•Responsible for SHE& Quality compliance in production department.
•Responsible for implementation of safety bi-system in production department.
•Department budget and cost management & KPIs including Variable cost / MOPEX / Coverage / Quality
•People Management of production department
•Continuous improvement in production
Requirements•5 years or above experience of production and related management experience
•English reading and verbal communication ability
•Knowledge of Microsoft office
•Knowledge of SHE/GMP
•Knowledge of chemical/process/equipment
Knowledge of Lean and six-sigmaBenefits
5 days working one week;
social insurance and housing fund;
Annual salary increase;
Annual outing;
free shuttlebus;
Skills Required
- 5+ years production and related management experience
- English reading and verbal communication ability
- Knowledge of Microsoft Office
- Knowledge of SHE/GMP
- Knowledge of chemical/process/equipment
- Knowledge of Lean and Six Sigma
What We Do
Centrient Pharmaceuticals is a global business-to-business manufacturer of foundational medicines, including antibiotics, next-generation statins, and anti-fungals. The company leverages proprietary enzymatic biotechnology to produce active pharmaceutical ingredients (APIs), intermediates, and finished dosage forms (FDFs). Headquartered in the Netherlands, Centrient focuses on sustainable, quality-driven manufacturing and supply chain security, serving as a key partner in the global healthcare system to improve patient lives through innovative medicine production.
