Senior CQV Engineer - Pharma Validation Lead

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

Benefits offered by this job

Competitive pay

Life, Short-Term & Long-Term Insurance

Tuition reimbursement

Job summary

Verista, Inc. is seeking an experienced CQV professional to lead commissioning, qualification and validation activities for pharmaceutical manufacturing.

You will develop validation plans, execute testing, and document results for capital equipment, systems and processes on client sites in the Boston area. Ideal candidates bring 4–6 years of CQV experience, GMP knowledge, and strong communication with clients.

Qualifications

• Bachelor’s degree or equivalent required
• 4-6 years of demonstrated role relevant experience
• Proven experience leading CQV activities for pharmaceutical manufacturing
• Strong communication and client-facing skills
• GMP and Good Documentation Practice

Responsibilities

• Lead CQV activities and develop validation strategies for pharma manufacturing equipment and processes
• Prepare and edit commissioning, qualification and validation documentation
• Run test scripts and document results with traceable records
• Collaborate with project teams and clients to ensure on-schedule delivery
• Mentor junior team members and communicate requirements clearly

Job description

Verista, Inc. is seeking an experienced CQV professional to lead commissioning, qualification and validation activities for pharmaceutical manufacturing.

You will develop validation plans, execute testing, and document results for capital equipment, systems and processes on client sites in the Boston area. Ideal candidates bring 4–6 years of CQV experience, GMP knowledge, and strong communication with clients.