Equipment Validation Specialist

Description Coordinate with department supervisors to ensure assigned tasks are completed according to established timelines. Develop, update, and maintain procedures and forms within the electronic document management system to accurately reflect processes and capture changes. Prepare and carry out engineering studies and validation activities for processes and equipment, including authoring protocols and final reports. Collect, interpret, and evaluate data to support engineering decisions and documentation. Initiate, manage, and support change control activities across applicable systems and processes. Provide training to staff on procedures, protocols, and related documentation as required. Support additional Engineering department needs, including general administrative and project-related tasks, as assigned. Excellent technical written and oral communication skills. Demonstrated critical thinking and problem-solving skills. Skills in presenting data clearly. Strong troubleshooting skills. Attention to detail and excellent organizational skills is essential.

• Ability to work both independently and in a cross-functional team environment.

Experience with an electronic document management system. Familiarity with statistical methods for data analysis is desired Skills Validation, equipment validation, gmp, process validation, Validation testing, Medical device, Technical writing Top Skills Details Validation,equipment validation,gmp,process validation Additional Skills & Qualifications

• Ideal candidate will have a minimum of a Bachelor's Degree in a Science or Engineering discipline or an equivalent combination of experience and/or education.
• At least 1 year of experience in the medical device, pharmaceutical, clean room, or biotech manufacturing industry.
• Experience working in a regulated environment.

Knowledge of FDA cGMP and/or ISO regulatory requirements a plus. Experience Level Intermediate Level Job Type & Location This is a Contract position based out of East Falmouth, MA. Pay and Benefits The pay range for this position is $45.00 - $50.00/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 East Falmouth,MA.

Application Deadline This position is anticipated to close on Mar 18, 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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.