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Remote Cdmo Jobs (NOW HIRING)

Fujifilm

Senior Counsel

$185K - $200K/yr

... to CDMO, Life Science/Pharma and Medical Device companies. Required Skills/Education * College ... Life Insurance * 401k * Paid Time Off *#LI-REMOTE EEO Information Fujifilm is committed to ...

synergy

New Business Development Manager

Dallas, TX · Remote

United States (Remote - National Territory) Travel: ~40-50% Overview Synergy Bioscience is a ... CRO * CDMO * Analytical testing labs * Pharmaceutical development services * Demonstrated success ...

Wilmington PharmaTech

Be Seen First

Sr. Business Development Director

San Diego, CA · Remote

This is a remote, field-based position ideally located in the Western region of the United States ... Experience: 7+ years of proven B2B sales experience, specifically within the contract API or CDMO ...

Danaher

Senior Product Manager - Core Proteins

OR · On-site +1

$100K - $130K/yr

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sr. Technical Sales Specialist

Madison, WI · On-site +1

$90K - $110K/yr

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Senior Product Manager - Core Proteins

$100K - $130K/yr

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Sr. Technical Sales Specialist

Fargo, ND · On-site +1

$90K - $110K/yr

At Aldevron, we deliver world-class CDMO services that accelerate the development of groundbreaking ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

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All JobsRemote Cdmo Jobs

Remote Cdmo information

How does a Remote CDMO professional typically collaborate with cross-functional teams while working remotely?

Remote CDMO professionals often work closely with diverse teams such as R&D, regulatory affairs, and supply chain management, using digital collaboration tools and regular virtual meetings to coordinate project milestones. Clear communication and proactive project management are crucial, as many tasks require input from multiple departments and external partners. While working remotely, staying organized and maintaining transparent progress updates help ensure seamless collaboration and project success.

What are the key skills and qualifications needed to thrive as a Remote CDMO (Contract Development and Manufacturing Organization) professional, and why are they important?

To thrive as a Remote CDMO professional, you need strong expertise in pharmaceutical or biotech process development, regulatory compliance, and project management, typically with a relevant science degree. Familiarity with systems such as LIMS (Laboratory Information Management Systems), electronic documentation tools, and quality management software is critical. Excellent communication, self-motivation, and problem-solving abilities are essential soft skills for remote collaboration and client interaction. These competencies ensure seamless project delivery, regulatory adherence, and successful partnerships in a virtual environment.

What is the difference between Remote Cdmo vs Remote Regulatory Affairs Specialist?

AspectRemote CdmoRemote Regulatory Affairs Specialist
Required CredentialsPharmaceutical or biotech degree, experience in drug development, regulatory knowledgeDegree in life sciences, regulatory affairs certification, understanding of compliance
Work EnvironmentCollaborates with R&D, manufacturing, and clinical teams in pharma/biotech companiesWorks with regulatory agencies, prepares submissions, ensures compliance
Employer & Industry UsagePharmaceutical companies, biotech firms, CDMOsPharma companies, regulatory consulting firms, biotech

The Remote Cdmo and Remote Regulatory Affairs Specialist roles share overlapping regulatory knowledge and industry context but differ mainly in focus. The Remote Cdmo handles drug development and manufacturing processes, while the Regulatory Affairs Specialist concentrates on compliance and submissions. Both roles require strong scientific credentials and industry experience, but their daily tasks and collaborations differ based on their core functions.

What is a Remote CDMO?

