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Project Manager Biotech Jobs in Kentucky (NOW HIRING)

Contract CRA

Covington, KY · On-site

$90 - $100/hr

... biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more ...

... and biotechnology? At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves ... in regional DP sales projects * Recruit, develop, and train sales associates with clearly ...

... and biotechnology? At Leica Biosystems, one of Danaher's 15+ operating companies, our work saves ... in regional DP sales projects * Recruit, develop, and train sales associates with clearly ...

Sr Mgr FP&A Business Partner

Boston, KY · On-site

$92K - $126K/yr

... biotechnology industry supporting Medical or R&D functions. * Strong knowledge of GAAP and IFRS ... Self-starter with the ability to manage competing priorities, meet deadlines, and drive projects ...

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Project Manager Biotech information

See Kentucky salary details

$18

$40

$66

How much do project manager biotech jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for project manager biotech in Kentucky is $40.16, according to ZipRecruiter salary data. Most workers in this role earn between $34.86 and $44.04 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a Project Manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a Project Manager in Biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Kentucky? For Project Manager Biotech jobs in Kentucky, the most frequently searched job titles are:
What cities in Kentucky are hiring for Project Manager Biotech jobs? Cities in Kentucky with the most Project Manager Biotech job openings:
Infographic showing various Project Manager Biotech job openings in Kentucky as of July 2026, with employment types broken down into 1% As Needed, 86% Full Time, 6% Part Time, 1% Temporary, 5% Contract, and 1% Summer. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $83,539 per year, or $40.2 per hour.
Senior Manager, Manufacturing Engineering

Senior Manager, Manufacturing Engineering

Danaher

Hebron, KY • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 18 days ago


Danaher rating

7.7

Company rating: 7.7 out of 10

Based on 29 frontline employees who took The Breakroom Quiz


Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.

You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory's role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making-we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

The Sr. Manufacturing Engineering Manager is responsible for leading our team of manufacturing engineers. This role is crucial for optimizing our production processes, ensuring efficient and high-quality manufacturing operations, and supporting the introduction of new products. The Sr. Manufacturing Engineering Manager will be responsible for driving continuous improvement initiatives, managing project execution, and fostering a culture of technical excellence and problem-solving within the team.

This position will report to the Director, Manufacturing Process Engineer, and is part of the Global Engineering team and will be an on-site role at our Hebron, KY site.

In this role, you will be responsible for:

  • Drive Process Improvement: Lead initiatives to enhance efficiency, reduce waste, and improve product quality using Lean and Six Sigma methodologies.
  • Support Production Operations: Provide hands-on engineering support to resolve manufacturing issues, minimize downtime, and ensure smooth operations.
  • Oversee New Product Introduction (NPI): Collaborate with R&D to ensure manufacturability and lead process validation and equipment qualification from pilot to full-scale production.
  • Implement Advanced Technologies: Evaluate and deploy new equipment and automation solutions to boost manufacturing capability and scalability.
  • Ensure Quality & Compliance: Partner with Quality teams to maintain process controls, conduct RCA/CAPA, and ensure regulatory compliance.
  • Manage Projects & Collaboration: Lead engineering projects and work cross-functionally with Production, Supply Chain, and R&D to drive operational excellence.

The essential requirements of the job include:

  • Education: Bachelor's degree in Manufacturing, Industrial, Mechanical, Electrical Engineering, or a related technical field.
  • Experience: 8+ years in manufacturing engineering within a GMP environment, including 4+ years in a leadership role.
  • Process Improvement: Proven success driving Lean Manufacturing and Six Sigma initiatives; Green or Black Belt certification preferred.
  • NPI Expertise: Hands-on experience with New Product Introduction, including process development, validation, and equipment qualification.
  • Technical Knowledge: Strong understanding of manufacturing processes such as assembly, machining, fabrication, automation, and inspection.
  • Leadership & Problem Solving: Excellent team-building, coaching, and analytical skills with a data-driven approach to decision-making.
  • Communication Skills: Strong verbal and written communication abilities, capable of conveying complex technical concepts to varied audiences.

Travel, Motor Vehicle Record & Physical/Environment Requirements: if applicable for role

  • Ability to travel ~ 20% travel
  • Must have a valid driver's license with an acceptable driving record

It would be a plus if you also possess previous experience in:

  • cGMP Medtech experience
  • Experience with CAD software and statistical analysis tools (e.g., Minitab, JMP).
  • Experience in the life sciences or healthcare industry.
  • Experience with industrial automation (e.g., PLCs, SCADA) if applicable to the industry.
  • Knowledge of AI/ML integration with automation.
  • Master's degree in engineering or an MBA.
  • Experience in a regulated industry
  • Knowledge of relevant quality systems (e.g., ISO 13485, AS9100, IATF 16949).
  • Experience implementing or working with Manufacturing Execution Systems (MES) or ERP systems.
  • Proficiency in project management

Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

The annual salary range for this role is $165K - $175K. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law.

Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.


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About Danaher

Sourced by ZipRecruiter

We are a science and technology innovator committed to helping our customers solve complex challenges, and improving quality of life around the world. A global family of more than 20 operating companies, we drive meaningful innovation in some of today's most dynamic, growing industries.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Washington, DC, US

Year founded

1984