QC Analyst I / Senior Analyst II - Micro Team at Greenfix Property Care

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

24 Feb, 26

Salary

0.0

Posted On

26 Nov, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Microbiological Testing, Analytical Test Methods, GLP Compliance, cGMP, Laboratory Equipment Maintenance, FDA Regulations, Team Collaboration, Pharmacopoeia Knowledge

Industry

Household Services

Description

About the job We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Ready to get started? Roles and Responsible Carry out microbiological testing for APIs, stability samples, QC check of media, water and environmental samples in compliance with specifications, analytical test methods, laboratory methods and pharmacopoeia requirements. Prepare reagents, solutions and microbiological media in compliance with GLP and laboratory SOP requirements. Planning and assurance of cGMP compliant quality testing and documentation according to schedule. Ensure that analyses are carried out and reported in accordance with GLP (Good Laboratory Practices, completed on time and are consistent with the business requirements.) Carry out analytical results and audit trail review. Assist in carrying out maintenance of laboratory equipment in compliance with established schedules. Ensure GMP documents e.g. specifications, lab methods, standard operating procedures and other GMP documents (i.e. raw data, logbooks) in the laboratory are well maintained. Responsible for electronic raw data handling in compliance with regulations and guidelines. Participate actively in efficiency management of the laboratory and contribute towards continuous improvement through teamwork, feedback and collaboration. Participate in regulatory inspection and customer audits preparedness at site with regards to cGMP Quality and EHS aspects. Ensure compliance with HSE and quality policies and site procedures. Ensure safe working in the laboratory by practicing and communicating safety. Bring out unsafe conditions and acts / procedures. Familiar with Pharmacopoeia such as USP, EP requirement. Jobs Requirement A Diploma in Microbiology or any other related scientific discipline with minimum 3 years' experience in pharmaceutical industry.; or A fresh graduate from Degree in Microbiology or any other related scientific discipline. Must be analytical, methodical, quality conscious and a good team player. Knowledge of FDA regulations and cGMP will be desirable. Why choose us? Bring the miracles of science to life alongside a supportive, future-focused team. Discover endless opportunities to grow your talent and drive your career, whether it's through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits. null

Responsibilities

The QC Analyst is responsible for carrying out microbiological testing and ensuring compliance with specifications and regulatory requirements. They will also prepare reagents and solutions, maintain laboratory equipment, and participate in audits and inspections.