Sr Quality Systems Specialist

Job DescriptionWill be the Subject Matter Expert for processes within the company's Quality System.Ensure regulatory compliance. Oversee CAPA, non-conformance, change control, document control and training compliance. Make recommendations for quality improvements. Work cross-functionally with various departments to ensure quality compliance. Ensuring compliance with cGMP, FDA, and other regulatory agency standards. Write, review, and maintain SOPs.Develop training for cGMP compliance.

MUST HAVES

5+ years experience in quality systems from FDA regulated manufacturing environmentExperience writing SOPsExperience with change control, deviation, CAPA

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.