Validation Associate

Job Title:

Validation Associate Job Description The Validation Associate supports equipment and process validation activities for a cosmetics and OTC manufacturing facility. This role assists with

IQ/OQ/PQ

execution, batching and compounding validation, and routine quality support activities such as batch record review. The position is well-suited for an early-career professional with exposure to regulated manufacturing environments and a desire to grow within Quality and Validation. Responsibilities Support execution of equipment validation protocols (IQ, OQ, PQ) for manufacturing, compounding, and support equipment. Assist with process and batching validation activities in partnership with the compounding and manufacturing teams. Leverage existing validation templates and approved protocols to execute repeatable validation activities. Collect, organize, and review validation data; ensure accurate and compliant documentation practices. Support batch record review for completeness, accuracy, and adherence to approved procedures. Assist with deviation documentation and investigation support related to validation or batch execution. Maintain validation files, logs, and controlled documents in accordance with GMP requirements. Participate in continuous improvement efforts related to validation processes. Assist during audits and inspections by retrieving validation and batch documentation as requested. Adhere to GMP, GLP, and company quality system requirements. Essential Skills Associate's or Bachelor's degree in Chemistry, Biology, Engineering, Life Sciences, or related field; equivalent experience may be considered. 1-3 years of experience in validation, quality, manufacturing, or laboratory support within a regulated industry. Basic understanding of

IQ/OQ/PQ

concepts and validation documentation practices. Strong attention to detail and ability to follow established procedures. Effective written and verbal communication skills. Additional Skills & Qualifications Exposure to OTC, pharmaceutical, cosmetic, medical device, or food manufacturing environments. Prior experience supporting compounding or batching operations. Familiarity with GMP regulations (FDA, 21 CFR Parts 210/211 a plus). Experience with batch record review or quality documentation. Ability to work cross-functionally with Manufacturing, Quality, and Engineering teams. Work Environment The work environment is a cosmetics and OTC manufacturing facility where adherence to GMP, GLP, and company quality system requirements is paramount. The role involves collaboration with compounding, manufacturing, and quality teams, supporting validation protocols and batch record reviews. The facility is equipped with advanced manufacturing and support equipment, requiring attention to detail and compliance with regulatory standards. Job Type & Location This is a Contract to Hire position based out of Moorpark, CA. Pay and Benefits The pay range for this position is $25.00 - $30.00/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 Moorpark,CA.

Application Deadline This position is anticipated to close on Apr 6, 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.