Quality Control

**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 proactively provides end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy, vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers. ProBio’s total cell and gene therapy solution covers CMC of plasmid and virus for IND filing as well as clinical manufacturing and commercial manufacturing.

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 production facility 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 and Chinese.
- 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.

GS

Europe

LI-AH1

GenScript USA Inc./ProBio Inc. maintains a drug-free workplace.