Experience: * 8+ years of technical experience in the pharmaceutical/biotechnology industry ... Direct experience designing end-to-end programs from technology transfer through validation within ...
Experience: * 8+ years of technical experience in the pharmaceutical/biotechnology industry ... Direct experience designing end-to-end programs from technology transfer through validation within ...
Experience: * 8+ years of technical experience in the pharmaceutical/biotechnology industry ... Direct experience designing end-to-end programs from technology transfer through validation within ...
Experience: * 8+ years of technical experience in the pharmaceutical/biotechnology industry ... Direct experience designing end-to-end programs from technology transfer through validation within ...
Beam is looking for a highly energetic Facilities & Maintenance Associate Director / Director for ... biotechnology/pharmaceutical/medical device manufacturing environment * In depth knowledge and ...
Beam is looking for a highly energetic Facilities & Maintenance Associate Director / Director for ... biotechnology/pharmaceutical/medical device manufacturing environment * In depth knowledge and ...
Labcorp is seeking an Executive Director of IT Quality & Compliance to join our team in Durham, NC ... biotechnology. * 10 or more years' experience leading/managing teams, developing strategies ...
New
Labcorp is seeking an Executive Director of IT Quality & Compliance to join our team in Durham, NC ... biotechnology. * 10 or more years' experience leading/managing teams, developing strategies ...
New
You will own, build, and run your startup in fields such as Biotech * You will embark on an extensive personal development journey crafted by unicorn founders and follow a fully customised programme ...
You will own, build, and run your startup in fields such as Biotech * You will embark on an extensive personal development journey crafted by unicorn founders and follow a fully customised programme ...
You will own, build, and run your startup in fields such as Biotech * You will embark on an extensive personal development journey crafted by unicorn founders and follow a fully customised programme ...
You will own, build, and run your startup in fields such as Biotech * You will embark on an extensive personal development journey crafted by unicorn founders and follow a fully customised programme ...
Regional Sales Director South Atlantic - Specialty MS Franchise
Raleigh, NC · On-site
$184K - $253K/yr
About This Role The Regional Sales Director, reporting into MS Director of Sales EAST, provides ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
Regional Sales Director South Atlantic - Specialty MS Franchise
Raleigh, NC · On-site
$184K - $253K/yr
About This Role The Regional Sales Director, reporting into MS Director of Sales EAST, provides ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
Regional Sales Director South Atlantic - Specialty MS Franchise
Raleigh, NC · On-site
$184K - $253K/yr
About This Role The Regional Sales Director, reporting into MS Director of Sales EAST, provides ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
Regional Sales Director South Atlantic - Specialty MS Franchise
Raleigh, NC · On-site
$184K - $253K/yr
About This Role The Regional Sales Director, reporting into MS Director of Sales EAST, provides ... As a mid-sized biotechnology company, we provide the stability and resources of a well-established ...
Speak with your direct manager to discuss your interest and alignment with your development goals ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Speak with your direct manager to discuss your interest and alignment with your development goals ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Director, Pathology
Durham, NC · On-site
Speak with your direct manager to discuss your interest and alignment with your development goals ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Director, Pathology
Durham, NC · On-site
Speak with your direct manager to discuss your interest and alignment with your development goals ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Medical Director Physician
Raleigh, NC · On-site
Description Medical Director, Surgical Optimization Clinic (Part time) Location: UNC Medical Group ... Raleigh boasts a diverse and rapidly growing economy, with a strong presence in technology, biotech ...
Medical Director Physician
Raleigh, NC · On-site
Description Medical Director, Surgical Optimization Clinic (Part time) Location: UNC Medical Group ... Raleigh boasts a diverse and rapidly growing economy, with a strong presence in technology, biotech ...
Director, Quality Control
Raleigh, NC · On-site
POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
Director, Quality Control
Raleigh, NC · On-site
POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
Description Medical Director, Surgical Optimization Clinic (Part time) Location: UNC Medical Group ... Raleigh boasts a diverse and rapidly growing economy, with a strong presence in technology, biotech ...
