Senior CSV Engineer​/Senior Validation Engineer

Verista’s 500 experts team up with the world’s most recognizable brands in the life science industry to solve their business needs. The nature of our business is to empower growth and innovation within the scientific community and to help researchers, organizations, and companies solve some of the world’s most pressing healthcare challenges. Verista provides innovative solutions and services that empower informed decision-making and are the result of our significant investment in our people and our capabilities.

Our ability to grow is driven by world-class people who thrive in a team environment and share our mission to enable life sciences clients to improve lives. Our talented and dedicated professionals are committed to making an impact every day.

• We empower and support our colleagues
• We commit to client success at every turn
• We have the courage to do the right thing
• We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
• We constantly acquire new skills and learn from our experiences to enhance our collective expertise

• Lead CSV remediation for laboratory and legacy systems, performing gap analyses against current regulatory and internal validation standards
• Develop and execute remediation strategies, supporting validation of 6–10 major laboratory systems
• Author, review, and approve CSV documentation including validation plans, protocols, reports, and risk assessments
• Support validation of GxP laboratory systems such as chromatography (HPLC, TLC), environmental monitoring, and other computerized lab systems
• Collaborate cross‑functionally with Quality, IT, Laboratory Operations, and Engineering to support system inventory definition, audit readiness, and continuous improvement initiatives

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline
• Senior‑level experience (5‑10 years) in Computer System Validation (CSV) within a regulated GxP environment, including legacy system remediation
• Demonstrated experience validating laboratory computerized systems (e.g., HPLC, CDS, environmental monitoring)
• Strong working knowledge of FDA, EMA, and GAMP 5 regulatory expectations
• Proven ability to independently perform gap assessments, drive remediation activities, and communicate effectively across stakeholders, with exposure to CQV/equipment validation considered a plus

For US geography, the salary range for this position is shown below. The actual salary is dependent upon a variety of job‑related factors such as professional background, training, work experience, location, business needs, market demand, and competitive market practice. Therefore, in some circumstances, the actual salary could fall outside of this expected range. This salary range is subject to change and may be modified in the future.

National (US) Range: $80,465 USD - $122,603 USD

Verista is an equal‑opportunity employer.

• High growth potential and fast‑paced organization with a people‑focused culture
• Competitive pay plus performance‑based incentive programs
• Company‑paid Life, Short‑Term, and Long‑Term Disability Insurance.
• Medical, Dental & Vision insurances
• FSA, DCARE, Commuter Benefits
• Supplemental Life, Hospital, Critical Illness and Legal Insurance
• Health Savings Account
• 401(k) Retirement Plan (Employer Matching benefit)
• Paid Time Off (Rollover Option) and Holidays
• As Needed Sick Time
• Tuition Reimbursement
• Team Social Activities (We have fun!)
• Employee Recognition
• Employee Referral Program
• Paid Parental Leave and Bereavement

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