Verista

6467 - Senior CSV Engineer / Senior Validation Engineer

Verista$80K — $131K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Computer Science or related field
  • Seven or more years of CSV, CSA or computerized-equipment validation experience
  • Hands-on experience with standalone GMP manufacturing equipment validation
  • Strong understanding of 21 CFR Part 11, EU Annex 11, GAMP 5
  • Experience testing electronic records, audit trails, and security
  • Ability to author and execute validation protocols
  • Experience with UNICORN, KlariFi, or Lucullus software

Responsibilities

  • Develop and execute CSV/CSA strategies for GMP equipment
  • Review software architecture and GxP impact
  • Author or review validation and risk assessment documents
  • Evaluate vendor testing documentation
  • Test user access, electronic records, and signature capabilities
  • Verify backup, recovery controls, and compliance with regulations
  • Support SOP development, change control, and training

Benefits

  • High growth potential in a fast-paced, people-focused culture
  • Competitive pay with performance-based incentives
  • Comprehensive insurance packages including medical, dental, and vision
  • 401(k) plan with employer matching
  • Paid Time Off and holidays, rollover option available
  • Tuition reimbursement and professional development opportunities
  • Team social activities and employee recognition programs
  • Paid parental leave and bereavement support
Full Job Description
Job Overview: We are seeking a Senior CSV/CSA Engineer to lead validation activities for standalone, computerized bioprocess equipment being installed in a single-use manufacturing facility. The equipment will utilize UNICORN, KlariFi and Lucullus software and will not be integrated with the site DeltaV system. The engineer will own or lead the computer-system validation lifecycle while coordinating with Process Engineering, CQV, Automation, Quality, IT, equipment vendors and system owners.

Senior Validation Engineer Responsibilities:
  • Develop and execute the CSV/CSA strategy for standalone GMP equipment systems
  • Review equipment and software architecture, intended use and GxP impact
  • Author or review validation plans, system assessments, risk assessments and supplier assessments
  • Review URS, functional specifications, configuration specifications and design documentation
  • Develop and execute risk-based test protocols
  • Evaluate vendor FAT, SAT, IQ and OQ documentation for leveraged testing
  • Test user access, roles, permissions and account administration
  • Test audit trails, electronic records and electronic signatures
  • Verify recipe, method and configuration controls
  • Test alarms, events, reports, data capture and record retention
  • Verify backup, restoration, archival, time synchronization and disaster-recovery controls
  • Assess compliance with 21 CFR Part 11, EU Annex 11 and applicable data-integrity requirements
  • Maintain requirements traceability and validation-documentation packages
  • Manage discrepancies, deviations, corrective actions and validation-summary reporting
  • Support change control, SOP development, training and system release

Job Requirements:
  • Bachelor's degree in Engineering, Life Sciences, Computer Science or a related discipline
  • Approximately seven or more years of CSV, CSA or computerized-equipment validation experience in a regulated life-sciences environment
  • Hands-on experience validating standalone GMP manufacturing equipment
  • Strong understanding of 21 CFR Part 11, EU Annex 11, GAMP 5 and data-integrity principles
  • Experience testing access security, audit trails, electronic signatures, recipes, reports and computerized records
  • Ability to review functional specifications, configuration specifications and system architecture
  • Strong protocol authoring, execution and deviation-management skills
  • Ability to work independently with equipment vendors, engineers and Quality representatives
  • Direct experience with UNICORN, KlariFi or Lucullus
  • Experience with chromatography, tangential-flow filtration or bioreactor systems
  • Experience validating PLC/HMI- or SCADA-controlled equipment
  • Familiarity with Kneat or another electronic validation lifecycle system
  • Experience supporting new-equipment installation and capital-project execution

This role requires the ability to be on-site, full-time in Devens, MA.

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-$131,685 USD

Benefits

Why Choose Verista?
  • 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

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

About Verista

Verista is a software company that provides a platform for managing and automating business processes. The company's platform uses artificial intelligence and machine learning to analyze data and optimize workflows. Verista's customers include companies in the healthcare, financial services, and manufacturing industries. The company was founded in 2017 and is headquartered in Palo Alto, California.
Learn more about Verista
Size
50 employees
Industry
Founded
2017

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