The role reports to the Director of Strategic and CDMO Marketing and is expected to bring strong ... At FUJIFILM Cellular Dynamics, we're unlocking the power of human cells to change lives. Using ...
The role reports to the Director of Strategic and CDMO Marketing and is expected to bring strong ... At FUJIFILM Cellular Dynamics, we're unlocking the power of human cells to change lives. Using ...
The role reports to the Director of Strategic and CDMO Marketing and is expected to bring strong ... At FUJIFILM Cellular Dynamics, you'll thrive in a collaborative and cutting-edge environment that ...
The role reports to the Director of Strategic and CDMO Marketing and is expected to bring strong ... At FUJIFILM Cellular Dynamics, you'll thrive in a collaborative and cutting-edge environment that ...
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At FUJIFILM Holdings America Corporation, we're redefining innovation across the industries we ...
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At FUJIFILM Holdings America Corporation, we're redefining innovation across the industries we ...
Global CDMO Compliance Officer
Morrisville, NC · On-site
$220 - $270/hr
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
Global CDMO Compliance Officer
Morrisville, NC · On-site
$220 - $270/hr
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
... at CDMO company. * Demonstrated familiarity with high-level CRM data architecture and technical CMC documentation workflows. * Experience collaborating across global time zones. * Ability and ...
Quick apply
... at CDMO company. * Demonstrated familiarity with high-level CRM data architecture and technical CMC documentation workflows. * Experience collaborating across global time zones. * Ability and ...
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145 - $165/hr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145 - $165/hr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Senior Radioanalytical Development Scientist
Boston, MA · On-site
$145K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
... CDMO Compliance Officer for its FUJIFILM Biotechnologies business, a world-leading contract ... At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways.
Director, Analytical Development
Cambridge, MA · On-site
$185 - $240/hr
... at CDMO. Provide person-in-plant support, as needed Develop, review, and approve analytical development source documents, and provide oversight for relevant CMC sections for regulatory submissions.
New
Director, Analytical Development
Cambridge, MA · On-site
$185 - $240/hr
... at CDMO. Provide person-in-plant support, as needed Develop, review, and approve analytical development source documents, and provide oversight for relevant CMC sections for regulatory submissions.
New
Properly clean and sanitize all mixers following the Standard Operating Procedure set by Swiss American CDMO. * Reassemble the mixer. * Provide DI Water at 80C in mobile kettle to the Production ...
Properly clean and sanitize all mixers following the Standard Operating Procedure set by Swiss American CDMO. * Reassemble the mixer. * Provide DI Water at 80C in mobile kettle to the Production ...
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159K - $195K/yr
Responsible for driving execution of the formulation development plan at CDMO (PO through delivery). * Champion a strong winning culture, fostering teamwork and commitment to excellence through ...
Associate Director, Formulation and Drug Product Development
Waltham, MA · On-site
$159K - $195K/yr
Responsible for driving execution of the formulation development plan at CDMO (PO through delivery). * Champion a strong winning culture, fostering teamwork and commitment to excellence through ...
This role involves leading the CDMO business and owning the commercial strategy for revenue growth ... Join a fast-growing organization at the forefront of radiopharmaceutical innovation. #J-18808 ...
This role involves leading the CDMO business and owning the commercial strategy for revenue growth ... Join a fast-growing organization at the forefront of radiopharmaceutical innovation. #J-18808 ...
Senior Program Manager, Cell Therapy CDMO GMP Projects
Forest, TX · On-site
$90 - $120/hr
The ideal candidate will have a Bachelor's degree in Life Science, at least 5 years of experience in a CDMO/GMP environment, and excellent communication skills to interact positively with internal ...
Senior Program Manager, Cell Therapy CDMO GMP Projects
Forest, TX · On-site
$90 - $120/hr
The ideal candidate will have a Bachelor's degree in Life Science, at least 5 years of experience in a CDMO/GMP environment, and excellent communication skills to interact positively with internal ...
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We're ... Summary of role We are seeking a CDMO Materials Management Senior Specialist. The Materials ...
New
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We're ... Summary of role We are seeking a CDMO Materials Management Senior Specialist. The Materials ...
New
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We're ... Summary of role We are seeking a CDMO Materials Management Senior Specialist. The Materials ...
At Lantheus we are purpose-driven, and every employee plays a vital role in our success. We're ... Summary of role We are seeking a CDMO Materials Management Senior Specialist. The Materials ...
