Job Description

　　When you're part of the team at Thermo Fisher Scientific, you'll do important work. Surrounded by collaborative colleagues, you'll have the support and opportunities that only a global leader can give you. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team, and help us make significant contributions to the world.

　　Work Location: Singapore, Gul Site

　　Working Hours: 8:00am to 5:15pm (Monday to Friday)

　　Operations:

　　Collaborate & participate in the successful transfer of new IPQC test methods from R&D.Responsible for writing up & execution of validation protocols for test method transfer.Ensure IPQC testing is in compliance with ISO 13485 and other relevant regulated guidelines.Ensure sufficient resources to support the release of incoming raw materials/reagents for production use.Provide timely updates of IPQC test results and participate in failure analysis of the array manufacturing process.To ensure junior staff are adequately trained to conduct IPQC testing.To coach and mentor the junior staff in the day-to-day activities.

　　Sustaining:

　　Ensure timely review and disposition of IPQC batch records for release to QA.Ensure laboratory equipment is maintained per the established schedule.Lead laboratory inventory to support IPQC testing.Development of new testing procedures/assays pertaining to the new products.Conduct investigation/trending of the materials/reagents performance failures. Identify and implement corrective and preventive actions.Other duties and tasks as may be assigned.

　　Education

　　Degree in Chemistry, Biochemistry, or, equivalent.Diploma holder with relevant experience.

　　Experience

　　Minimum 2 years of QC experience, preferably in pharmaceutical/biotech industries.Experience with people management.Proficiency in handling analytical laboratory equipment like HPLC, FTIR, and UV Vis Spectrophotometer.Proficiency in computer systems for laboratory tests, analysis, and data management.Validated understanding of cGMP and QSG preferred.

　　Knowledge, Skills, Abilities

　　Strong written and verbal skillsCan demonstrate an ability to meet the requirementCan work independently and be an effective teammate in a fast-paced environment.Requires keen attention to detail.Must be self-motivated, pragmatic, work well independently, and have a positive working demeanor with a matter of exigency.Good analytical abilitiesUnderstand the ISO requirements

　　Physical Requirements / Work Environment

　　Each one of our 70,000 outstanding minds has a remarkable story to tell.

　　Join us and supply our unusual mission.

　　Benefits

　　We offer beneficial remuneration, annual incentive plan bonuses, healthcare, and a range of employee benefits. The company offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer a delighted company culture that stands for integrity, intensity, involvement, and innovation!