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Supervisor, Manufacturing Operations (Warehouse) at Quva
Quva
Sugar Land, TX
Logistics
Posted 0 days ago
Job Description
Our Supervisor Manufacturing Operations (Warehouse) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training you are responsible for supervising warehouse technicians in the warehouse. Warehouse personnel are responsible for receiving and picking materials used in compounding. The Supervisor will ensure personnel are using current Good Manufacturing Practices. 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 set consistent schedule based on site in our XXXX 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 (Warehouse) Does Each Day:Supervises warehouse personnel on multiple shift operationOversees discrepancy and non-conformance investigations and documenting investigations on process/product deviations or non-conforming materialsMaintains records of movement of materials at the point of receipt in the warehouse to the point of useReviews documentation to ensure recording of processes logs batch records and accounting of materials complies with policies procedures and Good Documentation Practices (GDP)Monitors the daily use of products throughout the process to ensure people and processes are in a continuous state of compliance with DEA regulations company policies and procedures and safety requirementsUses ERP System Infor to input data reference orders for pickingResponsible for training adherence for warehouse personnelDevelops and provides oversight to identification and implementation of appropriate corrective actions and preventive actionsDocuments in a timely manner all tasks requiring written records as specified in Standard Operating ProceduresManages material handling and movement with a sense of urgency as neededEnsures picking of batches meets production schedule and customer demandOur Most Successful Supervisor Manufacturing Operations: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 objectivesApproaches 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 Role:High school Diploma or GED from recognized institution or organization required1 year of supervisory or management experience requiredSuccessful completion of certified in-house qualification programsAble and willing to walk stoop stand bend and lift up to 50 lbs. throughout each shift with or without reasonable accommodationMust 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 Edge: Bachelors Degree in Life Science or other related fieldExperience working with controlled substancesWorking knowledge of DEA regulatory requirements as well as all applicable SOPsWorking knowledge of safety standards and their application to continuously improve the safety culture and metricsBenefits of Working at Quva:Set 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 Quva:Quva 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 Pharmas multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStreampartners 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. Quvas 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. Quvas 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.Required Experience:Manager Key Skills Lean Manufacturing,Six Sigma,Continuous Improvement,FDA Regulations,Lean,Packaging,Production Planning,cGMP,Cell Culture,Leadership Experience,Supervising Experience,Manufacturing Employment Type : Full-Time Experience: years Vacancy: 1
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