Position Overview

The Manufacturing Manager is a critical leadership position responsible for leading teams to execute clinical and commercial GMP cell therapy manufacturing activities such as media preparation, master cell banks, viral vectors, cell separation, autologous and allogeneic cell therapy. The Manufacturing Manager is accountable in ensuring manufacturing execution is performed in compliance with all required procedures and expectations are always meet, ensuring successful and complaint delivery of cell therapy technologies.This is a full time on site position.

Company Overview

Join us! FUJIFILM Diosynth Biotechnologies is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community, and the world at large.

Job Description

The Manufacturing Manager is a critical leadership position responsible for leading teams to execute clinical and commercial GMP cell therapy manufacturing activities such as media preparation, master cell banks, viral vectors, cell separation, autologous and allogeneic cell therapy. The Manufacturing Manager is accountable in ensuring manufacturing execution is performed in compliance with all required procedures and expectations are always meet, ensuring successful and complaint delivery of cell therapy technologies.This is a full time on site position.

Department: Internal Manufacturing

Location: Thousand Oaks, CA

Reports To: Manufacturing Associate Director

MAJOR ACTIVITIES AND RESPONSIBILITIES:

• Oversee day to day cell therapy manufacturing operations ensuring supervisors leads their teams as expected

• Accountable for driving evaluation of day to day floor issues in collaboration with quality and applicable SME’s

• Provide guidance to shift supervisors in response to day-to-day issues, compliance, personnel management, shift schedules, aseptic behaviors, safety, inventory management and continuous improvement

• Responsible for development of robust and agile training plan as to ensure the demands of new technologies and processes can be supported without impact to schedule adherence

• Author and or revise manufacturing SOP’s Batch records, work instructions, validation protocols. Lead investigation of quality events including but not limited to; investigation records, CAPA’s and Effectiveness check records

• Collaborate with planning function, facilities, supply chain, program management and MSAT team to ensure on time execution of production plan commitments

• Ensure manufacturing lots conforms to applicable quality standards and batch records are reviewed within established timeframe

• Collaborate with Program Management and MSAT team to assist in tech transfer, scale up and transition activities

• Partner with people department in support of hiring, selection and retention process of manufacturing personnel by supporting interviews, onboarding process, team building and other employee engagement activities as needed

• Provide daily production updates at Work Center Team meetings, clients representatives and program management team as needed

• Provide guidance for implementation of continuous improvement efforts within manufacturing areas

• Represent the manufacturing department in interactions with FMEA’s, client visits, inspections and audits and cross-functional projects as needed

• Support with technical expertise in the development of new processes, techniques and standards.

• Assist facilities, engineering and validation teams in execution of maintenance, calibration and validation activities, as needed

• Provide suggestions and support implementation of process optimization and efficiencies

• Lead by example exhibiting our company values and 9 people fundamentals in day-to-day interactions

BACKGROUND REQUIREMENTS (Education, Behavioral, Professional & Technical Capabilities Experience):

Qualifications:

• 2-4 years’ experience in leading teams

• Master of Science (M.Sc.) with 4+ years applicable biopharma experience; or

• Bachelor of Science (B.Sc.) with 6+ years of applicable biopharma experience; or

• Associate degree with 8+ years of applicable biopharma experience; or

• High school diploma with 9+ years of applicable biopharma experience

Preferred Qualifications:

• Leadership experience in a GMP manufacturing environment

• Experience in applying Operational Excellence and Lean Manufacturing

• Excellent communication skills, drive, sense of urgency, energy level and problem-solving abilities

• Ability to forge and maintain positive relationships with other functional areas

• Ability to effectively develop and mentor staff and positively advance the culture of an organization

WORK ENVIRONMENT:

• Work is generally performed in an office environment with occasional entry into manufacturing environments

• Consists of frequent complete use, virtual and in person meetings, and interacting with cross functional teams

• The Manufacturing Environment is Good Manufacturing Practice (GMP) facility. A GMP facility is governed by regulatory agencies in which there are specific requirements for hygiene and acceptable clothing. The following items are restricted when accessing the GMP manufacturing area:

• Makeup, painted nails

• Hair products (spray, gel, wax)

• Perfume and cologne

• Jewelry (rings, watches, bracelets, fitness bands, necklaces, and facial/earpiercings, etc.)

• Donning of gowns requires ability to physically don gowns while balancing in a cleanroom environment

PHYSICAL REQUIREMENTS:

• Subject to extended periods of sitting and/or standing, vision to monitor and moderate noise levels

• Ability move about an office environment and to occasionally enter into the manufacturing environments

• Open to work various shifts as needed

• Required to work weekends and holidays

SALARY AND BENEFITS:

• $120,000 to $150,000, depending on experience

• Medical, Dental and Vision

• Life Insurance

• 401k

• Paid Time Off

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.

EEO Information

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.

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 (FDBCHR@fujifilm.com).

Job Locations US-CA-Thousand Oaks

Posted Date 3 days ago (1/29/2025 12:26 PM)

Requisition ID 2025-33138

Category Manufacturing

Company (Portal Searching) FUJIFILM Diosynth Biotechnologies