Grade: L1-1
Hiring Manager: Site QC Lead
Location: D9 Ho Chi Minh City
Opella, the Consumer Healthcare business unit of Sanofi, is the purest and third-largest player globally in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market. We have an unshakable belief in the power of self-care and the role it can play in creating a healthier society and a healthier planet. That’s why we want to make self-care as simple as it should be by being consumer-led always, with science at our core.
Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands. This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers. We are also proud to be the first major fast-moving consumer healthcare company to achieve B Corp certification.
Join us on our mission. Health. In your hands.
Job purpose:
Responsible for testing & sampling samples following QC team leader assignment. Responsible for compliance with safety requirement (HSE), orderliness and cleanliness of their work area simultaneously
Main responsibilities:
- Testing type of samples following QC team leader assignment: Finished product, stability, raw material samples
- Record adequately in analytical records, logbooks following requirements in QC
- Establishment of the secondary standard substances for QC
- Responsible for chemicals, reagents and medium preparation in testing.
- Create and update testing procedures following current pharmacopoeia or when required
- Perform validation in group such as: Test method validation/verification, cleaning validtaion, CDP, PET when required
- Respect strictly the standard operation procedures, HSE requirements and regulation in site
- Perform tasks as required GLP/ GMP according to allocation of QC team leader and report monthly on their tasks
- Attending to EHS activities according to company regulation
Qualification:
- Chemist, Chemist - biological bachelor/ Engineer or Pharmacist
- At least 6months- 1 years working in laboratory.
- Good knowledge of chemical analysis method and ability of working independently in accordance with current regulations
- Have knowledge and know how to use the modern QC Laboratory equipments such as HPLC, UV-vis, titrator, pH, Densitometer
- Good knowledge on GLP, GMP, HSE and high respect on GLP guidelines as well as current procedures in site
- Have Ability to read and understand documents in English
- Cautiousness, faithfulness and promptness
- Like studying and have continous improvement mindset
