Pharma CSV Engineer: Validation & Compliance

PSC Biotech

Singapore

On-site

SGD 70,000 - 100,000

Full time

14 days+

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Job summary

A global biopharmaceutical company is seeking an experienced candidate to develop and review validation plans, perform risk assessments, and ensure compliance with regulatory guidelines in Singapore. The ideal candidate has a Bachelor’s degree in a relevant field and 5-8 years of experience in computer system validation within a regulated industry. Strong documentation and collaboration skills are essential. This role offers a dynamic working environment and the opportunity to contribute to compliance and validation activities.

Qualifications

  • 5-8 years of experience in CSV within pharmaceutical manufacturing or regulated industries.
  • Strong understanding of GxP regulations.
  • Experience with PLC SCADA, MES, or pharma manufacturing Automation systems.

Responsibilities

  • Develop and review validation plans and protocols.
  • Perform risk assessments and impact analysis.
  • Ensure compliance with regulatory guidelines.
  • Collaborate with IT and Quality Assurance teams.
  • Manage change control and deviation investigations.
  • Support audits and inspections by regulatory authorities.
  • Maintain validation documentation.

Skills

Validation plans development
Risk assessment
Regulatory compliance
Collaboration with cross-functional teams
Change control management
Documentation skills

Education

Bachelor’s degree in Pharmacy, Life Sciences, Engineering, or Computer Science

Job description

A global biopharmaceutical company is seeking an experienced candidate to develop and review validation plans, perform risk assessments, and ensure compliance with regulatory guidelines in Singapore. The ideal candidate has a Bachelor’s degree in a relevant field and 5-8 years of experience in computer system validation within a regulated industry. Strong documentation and collaboration skills are essential. This role offers a dynamic working environment and the opportunity to contribute to compliance and validation activities.
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