Full Description

Position Summary: Roles is responsible for performing, managing, and tracking deliverables for batch disposition to include compiling batch and batch linked documentation required for final and conditional product release, accurately maintaining site tracking and communication trackers, and providing accurate disposition statuses to clients, site departments, and Site / Executive Leadership. The role interfaces and collaborates with clients, Project Management, Manufacturing, QC, Supply Chain, Facilities/Engineering and internal QA departments to set disposition priorities, execute disposition elements and meet disposition timelines. Additionally, the role tracks, trends, and reports QA batch release metrics at relevant operational meetings and to Senior Leadership as well as leads internal cross-functional batch disposition meetings: identifying and tracking actionable items and escalating / informing to assure resolution of obstacles. Supports external client review and resolution of comments related to batch documentation, deviations, and CAPAs as needed. Responsible for gathering and presenting data for disposition and relevant metrics to management. Position Responsibilities: Tracks, monitors, and reports on status of Batch disposition for each product. Maintains and reports related to metrics. Trends, reports on batch disposition and other area data. Reviews batch documentation and approve relevant documents as the QA Approver. Compiles final packages. Works directly with Manufacturing, Engineering, MS&T (Manufacturing Science and Technology), Quality Control, Quality Assurance, Supply Chain and Validation to resolve issues to support commercial and clinical batch disposition. Interfaces with the client. Reviews deviations, CAPA’s, Interim Reports and ECs as needed. Completes Change Controls, master and executed Batch Records, and technical documents including CPV reports upon need. Initiates, manages Quality Change Controls as needed. Supports Annual Product Review, Complaint process (Supplier Quality, Product), Internal and client Inspections. Performs as disposition and complaint SME during regulatory and Health Authority Inspections. Performs as back-up for Client Support as a Point of Contact (POC), working closely with the PM team, attending client / KBI Quality to Quality meetings, compiles disposition and document status for meetings; develops related presentations. Supports manufacturing, Supply Chain and Quality to improve and streamline relevant Quality systems, business processes, and manufacturing processes. Executes other assignments upon request. Minimum Requirements: BS and 18+ years' experience or MS and 15+ years' experience in a cGMP regulated environment within Biopharmaceuticals or equivalent. Experience with Quality Systems to include batch record review, batch disposition of biopharmaceuticals, and investigations and CAPAs. Knowledge of US, EU, and Row cGMP guidelines required. KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply. I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary. I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal. At KBI, we are constantly seeking to improve our team with accomplished individuals who share in our commitment to serve our clients as they seek to advance important medicines to the patients who need them. We offer our employees a challenging, rewarding and fast-paced environment along with the opportunity for career advancement through the development of one’s technical skills. At KBI, employees work in a collaborative, team environment, where sharing knowledge and expertise with one another is strongly encouraged. If you do not see a position that matches your background, we invite you to return to our site often as positions are updated frequently. Please Note: To 3rd Party Search Firms/Employment Agencies: All inquiries must be directed to staffinginquiry@kbibiopharma.com. Please do not call or email any KBI Biopharma employee about current or future job openings. All resumes submitted by search firms or employment agencies to any employee at KBI Biopharma via-email, telephone, social media or other means will be deemed to be the sole property of KBI Biopharma, unless the firm submitting the resume has previously entered into a written agreement with KBI Biopharma regarding recruitment services and has been approved by Human Resources to work on an open position. KBI Biopharma will not pay any fee or remuneration with respect to candidates without complying with this requirement.