Process Validation Engineer — Pharma/Biotech (1-year Contract)

GMP Technologies

Singapore

On-site

SGD 60,000 - 80,000

Full time

14 days+

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Job summary

A leading pharmaceutical firm in Singapore is seeking an Operations Engineer on a 1-year contract to develop and validate buffer and media preparation processes. The ideal candidate will have a bachelor's degree in Chemical Engineering, a minimum of 3-5 years of experience in a regulated manufacturing environment, and strong knowledge of cleaning validation. This role involves collaboration with production supervisors and creating validation documentation. Excellent technical writing, communication, and leadership skills are required to guide cross-functional teams.

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.

Responsibilities

  • Develop and validate buffer and media preparation processes.
  • Establish and execute equipment cleaning validation protocols.
  • Support new assembly and manufacturing process introductions.
  • Create validation protocols and reports.
  • Collaborate with production supervisors to monitor validation activities.
  • Ensure completion and documentation of protocols.
  • Contribute to improvements in operations efficiency.

Skills

Cleaning Validation principles
Technical writing
Teamwork
Leadership
Regulatory guidelines knowledge

Education

Bachelors degree in Chemical Engineering, Biomedical Engineering, Biotechnology

Job description

A leading pharmaceutical firm in Singapore is seeking an Operations Engineer on a 1-year contract to develop and validate buffer and media preparation processes. The ideal candidate will have a bachelor's degree in Chemical Engineering, a minimum of 3-5 years of experience in a regulated manufacturing environment, and strong knowledge of cleaning validation. This role involves collaboration with production supervisors and creating validation documentation. Excellent technical writing, communication, and leadership skills are required to guide cross-functional teams.
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