CSV Consultant

ORKA CONSULTING PARTNERS PTE. LTD.; Singapore; On-site; SGD 60,000 - 80,000; Full time

Job summary

A consulting firm focused on life sciences is seeking a consultant for Computer System Validation projects in Singapore. You'll be responsible for delivering CSV consulting services, drafting essential documentation, and ensuring compliance with regulatory standards. Ideal candidates should hold a Bachelor’s degree in Life Sciences or Engineering and have 2-4 years of relevant experience. Join a professional team that values collaborative work and offers opportunities for career development and impactful learning.

Benefits

Career development opportunities

Professional working environment

Access to training materials and mentorship

Qualifications

• 2-4 years of experience in CSV or related roles within a regulated environment.
• Experience in automation systems validation.
• Ability to work independently and produce results with minimal supervision.

Responsibilities

• Deliver CSV consulting projects for computerized system implementations.
• Draft and maintain CSV documentation to ensure compliance.
• Manage stakeholders to plan and implement validation activities.

Skills

Computer System Validation (CSV)

Stakeholder management

Project management

Regulatory compliance

Education

Bachelor’s degree in Life Sciences or Engineering

Job description

Key Responsibilities:

• Deliver CSV consulting projects to support implementation of computerized systems (e.g., DeltaV, Siemens PCS7, Rockwell PLCs) in the Life Sciences clients with compliance of GxP and other relevant regulatory standards.
• Deliver CSV consulting projects to support OS upgrade (e.g., Windows 11 upgrade) for laboratory and manufacturing equipment.
• Draft, review and maintain CSV documentation such as URS, FDS, Risk Assessment, Audit Trail Assessments, ERES assessments, Data Security Assessment, Validation Plans, IOPQ Protocols, RTM and any other lifecycle management documents.
• Provide expert consultation to ensure compliance with current regulatory requirements (e.g., GAMP5, 21 CFR Part 11, Annex 11).
• Support system configuration and computerised system (CS) activities such as backup and restore, access management, etc.
• Manage stakeholders from cross-functional teams (IT, Quality, Engineering, Operations) to plan and implement validation activities.
• Collaborate with other stakeholders including IT/OT, automation and quality teams to deliver validation projects on schedule.
• Draft, revise and review SOPs, forms and related operational and maintenance documents.

Requirements:

• Hold Bachelor’s degree in Life Sciences, Engineering or related field.
• Possess 2-4 years of experience in Computer System Validation (CSV), Automation, or related quality and compliance roles within a regulated environment (pharmaceutical, medical device, etc.)
• Familiar with CSV lifecycle management and automation systems validation.
• Had experience in leading a project from planning through execution and reporting.
• Able to manage stakeholders and deliverables within project timelines.
• Must be able to work independently and deliver results under minimal supervision.
• Understand computerised system regulatory requirements (e.g., 21 CFR Part 11, Annex 11) and industry best practice (e.g., ISPE GAMP5).
• Preferably with experience in change, incident and problem management.

Why Join Orka:

• Work that Matters: Support clients bringing innovative and life saving solutions to the population.
• Career Development: Build a consulting career in a professional consulting company with Life Sciences focus.
• Professional Environment: Work with similar professionals possessing Intelligent, Resourceful, Loyal and Teamwork characteristics.
• Impactful Learning and Mentoring: Develop yourself in an environment that heavily foster learning attitude and benefit from access to training materials, references, mentors and management with wide range of regulated industry experiences.