A Remote CDMO is a Contract Development and Manufacturing Organization (CDMO) that provides its services primarily through remote or virtual means, rather than requiring clients to be physically present on site. These organizations help pharmaceutical and biotechnology companies with the development, manufacturing, and sometimes commercialization of drugs, often utilizing digital platforms for project management, communication, and data sharing. Remote CDMOs are particularly valuable for clients who need flexible, efficient collaboration without geographical limitations.
More about Remote Cdmo jobs
What cities are hiring for Remote Cdmo jobs? Cities with the most Remote Cdmo job openings:
What are the most commonly searched types of Cdmo jobs? The most popular types of Cdmo jobs are:
What states have the most Remote Cdmo jobs? States with the most job openings for Remote Cdmo jobs include:
What job categories do people searching Remote Cdmo jobs look for? The top searched job categories for Remote Cdmo jobs are:
Remote Cdmo jobs near you
Infographic showing various Remote Cdmo job openings in the United States as of June 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.
Senior Counsel

Senior Counsel

Fujifilm

Remote

$185K - $200K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Fujifilm rating

8.3

Company rating: 8.3 out of 10

Based on 66 frontline employees who took The Breakroom Quiz

46th of 518 rated manufacturers

Job description

Position Overview
Senior Counsel will work, independently and collaboratively, on legal issues affecting FUJIFILM Holdings America Corporation and its Life Science/Pharma companies to minimize risks of legal liability and ensure maximum legal rights of the company.
Company Overview
At FUJIFILM Holdings America Corporation, we're redefining innovation across the industries we touch-from healthcare and photography to semiconductors and data storage. With roots in photosensitive materials and a legacy of groundbreaking technology, we now lead 23 diverse affiliate businesses across the Americas.
We're looking for mission-driven talents eager to join us to help create, market, and support a vast portfolio of products. At Fujifilm you'll have the opportunity to explore and grow your skills in new, exciting ways. Whether you're shaping tomorrow's tech or redefining today's processes, we'll provide a flexible work environment and dynamic culture where innovation thrives.
Our Americas HQ is nestled in Valhalla, New York, a charming town known for its excellent schools, beautiful parks, and easy access to the vibrancy of New York City.
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
Job Description
Responsibilities
  • Operating as a business partner, manage the day-to-day legal affairs of certain Fujifilm Life Sciences/Pharma companies under general supervision of Division General Counsel, Life Sciences and in coordination with other Fujifilm legal teams located within and outside the U.S.
  • Advise, counsel and report to management on legal and regulatory risks, including with respect to FDA regulations and other frameworks specific to Life Science/Pharma companies.
  • Directly draft, review and negotiate a variety of commercial contracts, including customer, distributor and vendor agreements, non-disclosure agreements, development, manufacturing and service agreements, and quality agreements, among others.
  • Work with outside counsel on a regular basis to review and handle large volume of contracts, to ensure agreements meet management/corporate objectives.
  • Champion and execute contracting and legal support process improvements, such as templates, contract management systems and other initiatives, to increase efficiency and improve service level.
  • Provide subject matter expertise and support for corporate and pre-litigation/litigation work to minimize risks and maximize legal rights.
  • Participate in the development and structuring of new business ventures and corporate transactions.
  • Keep abreast of legislative and regulatory changes that may affect HLUS and its subsidiary companies.
  • Provide training to HLUS and its subsidiary companies on substantive legal topics, including regulations specific to CDMO, Life Science/Pharma and Medical Device companies.

Required Skills/Education
  • College degree and juris doctorate from accredited law school. Academic honors preferred.
  • Admitted to at least one state bar in good standing.
  • 6-8 years of relevant experience in a corporate law firm and/or in-house legal department, preferably in the Life Science/Pharma, Medical Device or health care field.
  • Solid commercial contract background with extensive drafting experience.
  • Experience managing outside counsel and/or legal staff.
  • In-depth knowledge of FDA and related regulations, including requirements specifically applicable to the CDMO, Life Science/Pharma and Medical Device industries.
  • Strong contract drafting and negotiation skills.
  • Computer skills and appropriate applications.

Desired Skills
  • Management Skills
  • Business acumen
  • Follow-Up
  • Negotiation and Leadership Skills
  • Ability to Multi-Task
  • Collaboration
  • Analytical Ability
  • Autonomy
  • Budget Conscious

Salary and Benefits:
  • $185,000 - $200,000 depending on experience
  • Medical, Dental, Vision
  • Life Insurance
  • 401k
  • Paid Time Off

*#LI-REMOTE
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 (hlushrteam@fujifilm.com).

What Fujifilm employees say

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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

Social media

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