Process Safety Manager-gmp/pharma

**PROJECT MANAGER (VALUE ADDED SERVICES), PHARMA APAC**: Our team in **Singapore** currently has an opening for a **Project Manager (Value Added Services), Pharma APAC** **YOUR ROLE & RESPONSIBILITIES**: **Objective**: To support facilities management for Pharma Value Added Services (VAS) department and ensure regional pharma facilities are in compliance to...

My client is seeking an **Assistant Production Manager**to support manufacturing operations by driving GMP-compliant processes, leading continuous improvement initiatives, and enhancing production efficiency across all products. **Key Responsibilities**: - Lead Continuous Process Improvements, CAPAs, and Change initiatives - Improve employee capabilities...

**Responsibilities**: - Responsible for handling the development of operation protocols for upstream or downstream operations starting from the dispensary of raw materials up to end of manufacturing process. - Execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for...

About the Company: Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world class distribution, digital, and commercial services to support the growing healthcare needs in this region.The company was started a hundred years ago and has grown to become...

**About the Company**: Zuellig Pharma is a leading healthcare solutions company in Asia, and our purpose is to make healthcare more accessible to the communities we serve. We provide world class distribution, digital, and commercial services to support the growing healthcare needs in this region. The company was started a hundred years ago and has grown to...

**Responsibilities**: - Responsible to handle the development of operation protocols for upstream or downstream operations starting from the dispensary of raw materials up to end of manufacturing process. - Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for...

Support equipment, facilities, utilities qualifications Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and complete execution in a timely fashion Manage qualification execution and lead qualification deviation investigations encountered during...

Jobscope Support the site in identifying, assessing and managing process hazards by having detailed knowledge of relevant methods like HAZOP, LOPA, Consequence/Effects modelling, QRA initiating, leading and facilitating sessions to apply these methods when required being familiar with the PSM (Process Safety Management) standard and consulting the site...

**Responsibilities**: - Main responsibilities include overseeing batch record review and incoming material quality audit - Provide quality oversight of GMP manufacturing and manufacturing support, including technical operations, engineering, QC laboratory and supply chain activities - Review completed incoming material inspection packages, Batch Records,...

Quality Operations Associate must assist site management to oversee the quality system execution on the manufacturing and production areas at all times. The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of...