Description of Production Development Supervisor - PT BrightGene Biomedical Indonesia
Job Description
1. Responsible for production process in accordance with their quality specification and strict adherence to GMP and HSE regulation within the required time and cost
2. Manage and controls product’s quality and implementation of quality management system in all production areas and takes necessary action to improve the process to satisfy consumers
3. Analyzes resources utilization (Manpower, Machine, materials and energy) for production line to maximize the utilization of resources and smooth operations in line with approved budget
4. Manage & analyze production performances (KPI) and coordinate improvement action to achieve agreed performance target
5. Ensures the compliance and implementation of safety, health and harmonious relationship engagement of all workers in Production area in order to to comply with government regulation, company policy and standard certification
6. Involves and monitoring a continuous improvement process within the team to cover and develop all requirements concerning People & Organization, Quality & Quantity, Cost, and Regulations
Requirements
1. Apoteker or Bachelor degree specializing in Pharmacy, Chemical, Chemical engineering/ pharmaceutical industry/related with at least 2 years experience working in the pharmaceutical/ FMCG/ Cosmetics industry
2. Fluent in English
3. Able to operate computer especially Microsoft office softwares
4. Knowledge in GMP and HSE protocols is preferable
5. Experienced with automation system & SAP or others ERP system
6. Willing to work in West Karawang
Job Detail
1. Placement location in Karawang New Industry City, Trans Heksa
2. Pharmaceutical company that aims to be at the forefront as a developer and producer of high quality active pharmaceutical ingredients (API)
3. 3 month probation period
