Contract Process Engineer (Pharm MNC) – 1 Year / NORTH #HHL

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 67,000 - 89,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore invites a biochemical/biopharma professional to lead deviation investigations and Change Controls within a GMP environment. You will troubleshoot process equipment, support commissioning and qualification activities (IQ/OQ/PQ), and review engineering docs.

The role requires 3–5+ years in pharmaceutical/biopharmaceuticals, strong CAPA management, and familiarity with cGMP.

Qualifications

• 3–5+ years of relevant experience in Pharmaceutical/Biopharmaceutical industries.
• Strong experience in Deviation Investigation and Change Control.
• Good understanding of cGMP manufacturing and process equipment; upstream/downstream bioprocess experience preferred.
• CAPA management and timely closure of quality events.

Responsibilities

• Lead deviation investigations and Change Controls.
• Manage CAPAs and ensure timely closure of quality events.
• Troubleshoot process equipment and support engineering improvements.
• Support commissioning & qualification activities (IQ/OQ/PQ).
• Review P&IDs, URS and engineering documentation.
• Support Cell Culture / Purification process equipment projects.

Skills

Deviation Investigation

Change Control

CAPA Management

Process Equipment Troubleshooting

IQ/OQ/PQ

P&IDs & URS Review

Biopharma Experience

Education

Bachelor's degree

Tools

URS Documentation

P&IDs Review

Job description

Woodland
Mon–Fri, 8.00am–4.30pm
Up to $8,000/month

Job Scope:

• Lead deviation investigations and Change Controls
• Manage CAPAs and ensure timely closure of quality events
• Troubleshoot process equipment and support engineering improvements
• Support commissioning & qualification activities, including IQ/OQ/PQ
• Review P&IDs, URS and engineering documentation
• Support Cell Culture / Purification process equipment projects

Requirements:

• Min. Degree holder with 3–5+ years of relevant experience
• Prior experience in Pharmaceutical / Biopharmaceutical experience
• Strong experience in Deviation Investigation & Change Control
• Good understanding of cGMP manufacturing and process equipment
• Upstream / Downstream bioprocess experience preferred