A leading testing and certification company in Ireland is looking for an experienced QC Analyst to join their Scientific In-sourcing team. The role involves testing pharmaceutical substances using HPLC and GC techniques, ensuring compliance with GMP standards, and training other analysts. Candidates are required to have at least 2 years of experience in a GMP lab and a degree in Chemistry or a related field. This is a site-based role with a commitment to quality and safety, focused on delivering results and performance. #J-18808-Ljbffr
A leading testing and inspection company in Ireland is seeking an experienced QC Analyst for their Scientific In-sourcing team. This role involves testing pharmaceutical substances in a GMP environment, with a focus on GC and HPLC analysis. The ideal candidate has a minimum of 2 years of GMP lab experience and a degree in Chemistry. The company offers a supportive work environment and career development opportunities. #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. 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 Excellent communication skills both verbal & written 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 Benefits 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. Skills chemistry QC Analyst HPLC GC Routine Testing #J-18808-Ljbffr
Company Description SGS is the worlds 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 Bachelors 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 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 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 Excellent communication skills, both verbal & written Good time management & attention to detail Skills: HPLC Chromatography Analysis GC KF FTIR Wet Chemistry Benefits: Pension Fund Medical Aid / Health Care Paid Holidays Performance Bonus Parking Flexitime Group Life Assurance
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 150 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 Education and training: 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 Additional information 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. Skills: QC Analyst Chemistry HPLC UPLC #J-18808-Ljbffr
