Pharma/Biotech Project Coordinator

Key Responsibilities Coordinate project activities, schedules, and deliverables across engineering, QA, IT, and operations teams. Support the Project Manager in maintaining project plans, dashboards, and action trackers. Facilitate meetings, MOMs, risk registers, and follow-up actions. Manage document control and review workflows (URS, design docs,...

**Location** - Singapore, Central Singapore**Job Type** - Contract**Salary** - $3,000 - $5,000 Per Month**Date Posted** - 16 hours agoAdditional Details **Job ID** - 129610**Job Views** - 38Roles & Responsibilities **Responsibilities**: - Drive and assist Manufacturing MES deployment - Hand-on to work with cross functional teams to implement workflow...

**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,...

**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 Specialists must assist site management to oversight 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...

**Responsibilities**: - Coordinate with suppliers and verify supplier quality standards are in accordance to the requirements - Track and qualify or disqualify suppliers according to standards - Liaise with suppliers or support the senior supplier qual specialist to support documentation compilation and GMP/GDP review per procedural requirements - Monitor...

**Responsibilities**: - Process all Change Plan/Requests for creation or changing of site documents through the company Document Management System following applicable policies, process, and procedures - Perform proofreading of documents and approve submitted to the Documentation Area for further processing in company Document Management System - Notify...

The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and...

Responsible to deliver and ensure successful qualification of 2 types of new QC lab equipment with computerized software (2units each) within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory...

**Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system) - Responsible for overseeing execution of but not limited to IQ, OQ, PQ and ERES Test Scripts of QC laboratory equipment (lab...