QA Reviewer

Sgs; Munster; On-site; EUR 60,000 - 90,000; Full time

Job summary

SGS is seeking an experienced QA Reviewer to join its Scientific In-sourcing team in Ireland. The role involves deputising for the Analytical Team Leader, maintaining expertise on Agilent HPLCs, Empower, Winsotax, and LIMS, and performing method development, validations, and release testing.

You will review data, support audits, ensure GLP/GMP compliance, and contribute to CAPA actions while maintaining a high standard of documentation and traceability. Travel may be required.

Qualifications

• Minimum 5 years of experience in a GLP/GMP analytical laboratory environment within the pharmaceutical or medical device industry preferred.
• Strong technical knowledge with the ability to troubleshoot HPLC, dissolution and other standard analytical instrumentation.
• Proficient in audit trail review and data integrity assessment within regulated laboratory systems.
• Willingness and availability to travel for business purposes when required.

Responsibilities

• Deputize for the Analytical Team Leader and provide technical support to the team.
• Maintain knowledge of Agilent HPLCs, Empower, Winsotax and LIMS systems.
• Carry out project work implementing new specifications and analytical methods.
• Receive and log samples, schedule testing activities, and support release processes.
• Monitor and verify laboratory equipment and maintain records.
• Perform instrument calibration and maintenance and document results.
• Review calibration and maintenance documentation.
• Support development of new methods and validation activities.
• Review data and reports for release testing of finished products and raw materials.
• Participate in audits and CAPA actions.

Skills

HPLC troubleshooting

Empower

LIMS

GMP/GLP

Data integrity

Auditing

Tools

Empower software

Winsotax

LIMS

Agilent HPLC

Job description

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 QA Reviewer to join our growing Scientific In-sourcing team.

Job Description

• Deputize for the Analytical Team Leader as required, including providing technical and problem-solving support to the team.
• Maintain in-depth knowledge of Agilent HPLCs, Empower, Winsotax software and LIMS.
• Carry out project work associated with implementing new specifications and analytical methods required by pharmacopeial or customer requirements.
• Receive and log samples for testing, schedule testing activities and support laboratory release processes.
• Monitor and verify laboratory equipment and complete associated documentation.
• Perform instrument calibration and maintenance and complete associated records.
• Review and approve calibration and maintenance documentation as required.
• Support development of new methods and perform validation activities.
• Review and approve laboratory testing data and reports for release testing of finished products and raw materials.
• Review and approve laboratory investigations in a timely manner.
• Troubleshoot and investigate out-of-specification results.
• Participate in internal and external audits and support implementation of CAPA actions.
• Comply with GLP, GMP and safety requirements at all times.
• Maintain the laboratory in a clean and organised condition.
• Provide monthly reports and quality metrics as required.

Qualifications

• Minimum 5 years of experience in a GLP/GMP analytical laboratory environment within the pharmaceutical or medical device industry preferred.
• Strong technical knowledge with the ability to troubleshoot HPLC, dissolution and other standard analytical instrumentation.
• Proficient in audit trail review and data integrity assessment within regulated laboratory systems.
• Willingness and availability to travel for business purposes when required.

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 is an Equal Opportunity Employer, and as such we recruit, hire, train, and promote persons in all job classifications without regard to race, colour, religion, sex, national origin, disability, age, marital status, sexual orientation, gender identity or expression, genetics, status as a protected veteran, or any other characteristics protected by law.