SGS is the world’s leading Inspection, Verification, Testing and Certification company. We are recognised as the global benchmark for sustainability, quality and integrity. We have 99,600 employees across our 2,600 offices and laboratories worldwide, working together to enable a better, safer and more interconnected world. In 2021, SGS acquired the International Services Laboratory (ISL) in Ringaskiddy Cork, a centre of excellence for all aspects of pharmaceutical testing, including method development & transfer, reference standard testing, stability management and QC Release & Stability testing. SGS International Services Laboratory (ISL) is central to the SGS Global strategy for the Health & Nutrition sector, it is a significant component of the organisation’s global laboratories network. Our main focus is to ensure the safety of the medicine, for the millions of patients who take the products we test. This is achieved through a strong quality focus and an excellent Health Authority audit history and reputation SGS ISL has a dynamic team culture, committed to employee development.We have an exciting opportunity for a QC Analyst to join our growing teams in our state-of-the-art facility. The successful candidate will be an essential part of the chemistry team,testing pharmaceutical drug substances and raw materials in accordance with corporate procedures and in compliance with the current GMP standards. You will enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage, making the world a better, safer place for over 140 years. Job Description Key Responsibilities Carry out testing of drug substances in accordance to the valid testing procedures and regulatory requirements Ensurelaboratory equipment iswell maintained, and calibrations are carried out at the designated frequencies. Review results generated by other analysts for compliance with requirements. Ensure that all target dates are met. Communicate status of testing at Tier 1 Unit meetings. Keep laboratories to a high housekeeping standard. Carry out method transfers and participate in the validation of analytical test methods as required. Write and maintain necessary documentation (test protocols, SOPs, instrumentation manuals and checkout sheets, method transfer reports,) according to the existing SOPs and cGMP standards. Lead Laboratory investigations and deviations if required. Assessment of testing results generated in the laboratory and close out of batch analysis. Uphold a safe working environment, in a state of audit readiness. Maintain own knowledge of cGMPs and relevant analytical techniques (HPLC, GC, UV, PSD, XRPD, wet chemistry, dissolution, etc.). Identification and implementation of safety, environmental, quality and service improvements Work with your leader to ensure continuous self-development and progression At all times, adopt a safe behaviour by exercising due regard for the health and safety of yourself, colleagues, and clients, in line with the Company’s policies and procedures Ensure full compliance with the Company’s Code of Integrity, and act in accordance with SGS Ireland’s Equality & Diversity Policy Qualifications Science Graduate in Chemistry or equivalent education with a minimum of 2years’ experience in a GMP environment. Experience with analytical technologies anddemonstrated troubleshooting skills (HPLC, GC, UV, PSD, XRPD, wet chemistry, dissolution, etc.). Additional Information Integrity Strong analytical ability and associated problem solving Excellent interpersonal skills Good time management & attention to detail Results and performance driven Compliance with SGS policies and procedures Along with an attractive compensation and benefits package including bonus, healthcare, pension and enhanced annual leave, We offer you: A friendly, supportive, approachable working environment with a down-to-earth culture Continuous learning with the chance to expand and enrich your career with our dedicatedtraining team #J-18808-Ljbffr
A leading testing and certification company in Ringaskiddy is seeking a QC Analyst to test pharmaceutical drug substances. The role requires a Science Graduate in Chemistry with a minimum of 2 years’ experience in a GMP environment. Key responsibilities include conducting tests, maintaining equipment, reviewing results, and contributing to laboratory investigations. The company offers an attractive compensation package and a supportive working environment. #J-18808-Ljbffr
A pharmaceutical industry leader in Munster, Ireland is seeking a Senior QC Analyst to provide technical leadership within the Quality Control laboratory. This role focuses on chromatographic method development, optimization, and validation. The ideal candidate will ensure compliance with GMP regulations while leading complex analytical activities. You will receive attractive compensation and benefits, including a performance-related bonus, medical insurance, and enhanced vacation. Join a dynamic team committed to quality and innovation. #J-18808-Ljbffr