Description Medical Director, Surgical Optimization Clinic (Part time) Location: UNC Medical Group ... Raleigh boasts a diverse and rapidly growing economy, with a strong presence in technology, biotech ...
Quality Compliance, Director
Holly Springs, NC · On-site
$180 - $240/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital ...
New
Quality Compliance, Director
Holly Springs, NC · On-site
$180 - $240/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital ...
New
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... QUALITY COMPLIANCE, DIRECTOR What you will do Let's do this. Let's change the world. In this vital ...
Director, Quality Control
Raleigh, NC · On-site
$120 - $150/hr
The Director, Quality Control provides strategic and operational leadership for all Quality Control ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
New
Director, Quality Control
Raleigh, NC · On-site
$120 - $150/hr
The Director, Quality Control provides strategic and operational leadership for all Quality Control ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
New
POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
POSITION SUMMARY The Director, Quality Control provides strategic and operational leadership for ... Minimum 12 years of experience in pharmaceutical or biotechnology QC, with. 8 years in leadership ...
Director, Pathology
Durham, NC · On-site
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Director, Pathology
Durham, NC · On-site
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Director, Pathology
Durham, NC · On-site
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Director, Pathology
Durham, NC · On-site
Position Summary The Director Pathology serves as the lead for Translational Medicine Safety ... DVM with 6+ years of post-graduate experience in a pharmaceutical, biotech or academic organization
Biotech Director information
See Raleigh, NC salary details
$24.6K - $39.1K
8% of jobs
$39.1K - $53.6K
15% of jobs
$55.9K is the 25th percentile. Wages below this are outliers.
$53.6K - $68.1K
14% of jobs
The median wage is $82.6K / yr.
$68.1K - $82.6K
14% of jobs
$82.6K - $97.1K
13% of jobs
$97.1K - $111.6K
10% of jobs
$114.5K is the 75th percentile. Wages above this are outliers.
$111.6K - $126.1K
10% of jobs
$126.1K - $140.6K
6% of jobs
$140.6K - $155.1K
5% of jobs
$155.1K - $169.6K
3% of jobs
$169.6K - $184.1K
2% of jobs
$24.6K
$94K
$184.1K
How much do biotech director jobs pay per year?
What are some common challenges faced by Biotech Directors and how are they addressed?
Biotech Directors often encounter challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and adapting to fast-paced advancements in technology. Addressing these issues requires staying informed on industry regulations, fostering a culture of open communication, and implementing effective project management strategies. Directors typically work closely with scientists, regulatory specialists, and business development teams to align project timelines, budgets, and objectives. Overcoming these challenges is a rewarding aspect of the role and helps drive organizational success in a competitive industry.
What are the key skills and qualifications needed to thrive as a Biotech Director?
To thrive as a Biotech Director, you need advanced expertise in biotechnology, project management, and leadership, usually demonstrated by a relevant advanced degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance protocols (such as FDA or EMA), and certifications like PMP or Six Sigma are highly valued. Excellent communication, problem-solving, and team-building skills help Biotech Directors effectively coordinate multidisciplinary teams and drive innovation. These skills and qualities ensure projects are completed efficiently, regulatory standards are met, and company goals in research and product development are achieved.
What does a Biotech Director do?
A Biotech Director oversees research, development, and operational strategies in a biotechnology company or department. They manage teams, ensure regulatory compliance, and drive innovation to develop new products or therapies. Responsibilities often include budgeting, partnerships, and aligning company goals with scientific advancements. Strong leadership, technical expertise, and industry knowledge are essential for success in this role.

Full-time
Re-posted 23 days ago
Fujifilm rating
8.4
Based on 67 frontline employees who took The Breakroom Quiz
50th of 537 rated manufacturers
Job description
We're growing and seeking an accomplished biologics professional to join our Program Design team. In this role, you will partner closely with our global commercial sales organization and site technical/operations teams to shape winning, customertailored programs-from technology transfer through cGMP manufacturing and process validation.
You will lead technical discussions with prospective and current clients, translate complex needs into clear program designs and proposals, and help drive new business across FUJIFILM Biotechnologies sites.
