Pharma CQV Engineer: Validation Lead (Onsite Raleigh)

Veristainc; Durham (NC); On-site; USD 70,491 - 109,900; Full time

Benefits offered by this job

Health Insurance

401(k)

Paid Time Off

Tuition Reimbursement

Job summary

Verista is seeking a Senior CQV Engineer in the Raleigh/Durham area to lead validation activities for pharmaceutical manufacturing. You will design validation plans, conduct risk assessments, and maintain qualification documents as part of a collaborative project team.

Requirements include 4–6 years of CQV experience, a Bachelor's degree, strong communication, and the ability to work onsite. Travel up to 10–50% may be required; GMP experience is essential.

Qualifications

• Bachelors degree or equivalent required.
• 4-6 years of demonstrated CQV experience in pharmaceutical manufacturing.
• Willing to work onsite in the Raleigh/Durham metro area.
• Experience with GMP and Good Documentation Practice.

Responsibilities

• Designing validation plans.
• Conducting and documenting impact and risk assessments with understanding of equipment/system/software operation.
• Maintaining records of qualification and validation, and change control activities.
• Designing and executing studies for process parameter definition and verification.
• Authoring, editing, and executing commissioning, qualification and validation documentation.
• Running test scripts and documenting results.
• Adherence to project schedules for all activities.
• Documenting impact and risk assessments as part of a team.

Skills

CQV leadership

Communication

Documentation

GMP awareness

Problem solving

Team collaboration

Mentoring

Project management

Education

Bachelors Degree or equivalent

Tools

Microsoft Office

Job description

Verista is seeking a Senior CQV Engineer in the Raleigh/Durham area to lead validation activities for pharmaceutical manufacturing. You will design validation plans, conduct risk assessments, and maintain qualification documents as part of a collaborative project team.

Requirements include 4–6 years of CQV experience, a Bachelor's degree, strong communication, and the ability to work onsite. Travel up to 10–50% may be required; GMP experience is essential.