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130 - $165/hr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130 - $165/hr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
Scientist/Sr. Scientist, Radiopharma Development and Tech Transfer (Boston or Salt Lake City)
Boston, MA · On-site
$130K - $165K/yr
Occasional business travel may be required (approximately 10%, Contiguous US) to facilitate technology transfer and troubleshooting activities at CDMO and internal sites. * Author, review, and ...
At Cdmo information
See salary details
$15K - $48.8K
2% of jobs
$48.8K - $82.6K
2% of jobs
$82.6K - $116.5K
6% of jobs
$116.5K - $150.3K
5% of jobs
$150.3K - $184.1K
2% of jobs
$201K is the 25th percentile. Wages below this are outliers.
$184.1K - $217.9K
14% of jobs
The median wage is $245.3K / yr.
$217.9K - $251.7K
22% of jobs
$251.7K - $285.5K
13% of jobs
$297.6K is the 75th percentile. Wages above this are outliers.
$285.5K - $319.4K
22% of jobs
$319.4K - $353.2K
7% of jobs
$353.2K - $387K
3% of jobs
$15K
$241.3K
$387K
How much do at cdmo jobs pay per year?
What is the difference between At Cdmo vs Clinical Research Associate?
| Aspect | At Cdmo | Clinical Research Associate |
|---|---|---|
| Required credentials | Typically requires a degree in life sciences, pharmacy, or related field; certifications vary | Requires a degree in life sciences or healthcare; often requires GCP or ICH certifications |
| Work environment | Contract manufacturing or development labs, regulatory compliance settings | Clinical trial sites, hospitals, or research organizations |
| Employer and industry usage | Pharmaceutical, biotech, and contract manufacturing organizations | Pharmaceutical companies, CROs, research institutions |
While both roles involve the pharmaceutical industry, At Cdmo professionals focus on manufacturing and development processes within CDMOs, whereas Clinical Research Associates oversee clinical trial activities at research sites. The credentials and work environments overlap but serve different stages of drug development.
What cities are hiring for At Cdmo jobs?
Cities with the most At Cdmo job openings:
What states have the most At Cdmo jobs?
States with the most job openings for At Cdmo jobs include:
What job categories do people searching At Cdmo jobs look for?
The top searched job categories for At Cdmo jobs are:

Fujifilm rating
8.5
Based on 70 frontline employees who took The Breakroom Quiz
33rd of 545 rated manufacturers
Job description
FUJIFILM Cellular Dynamics, Inc. is seeking an Associate Director, Program Design to lead the scoping, design, and proposal development process for new CDMO business opportunities, from client request for proposal through contract signature. This individual contributor role serves as a key bridge between Commercial, Program Management, Site Leadership, Finance, Legal, R&D, Process and Analytical Development, Manufacturing, Supply Chain, Facilities, and Quality to translate client requirements into executable program scopes, assumptions, timelines, capacity plans, and pricing models. The role reports to the Director of Strategic and CDMO Marketing and is expected to bring strong technical, operational, and commercial judgment to support high-quality proposals, clear client communication, and efficient transition of awarded work into Program Management. Collaborates closely with the centralized Program Management group and serves as the local representative. This is an on-site position in Madison, Wisconsin.
At FUJIFILM Cellular Dynamics, we’re unlocking the power of human cells to change lives. Using revolutionary induced pluripotent stem cell (iPSC) technology, we drive advancements in drug discovery, disease modeling, cell therapy, research tools, and cell therapy manufacturing. Our mission is deeply meaningful, and we’re looking for bold innovators to join us.
At FUJIFILM Cellular Dynamics, you’ll thrive in a collaborative and cutting-edge environment that encourages creativity and celebrates breakthroughs. If you’re ready to do work that makes a real impact and propels healthcare forward, this is your chance to be part of something extraordinary for science, patients, and yourself.
Our headquarters is in Madison, Wisconsin, a dynamic city celebrated for its lakes, parks, cultural richness, biotech leadership, and access to world-class academia.
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 Job Functions
- Improve and sustain a harmonized process for authoring, managing, and delivering CDMO program proposals that support new business acquisition, in line with the central Program Design group.
- Partner with the Commercial Sales Team to review customer requests for proposals, clarify client requirements and assumptions, participate in client discussions, deliver FCDI proposals, and respond to follow-up questions.
- Define program scope, including technical requirements, materials, equipment, timelines, resource needs, and key assumptions in collaboration with technical functions and designated subject matter experts.
