Associate Scientist, Microbiology

About the Position

The position reports to the Microbiology Manager, 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 the 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.

Responsibilities

• Assist in the set-up, development and maintenance of a GMP QC-Microbiology Lab.
• Participate in EMPQ, cleanroom validation, and associated activities/documents.
• Responsible for following cGMP in carrying out functions related to QC testing.
• Functions may include, but 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.
• Testing of compounded sterile and non-sterile pharmaceuticals.
• Assist laboratory personnel in daily activities to maintain quality and compliance with SOPs, cGMP protocols, and safety standards.
• Conduct mycoplasma testing and various virology and microbial assays.
• Demonstrate the ability to learn new skills and achieve proficiency.
• Support optimization initiatives to improve QC department.
• Perform other duties, as assigned based on business needs.

Qualifications

• Master’s degree with 1 years 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 a plus.
• Experience with Environmental monitoring, cleanroom activities.
• Experience in Mycoplasma testing or other cell culture and viral assays.
• Experience with documentation, by way of authoring, reviewing and/or approving GMP documents, such as procedures, test methods, protocols, reports, etc.
• Ability to problem solve and work independently and as part of a team.