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.