to high-quality pharmaceutical production. The Next Step for you: Should this position be of interest to you please submit your CV to Jessica Maguire from Next Generation Recruitment using the apply button. Next Generation are specialists in Supply Chain, Procurement, Engineering, Quality, Technical and Operation (permanent, contract and temporary) positions. Applications are in strict confidence. Next Generation will never share your data outside of our organisation without your prior written consent. Please read our Data Protection Policy on our website.