Quality Control - Stability Coordinator I, Hamilton

Position Overview Summary : The QC Stability Coordinator I will construct, maintain, and oversee the Quality Control Testing of Stability programs to include developing a schedule of pull dates, overseeing testing of each pull, and generating summaries from the data. The Quality Control Coordinator I, under general direction, will be responsible for implementing a Quality Control Stability Program that will encompass the needs of the client for each program. The position will require frequent communication with the Chemistry, Cell Biology, Microbiology, and Quality Assurance groups to coordinate execution of testing, deviation management, and issuance of deliverables. The Coordinator will have visibility to method qualification to ensure timing of stability laydowns. Close attention to detail is required to oversee scheduling the stability testing and compiling data, to facilitate meeting deadlines and milestones. Other responsibilities may include but are not limited to: ownership of CAPA’s and deviations, client meetings, attending planning meetings, communication of changes, and utilizing new software.Company Overview The work we do at FUJIFILM Diosynth Biotechnologies has never been more important—and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people’s lives. Join FDB and help create the next vaccine, cure, or gene therapyin partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy, and drive - what FUJIFILM Diosynth Biotechnologies calls Genki.Job Description Essential Functions: Assists in preparing QC metrics on a monthly basis Performing pulls occur within the specified window Ensuring testing occurs within the specified window Assist in generating POs for external testing Work directly with Contract laboratories to coordinate and monitor testing and release schedulesWork directly with customers to update and confirm schedules and deadlines Attend daily briefings and update as needed Assist QC Director and QC Managers Ability to work cross-functionally with other Quality Control groups, Quality Assurance, Manufacturing, and Project Management to establish timelinesEstablish GMP documentation Review GMP documentation Update GMP documentation Follow all established laboratory, regulatory, safety, and environmental procedures Maintain and execute a minimum of 6 stability protocols Performs deviation management Perform other duties as assigned Required Skills&Abilities: Must be highly organized, driven, and possess the skills and capability to plan ahead and stay on schedule. Ability to evolve and adapt to new technologies to include electronic planning tools and Laboratory Information Management Systems (LIMS) Computer skills in Microsoft Office and Microsoft ProjectAbility to multi-task and prioritize work assignments with little supervision Excellent attention to detail Ability to work in a team or independent setting and collaborate with employees from various departments. Excellent analytical and planning skills Must have excellent organizational, written and oral communication skillsMinimum Qualifications: High school or GED and minimum of 4 years in GxP setting or coordinator/management position Associates degree and minimum of 2 years in GxP setting or coordinator/management position Bachelor’s degree and minimum of 1 year in GxP setting or coordinator/management positionMaster’s degree and no minimum GxP, coordinator/management experience Preferred Qualifications: Bachelor’s degree in a scientific discipline PMP Certificate Previous coordinator or management experience Analytical Background Working Conditions&Physical Requirements: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to:Experience prolonged standing, some bending, stooping, and stretching Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment is required Ability to sit for long periods to work on a computer Attendance is mandatoryEEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department ( or (979) 431-3500). #J-18808-Ljbffr