Senior CQV Engineer — Onsite Boston, Travel‑Ready

Verista; Boston (MA); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Competitive pay

Professional development opportunities

Team-focused culture

Job summary

Verista is seeking a Senior CQV Engineer to lead validation activities within pharmaceutical manufacturing projects. You will design validation plans, perform risk assessments, and document qualification activities with a focus on compliance and traceability.

The role requires coordinating with project teams to ensure timely delivery and maintain rigorous records. The candidate will mentor junior staff, communicate effectively with clients, and work onsite in the Boston area, with potential

Qualifications

• Bachelor's Degree or equivalent required.
• 4-6 years of role-relevant experience in CQV activities.
• Experience in GMP regulated environment and Good Documentation Practice.

Responsibilities

• Designing validation plans.
• Conducting risk assessments with understanding of equipment, systems, and software.
• Maintaining detailed records of qualification, validation, and change control for audits.
• Authoring testing documentation and executing test scripts on validated systems.
• Collaborating with project teams to meet schedules and deliverables.

Skills

Communication skills

Mentoring

Team player

Problem solving

Attention to detail

GMP awareness

Education

Bachelor's Degree

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

Verista is seeking a Senior CQV Engineer to lead validation activities within pharmaceutical manufacturing projects. You will design validation plans, perform risk assessments, and document qualification activities with a focus on compliance and traceability.

The role requires coordinating with project teams to ensure timely delivery and maintain rigorous records. The candidate will mentor junior staff, communicate effectively with clients, and work onsite in the Boston area, with potential