Validation Engineer

Job Description

Job Description

Job Title: Validation Engineer Job Description

This role involves providing advanced technical and engineering support for equipment and system initial validation and requalification. The engineer will be an integral part of teams focused on improving compliance and performance of plant systems, with a keen understanding of regulatory requirements for change control. The role includes coordinating HEPA filter integrity/velocity testing and critical air airflow pattern testing. A comprehensive understanding of cGMPs is essential, and the individual must become certified to enter controlled areas of the plant. The engineer will also provide direction to validation team members and contractors as necessary.

• Schedule and participate in equipment requalifications according to Standard Operating Procedures (SOPs), coordinating and communicating testing with affected functional groups.
• Execute validation studies, acting as a Project Manager, including protocol preparation, scheduling, execution, and final report preparation.
• Present results to Regulatory Agencies when necessary.
• Program, lead, and operate department instruments to perform controlled temperature/humidity chamber qualifications.
• Develop and improve validation programs to remain current with cGMPs and industry standards.
• Schedule and execute HEPA filter and critical area testing, and airflow pattern testing, using equipment such as smoke generators, photometers, and velocity meters.
• Represent the Validation department in teams responsible for specifying, installing, validating, troubleshooting, and maintaining systems and equipment.
• Conduct validation deviations and participate in deviation investigations to identify root causes and define corrective and preventative actions.
• Mentor lower-level engineers, professionals, and technician personnel.

• Experience with validation protocols and process validation.
• Knowledge of Installation, Operational, and Performance Qualifications protocol generation and execution.
• Competency with standard office applications (Word, Excel, PowerPoint, Project, Access).
• Understanding of cGMPs, industry guidance, and aseptic techniques.
• Familiarity with statistical analysis tools and methods.
• Knowledge of cGMP room classifications, HEPA filter testing, and airflow pattern testing tools and techniques.
• Experience in cGMP CA/PA, root cause analysis, risk assessment, and investigation tools and techniques.

• Experience with inspection machines and pharmaceutical equipment validation.
• Engineering background with a focus on validation.

The work environment involves working in controlled areas of the plant. The role requires wearing appropriate attire to comply with cGMP standards and may involve operating various testing instruments. Standard office applications are used frequently, and collaboration with various departments is essential.

This is a Contract position based out of Wilson, NC.

The pay range for this position is $47.00 - $52.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Wilson,NC.

This position is anticipated to close on Sep 9, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on ziprecruiter.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.