Senior Pharma Process Engineer — Design & Optimisation

Amaris Consulting Pte Ltd; Singapore; On-site; SGD 80,000 - 120,000; Full time

Benefits offered by this job

Internal Academy training

Team events

Global community

Job summary

Amaris Consulting drives process engineering in pharma/biopharma manufacturing, delivering design, qualification and continuous improvements across equipment and systems. You will own process design, qualification activities and critical change controls while partnering with MS&T, Automation, Manufacturing, Quality and Validation teams.

You will lead troubleshooting, drive yield and cycle-time improvements, and provide on-call support as needed to ensure safe, compliant site operations.

Qualifications

• Degree in Chemical Engineering, Process Engineering, Pharmaceutical Engineering, Biotechnology, Mechanical Engineering, or a related field.
• 5–8 years of experience in process engineering within regulated pharma/biopharma manufacturing.
• Experience with process design, P&ID development, URS, risk assessments, design reviews, and HAZOP.
• Understanding qualification/validation activities: FAT, SAT, IQ, OQ, PQ, requalification.
• Practical knowledge of CIP, SIP, washers, autoclaves or similar systems.
• Experience in managing change controls, deviations, investigations and CAPAs.
• Understanding automated manufacturing processes, including equipment modules and recipes.
• Ability to collaborate with MS&T, Automation, Manufacturing, Quality, Validation and Engineering teams.
• Strong troubleshooting, analytical, documentation and problem-solving skills.
• Ability to work independently, lead when required, and provide on-call support.

Responsibilities

• Develop process designs, P&IDs, URS, SRA, FRA and other engineering docs.
• Participate in design reviews, design qualification activities and HAZOP studies.
• Lead process engineering changes, deviations, and CAPAs.
• Support FAT, SAT, IQ, OQ, PQ and requalification activities.
• Translate process requirements into automation modules, recipes and parameters.
• Provide independent technical support for safe, reliable operations.
• Lead improvements for equipment performance, yield, and cycle time.
• Collaborate with MS&T, Automation, Manufacturing, Quality, Validation and Engineering teams.

Skills

Process design

P&ID development

Risk assessments

HAZOP

CAPAs

Automation collaboration

Education

Degree in Chemical/Process/Pharmaceutical/Biotech/Mechanical Eng

Job description

Amaris Consulting drives process engineering in pharma/biopharma manufacturing, delivering design, qualification and continuous improvements across equipment and systems. You will own process design, qualification activities and critical change controls while partnering with MS&T, Automation, Manufacturing, Quality and Validation teams.

You will lead troubleshooting, drive yield and cycle-time improvements, and provide on-call support as needed to ensure safe, compliant site operations.