Job Title

Job Description -QC Lab ManagerAbout UsEvergreen Theragnostics, Inc. is a radiopharmaceutical company headquartered in Springfield, NJ. We operate in a brand-new state-of-the-art facility, developing our own radiopharmaceutical products and providing contract development and manufacturing services for other radiopharmaceutical companies. We also operate our own cutting edge cancer research laboratories. The company expects rapid growth in the next few years.Evergreen is a small team, where all team members support each other in a variety of activities. We are looking for team members who are motivated to take on new challenges and excited to help build the company. Partial equity-based compensation packages possible.Summary: We are seeking a QC Lab Manager to support our growing QC team, reporting to our QC Manager.Job ResponsibilitiesOversee all day-to-day QC laboratory operations and related activities.Schedule and manage laboratory workload, managing utilization and efficiency of laboratory operations.Ensure QC laboratory procedures and standards are continuously updated and maintained.Establish training programs for new team members and ensure compliance to standard operating procedures, safety, GMP, and other regulatory requirements.Responsible for supervision of QC Team during investigation, resolution, and reporting of laboratory non- conformances, OOSs, OOTs, OOEs, and deviations.Provide QC Team with developmental feedback throughout the execution of routine operations, as well as new and challenging tasks.Develop a disciplined QC Team that adheres to all organization standard operating procedures and good laboratory practices.Participate, as well as supervise QC Team members, regarding all QC testing of finished product, product intermediates, and raw materials.Maintain QC Laboratory calibration records and preventive maintenance schedules for all analytical equipment.Provide technical assistance and information to customers, suppliers, and internal departments to ensure product quality.Manage safety and environmental regulations by ensuring that standards, policies, and procedures are adhered to in compliance with organizational, as well as state and local requirements.Responsible for establishing the requirements for raw material acceptance from suppliers and continuously monitoring their compliance.Participate in customer and regulatory authority audits, when requested by Head of QualityAs this is a position involving occupational exposure to radiation, candidates must not have an aversion to occupational radiation exposure (proper training to be provided).Be able to lift heavy objects (up to 70 lbs.)QualificationsSkills:Leadership and collaboration skillsStrong written and verbal communication skillsAnalytical and critical thinking skillsProject management skillsQC process skillsComputer knowledge and skillsEducation and Relevant ExperienceBS in appropriate discipline (STEM)Laboratory and QC experience preferredOperation of analytical equipment preferred (e.g., HPLC, GC, FTIR, etc.)3-5 years' experience in a QC managerial roleKnowledge of local and international regulations relating to QC testing of pharmaceutical productsWorking knowledge of QMS requirements and KPIsWorking knowledge of LIMS and associated regulatory requirementsExperience with MS Word, Excel, project management and analytics software