Quality Investigator 1st Shift

TX - Sugar Land 10751075 W Park One Dr #100Sugar Land, TX 77478, USAOur Quality Investigator 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 supporting all stages of manufacturing with conducting and writing incidents and deviation investigations. The candidate will work cross-functionally with Operations and various support groups to investigate root causes, implement effective corrective and preventative actions, and perform thorough product impact analyses. 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.This is a full-time role for our 1st shift, working Monday through Friday from 8:00 AM - 4:30 PM. This is a set, consistent schedule with minimum overtime requirements and 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 the Quality Investigator Does Each DayIndependently author and resolve deviations to meet production and product release requirementsCommunicating across multiple groups and levels to drive deviation closureIdentifying interdepartmental process improvements and working cross-functionally to-implement themUtilizing advanced root cause analysis techniques and technical impact analyses during the deviation investigation processManaging multiple priorities either independently or as part of a team to meet key deadlines and communicate issues and progress across all levels of organizationCommunicating (both written and verbal) progress and updates across multiple levels of the organizationPerforming more complex deviation investigationsParticipates in the training process and coaching of new team members and processesHelps assist with metric reporting and workload to meet the team's prioritiesOur Most Successful Quality InvestigatorsAre detail-oriented with strong verbal and written communications skillsExpresses energy, shows accountability, multi-tasks and works in a fast-paced, quality-rich environmentFulfills expectations, establishes sustainable relationships with team members, maintains effective and meaningful communication channelsHas good interpersonal skills and ability to work effectively and efficiently in a team environment to accomplish goalsUnderstands process flows, gap assessments and analysis of data to drive improvementEffectively identifies root causes and implement CAPAMinimum Requirements for this RoleAn associate degree and 3+ years' cGMP experience OR Bachelor's degree and 2+ years' cGMP experienceExperience with authoring, writing and leading deviation investigationsExperience working within a production or quality department of a pharmaceutical/ manufacturing companyKnowledge of continuous improvement techniques and problem-solving skills#J-18808-Ljbffr

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