CQV Engineer - On-site Validation Specialist (Devens)

Verista; Harvard (MA); On-site; USD 65,000 - 108,980; Full time

Benefits offered by this job

High growth potential

Performance-based incentive programs

Company-paid Life, Short-Term, and Long-Term Disability Insurance

Medical, Dental & Vision insurances

401(k) Retirement Plan with Employer Matching

Paid Time Off and Holidays

Tuition Reimbursement

Job summary

Verista is hiring a Validation Engineer for a full-time, on-site position in Devens, MA. The role requires expertise in executing IQ/OQ protocols and supporting commissioning activities, ensuring compliance with GMP/GDP practices.

Candidates must hold a Bachelor’s in a related field and have 1-3 years of experience in a pharmaceutical, biotech, or regulated environment. The position offers a robust benefits package including competitive pay, health insurances, a 401(k) plan, and paid parental leave.

Qualifications

• 1-3+ years of CQV, validation, commissioning or related experience.
• Familiarity with GMP/GDP documentation practices.
• Degree in Biomedical Engineering or Chemical Engineering preferred.

Responsibilities

• Support commissioning and qualification activities for equipment.
• Execute IQ/OQ protocols.
• Maintain GMP/GDP-compliant documentation.

Skills

Execution of IQ/OQ protocols

Commissioning and qualification activities

Documentation practices

Cross-functional collaboration

Education

Bachelor’s Degree in STEM

Tools

Validation tools

Job description

Verista is hiring a Validation Engineer for a full-time, on-site position in Devens, MA. The role requires expertise in executing IQ/OQ protocols and supporting commissioning activities, ensuring compliance with GMP/GDP practices.

Candidates must hold a Bachelor’s in a related field and have 1-3 years of experience in a pharmaceutical, biotech, or regulated environment. The position offers a robust benefits package including competitive pay, health insurances, a 401(k) plan, and paid parental leave.