Description:

　　-Prepare experimental materials using Standard Operating Procedures, Good Laboratory Practice, and safety guidelines.

　　-Maintain accurate records of procedures and experiments.

　　-Experience drafting technical SOPs, working knowledge of design control

　　-Perform experiments and analyses for multiple clinical research protocols

　　-Assist with analysis of experiments as assigned.

　　Additional Skills & Qualifications:

　　-Degree in Chemistry or Biology minimum

　　-Preferred experience in cGMP manufacturing setting

　　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

　　Actalent is an equal opportunity employer.

　　About Actalent

　　Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.