Analyst Ii, Quality Control

• Working in QC GLP and/or cGMP BSL-2 (and BSL 3) laboratory facilities and operations.
• Transfer test protocols from the Analytical development lab (or clients) to the cGMP-compliant QC laboratory.
• Perform QC release and in-process tests on many samples.
• Routine operation and management of BSL2 (and BSL3) labs.
• Prepare and review virology SOPs, protocols, and reports.
• Participate in other activities such as testing deviations, non-conformances, Out of Specification (OOS) failure investigations, etc.
• Timely development and qualification of viral and other in vitro assays
• Perform QC tests in support of Viral banking.

• All employees are expected to adhere to the Quality Management System established in the Quality Manual, Quality Policy, Standard Operating Procedures, Current Good Manufacturing Practices, and any other applicable regulations and standards to the duties within their role.

• Capable of working independently with minimal supervision.
• Experience with viral disinfection efficacy studies is a plus.
• Experience in basic molecular biology (RNA/DNA/plasmid extraction, qPCR, and Droplet Digital PCR).
• Experience working with mammalian cells, bacteria, live viruses, and viral-based vaccines preferred (different infectivity assays, plaque assays, TCID50, neutralization assays, etc.).
• Knowledge and experience of cGMP and GLP.
• Experience writing and reviewing test methods, SOPs, protocols, and reports.
• Willing to work in a teamwork environment where individual collaboration and accountability are valued.

• Bachelor’s degree in Biological Sciences, Virology, Microbiology, Biotechnology, or a related field. Advanced degree preferred.
• Four (4) years of related experience in a regulated laboratory environment.

• Stoop, crouch, reach, walk, pull, push, stand, lift, do repetitive motions, grasping, and talking. Sitting long hours performing assays working in biosafety cabinets
• Preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; working under microscopes for continuous hours.
• Exposure to the following hazards: Electrical current, moving mechanical parts, exposure to chemicals, packaging, shipping, handling, or decontamination of infectious agents assigned to risk group 2 and 3, including for emergency response. Laboratories, production rooms, waste holding areas, or other facilities where infectious agents are or may be handled or stored.
• On several occasions task may also require use of full face or half face respiratory protection like, Personal Air Purifying Respirators (PAPR)
• Occasionally be required to perform sedentary, light, medium, heavy, and very heavy work (Exerting in excess of 100 pounds of force occasionally, and/or in excess of 50 pounds of force frequently, and/or in excess of 20 pounds of force constantly to move objects).

Resilience offers employees a robust total rewards program including equity, an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target annualized base pay hiring range for this position is $69,000.00 - $87,000.00. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate’s geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.