The Associate Manager/Supervisor of DSM (Drug Substance Manufacturing) leads a team of manufacturing associates (MA’s) for manufacturing bulk drug substance. The Associate Manager is responsible for the departments training and regulatory  compliance, ensuring schedule adherence, and their associated activities to ensure compliant and reliable start up activities and production.

FUJIFILM Biotechnologies is building the future of bioproduction in Holly Springs, North Carolina. By end of 2025, we’ll open North America’s largest end-to-end CDMO biopharmaceutical manufacturing facility, offering drug substance production, fill-finish, and packaging under one roof.

We’re looking for passionate, mission-driven people to help us realize this exciting vision and deliver the next vaccine, cure, or therapy. We offer a dynamic work environment and we’re proud to cultivate a culture that will fuel your purpose, energy, and drive—what we call Genki. Ready to shape the future of medicine? Let’s transform healthcare together!

Holly Springs, North Carolina, combines small-town warmth with proximity to Raleigh’s thriving tech scene, making it the perfect blend of community and opportunity.

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

 What You’ll Do

• Provides on-the-floor leadership for a shift team of up to 7-10 manufacturing associates
• Coordinates the execution of the manufacturing schedule through daily shift assignments, lead daily huddles, and manages escalations
• Fosters an inclusive, people-first culture with regular communication, conducting 1:1s on a defined cadence with direct reports
• Maintains a safe and cGMP compliant environment by ensuring direct reports have correct and up-to-date training
• Supports manufacturing investigations and continuous improvement projects
• Coordinates with other functional areas for additional activities requiring access to the manufacturing space and equipment, such as but not limited to: maintenance, calibration activities and the use of manufacturing equipment
• Administers company policies, such as but not limited to: time reporting, time off, shift policies, and inclement weather that directly impact manufacturing employees
• Coaches and guides direct reports to foster individual and team professional development and growth
• Participates in the recruitment process and retention strategies to attract and retain talent
• Addresses performance gaps, employee concerns, and partners with HR as needed for resolution
• Leads peer department management in tactical and strategic development
• Supports and leads water and engineering batch schedule attainment as required for the tech transfer of new products
• Collaborates with partners, vendors, and key stakeholders, as needed while executing the day-to-day manufacturing activities
• Other duties, as assigned

Basic Requirements

• HS diploma or GED with 8+ years’ experience from similar role in large pharma/biotech operations or projects

• BA/BS Life Sciences Degree or associate degree with Bachelor’s degree and 4+ years’ experience from similar role in large pharma/biotech operations or projects OR
• Associate degree in Life-Sciences and 6+ years’ experience from similar role in large pharma/biotech operations or projects OR
• Or Military experience of equivalence
• Experience in in manufacturing of biological products, familiar with GMP/GLP requirements

Preferred Requirements

• High School Diploma/GED with 8 years of related experience; or
• Bachelor’s degree in Life Science, Engineering, or related field with 4 years of related experience; or
• Master’s degree in Life Science, Engineering, or related field with 2 years of related experience
• 2 years of experience managing a team
• Experience with regulatory inspections, investigations, and change
management

WORKING CONDITIONS & PHYSICAL REQUIREMENTS

• Will work in environment which may necessitate respiratory protection
  
• May work in Mechanical/Production spacesthat may require hearing protection and enrollment in a hearing conservation program
• Will work in environment operating a motor vehicle or Powered Industrial Truck
• Ability to discern audible cues
• Ability to stand for prolonged periods of time - up to 240 Minutes
• Ability to sit for prolonged periods of time - up to 240 Minutes
• Ability to conduct activities using repetitive motions that include wrists, hands and/or fingers
• Ability to operate machinery and/or power tools
• Ability to conduct work that includes moving objects up to 33 pounds
• Ability to bend, push or pull, reach to retrieve materials from 18” to 60” in height, and use twisting motions
• Will work in warm/cold environments

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.

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 (FDBN_PNC@fujifilm.com).