Lead CQV Engineer — Pharma Validation Leader (On-Site)

Verista; Harvard (MA); On-site; USD 87,780 - 145,307; Full time

Benefits offered by this job

Medical, Dental & Vision insurance

401(k) Retirement Plan

Paid Time Off

Tuition Reimbursement

Employee Referral Program

Job summary

Verista is seeking a Lead Validation Engineer to oversee CQV execution activities in Harvard, MA. The successful candidate will have over 8 years of validation experience in the pharmaceutical or biotech industry and will lead teams to ensure compliance with GMP standards.

This full-time on-site role offers a salary range of $87,780 to $145,307, plus comprehensive benefits in a fast-paced, people-focused culture.

Qualifications

• 8+ years of CQV/validation experience in pharma or biotech.
• Bachelor's degree in STEM, preferably Biomedical or Chemical Engineering.
• Hands-on experience with bioreactors and chromatography.

Responsibilities

• Lead CQV execution activities across multiple systems.
• Coordinate daily execution priorities.
• Ensure all documentation meets GMP/GDP standards.

Skills

CQV validation experience

Strong GMP/GDP knowledge

Process equipment handling

Leadership experience

Experience with eVal

Education

Bachelor’s Degree or equivalent

Tools

ValGenesis

Temperature mapping tools

Job description

Verista is seeking a Lead Validation Engineer to oversee CQV execution activities in Harvard, MA. The successful candidate will have over 8 years of validation experience in the pharmaceutical or biotech industry and will lead teams to ensure compliance with GMP standards.

This full-time on-site role offers a salary range of $87,780 to $145,307, plus comprehensive benefits in a fast-paced, people-focused culture.