Urgent - Contract Process Engineer - Biopharma Mnc #hms

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 81,000 - 97,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD in Singapore is seeking an experienced Contract Process Engineer for a biopharma MNC. The role is based in Kranji, walking distance from MRT, on a 1-year contract, Mon-Fri 8.00am-4.30pm, with immediate starters preferred.

You will lead deviation investigations, manage change controls, drive CAPA, and support commissioning, qualification, IQ/OQ/PQ, and equipment handover with cGMP compliance.

Qualifications

• Lead deviation/quality event investigations from initiation through closure.
• Lead change controls for equipment and facility modifications.
• Drive CAPA projects arising from deviation investigations.
• Troubleshoot and fault-find production equipment issues.
• Draft and execute commissioning and qualification protocols.
• Support IQ/OQ/PQ execution and equipment qualification activities.

Responsibilities

• Review P&IDs, URS, functional specifications and engineering drawings.
• Participate in equipment installation, commissioning and qualification.
• Review vendor and construction turnover packages.
• Work closely with Manufacturing, MSAT, Automation, Validation and external engineering consultants.
• Ensure engineering activities comply with cGMP and Good Engineering Practices.

Skills

Quality investigations

Change Controls

CAPA

Troubleshooting

Commissioning & Qualification

Job description

URGENT | CONTRACT PROCESS ENGINEER - BIOPHARMA MNC

Kranji | Walking distance from MRT

Up to $8,000/month

1-Year Contract

Mon-Fri | 8.00am-4.30pm

Immediate starters preferred

• Lead and manage Deviation / Quality Event investigations from initiation through closure
• Lead Change Controls for equipment and facility modifications
• Drive CAPA projects arising from deviation investigations
• Troubleshoot and fault-find production equipment issues
• Draft and execute commissioning and qualification protocols
• Support IQ/OQ/PQ execution and equipment qualification activities
• Review P&IDs, URS, functional specifications and engineering drawings
• Participate in equipment installation, commissioning and qualification
• Review vendor and construction turnover packages
• Work closely with Manufacturing, MSAT, Automation, Validation and external engineering consultants
• Support improvements and modifications within Cell Culture / Purification areas
• Ensure engineering activities comply with cGMP and Good Engineering Practices