Description:

Responsible for Master Validation Plans, project plans and test plans.

Facilities, utilities, instruments and equipment qualification and process for validation

Documentation for validation including requalification/revalidation for equipment and processes

Skills:

Validation, Pq, Oq, Iq, Gmp, life science, mechanical engineering, electrical troubleshooting, design drafting, solidworks

Additional Skills & Qualifications:

5+ years experience in Validation Engineering, Manufacturing Engineering or Process Engineering

First hand audit experience

FDA, cGMP, SOP and Specs documentation

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 actalentaccommodation@actalentservices.com for other accommodation options.