QC Specialist
GenScript/ProBio
Apply to this jobAbout 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.
Job Scope:
- Responsible for coordinating QC and QA work in the team
- Responsible for the completion of key orders and trouble shooting
- Responsible for statistics and analysis of production data, and assist the supervisor to optimize and improve the production process or technology
- Participate in or be responsible for the management of multiple promotion projects and promote the achievement of project objectives
- Responsible for the formulation and update of SOP, summarize and solidify work experience and train up junior employees
- Assist the supervisor to complete quality monitoring and safety inspection, and timely complete problem rectification
- Complete other tasks assigned by the supervisor
Key Requirements:
- Bachelor’s degree or above in cell biology, molecular biology, biomedicine and other related majors
- Familiar with the experimental operation of SDS-PAGE, Western blot, LC-MS, HPLC and other protein detection,
- Good trouble shooting and project management skills
- Good communication skills (verbal and written)
- Good collaboration skills
#GS
#LI-MF1
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.
Summary
Coordinate QC/QA tasks, troubleshooting, data analysis, SOP updates, and staff training
Job title
QC Specialist
Experience level
bachelor’s degree or above
Industry
biotech
Location requirements
Singapore, no remote work allowed
Salary
Not specified
Visa sponsorship
H-1B sponsor history
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Singapore