Please See Below for a Great Opportunity to advance your career with one of the top Scientific organizations in the Tewksbury, MA area!

　　Description:

　　Create, Edit, and Write Batch Record Review

　　Accurate review of GMP documents of batch records

　　Constant control and flow of GMP documentation

　　Work closely and help write SOPs for chemists and QA teams

　　Skills:

　　Document control, Gmp, batch record review, batch record, chemistry, Compliance, Quality assurance, Quality control, Erp

　　Additional Skills & Qualifications:

　　Associate's or bachelor's degree in a science

　　Experience working with Batch record review

　　Looking for someone with 2-3 years experience

　　Work Environment

　　30-32 hours a week. Either Monday-Thursday or Tuesday-Friday and the hours are 9:00am-5:00pm. This is a 100% onsite position. It is a business causal environment.

　　Experience Level:

　　Entry Level

　　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.