No deviation

Project Manager (Engineering)

No deviation  •  Singapore, SG (Onsite)  •  3 hours ago
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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

We are seeking an experienced Project Manager (Engineering) to lead and coordinate pharmaceutical engineering / CAPEX projects from project initiation through execution, commissioning and final handover.The successful candidate will be responsible for overall project planning, cost and schedule control, risk management, procurement, contractor management, construction execution and project governance, ensuring projects are delivered safely and in accordance with agreed scope, quality, budget and timeline requirements.

Key Responsibilities

  • Develop Project Charters, Business Cases, CAPEX requests and project initiation documentation.
  • Define project scope, execution strategy, delivery methodology and overall project objectives.
  • Develop and maintain:
  • Project schedules
  • Work Breakdown Structures (WBS)
  • Cost Breakdown Structures (CBS)
  • Cost estimates and forecasts
  • Project execution and controlling plans
  • Perform project risk assessments covering safety, quality, technical, functional and execution risks.
  • Establish project change control, risk management and reporting processes.
  • Develop sourcing and procurement strategies and support tendering, vendor selection and contract award.
  • Prepare technical specifications, Bills of Quantities and supporting procurement documentation.
  • Manage and coordinate engineering consultants, vendors, contractors and other third parties.
  • Lead project HSE planning and ensure contractor compliance with site safety requirements.
  • Conduct project reviews including Technical Quality Reviews, constructability reviews and Stage Gate assessments.
  • Monitor and report project performance against cost, schedule, scope, quality and risk.
  • Manage project changes, claims, deficiencies and deviations throughout execution.
  • Coordinate statutory approvals and permits where required.
  • Lead or oversee construction management and installation supervision activities.
  • Coordinate new equipment FAT, SAT, inspections and technical acceptance.
  • Develop project turnover and handover strategies and coordinate completion activities.
  • Ensure project documentation is properly managed, archived and transferred to the relevant operational teams.
  • Manage provisional and final project handover.
  • Prepare final project reports, benchmarking information and lessons learned.
  • Ensure investment projects are delivered in accordance with customer requirements for cost, schedule, functionality, safety and quality.

Required Qualifications

  • Degree in Engineering or a related technical discipline.
  • Strong experience in engineering project management / CAPEX project delivery, preferably within the pharmaceutical, biotechnology or regulated manufacturing industry.
  • Experience managing projects across multiple phases including:
  • Concept / Definition Design Procurement Construction Commissioning Handover.
  • Good understanding of project controls including budgeting, cost forecasting, scheduling, risk management and change control.
  • Experience managing engineering contractors, equipment vendors and construction activities.
  • Familiarity with FAT, SAT, equipment installation and commissioning activities.
  • Knowledge of pharmaceutical / GMP engineering environments would be highly advantageous.
  • Strong understanding of project HSE and contractor safety management.
  • Strong stakeholder management, communication and coordination skills.
  • Able to work independently and manage multiple project interfaces in a fast-paced environment.

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.

No deviation

About No deviation

Founded in 2007, No deviation is a trusted partner to pharmaceutical and biotech companies seeking smarter ways to deliver compliance. From engineering consultancy to CQV execution, regulatory compliance, and digital enablement, we support our clients across the entire project lifecycle in Asia, Europe.

We specialise in:

CQV (Commissioning, Qualification & Validation)

Lean, risk-based approaches aligned with GAMP 5, Annex 15, and ASTM E2500.

Quality, Compliance & Regulatory

Audit readiness, QMS remediation, documentation, and training.

Project Management & Technical Support

From operational readiness to vendor coordination.

Digital Enablement

Implementation of paperless validation (e.g. Kneat Gx), data integrity, and process digitalisation.

Specialised Training & Talent Support

Upskilling programs and resource placement to accelerate project success.

Our approach is rooted in patient safety, process understanding, regulatory compliance, and a constant drive for operational excellence in terms of safety, quality, delivery, and cost.

If you’re troubleshooting a deviation, planning a major CQV deployment, or scaling digital validation tools, we work side-by-side with your teams to deliver meaningful outcomes. Our methodology draws from ICHQ9 risk principles, with a hands-on framework: Understand - Observe - Define - Implement.

Want to learn more about paperless CQV, digital QMS, or project-ready resources? We’re happy to talk. Visit nodeviation.com to explore how we can support you.

Industry
Chemicals & Materials
Company Size
51-200 employees
Headquarters
Singapore, SG
Year Founded
2007
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