- Together with Program Management, assess site capacity, suite utilization, scheduling constraints, and operational readiness to inform proposal assumptions and support executable program designs.
- Together with finance and Program Management, develop proposed program pricing using approved cost allocation and pricing models, and secure appropriate approvals.
- Coordinate with Commercial, Site Leadership, Legal, and other stakeholders to deliver accurate, timely, and commercially competitive proposals to prospective clients.
- Review, upgrade and maintain proposal infrastructure in alignment with the central Program Design group, including databases for site services, labor assumptions, functional inputs, RFPs, proposal responses, assumptions, and related proposal history.
- Develop, monitor, and report key performance indicators for proposal volume, turnaround time, win/loss drivers, proposal quality, and other metrics related to Program Design responsibilities.
- Drive timely decision-making by completing analyses, identifying risks, proposing mitigations, and communicating tradeoffs clearly to stakeholders.
- Ensure clear and timely communication across teams as needed, including planning discussions, progress updates, issue escalation, proposal reviews, closure, and lessons learned.
- Translate approved proposals into initial Statements of Work once FCDI is selected, and ensure a structured handoff of scope, assumptions, commitments, and risks to Program Management.
- Maintain current knowledge of cell therapy industry standards, CDMO operating models, cGMP operations, corporate policies, and relevant best practices.
- Evaluate the suitability of new technologies, equipment, scalability, and manufacturability considerations for prospective client programs in partnership with R&D, Process and Analytical Development, Manufacturing, Supply Chain, Facilities, and Quality.
- Contribute to a culture of safety, quality, accountability, and patient focus by complying with company procedures, policies, and applicable cGMP cell culture manufacturing requirements.
- Perform other duties as assigned based on business needs.
Qualifications
- Bachelor’s degree in a scientific, engineering, business, or related discipline plus a minimum of 7 years of relevant experience; or Master’s degree plus a minimum of 5 years of relevant experience; or Ph.D. plus a minimum of 2 years of relevant experience. Relevant experience includes experience in CDMO, biologics, gene therapy, or cell therapy industry, including technical and regulatory familiarity with development, technology transfer, manufacturing, cell culture, and drug product.
- Demonstrated understanding of process development, analytical development, manufacturing, quality, supply chain, and/or technical operations within a biologics, gene therapy, or cell therapy environment is required.
Capabilities and Experience
- Ability to work independently, take ownership of complex assignments, and proactively engage cross-functional stakeholders to obtain required inputs and alignment.
- Strong technical writing skills, with experience developing clear proposals, scopes, assumptions, project plans, and client-facing materials.
- Critical thinking and problem-solving skills, including the ability to analyze complex technical and business issues, evaluate alternatives, and recommend practical solutions.
- Financial and business acumen, including experience with cost assumptions, pricing inputs, proposal economics, and business case considerations.
- Ability to synthesize and present complex technical, operational, and financial information clearly and concisely for internal stakeholders and external clients.
- Exceptional collaboration, communication, facilitation, project management, and organizational skills.
- Ability to operate effectively in a fast-paced, dynamic environment while managing multiple competing priorities and driving deliverables to completion.
- Demonstrated ability to develop, communicate, and execute project or proposal plans with clear ownership, timelines, milestones, and decision points.
- Experience supporting multiple simultaneous projects, proposals, or client opportunities with changing priorities and time-sensitive deliverables.
- Ability to lead through influence, interact effectively across functions and levels, resolve conflicts, and drive decisions among cross-functional teams.
- Continuous improvement mindset, with a commitment to standardization, innovation, operational discipline, and practical problem solving in an evolving CDMO environment.
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 (fcdi-hr@fujifilm.com).
About Fujifilm
Sourced by ZipRecruiter
With each Industry we enter, We’ve learned to Leverage and Adapt our knowledge, Expertise and rRsources to make the World a better place. When it comes to Innovating for a Healthier World and a more sustainable society, we’ll NEVER STOP. Fujifilm will contribute to the social challenges by creating new value in a wide range of business domains through innovation in Products, Services, and Technological Development. We launched our Healthcare Business with X-ray film in 1936. And now, We are developing our business in areas of prevention, diagnosis, and treatment as a Comprehensive Healthcare Company. We will never stop Innovating for a Healthier World.
Industry
Chemical manufacturing
Company size
10,000+ Employees
Headquarters location
Minato-ku, Tokyo, JP