Verista

6444 - Lead CQV Engineer / Lead Validation Engineer

Verista$87K — $147K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree or equivalent required
  • 10+ years aseptic filling, sterile manufacturing, isolator, or barrier-system CQV experience
  • Expertise in vial filler/capper, isolator, and environmental monitoring aligned with Annex 1 standards
  • Proven field execution experience in vendor SAT and punch item management
  • Comfortable collaborating with quality reviewers on sterile manufacturing risks
  • Strong technical writing and troubleshooting skills
  • ValGenesis experience is a plus

Responsibilities

  • Own QP/DQ/QRA/data integrity/ERES inputs for filler/isolator systems
  • Coordinate vendor documentation and execution for sterile manufacturing equipment
  • Support interface with cleanroom qualifications and environmental monitoring
  • Manage risks, test exceptions, and final report approvals
  • Lead C&Q scope for filler/isolator systems
  • Oversee vendor package reviews
  • Address VHP and sterile boundary questions as needed
  • Author and review IOQ/QSR/TM documentation

Benefits

  • High growth potential in a fast-paced, people-focused culture
  • Competitive pay with performance incentives
  • Comprehensive company-paid disability insurance
  • Health insurance offerings including Medical, Dental & Vision
  • Flexible spending accounts and commuter benefits
  • Retirement plan with employer matching
  • Generous Paid Time Off and Rollover option
  • Tuition reimbursement and team social activities
  • Employee recognition programs and referral incentives
  • Paid parental leave and bereavement support
Full Job Description
Job Overview: We are seeking a Lead Validation Engineer to lead C&Q scope for drug product filling, isolator, and related aseptic manufacturing equipment. This is a specialist role for someone who has qualified vial filling/capping and isolator systems and can manage sterile boundary risk, vendor package questions, SAT/IOQ execution issues, and quality-facing closeout.

Lead Validation Engineer Responsibilities:
  • Own filler/isolator-related QP/DQ/QRA/data integrity/ERES/configuration/traceability inputs as applicable, plus SAT leveraging, commissioning, IOQ, QSR, blue tag, and PQ readiness where required
  • Coordinate vendor documentation and execution windows for filler/capper, isolator, labeler, inspection equipment, and associated sterile manufacturing systems
  • Support interface with cleanroom/room qualification, environmental monitoring instruments, utilities, automation/IT, operations, MS&T, and quality
  • Manage sterile equipment risks, test exceptions, deviations, punch items, and closeout evidence through final report approval
  • Lead filler/isolator C&Q scope
  • Coordinate vendor package review
  • Support VHP/sterile boundary questions if in scope
  • Author/review IOQ/QSR/TM

Job Requirements:
  • Bachelor's Degree or equivalent required
  • 10+ years aseptic filling, sterile manufacturing, isolator, or barrier-system CQV experience
  • Direct vial filler/capper, isolator, inspection/labeling, VHP/decontamination, glove integrity, leak testing, sterile boundary, environmental monitoring, or Annex 1-aligned experience
  • Strong field execution profile: can coordinate vendor SAT, manage punch items, document discrepancies, support deviations, and drive final qualification reports
  • Comfort working with quality reviewers on sterile manufacturing risks, critical parameters, acceptance criteria, and evidence expectations
  • Strong technical writing and problem-solving abilities
  • ValGenesis experience a plus

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

$87,780-$147,123 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

Verista collects and processes personal data in accordance with applicable data protection laws. If you are a California Job Applicant, see the privacy notice for further details.

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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