DescriptionThe Validation Engineering Technician is responsible for providing engineering support to production and product development. Key duties include formulating manufacturing batches and solutions used during the manufacturing process, preparing technical reports, drawings, and specifications, and updating them as necessary. The technician also assists with the execution of IQ, OQ, PQ validations, performs recurring validations of equipment, tooling, processes, and products, and works with cross-functional teams to help with the qualification of medical devices (design verification, validation, transfer). Other responsibilities include assisting in selecting, developing, and improving processes, tooling, and equipment to reduce costs or improve quality, maintaining and repairing equipment, conducting tests on prototypes or systems, troubleshooting production equipment and process problems, and supporting calibration, maintenance, and repair of production equipment.SkillsManufacturing, formulation, technical report, validation, iqoqpq, equipment validation, process validation, report writing, testing, troubleshooting, medical device, pharmaceutical industry, aerospace, cleanroom, iso 9001Top Skills DetailsManufacturing,formulation,technical reportAdditional Skills & QualificationsEDUCATION B.S. in Engineering or a related technical field EXPERIENCE 1-2 years of experience in a regulated manufacturing environment Experience with basic clean room laboratory technology and hands-on knowledge Experience within Medical Device, Pharmaceutical, or another regulated industry Experience preparing technical reports Experience supporting execution of Validation Protocols strongly preferredExperience LevelIntermediate LevelPay and BenefitsThe pay range for this position is $33.00 - $36.00/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 TypeThis is a fully onsite position in Glendora,CA.Application DeadlineThis position is anticipated to close on Mar 31, 2025.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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are 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
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] (%[email protected]) for other accommodation options.