**Overview** **Follow Your Genki to North America's largest, state-of-the-art Life Science Manufacturing Facility & CDMO** The work we do at FDB 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 manufacture the next vaccine, cure, or gene therapy in 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 we call Genki. **Join us** We are growing our locations and are investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of our Bio CDMO (Contract and Development Manufacturing Organization) business. This will be the largest end-to-end cell culture CDMO provider in North America. The new site will offer end-to-end solutions to our customers looking to manufacture biopharmaceuticals in the US. In addition to drug substance manufacture, it will also provide automated fill-finish and assembly, packaging, and labeling services. The new state-of-the-art facility is located in Holly Springs, North Carolina, United States. **External US** **About the Role** The Associate Manager, QA for QC is responsible for supervising the QA team in the quality oversight of the Quality Control (QC) area. They help drive the quality oversight for the direction of all QC Laboratory processes, from project phase through operational readiness, as well as provide oversight of validation program execution for these processes. This role collaborates with other project teams and QA departments at other sites to align strategies and procedures. The role serves as the primary point of contact for their team and the first-line escalation point in areas of their responsibility. This role requires collaboration with leadership, site-based customers, and global colleagues. **What You'll Do** • Provides supervision of the QA for QC Compliance team. • Ensures allocation of adequate resources for shop floor QA activities (e.g., document review and approval, data review and approval, event triage), QA support activities (e.g., DR/CAPA review and approval, raw materials onboarding and release) and technical QA activities (e.g., CC review and approval, WO oversight). • Leads cross-functional teams to achieve operational readiness objectives and new product introduction goals using a risk-based, right-size approach. • Collaborates with Responsible Person(s) to facilitate timely disposition of GMP materials. • Serves as Subject Matter Expert in audit and inspections for their area of responsibility. • Establishes and maintains internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements. • Provides training, coaching, and mentorship of their team and peers as applicable. Works with their team to identify areas of improvement, reduce blind spots, and give opportunities for increasing responsibility as appropriate for each individual's career objectives. • Identifies and leads process optimization initiatives and continuous improvement tasks in their area of responsibility. • Establishes and maintains internal and external training goals for self and team to ensure compliance with cGMPs and regulatory requirements. • Applies expertise in Laboratory QA concepts and business knowledge to act as the primary point of contact for their team and the first-line escalation point in areas of their responsibility. • Gathers recommendations for enhancements and gaps related to their areas of responsibility and, in collaboration with leadership, prioritizes and implements solutions accordingly. • Maintains relationships with site-based customers and global colleagues and provides updates to leadership as requested. • Performs other duties, as assigned. **Minimum Requirements** • Bachelor’s degree in Life Sciences or Engineering and 8+ years of experience in GMP quality assurance and/or similar role OR • Master’s degree in Life Sciences or Engineering and 6+ years of experience in GMP quality assurance and/or similar role. • 2+ years of direct supervisory experience • Excellent oral and written communication skills **Preferred Requirements** • Working knowledge of ASTM E2500, Smartsheet, Trackwise, MasterControl and/or Kneat validation software is a plus • Understanding of the following processes preferred such as cell culture or fermentation. • Experience with complex projects and the ability to keep work paceand meet deadlines with good organization and planning skills. • High level of familiarity/understanding of production equipment, hygienic utilities, quality systems, automation, manufacturing & IT Systems, and/or validation methodologies • Understanding of GAMP5, Data Integrity, and application of 21 CFR Part 820 and Part 11 • Training and/or familiarity with Quality Risk Management principles preferred **Working & Physical Conditions** May work in Mechanical/Production spaces that may require hearing protection and enrollment in a hearing conservation program. Ability to ascend or descend ladders, scaffolding, ramps, etc. Ability to stand for prolonged periods of time up to 60 minutes. Ability to sit for prolonged periods of time up to 30 minutes. Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers. _FDBN is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation, gender identify or any other protected class. If an accommodation to the application process is needed, please email_ FDBN_PNC@fujifilm.com _._ _To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid._ **Job Locations** _US-NC-Holly Springs_ **Posted Date** _4 days ago_ _(12/10/2024 1:18 PM)_ **_Requisition ID_** _2024-28140_ **_Category_** _Quality Assurance_ **_Company (Portal Searching)_** _FUJIFILM Diosynth Biotechnologies_