Overview SGS are the world’s leading testing, inspection and certification company. We deliver solutions to a wide range of industry sectors in Ireland. Enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage that has been making the world a better, safer place for over 140 years. Our client services include providing SGS QC analysts and technical support staff on-site to fulfill staffing requirements (Scientific In-sourcing), all under the supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test. Due to growth, we have an exciting opportunity for an experienced QC Analyst to join our growing Scientific In-sourcing team. Main Purpose of Role Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with clients' procedures and quality systems. The main focus will be GC and HPLC analysis , along with a range of other analytical techniques as required. Key Accountabilities Receive training from SGS and client and get trained in relevant analytical techniques. Train other analysts where appropriately qualified. Carry out testing in accordance to the valid testing procedures and regulatory requirements. Ensure that laboratory equipment is well maintained, and calibrations are carried out at the designated frequencies. Manage inventory and status of materials required for analysis. When qualified to do so, verify and review results generated by other analysts for compliance with requirements. Ensure correct data entry to LIMS. Assessment of testing results generated in the laboratory and close out of batch analysis. Ensure that all target dates are met. Update visibility tools and communicate status of testing at meetings. Maintain laboratories to a high housekeeping standard. Ensure high standard of lab records, with work completed Right First Time and on time. Write and maintain necessary documentation (SOPs, methods, reports, etc.). Work as part of the team ensuring customer expectations are met and exceeded. Support achievement of client and SGS Key Performance Indicators, such as around investigations, training, productivity and on-time testing. Notify appropriate contact and document results and investigations for any atypical or aberrant results. Lead Laboratory investigations and deviations if required. Maintenance of a safe working environment, in a state of audit readiness. Identification and implementation of safety, environmental, quality and service improvements . Work with their leader to ensure self-development and progression. Adopt safe behaviour by exercising due regard for health and safety of yourself, colleagues, and clients, in line with the Company’s policies and procedures. Ensure full compliance with the Company’s Code of Integrity, and act in accordance with SGS Ireland’s Equality & Diversity Policy. Qualifications Science Degree in Chemistry or equivalent (Level 7 minimum). 2 years experience in a GMP laboratory. Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, X-ray, Wet chemistry). Team player, flexible to evolving needs with a strong customer service mentality. Excellent quality and safety standards. Aptitude in lab computer systems, including LIMS and Trackwise. Additional Information Integrity. Strong analytical ability and associated problem solving. Excellent communication skills both verbal and written. Good time management and attention to detail. Results and performance driven. Compliance with SGS policies and procedures. Compliance with SGS and client policies and procedures. SGS offer a friendly, supportive, approachable working environment with a down-to-earth culture. A friendly, supportive, approachable working environment with a down-to-earth culture. Continuous learning with the chance to expand and enrich your career with our dedicated training team. Career development opportunities across SGS. SGS is an equal opportunities employer. #J-18808-Ljbffr
SGS is the world’s leading Inspection, Verification, Testing and Certification company, with over 98,000 employees in 2,600 locations around the world, including 24 labs in the Pharmaceutical sector. We deliver solutions to a wide range of industry sectors in Ireland. In 2021, SGS acquired the International Services Laboratory (ISL) in Ringaskiddy Cork, a centre of excellence for all aspects of pharmaceutical testing. This includes method development & transfer, release and stability testing, stability program management and support of our Scientific Insourcing We are seeking a highly experienced Senior QC Analyst to provide technical leadership within the Quality Control laboratory, with a strong focus on chromatographic method development, optimization, and validation . The successful candidate will act as a subject matter expert for analytical methods, ensuring robust, compliant, and scientifically sound testing in accordance with GMP and ICH guidelines. This role requires a hands‑on analytical scientist capable of independently leading complex analytical activities within a regulated pharmaceutical environment. We also will ensure the focus on you and your development. You will receive attractive compensation and benefits, with pharma benchmarked salary, performance related bonus , medical insurance, pension, illness income protection and enhanced vacation . This role is working typical office hours, with flexitime arrangements Job Description Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with ISL procedures and quality systems. Focus will be chromatography analysis , along with a range of other analytical techniques as required. Key Accountabilities Lead and execute