Position Overview

Job Title:QA Supervisor - Regulatory Affairs

Worksite: Bryan, TX

Requisition # 2026-38809

Job Description: QA Supervisor - Regulatory Affairs for FUJIFILM Diosynth Biotechnologies Texas LLC, Bryan, TX. Responsible for supporting the electronic publishing of regulatory submissions for national and regional regulatory agencies, and FUJIFILM Diosynth partner companies with the primary focus on moderate to complex regulatory submissions in both eCTD and non-eCTD format. Supports all CMC regulatory affairs activities for FUJIFILM Diosynth partner companies' products, summarize regulatory intelligence, provides CMC regulatory input for regulatory submissions, and manages the compilation and SME review of CMC sections of all submissions for completeness and quality.(25%). Specific job duties include the following: Obtain data/documents from multiple internal teams for exchange and/or communication with FUJIFILM Diosynth partner companies. Upload information to the Regulatory documentation management location for future use.(25%) May be required to compile and report key information to pertinent stakeholders within the Quality team to ensure proper visibility and communication. Support a vibrant regulatory culture, working among functional groups as a teammate and collaborator to develop successful regulatory strategies.(10%). Produce and manage the generation of documentation to be submitted to worldwide governmental regulatory agencies to secure approvals for marketing products manufactured and/or distributed by FUJIFILM Diosynth partners. (15%) Support development teams working towards modifying existing processes or creating new processes; ensure compliance with existing design controls, risk management, and domestic and international regulations.(5%) Ensure timely approvals, communicate, and support negotiations with the FDA and other regulatory bodies as needed to identify pre-submission requirements and strategy and to resolve post-submission queries and issues.(5%) Maintain proficiency on regulatory requirements; and FDA/Notified Body published reviews as applicable.(5%) Provide continuing regulatory education and disseminate regulatory information to the product development, marketing, and clinical groups. Ensure that regulatory intelligence communications are disseminated in a timely manner to the appropriate business functions. (5%) Be responsible for ensuring personal and Company compliance with all Federal, State local, and Company regulations, policies, and procedures. Support the review and negotiation of Master Service Agreements (MSA) and Quality Agreements (QAg).(5%)

Job Description

Requirements: Master's degree in Material Science, Biochemistry, Quality Assurance or related biology/science field and three (3) years experience as a senior regulatory affairs analyst, senior quality control/assurance analyst or related occupation in regulatory affairs; OR Bachelor's degree and five (5) years experience as a senior regulatory affairs analyst, senior quality control/assurance analyst or related occupation in regulatory affairs.

Must possess two years of experience in the following:

• Regulatory experience in a pharmaceutical or regulated industry;
• GMP/GXP or a comparable heavily regulated environment;
• Regulatory Information Systems, planning and/or publishing tools.

Must possess one year of experience in the review and preparation of regulatory documentation for regulatory intelligence/compliance, supporting e-CTD publishing, maintenance of the company regulations and CDMO-related regulatory obligations

Must possess the following knowledge/skills: Cell & Gene Therapy area and biologics product knowledge; Product science and product development

Salary: $80,400 - $115,000 / year

Application Instructions: For confidential consideration, apply at https://www.fujifilm.com/us/en/about/region/careers. Requisition # 2026-38809

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