PMO MSAT Project Manager

No deviation Pte Ltd; Singapore; On-site; SGD 80,000 - 120,000; Full time

Job summary

A leading pharmaceutical consultancy in Singapore is seeking a PMO – MSAT Project Manager. The role involves leading project management for Manufacturing Science and Technology initiatives within a GMP-regulated environment. The ideal candidate has 8–10 years of experience in the pharmaceutical or biopharmaceutical sector, strong project management skills, and expertise in process optimization. Join a company that values innovation, collaboration, and professional development opportunities, offering comprehensive health coverage and a generous leave policy.

Benefits

Generous Leave Policy

Comprehensive Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Qualifications

• 8–10 years of experience in pharmaceutical or biopharmaceutical manufacturing.
• Prior experience in MSAT, Manufacturing, or Technical Operations.
• Hands-on exposure to drug substance and/or drug product manufacturing.

Responsibilities

• Lead end-to-end project management for MSAT-related initiatives.
• Coordinate the review and approval of protocols and reports.
• Maintain project documentation including charters and logs.

Skills

Project management

Process optimization

Cross-functional coordination

Risk management

Education

Bachelors degree in Chemical Engineering

Pharmaceutical Sciences

Job description

About No deviation

At 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 projects and drive innovation.

We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That's why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

Position Overview

The PMO – MSAT Project Manager is responsible for leading end-to-end project management for Manufacturing Science and Technology (MSAT) initiatives within a GMP-regulated pharmaceutical or biopharmaceutical manufacturing environment. This role oversees cross-functional projects including process improvements, technology transfer support, new equipment introduction, and process optimization and troubleshooting. Acting as a key coordination point between MSAT, Manufacturing, Engineering, Quality, and Supply Chain, the Project Manager ensures projects are delivered on time, within scope and budget, and in full compliance with regulatory and quality requirements. The role also provides strong governance, risk management, and communication to support site readiness, inspection preparedness, and successful project execution.

Key Responsibilities

• Lead end-to-end project management for MSAT-related initiatives, including process improvements, tech transfer activities, equipment introduction, and process optimization
• Develop, maintain, and control project plans, timelines, milestones, and budgets
• Track and manage cross-functional dependencies across Manufacturing, QA, QC, Engineering, and Supply Chain
• Act as the primary coordination point between MSAT, Manufacturing, Engineering, and Quality teams
• Facilitate alignment on process changes, validation and qualification activities, and scale-up or site readiness initiatives
• Support MSAT teams in planning process characterization, routine process monitoring, and equipment/process readiness for manufacturing campaigns
• Ensure all project activities comply with GMP, data integrity requirements, and site procedures
• Coordinate the review and approval of protocols, reports, technical justifications, change controls, deviations, and CAPAs
• Identify, assess, and mitigate project risks; manage issues and changes through formal governance processes
• Escalate risks and issues impacting manufacturing schedules, product quality, or regulatory commitments
• Lead regular cross-functional project meetings and provide clear, concise updates to site leadership and global stakeholders
• Maintain project documentation including project charters, RAID logs, action trackers, and decision logs
• Prepare management dashboards, progress reports, and support effective knowledge transfer and project close-out
• Coordinate vendors and external partners as required

Required Qualifications

• Bachelors degree in Chemical Engineering, Biotechnology, Pharmaceutical Sciences, Life Sciences, or a related discipline
• 8–10 years of experience in pharmaceutical or biopharmaceutical manufacturing
• Prior experience in MSAT, Manufacturing, Process Engineering, or Technical Operations
• Demonstrated project management experience within a GMP-regulated environment
• Hands-on exposure to drug substance and/or drug product manufacturing
• Experience supporting technology transfer, scale-up, and process improvement initiatives

Why join us?

• Generous Leave Policy.
• Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
• Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
• Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
• Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How to apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions? If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.