Process Engineer

JUPITER RECRUITMENT AGENCY PTE. LTD.; Singapore; On-site; SGD 55,000 - 75,000; Full time

Job summary

A leading recruitment agency in Singapore is looking for a Process Engineer specializing in pharmaceutical manufacturing. The role involves designing, optimizing, and ensuring compliance of process systems with GMP standards and customer specifications. Candidates should have a degree in Chemical or Process Engineering, along with experience in biotech or cleanroom environments. Strong problem-solving and analytical skills are essential. This position offers a dynamic work environment where collaboration and technical documentation are key.

Qualifications

• Degree in Chemical Engineering, Process Engineering, or related field.
• Experience in pharmaceutical, biotech, or cleanroom-based process environments.
• Knowledge of cGMP, GAMP, ISPE guidelines.

Responsibilities

• Design and develop process flows, P&IDs for pharmaceutical production lines.
• Support installation and commissioning of process equipment.
• Conduct process risk assessments and qualification activities.
• Collaborate with teams to ensure compliance with cGMP standards.
• Troubleshoot process deviations and provide solutions.
• Prepare technical documentation and reports for audits.

Skills

Analytical skills

Problem-solving skills

Education

Degree in Chemical Engineering

Degree in Process Engineering

Job description

Process Engineer – Pharmaceutical

The Process Engineer will be responsible for designing, optimizing, and supporting the installation of process systems used in pharmaceutical manufacturing. This role ensures all installed systems comply with GMP standards, regulatory requirements, and customer specifications.

Key Responsibilities

• Design and develop process flows, P&IDs, material and energy balances forpharmaceutical production lines.
• Support installation and commissioning of process equipment (mixing vessels, bioreactors, filtration systems, CIP/SIP systems, etc.).
• Conduct process risk assessments, FAT/SAT, and qualification activities (IQ/OQ).
• Collaborate with QA, validation, mechanical/electrical teams to ensure compliance withcGMP and industry standards.
• Troubleshoot process deviations and provide technical solutions.
• Prepare technical documentation, SOPs, and reports for regulatory audits.

Requirements

• Degree in Chemical Engineering, Process Engineering, or related field.
• Experience in pharmaceutical, biotech, or cleanroom-based process environments.
• Knowledge of cGMP, GAMP, ISPE guidelines.
• Strong analytical and problem-solving skills.