Regulatory Affairs Specialist II

College Station, TX - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Position Overview

The Regulatory Affairs Specialist II is responsible for supporting the Regulatory Intelligence deliverables the electronic publishing of regulatory submissions for national and regional regulatory agencies and FUJIFILM Biotechnologies partner companies. The primary focus of this position is on moderate to complex regulatory submissions in both eCTD and non-eCTD format and working with site functional groups with their response to changes in relevant Regulatory Intelligence. Actual work assignments are based on the FUJIFILM Biotechnologies portfolio of work along with the incumbents experience knowledge demonstrated technical skills and competencies or as part of an individuals development plan.

The Regulatory Affairs function supports all FUJIFILM Biotechnologies Texas - related regulatory affairs activities for FUJIFILM Biotechnologies partner companies products summarize regulatory intelligence provides regulatory-compliance input for regulatory submissions and manages the FUJIFILM Biotechnologies Texas response to changes in the regulatory landscape.

Company Overview

The work we do at FUJIFILM Biotechnologies Texas has never been more importantand we are looking for passionate mission-driven people like you who want to make a real difference in peoples lives.

From developing the next vaccine to advancing cell and gene therapies we collaborate with industry leaders to tackle complex challenges and deliver meaningful solutions.

If youre ready to help transform the future of medicine join FUJIFILM Biotechnologies. We offer a flexible work environment and were proud to cultivate a culture that will fuel your passion energy and drivewhat we call Genki.

Our state-of-the-art biomanufacturing facility is located in in College Station Texas which combines a small-town feel with vibrant culture top-notch schools and close proximity to big city life. Nestled between major hubs its a dynamic location that blends convenience with innovation.

Fujifilm is globally headquartered in Tokyo with over 70000 employees across four key business segments of healthcare electronics business innovation and imaging. We are guided and united by our Group Purpose of giving our world more smiles. Visit: Description

Reports to Director Regulatory Affairs

Work Location College Station TX

Primary Responsibilities:

Obtain data/documents from multiple internal teams for exchange and/or communication with FUJIFILM Biotechnologies partner companies.
Upload information to the Regulatory documentation management location for future use.
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.
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 Biotechnologies partners.
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.
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.
Maintain proficiency on regulatory requirements; and FDA/Notified Body published reviews as applicable.
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 and appropriate actions are taken by the respective stakeholders.
Be responsible for ensuring personal and Company compliance with all Federal State local and Company regulations policies and procedures.
May support the review and negotiation of Master Service Agreements (MSA) and Quality Agreements (QAg).

Qualifications:

Bachelors degree from accredited university with 1 year of GMP working experience.
Associate degree from accredited university with 3 years of GMP working experience.
Working knowledge of Regulatory Information Systems planning and /or publishing tools.
Working knowledge of and experience with various submission and application types publishing templates and relevant regulatory agency and industry guidelines.
Effective interpersonal teamwork networking and communication skills.
Proficiency in applying submission-readiness and publishing standards via Adobe Acrobat MS Word and related applications.
Proficiency with various aspects of the PQS specifically Change Controls CAPAs Deviation Management.
Demonstrated ability to build productive relationships across an organization and with FUJIFILM Biotechnologies partner companies is required.
Problem-solving capability including trouble shooting and adaptability required.
Understanding of the drug development process.
Skill to apply knowledge of submission-readiness and publishing standards.
Cell & Gene Therapy area and product knowledge strong understanding of product development process.
Fluency in English proofreading and strong negotiation skills.
Ability to work or lead in a matrix environment.
Ability to execute assignments independently as assigned.
Must possess strong organization skills strong written and verbal communication skills.
Demonstrated ability to handle multiple competing priorities simultaneously.
Role model for company core values of trust delighting our customers and Gemba.

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 essential functions. While performing the duties of this job the employee is required on a regular basis to:

Experience prolonged standing some bending stooping and stretching.
Ability to sit for long periods to work on a computer.
Potential for exposure to chemicals gases fumes odors dusts and other hazardous materials.
Ability to wear personal protective equipment including but not limited to safety glasses lab coat gloves specialized clothing including laboratory scrubs (pants and shirt) cleanroom (ISO 8 to ISO 5) gowning material and appropriate shoes required in most areas associated with this position.
Lifting to 25 pounds on occasion.
Use hand-eye coordination and manual dexterity sufficient to operate a keyboard photocopier telephone calculator and other office equipment is required.
Must be willing to work flexible hours.
Ability to work weekends and off-shift hours as needed to support manufacturing activities.
Must be willing to travel occasionally as needed.
Attendance is mandatory.

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 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.

EEO Information

Fujifilm is committedto 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 ).

Required Experience:

Position OverviewThe Regulatory Affairs Specialist II is responsible for supporting the Regulatory Intelligence deliverables the electronic publishing of regulatory submissions for national and regional regulatory agencies and FUJIFILM Biotechnologies partner companies. The primary focus of this pos...