Process Safety Manager-gmp/pharma

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PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational...

**Manufacturing Biotechnologist upstream/downstream/central services (Pharma/Biotech) **Responsibilities**: - Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.) - Support day to day production activities and record data according to Electronic Batch Record (EBR) in compliance with GMP, Environmental, Health and Safety...

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...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational...

**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...

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 qualification -...

**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,...