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Quality Assurance Specialist

Company: QuVa Pharma Inc.
Location: Temple
Posted on: May 3, 2021

Job Description:

Job DetailsLevelEntryJob LocationTemple - Temple, TXPosition TypeFull TimeEducation LevelHigh School Diploma or GED EquivalentTravel PercentageNoneJob ShiftAnyJob CategoryQA - Quality ControlDescriptionPosition Overview:The Quality Assurance Specialist supports in oversight and performance of functional areas, and training in regards to processes, documentation as they pertain to quality standards and governmental regulations. Responsibilities may include: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 responsibilitiesEnsures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPsDemonstrates 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 processes Maintenance 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 productsOther duties as designated by the Quality Assurance SupervisorQualifications:Legally authorized to work in the job posting countryHigh school Diploma or GED from recognized institution or organization requiredBachelors Degree in life science or related field preferred but not required1 to 2 years experience in Quality Assurance, Sterile Compounding and/or GMP production facility preferred1 to 2 years experience with FDA-regulated operations (cGMP processes) preferredStrong Microsoft Word and Excel skillsTo be considered:In order to be considered for this position you must complete the entire application process, which includes answering all prescreening questions and providing your eSignature on or before the requisition closing date.Candidates for regular U.S. positions must be a U.S. citizen or national, or an alien admitted as permanent resident, refugee, asylee or temporary resident under 8 U.S.C. 1160(a) or 1255(a)(1). Individuals with temporary visas such as E, F-1, H-1, H-2, L, B, J, or TN or who need sponsorship for work authorization now or in the future, are not eligible for hire.It is the policy of QuVa Pharma to afford equal opportunity for employment to all individuals regardless of race, color, age, national origin, physical or mental disability, history of disability, ancestry, citizenship status, political affiliation, religion, gender, transgender, gender identity, marital status, status as a parent, sexual orientation, veteran status, genetic information or other factors prohibited by law, and to prohibit harassment or retaliation based on any of these factors.

Keywords: QuVa Pharma Inc., Temple , Quality Assurance Specialist, Other , Temple, Texas

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