Intern - QA

About GenScript
Founded in 2002 in New Jersey, GenScript Biotech Corporation accelerates innovation in biotech and healthcare by providing researchers and companies with the building blocks needed to develop groundbreaking treatments and products. Guided by its mission to Make People and Nature Healthier Through Biotechnology, and its role as a well-recognized biotechnology company, GenScript has a team of approximately 6,165 employees and has served more than 200,000 customers across over 100 countries and regions.
Key Responsibilities
Responsible for reviewing of product CoA and any other product release document to ensure it meet the customer requirement.
Responsible for management of controlled SOP to ensure it meet ISO 9001 requirement.
Responsible for in-coming material and work closely with key stakeholder to ensure timing testing and release of material.
Participate in material non-conformance investigation and follow up with procurement timely on the supplier investigation outcome.
Complete other tasks assigned by the supervisor.
Key Requirements
Diploma / Bachelor’s degree in Biological Sciences or equivalent
Familiar with the reading and interpreting of SDS-PAGE, LC-MS, HPLC and other protein detection report
Detail oriental
Good problem-solving skills
Good communication skills (verbal and written)
Good team working skills