Supervisor, Manufacturing Operations (ILP) 2nd Shift

Supervisor, Manufacturing Operations (ILP)Our Supervisor, Manufacturing Operations (ILP) 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 Inspection, Labeling and Packaging Operations and Label Printing Operations (as applicable). 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 2nd shift, working Wednesday through Saturday from 3:30PM to 1:30AM.

This is a set, consistent schedule based on site in our Bloomsbury, NJ 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 (ILP) Does Each Day:Supervise ILP operations and label printing activitiesSupervises ILP schedule in accordance with production schedule and customer demandPrepares and submits daily/weekly/monthly reports, prepares metrics and trends data to identify and prioritize continuous improvement opportunitiesParticipates in safety meetings, investigates accidents, and takes appropriate corrective action to eliminateOversee production activities to assure performance to plan is achievedEffectively arranges for work to be completed, schedules workflow and assignments to ensure delivery performance objectives for product or projects are met or exceededManages front line leadership in completion of daily operational tasks and assignmentsDrives Quality Management System assignmentsReviews 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 training programs & assures training is conductedReports & initiates production schedule changes, requests equipment and facility repairs, or modificationsOur Most Successful Supervisor, Manufacturing Operations (ILP):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 Role:High 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 Edge:Bachelor's Degree in Life Science or other related fieldStrong technical writing and verbal/written communication ability, including presentation skillsUnderstanding of process flows, gap assessments and analysis of data to drive improvementProficiency with computerized tracking toolsComprehensive knowledge of Adult learning techniquesBenefits 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 opportunitiesSalary Range $56,541- $77,744 Shift Differential- $5200yrAbout 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 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 EmployeesEqual Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws.

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