Jobs at QuVa Pharma, Inc.

Supervise QC Microbiology laboratory operations, mentor staff, and ensure cGMP compliance. Oversee sterility, endotoxin, and environmental testing, review/approve data, investigate OOS results, manage SOPs and LMS documentation, coordinate with contract labs, and lead continuous improvement to maintain product quality and regulatory compliance.

Manage and coordinate DEA compliance across multiple manufacturing sites: inventories, ARCOS reporting, CSOS and DEA 222 processing, controlled substance movement, training, registrations, audits, quota submissions, and regulatory updates to ensure pharmaceutical regulatory adherence and security.

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.

Lead end-to-end customer onboarding and implementation programs, build scalable project plans and PMO frameworks, coordinate cross-functional teams, track milestones/risks, and ensure delivery meets scope, timelines, and success metrics through structured communication and escalation.

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

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.