Computer System Validation Engineer

PHARMENG TECHNOLOGY PTE. LTD.; Pasir Panjang; On-site; MYR 80,000 - 120,000; Full time

Job summary

A leading healthcare services company is seeking a Computer System Validation Engineer with over 5 years of experience in pharmaceutical engineering. This role involves providing technical guidance, developing qualifications, and coordinating projects. Ideal candidates will have strong knowledge of cGMP operations and experience in validation projects. Competitive wages and opportunities for career growth are offered.

Benefits

Continuous career growth

Opportunities for travel

Competitive wages

Qualifications

• 5+ years of experience in commissioning, qualification or validation of systems.
• Experience with Qualification or Validation of clean utilities.
• Possess the ability to undertake leadership and mentorship duties.

Responsibilities

• Provide technical guidance in the commissioning and qualification of equipment.
• Lead the development of qualification deliverables.
• Prepare protocols and summarize data.
• Coordinate cross-functional meetings to drive project progress.

Skills

Excellent written and spoken English

5+ years in commissioning, qualification, or validation

Knowledge of cGMP operations

Experience in developing validation projects

Knowledge of GAMP and Data Integrity

Leadership skills

Mentorship skills

Strong multi-tasking skills

Ability to lift 50 lbs

Ability to handle multiple projects

Education

Engineering or Science degree

Job description

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking for a Computer System Validation Engineer with experience in pharmaceutical engineering for a role in Singapore.

Responsibilities

• Provide technical guidance into the commissioning, qualification and start-up of various equipment and facilities.
• Lead the development of key qualification deliverables during the project lifecycle to ensure project is well defined, and the action plan to test the system is applicable and relevant.
• Prepare protocols, execute protocols, summarize data, resolve deviations, prepare final reports.
• Experience in bioprocess systems, or other process equipment, utilities, facilities in pharma, biologics, aseptic fill-finish is considered a strong asset.
• Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, provide updates.
• Engage other departments, as required, for design reviews and decisions.
• Travel may be occasionally required for meetings with clients, equipment fabrication vendors or Factory Acceptance Testing (FATs).
• Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases.
• Visit construction and installation sites.
• Supervise contractors during critical testing of system and equipment.
• Other duties as assigned by client, and/or PharmEng, based on workload and project requirements.

Qualifications

• Excellent written and spoken English is required including the preparation of technical documents in English
• Years of experience: 5+ years for years of experience in commissioning, qualification or validation of various systems within the pharmaceutical/biotech industry.
• Knowledge of requirements for a cGMP operations, including SOPs, Change Controls, Validation.
• Experience with developing and executing validation projects.
• Knowledge of GAMP and Data Integrity requirements.
• Previous Pharmaceutical/Biotech experience is mandatory for this role.
• Experience with Qualification or Validation of clean utilities
• Experience with thermal Validation is considered an asset.
• Lead teams of Validation staff, manage staff priorities, provide mentorship/oversight, help staff resolve issues. Leadership is considered an asset, but not required.
• Possess leadership skills, and be able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.
• Possess mentorship skills, to coach and develop junior and intermediate employees.
• Engineering or Science degree, preferably in Automation, Instrumentation, Mechanical, Electrical, Electromechanical, Chemical, Biochemical or a related discipline.
• Ability to lift 50 lbs.
• Travel may be required on occasion.
• Ability to handle multiple projects and work in a fast-paced environment.
• Strong multi-tasking skills.

Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.

EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.