Process Engineer

NO DEVIATION PTE. LTD.; Singapore; On-site; SGD 60,000 - 90,000; Full time

Benefits offered by this job

Generous leave

Health coverage

Professional development

Inclusive culture

Career impact

Job summary

No deviation is a pharmaceutical-focused consultancy expanding its manufacturing footprint in Singapore. We seek a Process Engineer to support introduction, qualification, and commercialization of new products, ensuring readiness and compliance across manufacturing operations.

You will collaborate with Quality, Supply Chain, Production, Engineering, and Regulatory teams, coordinating PQ activities, document development, and MES system setup to enable smooth product transfers and launches.

Qualifications

• Bachelor's degree in Chemical Engineering or related discipline.
• 2–5 years in manufacturing, process engineering, tech transfer or PQ environments.
• Experience with MES systems, BOM management, and manufacturing documentation preferred.
• Knowledge of GMP, quality systems and manufacturing validation processes is advantageous.

Responsibilities

• Assess QC buffer requirements and feasibility for Singapore production.
• Evaluate process capabilities and equipment fit for local production implementation.
• Coordinate PQ activities and manage raw material requests for qualification runs.
• Develop and maintain Production Instructions and Bills of Materials.
• Configure MES, verify master data, and support MES-related issues during implementation.

Skills

Process engineering

Cross-functional collaboration

Quality systems

Education

Bachelor's Degree in Chemical Engineering

Tools

MES systems

BOM management

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 Process Engineer is responsible for supporting the introduction, qualification, and commercialization of new products and processes within the manufacturing facility. This role ensures production readiness through process assessment, material planning, system setup, and manufacturing execution support, while maintaining compliance with quality and operational requirements.

Key Responsibilities

Process Assessment & Manufacturing Readiness

• Assess QC buffer requirements and manufacturing feasibility for products to be produced in Singapore.
• Evaluate process capabilities, equipment suitability, and manufacturing constraints to support local production implementation.
• Perform Facility Fit Assessments (FFA) to ensure product and process compatibility with existing manufacturing infrastructure.

Process Qualification (PQ) Support

• Coordinate and support Process Qualification (PQ) activities to ensure manufacturing readiness.
• Raise requests for raw materials required for qualification runs and production startup.
• Ensure proper segregation, identification, and management of raw materials in accordance with quality and regulatory requirements.
• Work closely with Supply Chain, Warehouse, Quality, and Production teams to ensure material availability for qualification activities.

Manufacturing Documentation Development

• Create and maintain Production Instructions (PIs) to support manufacturing operations.
• Develop and manage Bills of Materials (BOMs) to ensure accurate material planning and production execution.
• Review documentation accuracy and alignment with product specifications and manufacturing requirements.

MES & System Implementation

• Configure and set up products, processes, and workflows within the Manufacturing Execution System (MES).
• Verify MES master data, process routes, and system parameters to support production and qualification activities.
• Troubleshoot and resolve MES-related issues during implementation and startup phases.

Cross-Functional Collaboration

• Collaborate with Quality, Supply Chain, Production, Engineering, and Regulatory teams to ensure smooth product transfers and launches.
• Support investigations, change controls, and continuous improvement initiatives related to manufacturing processes.
• Participate in project meetings and provide technical expertise during product introduction activities.

Required Qualifications

• Bachelor's Degree in Chemical Engineering, Process Engineering, Manufacturing Engineering, Biotechnology, or a related discipline.
• 2-5 years of experience in manufacturing, process engineering, technology transfer, or process qualification environments.
• Experience with MES systems, BOM management, and manufacturing documentation is preferred.
• Knowledge of GMP, quality systems, and manufacturing validation processes is an advantage.

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.