routine and non‑routine QC testing in compliance with cGMP , regulatory requirements, and approved analytical methods. Serve as a technical SME for chromatographic techniques, including HPLC, UPLC, and GC , with detectors such as UV/Vis, PDA , and MS (desirable) . Independently develop, optimize, and troubleshoot chromatographic methods , including selection of mobile phases, gradients, columns, flow rates, temperatures, and injection parameters. Design and execute analytical method development studies assessing specificity, robustness, linearity, sensitivity , and overall method performance. Lead and perform forced degradation and stability‑indicating studies to demonstrate method specificity and product knowledge. Plan, execute, and review full analytical method validation packages in alignment with ICH Q2 (R2) , including: Accuracy and Precision Specificity Linearity and Range Robustness and Ruggedness LOD and LOQ Author, review, and approve method development reports, validation protocols, validation reports, and technical justifications . Provide technical oversight for method transfers , analytical lifecycle management, and continuous improvement initiatives. Perform advanced data analysis including chromatographic integration, impurity profiling, and data trending . Lead or support OOS/OOT investigations , root cause analysis, and implementation of CAPAs. Ensure data integrity , high‑quality documentation, and strict adherence to GMP, SOPs, and regulatory expectations. Support regulatory inspections, client audits, and internal audits as a QC representative. Mentor and provide technical guidance to junior QC analysts as required. Qualifications Expert‑level hands‑on experience with HPLC, UPLC, and GC Detector experience including UV/Vis, PDA , and MS (desirable) Advanced chromatographic method development, optimization, and troubleshooting Full analytical method validation execution and documentation Impurity profiling, forced degradation, and stability‑indicating methods GMP documentation, data integrity, and regulatory inspection readiness Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or related discipline (advanced degree preferred). 4+ years of experience in a pharmaceutical GMP QC or analytical development laboratory. Proven leadership in analytical method development, optimization, and validation activities. Strong working knowledge of ICH Q2 (R2), GMP regulations, and data integrity expectations. Demonstrated ability to work independently, lead complex analytical studies, and mentor junior staff. Manufacturing Practices, Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, Xray, Wet chemistry) Good organizationalskills and strong communication – written and verbal Team player, flexible to evolving needs with a strong customer service mentality Excellent quality and safety standards Aptitude in lab computer systems, including LIMS and Trackwise Additional Information Additional information Expected Behaviors: Integrity, consistency and flexibility Professionalism; with the client, contractors and colleagues at all times Compliance with SGS policies and procedures Participate in team meetings / Team player Strong analytical ability and associated problem solving Results and performance driven Good time management & attention to detail #J-18808-Ljbffr
SGS are the world’s leading testing, inspection and certification company SGS Group. We deliver solutions to a wide range of industry sectors in Ireland. Enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage that has been making the world a better, safer place for over 140 years. Our client services include providing SGS QC analysts and technical support staff on-site to fulfill staffing requirements (Scientific In-sourcing), all under the supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test. Due to growth, we have an exciting opportunity for an experienced QC Analyst to join our growing Scientific In-sourcing team. Job Description Main Purpose of Role Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with clients\' procedures and quality systems. The main focus will be GC and HPLC analysis , along with a range of other analytical techniques as required. Key Accountabilities Receive training from SGS and client and get trained in relevant analytical techniques. Train other analysts where appropriately qualified Carry out testing in accordance to the valid testing procedures and regulatory requirements Ensure that laboratory equipment is well maintained, and calibrations are carried out at the designated frequencies Manage inventory and status of materials required for analysis When qualified to do so, verify and review results generated by other analysts for compliance with requirements Ensure correct data entry to LIMS Assessment of testing results generated in the laboratory and close out of batch analysis Ensure that all target dates are met. Update visibility tools and communicate status of testing at meetings Maintain laboratories to a high housekeeping standard Ensure high standard of lab records, with work completed Right First Time and on time Write and maintain necessary documentation (SOPs, methods, reports etc) Work as part of the team ensuring customer expectations are met and exceeded. Support achievement of