Qc Analyst
3 weeks ago
Job PurposeJob Purpose:This position is responsible for daily laboratory testing of raw materials, in process and finished products.In addition, this position is responsible for providing support for environmental testing, validation, stability and other various laboratory and production testing.Key ResponsibilitiesAdhering to all Quality and Safety requirements on site and supporting Quality and Safety initiatives as requiredPerform chemical testing using analytical instrumentation including HPLC, GC, FTIR, UV-VIS, etcAssist in sampling of raw materials upon receipt, when needed.Aid in maintaining quick turnaround time of raw material releaseFamiliar with Quality GMP documentation (hard copy and electronic) of testing results and assurance of laboratory data integrityMaintain accurate lab notebooks and complete all related analytical reports, write summaries, and keep proper documentation in compliance with SOPs.Experience with USP interpretation and testing.Support QC audit readiness with understanding of FDA and ISO regulations and requirements.Support on-time performance in the QC lab against the Production and laboratory schedules.Assist with maintenance and troubleshooting of QC lab equipment to minimize downtime.Assist with out of specification investigations.Maintain a safe, clean, and organized environment (5S) for all QC areas.Employ sound and compliant laboratory techniques and logic per industry standards (e.g., FDA, USP/NF, ISO, ANSI) and internal and customer requirements.Troubleshooting laboratory instrumentation.Review batch records to ensure they are compliant with SOPs, WIs, and cGMPsFollow all SOPs and Safety Guidelines to ensure compliance with a cGMP environment and Safety Practices.Any additional functions as assigned by the Laboratory LeadEducation and ExperienceMinimum of a Bachelor's degree in Chemistry or related scientific fieldExperience working in an ISO or FDA regulated environment preferredFamiliarity with EmpowerExcellent communication skills, including the ability to speak clearly, listen and gain clarification, respond well to questions, and write clearly and informatively.Ability to deal with problems involving several concrete variables in standardized situationsProficiency with Microsoft Word, Excel, and Access.#J-*****-Ljbffr
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QC Analyst
4 weeks ago
Limerick, Ireland SGS Full timeMain 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...
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[Urgent] QC Analyst
4 weeks ago
Limerick, Ireland SGS Ireland Ltd Full timeSGS is the world's leading Inspection, Verification, Testing and Certification company. We are recognised as the global benchmark for quality and integrity. With more than 98,000 employees, we operate a network of more than 2,650 offices and laboratories around the world. We deliver global service with local expertise, to market leading clients across 10...
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QC Analyst
1 week ago
Limerick, Ireland Regeneron Ireland Full timeAs a QC Analyst in HPLC Chemistry you will perform a wide variety of chemical or biological analyses on products, in-process materials, or stability samples in support of the company's quality program. In this role a typical day might include, but is not limited to, the following: Gathering data and documenting test results Reviewing test results to ensure...
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Compliance Specialist
1 week ago
Limerick, Ireland Regeneron Ireland Full timeAs a Compliance Specialist within QC you will support the QC organisation in meeting compliance targets through laboratory investigation and deviation management. The Compliance Analyst will report quality system metrics to the group and identify improvements that can be made in all quality system inputs. A typical day might include, but is not limited to,...
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QC Analyst
4 weeks ago
Limerick, Ireland Regeneron Ireland Full timeAs a QC Analyst you will perform a wide variety of analytical chemistry testing to support in-process and bulk drug substance manufacture in a cGMP regulatory environment. . Please note this is a 24/7 shift position. The successful candidate will be required to work shift which includes days & nights. A typical day might include, but is not limited to, the...