Supervisor, Manufacturing Operations (Compounding) 3rd Shift

Our Supervisor, Manufacturing Operations (Compounding) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you will be responsible for daily coordination and working schedules of people and equipment in Compounding Operations. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.This is a full-time role for our 3rd shift, working Monday through Friday from 10:00 PM to 6:30 AM. This is a set, consistent schedule based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.What The Supervisor, Manufacturing Operations (Compounding) Does Each DayRuns operation to meet or exceed delivery performance objectives for product or projectsSupervises staff in execution of daily work; assures operators comply with validated parameters and standard operating procedures, cGMP regulations and safety requirements; provides constructive operator feedbackCounsels, trains, & develops technicians for efficient performance; creates an atmosphere of team effort & open communicationCompletes in-process checks & verifications in alignment with Standard Operating ProceduresReviews documentation such as batch records and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation PracticesDevelops technician training programs & assures operator training is conductedTroubleshoots or resolves issues impeding daily/weekly deliverables; proactively demonstrates the ownership to achieveReviews operational performance and drives improvement opportunitiesInitiates & executes change control assignments in support of continuous improvement initiatives for equipment, documentation, or processesDrives Quality Management System assignments (CAPA, Deviation, Change Control, GMP tasks) to on-time closureReports & initiates production schedule changes, requests equipment and facility repairs, or modificationsOur Most Successful Supervisor, Manufacturing Operations (Compounding)Meets productivity standards; Completes work in timely manner; Strives to increase productivityFollows policies and procedures; completes administrative tasks correctly and on timePrioritizes and plans work activities; Sets goals and objectives; Organizes or schedules other people and their tasksApproaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitmentsMinimum Requirements For This RoleHigh school Diploma or GED from recognized institution or organization required2-3 years prior experience in cGMP / FDA regulated industry1 year of supervisory or management experience requiredSuccessful completion of certified in-house qualification programsExperience training personnel on aseptic techniques and appropriate gowning techniquesAble and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodationWell versed in the compliance & quality requirements of 503B pharmaceutical industry and CGMP's and have demonstrated strength in problem solving and resolutionMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visasAny Of The Following Will Give You An EdgeBachelor’s Degree in Life Science or another related fieldComputer SkillsTraining SoftwareMicrosoft SuiteERP softwareBenefits Of Working At QuvaSet, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match22 paid days off plus 8 paid holidays per yearNational, industry-leading high growth company with future career advancement opportunitiesAbout QuvaQuva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma’s multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva’s overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”California Consumer Privacy Act (CCPA) Notice for Applicants and Employees