client and SGS Key Performance Indicators, such as around investigations, training, productivity and on-time testing Notify appropriate contact and document results and investigations for any atypical or aberrant results Lead Laboratory investigations and deviations if required Maintenance of a safe working environment, in a state of audit readiness Identification and implementation of safety, environmental, quality and service improvements Work with their leader to ensure self-development and progression At all times, adopt a safe behaviour by exercising due regard for the health and safety of yourself, colleagues, and clients, in line with the Company’s policies and procedures Ensure full compliance with the Company’s Code of Integrity, and act in accordance with SGS Ireland’s Equality & Diversity Policy Qualifications Science Degree in Chemistry or equivalent (Level 7 minimum) 2 years experience in a GMP laboratory. Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, Xray, Wet chemistry) Team player, flexible to evolving needs with a strong customer service mentality Excellent quality and safety standards Aptitude in lab computer systems, including LIMS and Trackwise Additional Information Integrity Strong analytical ability and associated problem solving Good time management & attention to detail Results and performance driven Compliance with SGS policies and procedures Compliance with SGS and client policies and procedures SGS offer a friendly, supportive, approachable working environment with a down-to-earth culture A friendly, supportive, approachable working environment with a down-to-earth culture Continuous learning with the chance to expand and enrich your career with our dedicated training team #J-18808-Ljbffr
A leading testing and certification company in Kinsale seeks an experienced QC Analyst for their Scientific In-sourcing team. This role focuses on testing pharmaceutical substances using techniques like GC and HPLC in compliance with GMP standards. Candidates should have a Science Degree and 2+ years of relevant experience. Opportunities for continuous learning and a supportive work environment are offered. #J-18808-Ljbffr
A leading testing and certification company in Ireland is seeking an experienced QC Analyst. The role involves testing pharmaceutical substances in a GMP environment, managing laboratory equipment, and ensuring compliance with regulatory requirements. Ideal candidates have a Science degree in Chemistry and at least 2 years of GMP laboratory experience. Strong organizational and analytical skills are essential, along with expertise in analytical technologies like HPLC and GC. Immediate eligibility to work in Ireland is required. #J-18808-Ljbffr
SGS are the world’s leading testing, inspection and certification company SGS Group. We deliver solutions to a wide range of industry sectors in Ireland. Enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage that has been making the world a better, safer place for over 140 years. Our client services include providing SGS QC analysts and technical support staff on-site to fulfill staffing requirements (Scientific In-sourcing), all under the supervision and guidance of ISL technical and operational teams. Like all SGS personnel, they are committed to upholding stringent technical and GMP standards, ensuring the safety of medications for the multitude of patients relying on the products we test. Due to growth, we have an exciting opportunity for an experienced QC Analyst to join our growing Scientific In-sourcing team. Job Description Testing of pharmaceutical substances e.g. raw materials and drug substances in a GMP environment in accordance with clients' procedures and quality systems. Main focus will be GC and HPLC analysis , along with a range of other analytical techniques as required. Key Accountabilities Receive training from SGS and client and get qualified in relevant analytical techniques. Maintain own training 100% current. Train other analysts where appropriately qualified. Carry out testing in accordance to the valid testing procedures and regulatory requirements. Ensure that laboratory equipment is well maintained, and calibrations are carried out at the designated frequencies. Manage inventory and status of materials required for analysis. When qualified to do so, verify and review results generated by other analysts for compliance with requirements. Ensure correct data entry to LIMS. Assessment of testing results generated in the laboratory and close out of batch analysis. Ensure that all target dates are met. Update visibility tools and communicate status of testing at meetings. Maintain laboratories to a high housekeeping standard. Ensure high standard of lab records, with work completed Right First Time and on time. Write and maintain necessary documentation (SOPs, methods, reports etc). Work as part of the team ensuring customer expectations are met and exceeded. Support achievement of client and SGS Key Performance Indicators, such as around investigations, training, productivity and on-time testing. Notify appropriate contact and document results and investigations for any atypical or aberrant results. Lead Laboratory investigations and deviations if required. Maintenance of a safe working