For nearly 70 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
We are seeking an experienced Project Manager for our Biologics Testing Solutions site located in Wilmington, MA.
Serve as study director for GMP studies, responsible for technical review of data and report compilation. Provide project leadership and coordination, including oversight of staff members involved in assigned projects and interact with clients regarding sample submission, scheduling, execution and reporting. Assures that study or assay protocols, including any changes, are approved as provided by applicable regulatory requirements and that the protocols are followed. Provide technical guidance to laboratory personnel, mentor staff in areas such as protocol and data interpretation and project related problem resolution. Verifies that all applicable manufacturing practice regulations are followed.Qualifications
- Education: Bachelor’s degree (B.A. /B.S.) or equivalent in a technically related discipline.
- Experience: Five to seven years related technical experience.
- An equivalent combination of education and experience may be accepted as a satisfactory substitute for specific education and experience listed above.
- Certification/Licensure: Appropriate for the area of expertise.
Equal Employment Opportunity
Charles River Laboratories, Inc. is an Equal Opportunity Employer M/F/Disabled/Vet