Job title: QC Analyst I / Senior Analyst II - Micro Team
Hiring Manager: Team Supervisor
Location: Aventis Pharma Manufacturing, Jurong, Singapore
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.
About You
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.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
Top Skills
Similar Jobs
