QuVa Pharma
Technical Operations Support Specialist: About This RoleOur Technical Operations Support 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 hands on support in the generation and execution of Technical Operations deliverables to include, but not limited to, process development/proof of concept studies, execution of process validation studies, new product transfers and API Conversions, process investigations, and process improvement initiatives. This individual will also provide support in the detection and resolution of difficult to detect process errors and frequently interact with individuals from other functions within the company. This position requires knowledge of existing processes and a comprehensive acquaintance with generation and approval of cGMP documentation to include Master Batch Records and Validations. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.What the Technical Operations Support Specialist Does Each Day:Report directly to the Manager, Technical Operations with minimal supervision in the execution of assigned deliverables required to fulfill Tech Ops commitmentsGenerate technical information, often in the form of process data, required to fulfill assigned deliverables without the support of established proceduresGenerate and execution of development, validation, and engineering documentation necessary to formally capture product introductions, process investigations, and process improvementsGenerate Knowledge Transfer and Training Plans to support the transition of knowledge from the Tech Ops community into routine production environmentProvide compounder and formulator training with respect to new products or processes as necessary to fulfill planned knowledge transfer requirementsEngage with Pharmacy Services, Quality, Operations, and R&D to support development and approval of Master Batch Records and associated labels for new products being introducedComplete training curricula and any Competency Assessment requirements to perform routine product formulation process steps to ensure new products and/or processes are designed in accordance with current standard operating proceduresRoutinely communicate with Tech Ops individuals at other Quva Pharma sites to leverage process knowledge to ensure similar process are aligned and consistent with best practices and company standardsGenerate change control documentation as necessary to support introduction of new products or process improvementsProvide experienced input for continued process improvement initiatives designed to support efficiency.Provide experienced input with Root Cause Investigations related to process variances or customer complaints and lead the execution of Root Cause Analysis cross functional teams as assigned. Once completed, summarize the root cause investigational activity in the form of cGMP investigation reportSupport the development and update of Standard Operating Procedures required to implement new products or processes and/or process improvementsProvide Quality Partners, Commercial Operations, and Executive Management visibility of shop floor concerns related to scheduled technical operations lots or routine production performance concernsOur Most Successful Technical Operations Support Specialist: Have strong problem-solving skills, including use of the scientific methodHave strong analytical skillsMake decisions in a constantly changing environmentDemonstrates great interpersonal communication skillsIs proficient in technical writing.Motivates cross functional teams to meet aggressive timelinesMinimum Requirements for this Role:Minimum High School Diploma3+ years' experience in the manufacture and distribution of sterile Pharmaceutical/Biological productsExperience in site-based manufacturing, quality operations, and/or research and development rolesExecution of product transfer and validation of formulation, manufacture, and distribution of sterile Pharmaceutical/Biological productsIncumbent must possess extensive knowledge of cGMPsGood working knowledge of regulatory guidance as it pertains to APIs and injectable drug productsExperience in Aseptic Operator Qualification and Process Simulation programsExperience with personnel and material flow patterns required for sterile environmentsAble 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 visasThe 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: $49,000- $68,000 per YearAny of the Following Will Give You an Edge: Experience at multiple sites and across multiple functionsExperience with product and/or process validation conceptsBenefits of Working at Quva:Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company matchA minimum of 17 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 medicines and 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 BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's 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. 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." Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.