Validation Engineer

PSC Biotech; New York (NY); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

Medical benefits

Sick time

Job summary

PSC Biotech in Columbia, MO seeks a Validation Engineer to support qualification of computerized systems within a regulated life sciences environment. The role focuses on lifecycle activities to ensure systems are properly qualified, documented, and maintained. This is a 6-month W2 temp contract with potential extension. Applicants must be legally authorized to work in the United States. Travel to project sites nationwide may be required, and Corp-to-Corp is not accepted.

Qualifications

• Experience validating computerized systems in regulated settings.
• Knowledge of GMP and quality requirements.
• Ability to develop and review validation documents.
• Strong technical writing and organization.
• Experience collaborating with Quality, Engineering and IT teams.

Responsibilities

• Support qualification/validation of computerized systems.
• Develop, review, and execute validation protocols and documentation.
• Support validation throughout system lifecycle.
• Review requirements for completeness and compliance.
• Document results and resolve discrepancies.
• Coordinate with cross-functional stakeholders.
• Support change control and validation-related assessments.
• Maintain traceable validation records.
• Assist audits and inspections readiness.

Skills

CSV validation

Quality documentation

Technical writing

Cross-functional collaboration

GMP awareness

Education

Bachelor's degree or equivalent

Job description

Columbia, United States | Posted on 11/02/2026

PSC Biotech providesthe life sciences with essential services to ensure thathealth care products are developed, manufactured, anddistributed to the highest standards, in compliance with allapplicable regulatory requirements.

Our goal is toskyrocket ourclients’ success, and you can be a part of ourteam’s achievements. Employing a global team of skilledprofessionals and experts that span across strategicallylocated offices in North America, Europe, Asia and the MiddleEast, we are proud of the roles we have fulfilled to help ourclients achieve success.

TheExperience

With operationsspanning the globe and featuring a multi-cultural team, PSCBiotech® is passionate about bringing the best and brightesttogether in an effort to form something truly special. Whenyou make the decision to join our team, you will be offeredthe ability to feel inspired in your career, explore yourprofessional passions, and work alongside a group of peoplewho will value and nurture your talents.

We are firm believersin coaching and developing the next generation of industryleaders and influencers. As such, you will not only beoffered compensation and benefits structure that rewards you,but also be provided with the tools that will help you growand learn.

At PSC Biotech®, it’sabout more than just a job—it’s about your career and yourfuture.

Your Role

The Validation Engineer is responsible for supporting the qualification of computerized systems within a regulated life sciences environment. This role will support computerized system lifecycle activities to help ensure systems are appropriately qualified, documented, and maintained in accordance with applicable quality and regulatory requirements.

This is a 6-month W2 temp contract opportunity based in Columbia, MO, with potential for extension. Applicants must be legally authorized to work in the United States. Employer-sponsored work authorization is not available for this position, and Corp-to-Corp (C2C) arrangements will not be considered.

• Support the qualification and validation of computerized systems.
• Develop, review, and execute computer system validation and qualification documentation.
• Support validation activities throughout the computerized system lifecycle.
• Review system requirements and associated documentation for completeness and compliance with established procedures.
• Develop and execute validation protocols and document results in accordance with approved procedures.
• Identify, document, and support the resolution of discrepancies or deviations encountered during qualification and validation activities.
• Collaborate with cross-functional stakeholders, including Quality, Engineering, IT, and system owners, to coordinate validation activities.
• Support change control and assessment activities associated with validated computerized systems.
• Maintain accurate and complete validation documentation in accordance with applicable quality requirements.
• Support inspection and audit readiness by ensuring computerized system validation records are complete and traceable.
• Ensure validation activities are performed in alignment with applicable GMP requirements and site procedures.
  

Requirements

• Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related technical discipline, or equivalent relevant experience.
• 5+ years of experience with computerized system validation (CSV) and/or computerized system qualification in a regulated environment.
• Working knowledge of validation lifecycle principles and documentation.
• Understanding of GMP-regulated systems and applicable quality requirements.
• Experience developing, reviewing, and/or executing validation or qualification documentation.
• Ability to identify and document discrepancies and support resolution of validation issues.
• Strong technical writing, documentation, and organizational skills.
• Effective communication skills with the ability to collaborate across Quality, Engineering, IT, and other functional groups.
• Ability to manage multiple validation activities and priorities while maintaining a high level of attention to detail.
  
• At PSC Biotech,many of our projects and clients are located invarious regions around the country. Therefore, wevalue candidates who are willing and able to travelas needed for project assignments and clientengagements. The ability to adapt to differentlocations, cultures, and work environments is essential, as itallows our team members to collaborate effectively withclients and colleagues nationally.
  
• Must be authorized towork in the US.
  
• No C2C at thistime.
  

W2 Temp roles include our Medical and Sick Time benefits

EqualOpportunity Employment Statement

PSC is committed to a policy of Equal Employment Opportunity with respectto all employees, interns, and applicants for employment.Consistent with this commitment, our policy is to comply with allapplicable federal, state and local laws concerning employmentdiscrimination. Accordingly, the Company prohibits discriminationagainst qualified employees, interns and applicants in all aspectsof employment including, but not limited to: recruitment,interviewing, hiring (or failure or refusal to hire), evaluation,compensation, promotion, job assignment, transfer, demotion,training, leaves of absence, layoff, benefits, use of facilities,working conditions, termination and employer-sponsored activitiesand programs, including wellness, social and recreationalprograms. Employment decisions will be made without regard to anapplicant’s, employee’s, or intern’s actual or perceived: race,color, religion, sex (including pregnancy, gender identity, andsexual orientation), national origin, age (40 or older),disability, genetic information, or any other status protected bylaw.