6421 - CSV Engineer (Laboratory) / Validation Engineer 2

Veristainc; New Jersey; Hybrid; USD 65,000 - 105,000; Full time

Benefits offered by this job

High growth potential

Competitive pay plus performance-based incentives

Company-paid disability insurance

Medical, dental & vision insurances

401(k) Retirement Plan

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Veristainc is seeking an experienced CSV Engineer in New Jersey to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The role involves managing multiple validation activities while ensuring compliance with GxP standards.

Ideal candidates will possess strong CSV experience in regulated environments, prior laboratory instrument validation experience, and excellent communication skills. The position includes benefits and a salary range of $65,000 to $105,000 USD.

Qualifications

• Strong CSV experience in a GxP laboratory or regulated life sciences environment.
• Prior experience with laboratory instrument implementation and validation.
• Experience with ELLA and Synergy Neo2 is strongly preferred.

Responsibilities

• Support CSV activities for ELLA and Synergy Neo2 instrument implementation.
• Develop and execute validation deliverables including validation plans and test protocols.
• Partner with lab, Quality, IT, and project stakeholders to ensure validation activities.

Skills

CSV experience in GxP laboratory

Managing multiple validation activities

Strong communication skills

Experience with ELLA and Synergy Neo2

Job description

Description

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.

Company Culture Guidelines & Values

• 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

Job Overview

We are seeking an experienced CSV Engineer to support the implementation and validation of ELLA and Synergy Neo2 laboratory instruments. The ideal candidate should have hands‑on experience supporting GxP laboratory instrument implementations and be comfortable managing validation activities for both technologies in parallel.

Validation Engineer Responsibilities

• Support CSV activities for ELLA and Synergy Neo2 instrument implementation
• Develop, review, and/or execute validation deliverables including validation plans, risk assessments, test protocols, traceability matrices, summary reports, and related documentation
• Partner with laboratory, Quality, IT, and project stakeholders to ensure validation activities are completed on schedule
• Support GxP compliance, data integrity, and 21 CFR Part 11 considerations as applicable
• Manage validation workstreams for both instruments simultaneously
• Identify and elevate risks, gaps, delays, or documentation issues
• Support deviation resolution and documentation updates during protocol execution

Job Requirements

• Strong CSV experience in a GxP laboratory or regulated life sciences environment
• Prior experience with laboratory instrument implementation and validation
• Experience with ELLA and Synergy Neo2 strongly preferred
• Ability to manage multiple validation activities or technologies concurrently
• Familiarity with IQ/OQ/PQ, CSV lifecycle documentation, risk‑based validation, data integrity, and Part 11 expectations
• Strong communication skills and ability to work effectively with cross‑functional teams
• Experience supporting ECQ or lab equipment qualification
• Experience in biotech, pharma, plasma, or manufacturing laboratory environments
• Prior experience working in client‑facing hybrid/onsite roles

This role can be a local/hybrid setup. At minimum, a 50% on‑site presence is required.

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.

*Verista is an equal opportunity employer.

National (US) Range

$65,000 — $105,000 USD

Benefits

• 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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For more information about our company, please visit us at Verista.com