QC Scientist - Microbiology

Job Description

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 (CGT), 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.

Job Scope:

The position reports to the Director of QC and is ideally suited for a professional with extensive technical knowledge and a proven track record of developing and carrying out processes suitable for use in GMP manufacturing of a wide range of clinical trial materials, and participating in technology transfer. There is a great opportunity to lead and evolve this function within a CDMO business, to support a broad portfolio and advance the manufacturing capabilities to deliver products to the client projects that transform the lives of patients.

Key Responsibilities:

1. Assist in the set-up, development, and maintenance of a GMP QC-Microbiology Lab.
2. Support QC-Microbiology testing and development of governing procedures and methods.
3. Participate in EMPQ, cleanroom validation, and associated activities/documents.
4. Responsible for following cGMP in carrying out functions related to QC testing.
5. Functions may include, but are not limited to, activities such as Environmental Monitoring, Plate Reads, Water Testing, Gas Testing, Gram Staining, Growth Promotion, Bioburden, Gowning Qualifications, and other QC-Microbiology activities.
6. Support optimization initiatives to improve QC department.
7. Perform other duties as assigned based on business needs.
8. Up to 15% travel to support CDMO projects or business development activities.

Qualifications:

1. Master's degree with 1 year of relevant work experience, or Bachelor's degree with 3 years of relevant work experience. Degree in Microbiology, Molecular Biology, Biochemistry, or related scientific field. Experience in gene and cell therapy recombinant plasmid DNA products is a plus.
2. Experience with EMPQ, cleanroom validation, lab optimization, and EM development.
3. Experience with documentation, by way of authoring, reviewing, and/or approving GMP documents, such as procedures, test methods, protocols, and reports.
4. Experience with Laboratory Information Management Systems (LIMS) or relevant data management software.
5. Experience as a trainer is a plus.
6. Ability to problem-solve and work independently and as part of a team.
7. Strong interpersonal, verbal, and written communication skills.

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 any characteristic protected by law.

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