Summary:  The Manufacturing Supervisor – Drug Product Operations will work directly with the processes associated with the Vanrx SA25 Automated Filling machine.   This includes but is not limited to formulation, aseptic filling, vial inspection and vial labeling following cGMP procedures.  This individual will also supervise a team of employees directly or indirectly in the production of Drug Product at FUJIFILM Diosynth.  

The work we do at FUJIFILM Diosynth Biotechnologies Texas has never been more important—and we are looking for passionate, mission-driven people like you who want to make a real difference in people’s 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 you’re ready to help transform the future of medicine, join FUJIFILM Diosynth Biotechnologies. We offer a flexible work environment and we’re proud to cultivate a culture that will fuel your passion, energy, and drive—what 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, it’s a dynamic location that blends convenience with innovation.

Fujifilm is globally headquartered in Tokyo with over 70,000 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: https://www.fujifilm.com/us/en/about/region/careers

Essential Functions: 

• Responsible for the operation of Vanrx SA25 Vial Filling Isolator. 
• Responsible for overseeing the formulation of the bulk drug product in accordance to procedures. 
• Responsible for visual inspection and labeling of filled bulk drug product vials in accordance to procedures. 
• Responsible for writing, reviewing, and/or updating Standard Operating Procedures (SOPs) and Batch Production Records (BPRs). 
• Document and maintain activity records according to cGMP regulations and ensure team members are trained. 
• Help implement project safety and quality assurance programs in collaboration with senior staff and EH&S.  
• Ensure proper documentation and execution of Batch Production Records for assigned projects. 
• Maintain confidentiality of proprietary company information. 
• Participate in incident investigations. 
• Maintain an effective working relationship with others. 
• Perform all other duties as assigned. 

Required Skills & Abilities: 

• Excellent oral and written communication skills as well as excellent interpersonal and organizational skills. 
• Demonstrated leadership, coaching and mentoring skills. 
• Ability to train others to perform and maintain cGMP standards 
• Strong proficiency with Microsoft Office applications. 
• Experience working in cleanroom environments. 
• Must have flexible work hours, and be willing to work outside of normal, scheduled hours, as necessary.  Must be able to work alternative shift hours and weekends as required. 
• Self-discipline and good attention to detail. 
• Excellent math and computer skills. 
• Must have exceptional planning skills and be willing to interface with colleagues in many different roles and functions throughout the manufacturing facilities and lead projects. 

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, pushing, pulling, reaching above the shoulder, stooping, and stretching.
• Use hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. 
• Potential for exposure to hazardous chemicals, gases, fumes, odors, mists, and dusts, and other hazardous materials.
• Ability to wear personal protective equipment including safety glasses, lab coat, safety shoes and gloves.  
• Ability to lift/pull/push up to 25 pounds frequently and up to 50 pounds on occasion.
• Attendance is mandatory.

Minimum Qualifications:

• Master’s degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or related field with three (3) years of relevant experience; OR
• Undergraduate degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or related field with five (5) years of relevant experience; OR
• Associates degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering, or other related field and seven (7) years of relevant experience; OR 
• High School/GED with nine (9) years of relevant experience.
• A minimum of two (2) years of formal or informal leadership experience required. 
• A minimum of three (3) years of experience in a GMP environment.

Preferred Qualifications:

• Biotechnology Certificate
• Green-Belt Certification
• Experience with mammalian, insect, yeast, or bacterial cell lines and their cultivation and/or purification of biologics or viral vectors produced from such

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.

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 (FDBTHR@fujifilm.com or (979) 431-3500).