Jobs at QuVa Pharma, Inc.

Monitor aseptic processing and sterility assurance activities in a clean room, including gown qualification, EM/PM sampling and plate reading, media fills proctoring, sterility investigations, and documentation. Ensure compliance with SOPs, cGMP and 21 CFR Part 211, support qualification activities, and provide feedback to compounding staff to maintain product quality and safety.

Lead cross-functional teams to design and implement process improvements, airflow visualization programs, validations, and tech transfers for sterile drug manufacturing. Perform feasibility and scale-up studies, root-cause investigations, CAPA, process characterization, and technical writing. Support regulatory readiness, contamination control, and production performance to improve yield, reduce deviations, and ensure compliance with GMP/ICH/QbD expectations.

The Principal Scientist ensures QC compliance with regulatory standards, enhances performance, leads investigations, and mentors staff while driving continuous improvement in laboratory operations.

The Sales Executive is responsible for pipeline growth, managing sales processes, closing deals, and collaborating with teams to achieve revenue targets in healthcare solutions.

The Manager Quality Control Lab oversees lab operations, ensures compliance with quality standards, manages staff, conducts testing, and coordinates analytical activities to maintain high safety and efficacy standards for medications.