environment, in a state of audit readiness. Identification and implementation of safety, environmental, quality and service improvements. Work with their leader to ensure self-development and progression. Qualifications Science Graduate in Chemistry or equivalent science education (Level 7). Necessary job experience: At least 2 years' experience in a GMP laboratory. GMP experience is a minimum requirement for this position. Professional requirements: Demonstrated experience with current Good Manufacturing Practices, Data Integrity and sound knowledge of analytical technologies (HPLC, GC, KF, IR, PSD, Xray, Wet chemistry). Good organizational skills and strong communication – written and verbal. Team player, flexible to evolving needs with a strong customer service mentality. Excellent quality and safety standards. Aptitude in lab computer systems, including LIMS and Trackwise. Expected Behaviors Integrity, flexibility, working under own initiative. Strong analytical ability and associated problem solving. Results and performance driven. Good time management & attention to detail. Professionalism; with the client, contractors and colleagues at all times. Compliance with SGS and client policies and procedures. To apply please submit your CV. Candidates must be immediately eligible to work in Ireland, this is a site based role. We are an equal opportunity employer and value diversity at our company. #J-18808-Ljbffr
SGS is the world’s leading Inspection, Verification, Testing and Certification company. We are recognised as the global benchmark for sustainability, quality and integrity. We have 99,600 employees across our 2,600 offices and laboratories worldwide, working together to enable a better, safer and more interconnected world. In 2021, SGS acquired the International Services Laboratory (ISL) in Ringaskiddy Cork, a centre of excellence for all aspects of pharmaceutical testing, including method development & transfer, reference standard testing, stability management and QC Release & Stability testing. SGS International Services Laboratory (ISL) is central to the SGS Global strategy for the Health & Nutrition sector, and a significant component of the organisation’s global laboratories network. Our main focus is to ensure the safety of medicine for the millions of patients who take the products we test. This is achieved through a strong quality focus and an excellent Health Authority audit history and reputation. SGS ISL has a dynamic team culture, committed to employee development. We have an exciting opportunity for a QC Analyst to join our growing teams in our state-of-the-art facility. The successful candidate will be an essential part of the chemistry team, testing pharmaceutical drug substances and raw materials in accordance with corporate procedures and in compliance with current GMP standards. You will enjoy a truly rewarding career in a global, multicultural organisation with a proud heritage, making the world a better, safer place for over 140 years. Job Description Key Responsibilities Carry out testing of drug substances in accordance with valid testing procedures and regulatory requirements. Ensure laboratory equipment is well maintained, and calibrations are carried out at the designated frequencies. Review results generated by other analysts for compliance with requirements. Ensure that all target dates are met. Communicate testing status at Tier 1 Unit meetings. Maintain high housekeeping standards in laboratories. Carry out method transfers and participate in the validation of analytical test methods as required. Write and maintain necessary documentation (test protocols, SOPs, instrumentation manuals, method transfer reports) according to SOPs and cGMP standards. Lead laboratory investigations and deviations if required. Assess testing results and close out batch analysis. Uphold a safe working environment, ensuring audit readiness. Maintain knowledge of cGMPs and analytical techniques (HPLC, GC, UV, PSD, XRPD, wet chemistry, dissolution, etc.). Identify and implement safety, environmental, quality, and service improvements. Work with leadership for continuous self-development and progression. Adopt safe behaviors, exercising due regard for health and safety in line with company policies. Ensure compliance with SGS Ireland’s Code of Integrity and Equality & Diversity Policy. Qualifications Science Graduate in Chemistry or equivalent with a minimum of 2 years’ GMP experience. Experience with analytical technologies and troubleshooting skills (HPLC, GC, UV, PSD, XRPD, wet chemistry, dissolution, etc.). Additional Information Integrity Strong analytical and problem-solving skills Excellent interpersonal skills Good time management and attention to detail Results and performance driven Compliance with SGS policies and procedures Excellent verbal and written communication skills Along with an attractive compensation and benefits package including bonus, healthcare, pension, and enhanced annual leave, we offer: A friendly, supportive, approachable working environment with a down-to-earth culture. Continuous learning with opportunities to expand and enrich your career with our dedicated training team. Development opportunities across SGS. SGS is an equal opportunities employer. #J-18808-Ljbffr
