Manager, Quality Control Lab

Manager Quality Control - Lab Our role plays a vital part within our organization. After completing training, you will manage daily activities, performance, and coaching development of staff. You will coordinate analytical activities, perform release testing, and help ensure our medications meet the highest standards of safety, efficacy, and quality. What The Manager Quality Control - Lab Does Each Day Test and release finished product routinely for commercial lots for potency, endotoxin, and sterility Maintain accurate and complete notebook records for all method validation and investigational studies in accordance with SOPs, cGMP, and current GdP Implement improvements to analytical test methods or instrumentation Write investigation report for OOS for sterility results Provide quality oversight of laboratory Responsible for assigned testing and work from beginning to end with minimal supervision Write SOPs and follow policy, procedure and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements Communicate with operations for scheduling the QC samples Ensure that analytical methods are validated as efficiently as possible to meet business milestones Provide technical support on an as‑needed basis as directed by Director of the Laboratories Manage the budget for the labs Ensure testing is conducted safely, including proper PPE and ventilation; report any safety issues to the Director immediately Our Most Successful Manager Quality Control - Lab Has a sense of urgency, accountability and resourcefulness (e.g., works well in a changing environment) Is a self‑starter and independent learner Promotes active listening with team members; contributes appropriately to conversations; has strong verbal and written communication skills with the ability to work with other departments and people at all levels Understands how various issues affect each other and the outcome of projects; improves existing approaches by seeking opportunities to creatively transform Minimum Requirements For This Role BS or MS degree in chemistry, biology or related field 5 years prior experience in Quality Assurance / Laboratory / cGMP / FDA‑regulated industry 3 years supervisory or management experience 18+ years of age Able to successfully complete a drug and background check Must be currently authorized to work in the United States on a full‑time basis; Quva does not sponsor work visas Any Of The Following Will Give You An Edge Prior experience in Quality Assurance / Laboratory / cGMP / FDA‑regulated industry Benefits Of Working At Quva Set, full‑time, consistent work schedule Comprehensive health and wellness benefits including medical, dental and vision 401k retirement program with company match 5 paid PLP and 17 PTO days off plus 8 paid holidays per year Occasional weekend and overtime opportunities with advance notice National, industry‑leading high growth company with future career advancement opportunities Base compensation estimated within the range described Range: $98,891 – $135,975 annually Eligible for annual incentive bonus subject to program terms and guidelines 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 #J-18808-Ljbffr