Lab CQV Specialist

Job Title:

Lab CQV Specialist Job Description The QC Laboratory Equipment Qualification & Validation Specialist is responsible for the full lifecycle management of laboratory equipment within the Quality Control organization. This role supports the installation, commissioning, qualification, decommissioning, and re-commissioning of analytical and support equipment in a GMP-regulated pharmaceutical environment. The specialist ensures that all QC laboratory instruments and systems are qualified, maintained, and compliant with applicable regulatory requirements, internal procedures, and data integrity standards. This position partners closely with QC, QA, Engineering, Metrology, IT, and external vendors to support laboratory readiness, inspection preparedness, and continuous improvement initiatives. Responsibilities Lead and execute

IQ/OQ/PQ

activities for QC laboratory equipment in accordance with approved protocols and regulatory expectations. Develop, review, and approve qualification documentation, including validation plans, risk assessments, protocols, and final reports. Perform commissioning and decommissioning activities for laboratory instruments, ensuring proper documentation and change control. Support re-qualification and periodic review of existing laboratory equipment. Coordinate and support the installation, relocation, and startup of new and existing QC laboratory equipment. Manage equipment lifecycle events including upgrades, replacements, retirements, and obsolescence planning. Interface with vendors during FAT/SAT, installation, and service activities. Ensure all activities comply with c

GMP, FDA, ICH, USP, EU

Annex 11, and data integrity requirements. Initiate and support deviations, investigations, CAPAs, and change controls related to laboratory equipment. Author, review, and revise SOPs, work instructions, and validation templates supporting equipment management. Maintain audit-ready documentation and actively support internal, client, and regulatory inspections. Partner with QC analysts, QA, Engineering, Metrology, and IT to ensure successful qualification and ongoing compliance. Provide technical guidance and training to QC laboratory staff on equipment use and qualification status. Support laboratory expansions, tech transfers, and continuous improvement initiatives. Essential Skills Bachelor's degree in Chemistry, Biology, Engineering, or a related scientific discipline, or equivalent experience. 3-7+ years of experience in CQV, equipment qualification, or validation within a pharmaceutical, biotech, or regulated laboratory environment. Demonstrated experience qualifying QC laboratory equipment (analytical instruments and lab systems). Hands-on experience with

IQ/OQ/PQ

execution and documentation. Strong understanding of cGMP regulations, data integrity principles, and regulatory expectations for laboratory equipment. Experience with change control systems, deviation management, and CAPA processes. Familiarity with electronic systems such as LIMS, CMMS, validation management systems, or document management systems. Excellent technical writing, organizational, and communication skills. Job Type & Location This is a Contract position based out of Wilson, NC. Pay and Benefits The pay range for this position is $50.00 - $60.00/hr. 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) Workplace Type This is a fully onsite position in Wilson,NC.

Application Deadline This position is anticipated to close on Apr 30, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people Actalent is an equal opportunity employer. About Actalent Actalent is a global leader in engineering and sciences services. For more than 40 years, we've helped visionary companies advance their goals. Headquartered in the United States, our teams span 150 offices across North America, EMEA, and APAC—with four delivery centers in India led by 1,000+ extraordinary employees who connect their passion with purpose every day. Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.