Aegis is currently partnered with a bio medical manufacturer.
Requirements
Bachelor’s degree in Chemistry, Science, or related field required. Relevant experience may be considered in lieu of degree.
10+ years of relevant experience required with prior supervisory experience preferred.
Strong knowledge of cGMP laboratory operations and major laboratory instrumentation.
Ability to interpret laboratory data and make sound compliance decisions.
Proven leadership, communication, coaching, and conflict management skills.
Strong analytical, problem-solving, and decision-making abilities with capacity to manage multiple priorities.
Ability to work in a radioactive manufacturing environment and meet physical demands including lifting up to 70 pounds, wearing PPE, standing for extended periods, and working off-shift, weekends, or holidays as needed.
Responsibilities
Ensure compliance with all applicable US and international regulatory standards including FDA, EU, ISO, USP, NRC, and cGMP guidelines.
Coordinate cross-functionally to align QC testing schedules with production plans and ensure all testing and maintenance activities are completed on time.
Perform and oversee testing of finished product, raw materials, components, stability samples, validation batches, and experimental samples.
Review, approve, and maintain controlled documents within area of responsibility.
Lead and support investigations related to deviations, product failures, and customer complaints.
Author and review quality and safety reports and drive timely corrective actions.
Ensure safe handling of radioactive materials and maintain exposure levels As Low As Reasonably Achievable (ALARA).
Coach, develop, and manage team performance while aligning goals with site objectives and KPIs.
Conduct daily huddles and communicate performance metrics.
Manage department overtime, maintain 5S standards, and ensure training and qualification compliance.