Associate Director or Director will be aligned to your experience; the Director level may include people leadership and broader crosssite improvement initiatives.
Company OverviewThe work we do at FUJIFILM Biotechnologies has never been more important-and we are looking for talented candidates to join us. We are growing our locations, our capabilities, and our teams, and looking for passionate, mission-driven people like you who want to make a real difference in people's lives. Join FUJIFILM Biotechnologies and help make the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. We are proud to cultivate a culture that will fuel your passion, energy, and drive - what we call Genki. 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 DescriptionWhat You'll Do
- Lead the technical aspects of customer meetings and teleconferences, projecting FUJIFILM's experience and expertise.
- Review RFPs and design customer programs spanning process development, technology transfer, cGMP manufacturing, and process validation.
- Assess customer programs for fit with FUJIFILM Biotechnologies' capabilities and site requirements.
- Partner with site operational/technical teams to evaluate program feasibility and requirements.
- Prepare high-quality proposals in response to RFPs, tailored to customer goals and constraints.
- Define program scope, siting/location, timelines, and resource needs in alignment with internal and client stakeholders.
- Support the overall sales process as needed, including SoW development, internal commercial processes, and customer requests.
- Engage proactively with internal stakeholders and manufacturing teams to promote open communication and enhance our service offerings.
- Stay current with industry advancements; attend webinars and conferences in support of FUJIFILM commercial teams.
- At the Director level, lead and direct Program Design team improvement efforts, including harmonization of work practices across sites.
- At the Director level, manager 1-3 direct reports supporting the FUJIFILM Biotechnologies business.
- Other duties as assigned.
Required Qualifications (Education and Experience)
- Education: Scientific degree (Bachelor's degree) in relevant biological science field.
- Experience:
- 8+ years of technical experience in the pharmaceutical/biotechnology industry.
- Broad understanding of CDMO business models and Biologics manufacturing (Microbial and/or Mammalian).
- Working knowledge of the regulatory environment, process development, and analytical technologies for biopharmaceutical manufacturing.
- Demonstrated understanding of, and experience with, cGMP manufacturing and associated requirements.
- Excellent written and verbal communication skills with the ability to interact with external customers in a professional and personable manner and to present a competent image of FUJIFILM at all times.
- Proven ability to analyze complex technical problems and present clear, actionable solutions.
- Ability to influence and collaborate effectively with customers and colleagues at all levels.
- Any combination of education and experience, which would provide an equivalent background to deliver against role expectations.
Preferred Qualifications
- Education: Advanced scientific degree (e.g. MSc or PhD) in a relevant biological science field.
- Experience:
- 6+ years of technical experience in a CDMO or closely related biopharmaceutical environment; experience working directly with customers in a client-facing capacity.
- Prior experience within FUJIFILM Biotechnologies or another biologics CDMO.
- Direct experience designing end-to-end programs from technology transfer through validation within a commercial environment.
- Leadership experience, especially cross-site harmonization and/or managing a small team (for Director consideration).
Who You Are:
- A customer-centric problem solver who thrives at the intersection of science, operations, and business development.
- A clear communicator who can translate complex scientific concepts into compelling, solution-oriented proposals.
- A collaborative partner who builds trust with technical, quality, and commercial teams to deliver on shared goals.
Why Join FUJIFILM Biotechnologies
- Impact: Shape high-value biologics programs and help customers bring important therapies to patients.
- Growth: Role scope and title (Associate Director or Director) tailored to your background, with opportunities to lead cross-site initiatives and people.
- Collaboration: Work with a global, multidisciplinary team across leading biologics sites.
Research shows that some candidates hesitate to apply unless they check every box. If you're excited about this role and have relevant experience in biologics/CDMO environments-even if your past experience doesn't align perfectly with every requirement-we encourage you to apply. We're committed to building a diverse, inclusive, and authentic workplace and welcome applicants from all backgrounds, including internal candidates exploring career growth.
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 InformationFujifilm 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 InformationIf 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 (fdbglobaltalent@fujifilm.com).
Employment Type: OTHERAbout 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