Jobs Companies GenScript/ProBio Biotechnologist (Gene)

Über diese Biotechnologist (Gene) Stelle bei GenScript/ProBio

GenScript/ProBio · Vor Ort · 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.

Job Responsibilities:

  • Operation and ensuring the completion of daily experimental task for the assigned team (Oligo/PCR/Ligation/Screening/Plasmid/Sequencing/QC/Reagent) 
  • Operation of experimental technology: Perform daily operation of tasks and any equipment with strict accordance to relevant Standard Operating Procedures in the role  
  • Be responsible for the arrangement of the daily order sheet, sorting out and summarizing the schemes that need to be done on the day, recording the reagents/products that need to be prepared  
  • Record all experimental data and results in specified forms (paper and electronic) with accuracy and responsibility 
  • Monitor and report the status of all delegated experiments and tasks, ensuring that any handover of incomplete experiments, abnormality analysis and daily order status report is thoroughly conveyed to the supervisor or handed over to relevant personnel 
  • Monitor equipment status daily and report back to the team’s supervisor should abnormalities occur 
  • Ensure that all safety guidelines are followed strictly at all times and  
  • Be responsible for maintaining a clean and orderly environment, and to provide suggestions to the supervisor on 5S improvement and maintenance 
  • Provide support for the team’s optimization and innovation projects 
  • Be responsible for any other tasks the supervisor assigns 

Qualifications:

  • Bachelor’s Degree in Biological Sciences / Life Sciences / Bioengineering / Chemistry or related courses
  • Solid foundation in Molecular Biology and Cell Biology; strong background in experimental operation; familiar with Conventional techniques of genetic engineering, such as Isolation and Manipulation of DNA (i.e: Primer Design, Plasmid Design, PCR, Restriction Digestion, Homologous Recombination, CRISPR/Cas9 Gene Editing, Transformation, Plasmid Isolation, Sequence Analysis and etc.) is preferred
  • Strong sense of achievement; resilient and able to perform under the pressure
  • Team player with good communication skills (verbal and written)
  • Available to work 8-hour shifts, 5 days a week, with 2 rest days that may not always fall on weekends

#GS

#LI-MF1

 

Your Privacy and Fairness in Our Recruitment Process
We are committed to protecting your data, ensuring fairness, and adhering to workplace fairness principles in our recruitment process. To enhance hiring efficiency and minimize bias, we use AI-powered tools to assist with tasks such as resume screening and candidate matching. These tools are designed and deployed in compliance with the Tripartite Guidelines on Fair Employment Practices and internationally recognized AI governance frameworks. We continuously validate our systems to uphold fairness, transparency, and accountability, ensuring they do not result in unfair or discriminatory outcomes. Your personal data is handled securely and transparently, and final hiring decisions are made by our recruitment team to ensure a human-centered approach. If you have questions about how your data is processed or wish to report concerns about fairness, please contact us at [email protected]

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. 

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Über GenScript/ProBio

About GenScript

GenScript Biotech Corporation (Stock Code: 1548.HK) is a global biotechnology group. Founded in 2002, GenScript has an established global presence across North America, Europe, the Greater China, and Asia Pacific. GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.

GenScript is committed to striving towards its vision of being the most reliable biotech company in the world to make humans and nature healthier through biotechnology.

 

About ProBio

ProBio is a New Jersey-based fully integrated end-to-end contract development and manufacturing organization (CDMO) that focuses on enabling biotech and pharmaceutical companies to accelerate novel drug development and supply for clinical trials through to commercialization.

ProBio develops technology-driven proprietary platform processes to support the full lifecycle of biologics drug development and manufacturing of next generation medicine: biologics and advanced therapies. Our technical and operational expertise spans the discovery, development, and drug substance or drug product (DS/DP) manufacturing of antibody-based therapeutics, including monoclonal, bispecific, and multi-specific antibodies, recombinant proteins, plasmid DNA, viral vectors, mRNA, and vaccines. Additionally, we provide specialized integrated services in process development, bioanalytical development, formulation and in vitro/in vivo pharmacology.

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