Process/ms&t Engineer-pharma/biopharma

**Role Overview**: We are seeking a passionate, proactive, strategic and results-driven Pharma/ Biopharma Business Development Specialist to join our team. In this pivotal role, you will focus on driving revenue growth and market expansion for pharmaceutical or biopharmaceutical markets in **South Asia Pacific, Australia, New Zealand, Japan and Korea**. This...

Join to apply for the Senior Process Engineer (Pharma) role at Wood 2 days ago Be among the first 25 applicants Join to apply for the Senior Process Engineer (Pharma) role at Wood Get AI-powered advice on this job and more exclusive features. Job DescriptionWood is currently recruiting for a Process Engineer with extensive experience in pharmaceutical and...

A leading engineering services company in Singapore is seeking a Senior Process Engineer to work on downstream processes in the bio-pharma sector. Candidates must have at least 5 years of relevant experience, including knowledge of chromatography and sterile filtration. The position involves process mapping, troubleshooting, and working during the...

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...

**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...

**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,...

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...

About No deviationAt No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful...

**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 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...