Vyriad Rochester , MN 55905
Posted 4 days ago
Biotechnology Quality Control Analyst
Company Overview
Vyriad is an early-stage biotechnology company focused on curing cancer using potent, safe and cost-effective cancer therapies utilizing engineered replication competent viruses designed to selectively and rapidly destroy cancer. Revolutionizing cancer treatment is our long-term goal, requiring curiosity, perseverance, an openness to challenging convention and a commitment to excellence. The challenges are complex, the work pace is fast, and progress is seldom a straight line. All of this makes for an exhilarating environment of collaboration, discovery, and fun.
Position Overview
Responsible for performing and validating analytical methods essential for quality control and release of drug product and performing environmental monitoring of critical manufacturing areas, thus ensuring that manufacturing processes and products meet quality specifications. The analyst shall maintain quality assurance processes, be responsible for testing products, recording, and analyzing data during product development and manufacturing. The analyst will follow through on set processes and ensures adherence to best production practices and product quality standards, as well as monitors the efficiency and cost-effectiveness of product output.
Key Responsibilities
Perform and maintain test systems for GMP manufacturing, and responsible for performing assays related to in-production and post-production product quality
Performs qualification/validation processes to maintain analytic validity of test methods
Monitor aseptic manufacturing suites for contamination.
Maintain and monitor equipment and instruments, diagnoses, and troubleshoots minor issues with laboratory instruments and equipment.
Other Responsibilities
Monitor production processes for compliance with processes and procedures and participates in non-conformance and complaint investigations, and develops, coordinates, and implements corrective and preventive actions
Support other manufacturing work areas including supply chain staff in raw material inspections, maintenance of the supply records, supplier management program and recall activities, as needed
Assists Quality Assurance staff in collating records for the final batch record review, as needed
Education Requirements
Experience and Skill Requirements
Knowledge and experience in FDA current Good Manufacturing Practices for product manufacturing and testing is required
Additional experience with other requirements (Good Laboratory Practices, ISO, etc.) is highly desirable
Exceptional human relations and communication (written, verbal, and listening) skills are required
Should be very detail-oriented and have the ability to work independently and productively with minimal direction, and routinely exercise initiative and sound judgment
Strong analytic skills coupled with critical thinking skills are essential in this role
Must have demonstrated capacity to write and comprehend complex protocols and reports, programs, and situations
The ability to exercise good judgment while under pressure and tight deadlines, and strong coping skills are required
Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities
Job Type
Location
Work Authorization
Vyriad