Senior CQV Engineer - Onsite Bioprocess Validation

Verista; Harvard (MA); On-site; USD 70,491 - 118,062; Full time

Benefits offered by this job

Medical, Dental & Vision insurances

401(k) Retirement Plan

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Verista is looking for a Senior Validation Engineer to join their team in Devens, MA. This role involves executing IQ/OQ protocols, performing equipment and drawing verifications, and supporting temperature mapping activities. Ideal candidates have 3–8 years of CQV/validation experience and a Bachelor's degree in a relevant STEM field.

The role offers competitive pay, performance-based incentives, and comprehensive benefits including medical, dental, and 401(k) plans. Join Verista's mission to empower growth in the life sciences industry!

Qualifications

• 3–8 years of experience in CQV/validation.
• Hands-on experience with bioprocess equipment preferred.
• Exposure to temperature mapping is a plus.

Responsibilities

• Execute IQ/OQ protocols and support operational verification activities.
• Perform drawing walkdowns and equipment verification.
• Identify and document deviations in compliance with GMP/GDP.

Skills

CQV/validation experience

GMP/GDP fundamentals

Process equipment validation

IQ/OQ execution

Field verification activities

Education

Bachelor’s Degree in STEM

Tools

eVal

ValGenesis

Temperature mapping tools

Job description

Verista is looking for a Senior Validation Engineer to join their team in Devens, MA. This role involves executing IQ/OQ protocols, performing equipment and drawing verifications, and supporting temperature mapping activities. Ideal candidates have 3–8 years of CQV/validation experience and a Bachelor's degree in a relevant STEM field.

The role offers competitive pay, performance-based incentives, and comprehensive benefits including medical, dental, and 401(k) plans. Join Verista's mission to empower growth in the life sciences industry!