1

Biotech Project Management Jobs in Florida (NOW HIRING)

Experience working in healthcare, medical devices, biotechnology, life sciences, or another regulated industry. * Exceptional organizational and project management skills. * Strong written and verbal ...

New

... of facilities management experience, preferably in agriculture, biotech, cannabis, or regulated manufacturing. * Demonstrated experience managing contractors and major capital projects.

... of facilities management experience, preferably in agriculture, biotech, cannabis, or regulated manufacturing. * Demonstrated experience managing contractors and major capital projects.

Facilities Engineer 2

Alachua, FL · On-site

$80K - $95K/yr

Provides engineering support for maintenance of a biotech manufacturing plant with a focus on ... Experience * 4-6 years of experience in project management, critical engineering systems, or ...

... of facilities management experience, preferably in agriculture, biotech, cannabis, or regulated manufacturing. * Demonstrated experience managing contractors and major capital projects.

... Biotechnology) or related field Proven experience in a laboratory setting, preferably in a research ... Strong project management skills, including experience with project management software Experience ...

Showing results 41-60

Biotech Project Management information

What are the key skills and qualifications needed to thrive in biotech project management?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in biotech project management?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.

What is a biotech project management?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are the most commonly searched types of Biotech Project Management jobs in Florida? The most popular types of Biotech Project Management jobs in Florida are:
What are popular job titles related to Biotech Project Management jobs in Florida? For Biotech Project Management jobs in Florida, the most frequently searched job titles are:
What cities in Florida are hiring for Biotech Project Management jobs? Cities in Florida with the most Biotech Project Management job openings:
Infographic showing various Biotech Project Management job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Bioprocess Manager

Goodwin Biotechnology Inc

Fort Lauderdale, FL • On-site

Full-time

Re-posted 18 days ago


Job description

Description:

Scope of Function:

The Bioprocess Manager position reports to the Vice President of Technical Operations and act as the Upstream Manufacturing, Manager. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are prerequisites. This role is responsible for overseeing end-to-end Upstream cGMP process for antibody and human cells production, including media/buffer preparation, seed train, medium to large scale bioreactor runs through the application of broad knowledge of theories and principles utilized to solve operational, as well as routine tasks in the production of bulk biologics from mammalian and cell culture systems for Phase I/II/III and commercial cGMP manufacturing.


Specific Duties:

• Collaborate with R&D and Process Development to transfer new monoclonal antibody processes and tech-transfers

• Foster a culture of safety, accountability, and innovation within the team

• Develop and implement robust production schedules, ensuring all deliverables align with project deadlines and quality standards

• Operates pharmaceutical manufacturing equipment such as: incubators, wave reactors, single-use and stainless-steel bioreactors, single use mixers, depth filtration skids, TFF skids, chromatography skids and in process testing equipment.

• Executes all Upstream Clinical Manufacturing and Development operations, including but not limited to work functions in cell culture, cell banking, media optimization, seed train preparation, bioreactor operations, harvest/clarification, and technology transfer to manufacturing.

• Demonstrates, understands, and adheres to Goodwin Biotechnology policies, GMP standards and safety procedures.

• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulation.

• Author and/or oversee the development of batch records, SOP’s and protocols as required.

• Supports other manufacturing processes teams and other GBI groups as necessary to achieve manufacturing goals.

• Conduct performance reviews, identify training needs, and provide professional development opportunities to team members.

• Lead cross-functional meetings to align upstream production with other departments, including downstream processing, QC, and supply chain

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice.

Requirements:

Education and Experience Required:

• Bachelor’s or Master’s degree in Biochemical Engineering, Biotechnology, Biochemistry, or a closely related life sciences discipline.

• Minimum of seven (7) years of experience with biologic Upstream production processes under GMP compliance with a minimum of two (2) years of supervisor/manager experience

• Excellent documentation skills including comprehension and review & establishing batch production records.