Lead Quality Assurance Specialist 2nd Shift at Quva

Our Lead Quality Assurance Specialist plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training your responsibilities will include oversight and performance of functional areas and training in regard to processes and documentation as they pertain to quality standards and governmental regulations. 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 Monday through Friday from 2:00 PM to 10:30 PM. 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 Lead Quality Assurance Specialist Does Each Day:Ensures company compliance to QuVa Pharmas Standard Operating Procedures (SOPs) and Quality Management System (QMS)Follows all regulatory guidelines cGMP guidelines and aseptic techniques as required by the job functionWorks in accordance with area Supervision to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMPs) including warehouse manufacturing processes inspection labeling and packaging batch record review batch disposition and product distribution as applicableSupports department supervision in oversight and prioritization of day-to-day responsibilities.Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPDemonstrates a high level of discretion in the timely identification and resolution of events potentially impacting the Quality of products and processesProvides an established technical expertise for current processes and oversees training of department personnel on new processesMaintenance of retained sample storageReviews routine manufacturing environmental monitoring and quality control data for in-process and finished productsEvaluation of batches / product for compliance with defined specificationsSampling inspection and control of commercial product labelsReview and approval of shipping documentation for commercial productsOur Most Successful Lead Quality Assurance Specialists:Work to create an environment of open communication participation and information-sharing within and between teams within Quality Assurance and throughout facilityAre detail-oriented with strong verbal and written communications skillsSupport the development of a climate of quality and safety within the teams by identifying and monitoring quality and safety standardsAct decisively with purposeful pursuit of goals or objectives and thinks strategically in terms of solutionsDrive achievement expresses energy shows accountability ability to multi-task and work in a fast-paced quality-rich environmentMotivate others share knowledge build high performing teams show respect towards others and give constructive feedbackMinimum Requirements for this Role:A High School diploma or equivalentAble to successfully complete a drug and background checkAble and willing to walk stoop stand bend and lift up to 50 lbs. throughout each shift with or without reasonable accommodation18 years of age20/20 vision (with or without corrective lenses) and the ability to successfully pass a color vision testDemonstrated performance with direct supervision of a team is requiredAt least 2 years experience in Quality Assurance Sterile Compounding and/or GMP production facility preferredStrong Microsoft Word and Excel skillsMust 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 related field preferred but not requiredAt least 1 year experience at Quva Pharma preferredAt least 2 years experience with FDA-regulated operations (cGMP processes) preferredBenefits of Working at Quva:Set full-time consistent work scheduleComprehensive health and wellness benefits including medical dental and vision401k retirement program with company match17 paid days off plus 8 paid holidays per yearNational industry-leading high growth company with future career advancement opportunitiesAbout Quva:Quva is a national industry-leading provider of compounded injectable medicinesand software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStreampartners with health-systems to analyze large amounts of data and through AI and machine learningdevelops softwaresolutions that turns the data into insights that are used to better run their pharmacy operation. Quvas overall product and technology offerings help health-systems achieve greater value and deliver the 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:IC Key Skills Invoicing,Information Technology Sales,IT Support,Audio Visual,Database Administration Employment Type : Full-Time Experience: years Vacancy: 1