Operation Engineer (1 year contract) | UK Pharma | West

GMP Technologies; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading biotech company in Singapore is seeking a skilled professional to develop and validate processes in a regulated manufacturing environment. The ideal candidate will have 3-5 years of experience, particularly in New Product Introduction and Cleaning Validation. Strong communication and technical writing abilities are essential for this role, which supports continuous improvement and operational efficiency.

Qualifications

• Min. 3-5 years of experience in a regulated manufacturing environment.
• Direct, hands-on experience in New Product Introduction (NPI) or Process Validation.
• Strong knowledge of Cleaning Validation principles and regulatory guidelines.

Responsibilities

• Develop and validate buffer and media preparation processes.
• Establish and execute equipment cleaning validation protocols.
• Support new assembly and manufacturing process introductions.

Skills

Process Validation

Cleaning Validation

Technical Writing

Communication

Teamwork

Leadership

Education

Bachelors degree in Chemical Engineering, Biomedical Engineering, Biotechnology, or related field

Job description

Jobscope:

• Develop and validate buffer and media preparation processes, ensuring smooth process transfer to production.
• Establish and execute equipment cleaning validation protocols to meet operational and quality standards.
• Support new assembly and manufacturing process introductions, ensuring readiness and compliance.
• Create validation protocols and reports in alignment with project requirements and timelines.
• Collaborate closely with production supervisors to plan, execute, and monitor validation activities.
• Ensure timely completion and proper documentation of protocols, reports, and related records.
• Contribute to continuous improvement in operations efficiency and process reliability.

Requirements:

• Bachelors degree in Chemical Engineering, Biomedical Engineering, Biotechnology, or a related field.
• Min. 3-5 years of experience in a regulated manufacturing environment (Biotech, Pharma, or Medical Device).
• Direct, hands‑on experience in New Product Introduction (NPI) or Process Validation.
• Strong knowledge of Cleaning Validation principles and regulatory guidelines (e.g., residue limits, analytical testing).
• Familiarity with cGMP standards and compliance practices.
• Excellent technical writing skills for drafting validation protocols and reports.
• Strong communication, teamwork, and leadership abilities to guide cross‑functional validation teams.

To apply, please visit www.gmprecruit.com

To learn more about this opportunity, please contact Fiona Koh; [e-mail]

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R11092398

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By applying for this role, you consent to GMP Recruitment Services (S) Pte Ltds PDPA and e2is PDPA