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Project Manager Biotech Jobs in Florida (NOW HIRING)

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring ... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ...

IQVIA Biotech is seeking Sr. CRA 1 candidates with a minimum of 2 years of on-site monitoring ... manage ongoing project expectations and issues. Evaluate the quality and integrity of study site ...

Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, or a related field. * Minimum of 5 ... Project management experience in a cross-functional environment. * Regulatory Affairs Certification ...

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Project Manager Biotech information

See Florida salary details

$16

$34

$57

How much do project manager biotech jobs pay per hour?

As of Jun 27, 2026, the average hourly pay for project manager biotech in Florida is $34.56, according to ZipRecruiter salary data. Most workers in this role earn between $30.00 and $37.88 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 Florida? For Project Manager Biotech jobs in Florida, the most frequently searched job titles are:
What cities in Florida are hiring for Project Manager Biotech jobs? Cities in Florida with the most Project Manager Biotech job openings:
Sr. Project Engineer

$94K - $123K/yr

Other

Posted 23 days ago


West Pharmaceutical Services rating

8.4

Company rating: 8.4 out of 10

Based on 31 frontline employees who took The Breakroom Quiz

15th of 110 rated packaging manufacturers


Job description

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  

There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.  

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.  

Job Summary
This role will work closely with production, maintenance, engineering, IT, and vendors to design, construct, install, validate, and maintain equipment, software, and data acquisition systems throughout their lifecycles.
Essential Duties and Responsibilities
  • Lead the planning, execution, and coordination of Facility & Equipment work packages from design through installation, commissioning, and handover, ensuring alignment with overall project milestones.
  • Develop and manage detailed work package schedules, integrating with the program master schedule and identifying interdependencies with other work packages.
  • Prepare and maintain Work Package Management Plans, defining how cost, schedule, risk, and quality will be controlled and reported.
  • Work closely with the Project Manager and Work Package Sponsors to define scope, objectives, and deliverables, ensuring alignment with program goals and business case.
  • Coordinate supplier, contractor, and engineering activities to ensure execution meets West standards, design intent, and safety expectations.
  • Lead regular progress reviews, reporting on costs, schedule adherence, risks, and change management; initiate mitigation plans for schedule or cost deviations.
  • Ensure all aspects of safety, quality, and compliance are proactively managed in alignment with West Engineering procedures and EHS policies.
  • Facilitate effective communication across stakeholders, bridging technical teams, project integration groups, and external service partners to achieve timely and coordinated delivery.
  • Ensure Commissioning, Qualification, and Handover plans are developed and integrated with site operations and validation teams.
  • Support the Project Manager with status reporting and risk escalation to the Steering Committee when high-level alignment or direction is required.
  • Promote standardization and harmonization of facility and equipment designs, leveraging global best practices in collaboration with Global SME and Site Engineering teams.
  • Ensure project documentation is complete, up to date, and properly handed over to operations or sustaining engineering functions at project completion.
  • Maintain alignment with West's Project & Program Management processes and contribute to ongoing improvements in project governance and technical delivery.
  • Any other duties as required.
Education
  • Bachelor's Degree in Engineering, Project Management, Science, or a related technical discipline; a Master's degree is an advantage.
  • Minimum of 5 years of experience in project delivery, construction, or engineering management in a manufacturing or regulated environment (pharmaceutical, biotech, or medical device preferred).
  • Demonstrated experience in managing facility and equipment projects from design to qualification, including vendor management and capital project control.
  • Strong leadership and coordination skills, with the ability to influence cross-functional and cross-site teams.
Work Experience
  • Minimum 5 years related work experience required and
  • previous experience in a manufacturing working environment and/or industrial setting required and
  • experience with Project Management processes and techniques preferred
Preferred Knowledge, Skills and Abilities
  • Knowledge of project management frameworks and tools (MS Project, Dashboards, cost control systems).
  • Understanding of GMP facility design, cleanroom construction, and equipment integration.
  • Familiarity with commissioning and validation principles in regulated environments.
  • Strong analytical and problem-solving capability; consistent record of delivering to cost, quality, and timeline targets.
  • Effective communicator, capable of engaging diverse stakeholders and providing clear direction in a matrix organization.
  • Demonstrated ability to manage risks and implement structured change control.
  • Working knowledge of ISO, FDA, and cGMP standards.
  • Strong project and stakeholder management skills with the ability to manage multiple priorities under pressure.
  • Excellent communication and interpersonal capabilities.
  • Ability to lead multidisciplinary teams and drive accountability.
  • High attention to detail and organizational skills, ensuring structured project execution and documentation.
  • Demonstrates adaptability, ownership, and a continuous improvement mindset.
  • Occasional travel (up to 15%) may be required to meet vendors, West SMEs, or other project teams.
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Self-motivated and solution-oriented personality.
  • Excellent written and verbal skills.
  • Good communication, project management, and interpersonal skills.
  • Good organizational skills.
  • Effective problem-solving skills.
  • Must wear safety toe shoes, safety goggles, and hearing protection, as required, in production areas.
  • Must follow and comply with Plant's Dress and Hygiene Code (SOI).
  • Must follow and comply with all Company and Plant policies, procedure (SOIs), rules and State and Federal laws

#LI-TH1

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com.  Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.


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