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Quality Control (QC) Technician, mRNA
Posted 5 hours 8 minutes ago by GenScript
GenScript's Europe division, headquartered in Rijswijk, Netherlands, with a branch office in Oxford, UK, was established in 2019 to serve as a hub for commercial, technical support, and logistics in the European and UK regions. As part of our ongoing commitment to enhancing service for our EU clients, we are excited to announce the opening of our first brand new laboratory in Delft, Netherlands. We are currently seeking a QC Technician to join our RNA service team. This position will be focusing on performing verities of experiment following protocol and guidance of manager for ensuring the quality of product under production and research in RNA team.
Job Title: QC Technician
Working Location: Delft, South Holland, Netherlands
Working Arrangement: On-site
Working Hours: Full-time, 40 hours per week
Main Responsibilities:
- Responsible for supporting communication with production manager and team, support a working environment that encourages employee involvement and collaboration.
- Operate QC assays as needed.
- Report out-of-specification results and deviations to the manager. Assists with investigations, root cause analysis, and reports for out-of-specification results and deviations.
- Responsible for timely completion of QC report after production job is finished. Accountable for the QC report compliance with good documentation practices.
- Design plasmids to insert customer ORF's into vectors used for IVT
- Order Gene Synthesis, Subcloning, Plasmid Preps, and Linearization strategically from manufacturing facilities.
- Support process improvement initiatives within in scope of responsibility.
- Monitor supply inventory and identify any products required.
- Maintain work area, equipment, department and all storage areas in a clean, neat and orderly manner.
- Perform other duties as needed.
Key Requirements:
- A Bachelor's or Master's degree in Molecular biology, Chemistry, Biochemistry, Pharmaceutical science or related field.
- Proficiency in English; fluency in Chinese is highly desirable.
- Experience with HPLC, FPLC, q-PCR is preferred.
- Ability to communicate efficiently in verbal and writing.
- Ability to follow detailed instructions, maintains accurate records and notes, and carry out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices.
- A sense of humility and an eagerness to continue to learn and contribute to a supportive team.
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.