Operation Engineer (1 year contract) | BioPharma | West

GMP TECHNOLOGIES (S) PTE LTD; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

A leading biotechnology firm in Singapore is seeking a professional to develop and validate buffer and media preparation processes, ensuring compliance and operational efficiency. The ideal candidate should have a Bachelor’s degree in Chemical Engineering or related fields, with 3-5 years of experience in regulated manufacturing environments. This role will involve hands-on process validation, collaboration with production supervisors, and strong technical writing skills. Competitive salary and benefits on offer.

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

Education

Bachelors degree in Chemical Engineering, Biomedical Engineering, Biotechnology

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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This is in partnership with the Employment and Employability Institute Pte Ltd (e2i).

e2i is the empowering network for workers and employers seeking employment and employability solutions. e2i serves as a bridge between workers and employers, connecting with workers to offer job security through job-matching, career guidance and skills upgrading services, and partnering employers to address their manpower needs through recruitment, training, and job redesign solutions. e2i is a tripartite initiative of the National Trades Union Congress set up to support nation-wide manpower and skills upgrading initiatives.

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