{"schemaVersion":"jobsearcher.job.v1","id":"59a68a706e938f02279bb310","url":"https://jobsearcher.com/jobs/59a68a706e938f02279bb310","canonicalUrl":"https://jobsearcher.com/jobs/59a68a706e938f02279bb310","title":"Manager, Quality Control Lab","description":"Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching and developing staff. Coordinate analytical activities including method transfers and stability testing. Perform release testing for analytical studies. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement 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. What the Manager Quality Control -Lab Does Each Day:Test and Release Finished Product routinely for Commercial lots for Potency, Endotoxin, and SterilityMaintain accurate and complete notebook records for all method validation and investigational studies in accordance with SOPs, cGMP, and current GdPImplement improvements to analytical test methods or to instrumentationWrite investigation report for OOS for Sterility resultsProvide quality oversight of LaboratoryResponsible for assigned testing and work from beginning to end with minimal supervisionWrite SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirementsCommunicate with Operation for Scheduling the QC SamplesEnsure that analytical methods are validated as efficiently as possible to ensure business milestones are metProvide technical support on an as-needed basis as directed by Director of the LaboratoriesManage the budget for the LabsEnsure testing is conducted in a safe manner including but not limited to the proper PPE and ventilation; Any safety issue must be brought to the attention of the Director immediatelyOur Most Successful Manager Quality Control- Lab:Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)Is a self-starter and independent learnerPromotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organizationUnderstands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transformMinimum Requirements for this Role:BS. or M.S. degree in chemistry, biology or related field required5 years prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry3 years of supervisory or management experience required18+ years of ageAble to successfully complete a drug and background checkMust 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: Prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industryBenefits of Working at Quva:Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match5 paid PLP and 17 PTO days off plus 8 paid holidays per yearOccasional weekend and overtime opportunities with advance noticeNational, industry-leading high growth company with future career advancement opportunitiesThe base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditionsRange: $98,891 - $135,975 AnnuallyThis role is also eligible for an annual incentive bonus, subject to program terms and guidelinesAbout 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 EmployeesJob SummaryRequisition Number: MANAG005903Job Category: 8000-QualitySchedule: Full-Time","company":"Quva Pharma","rawCompany":"quva pharma","city":"Bloomsbury","state":"NJ","isRemote":false,"isActive":true,"createdAt":"2026-08-18T05:12:31.491Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-9121.00","title":"Natural Sciences Managers","slug":"natural-sciences-managers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"},{"code":"325998","title":"All Other Miscellaneous Chemical Product and Preparation Manufacturing","slug":"all-other-miscellaneous-chemical-product-and-preparation-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Manager, Quality Control Lab","description":"Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our training, your responsibilities will include managing daily activities, performance, and coaching and developing staff. Coordinate analytical activities including method transfers and stability testing. Perform release testing for analytical studies. At Quva, you will be an essential part of a mission-driven organization dedicated to expanding critical access to quality, affordable medication and data insights while promoting a culture of innovation, collaboration, and continuous improvement 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. What the Manager Quality Control -Lab Does Each Day:Test and Release Finished Product routinely for Commercial lots for Potency, Endotoxin, and SterilityMaintain accurate and complete notebook records for all method validation and investigational studies in accordance with SOPs, cGMP, and current GdPImplement improvements to analytical test methods or to instrumentationWrite investigation report for OOS for Sterility resultsProvide quality oversight of LaboratoryResponsible for assigned testing and work from beginning to end with minimal supervisionWrite SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirementsCommunicate with Operation for Scheduling the QC SamplesEnsure that analytical methods are validated as efficiently as possible to ensure business milestones are metProvide technical support on an as-needed basis as directed by Director of the LaboratoriesManage the budget for the LabsEnsure testing is conducted in a safe manner including but not limited to the proper PPE and ventilation; Any safety issue must be brought to the attention of the Director immediatelyOur Most Successful Manager Quality Control- Lab:Has a sense of urgency, accountability and resourcefulness (e.g., work in changing environment)Is a self-starter and independent learnerPromotes active listening with team members; Contributes appropriately to conversations; Has strong verbal and written communication skills with the ability to work effectively with other departments within the organization and with people at all levels of the organizationUnderstands how various issues affect each other and the outcome of projects; Improves upon existing approaches by seeking opportunities to creatively transformMinimum Requirements for this Role:BS. or M.S. degree in chemistry, biology or related field required5 years prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industry3 years of supervisory or management experience required18+ years of ageAble to successfully complete a drug and background checkMust 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: Prior experience in Quality Assurance /Laboratory/ cGMP / FDA regulated industryBenefits of Working at Quva:Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match5 paid PLP and 17 PTO days off plus 8 paid holidays per yearOccasional weekend and overtime opportunities with advance noticeNational, industry-leading high growth company with future career advancement opportunitiesThe base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditionsRange: $98,891 - $135,975 AnnuallyThis role is also eligible for an annual incentive bonus, subject to program terms and guidelinesAbout 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. 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