Process Engineer

No deviation; Singapore; On-site; SGD 70,000 - 110,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Wellness Coverage

Professional Development Opportunities

Inclusive Culture

Shape the Future

Job summary

No Deviation is seeking a Process Engineer with a strong biologics manufacturing background to support routine manufacturing and New Product Introduction (NPI) activities. The role emphasizes SUS activities, deviation investigations, CAPA, and cross-functional collaboration with Manufacturing, MSAT, Quality, Engineering and Validation teams.

The ideal candidate holds a degree in Chemical/Biochemical Engineering or related field with 3–6 years of biologics experience and hands-on work with

Qualifications

• Degree in Chemical/Biochemical Engineering, Biotechnology, Life Sciences or related discipline.
• 3–6 years of relevant experience in biologics/biopharmaceutical manufacturing.
• Experience with Single-Use Systems, deviations, change controls and troubleshooting.
• NPI or technology transfer experience would be advantageous. Good understanding of GMP manufacturing requirements.

Responsibilities

• Act as Process Engineer for Single-Use System (SUS) activities and support routine biologics manufacturing operations.
• Troubleshoot single-use defects, process issues and decontamination-related activities.
• Support deviation investigations, root cause analysis and CAPA implementation.
• Own/support change controls related to manufacturing processes, single-use systems and NPI activities.
• Support NPI and manufacturing readiness, including process assessments, documentation and implementation of process changes.
• Provide technical and shop-floor support during manufacturing and new product introduction.
• Collaborate with Manufacturing, MSAT, Quality, Engineering and Validation teams.

Skills

Process troubleshooting

Collaboration

Quality mindset

Education

Chemical/Biochemical Engineering or related

Biologics/biopharmaceutical manufacturing experience

Tools

Single-Use Systems

CAPA implementation

NPI / tech transfer

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.

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 looking for a Process Engineer with a strong biologics manufacturing background to support routine manufacturing and New Product Introduction (NPI) activities.

Key Responsibilities

• Act as Process Engineer for Single-Use System (SUS) activities and support routine biologics manufacturing operations.
• Troubleshoot single-use defects, process issues and decontamination-related activities.
• Support deviation investigations, root cause analysis and CAPA implementation.
• Own/support change controls related to manufacturing processes, single-use systems and NPI activities.
• Support NPI and manufacturing readiness, including process assessments, documentation and implementation of process changes.
• Provide technical and shop-floor support during manufacturing and new product introduction.
• Collaborate with Manufacturing, MSAT, Quality, Engineering and Validation teams.

Required Qualifications

• Degree in Chemical/Biochemical Engineering, Biotechnology, Life Sciences or related discipline.
• 3–6 years of relevant experience in biologics/biopharmaceutical manufacturing.
• Experience with Single-Use Systems, deviations, change controls and troubleshooting.
• NPI or technology transfer experience would be advantageous. Good understanding of GMP manufacturing requirements.

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.