Process/ms&t Engineer-pharma/biopharma

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide. - This role will be responsible for design, plan, perform, interpret, and report scientific experiments to support overall MS&T strategies and objectives.**Key Responsibilities** - Lead / participate in...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide. - This role will be responsible for design, plan, perform, interpret, and report scientific experiments to support overall MS&T strategies and objectives.**Key Responsibilities** - Lead / participate in...

Roles & ResponsibilitiesES 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...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide. - This role will be responsible for design, plan, perform, interpret, and report scientific experiments to support overall MS&T strategies and objectives.**Key Responsibilities** - Lead / participate in...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide. - This role will be responsible for design, plan, perform, interpret, and report scientific experiments to support overall MS&T strategies and objectives.**Key Responsibilities** - Lead / participate in...

More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide.**Key Responsibilities** - Responsible for process engineering design related deliverables such as Piping and Instrumentation Diagrams (P&IDs), Block Flow Diagrams (BFDs), Process Flow Diagrams (PFDs),...

Job Scope - Performing technical assessment and sizing for safety relief valves, rupture discs, vent devices and others. - Originating and checking PRD sizing calculations for Pressure Relief Valves, Bursting/Rupture Discs and Conservation & Breather Vents as per International Standards in API. - Specification for purchasing PRDs - Drafting Pressure Relief...

Roles & Responsibilities: - Responsible for the Project leading and managing for Pharma or Biopharma clients for DCS system (Emerson DeltaV). - Team lead and mentor for automation engineers and graduates trainees. - Defining project infrastructure Scope and requirements, Planning shopfloor network architecture, networking, and hardware deployment in Clean...

**Scope of work for Technical MS&T support** Responsible in conducting the gap analysis of sending unit versus receiving unit and risk assessment includes but not limited to material, process, equipment, utilities, contamination strategy and etc for GMP readiness, successful water run and engineering run Support on the preparation (author or reviewer) of...

**Scope of work for Technical MS&T support** Responsible in conducting the gap analysis of sending unit versus receiving unit and risk assessment includes but not limited to material, process, equipment, utilities, contamination strategy and etc for GMP readiness, successful water run and engineering run Support on the preparation (author or reviewer) of...

Overview / Responsibilities: - Driving technical excellence and assurance. - Carry out process engineering design activities, following client and Amec Foster Wheeler standards and procedures to schedule and budget - Develop, review, and take responsibility for the quality and accuracy of Process engineering deliverables. - Ensure Amec Foster Wheeler and...

**REGIONAL COMMERCIAL DIRECTOR, BIOPHARMA & REGULATED SYNTHESIS**: Our team in **Singapore** currently has an opening for a **Regional Commercial Director, Biopharma & Regulated Synthesis** **YOUR ROLE & RESPONSIBILITIES**: **Job Summary**: Drive topline growth in the Biopharma business and manage assigned internal & external account manager teams. Define...

Role Title: Validation Engineer (BioPharma) Duration: 1 year contract **Responsibilities **. - Support project execution from Feasibility through to project completion/handover, including all project stages such as: - Feasibility - Concept Design, Basic Design, Detailed Design - Commissioning & Qualification - Prepare/perform/review process engineering...

**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,...

Roles & ResponsibilitiesAbout our client: Our client is a leading global biopharma manufacturing company. *Please note that this role will be hired on a 6 months' contract basis to support our client's project. About the role: Support the Quality Event (Deviation) process together with the Process Engineering team and ensure timely creation, analysis, and...

Roles & ResponsibilitiesAbout our client: Our client is a leading global biopharma manufacturing company. *Please note that this role will be hired on a 6 months' contract basis to support our client's project. About the role: Support the Quality Event (Deviation) process together with the Process Engineering team and ensure timely creation, analysis, and...

**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**: - 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...

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...

MS&T Junior Consultant **Responsibilities**: - Perform risk-based commissioning, qualification and validation of pharmaceutical and biopharmaceutical equipment, utilities and process. - Executed / develop validation protocols using a risk-based approach that meets regulatory requirements and industry best practices. - Develop risk assessment, system impact...