Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

Process Engineer-C&Q (Pharmaceutical Manufacturing Operations) at Unison Group

Singapore, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

31 Dec, 25

Salary

0.0

Posted On

02 Oct, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process Engineering, C&Q Execution, Qualification Protocols, FAT/SAT Activities, Commissioning, Troubleshooting, DeltaV, GMP Compliance, Regulatory Requirements, Collaboration, Risk Assessments, Documentation, Pharmaceutical Manufacturing, Batch Execution, Operational Input, Process Knowledge

Industry

Business Consulting and Services

Description

· Support C&Q execution for process equipment, utilities, and manufacturing systems. · Review and execute qualification protocols (IQ, OQ, PQ) and support FAT/SAT activities. · Provide process and operational input during commissioning and troubleshooting. · Support DeltaV-related activities (recipes, phases, batch execution understanding). · Develop/review C&Q documentation (URS, risk assessments, protocols, reports). · Ensure adherence to GMP, regulatory, and data integrity requirements. · Collaborate with operations, QA, and automation teams to meet project deliverables. · Bachelor’s degree in chemical / Biochemical / Process / Mechanical Engineering or related field. · 4–6 years’ experience in pharmaceutical/biotech manufacturing or operations, with exposure to C&Q. · Strong process knowledge of pharmaceutical manufacturing. · Working knowledge of DeltaV – recipes, batch execution, troubleshooting. · Hands-on experience with C&Q documentation and execution (IQ, OQ, PQ). · Good knowledge of cGMP, FDA/EMA guidelines, and industry practices.

Responsibilities

Support C&Q execution for process equipment, utilities, and manufacturing systems. Collaborate with operations, QA, and automation teams to ensure project deliverables are met.