Strong fit for candidates with a background in biological sciences who can manage documentation and collaborate with stakeholders in a regulated environment.
Derived from job-description analysis by Serendipath's career intelligence engine.
Original posting from GenScript via Greenhouse
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 of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and company holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
GenScript USA Inc/ProBio Inc. is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is the Company's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.
GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.
Please note: Genscript USA Inc./ProBio Inc. will only contact candidates through verified application sources. GenScript/Probio does not request personal information from candidates through individual email or any other platform.
Source: GenScript careers (Greenhouse)