genscript · Singapore
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 Key Learnings By the end of this internship, you will: Develop a good understanding of ISO 9001:2015 requirements and the role of a Quality Management System (QMS). Gain hands-on experience in critical material management, document control, and product release processes. Enhance problem-solving skills by conducting non-conformance investigations using quality tools such as Fishbone Diagrams, 5 Whys, and Root Cause Analysis (RCA). Benefits: Benefits include medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer paid parental leave after just three (3) months o…
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