1

Process Development Jobs in Florida (NOW HIRING)

Sr Engineer, Process Development

Sunrise, FL · On-site

$99.20K - $128.30K/yr

... process validations such as IQ, OQ, PQ protocols and reports Lead the design transfer phase including product development, validation planning, design for manufacturability and assembly, Design of ...

Sr. Engineer, Process Development

Sunrise, FL · On-site

$99.10K - $128.10K/yr

Terumo Aortic is focused on the continuing development of new and innovative products driving the ... Lead and manage key process items to bring new components through the design phase into efficient ...

next page

Showing results 1-20

Process Development information

See Florida salary details

$14

$25

$37

How much do process development jobs pay per hour?

As of May 29, 2026, the average hourly pay for process development in Florida is $25.17, according to ZipRecruiter salary data. Most workers in this role earn between $20.67 and $30.91 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Process Development professional, and why are they important?

To thrive in Process Development, you need a strong background in engineering, chemistry, or a related scientific field, often with a bachelor's or advanced degree. Familiarity with process simulation software, statistical analysis tools, and industry-specific quality standards or certifications like Six Sigma is typically required. Analytical thinking, problem-solving abilities, and effective cross-functional communication are crucial soft skills for success in this role. These skills and qualifications are vital for designing efficient, scalable processes that improve productivity and ensure product quality.

What are the main challenges faced by professionals in Process Development, and how are they typically addressed?

Professionals in Process Development often encounter challenges such as scaling laboratory processes to full production, troubleshooting unexpected technical issues, and ensuring process consistency while meeting regulatory requirements. These challenges are typically addressed by collaborating closely with cross-functional teams—including R&D, Quality Assurance, and Manufacturing—to share expertise and implement robust validation protocols. Continuous learning, strong project management skills, and adaptability are important for overcoming these hurdles and ensuring successful process implementation.

What is process development?

Process development is the systematic approach of designing, optimizing, and scaling up manufacturing or business processes to improve efficiency, quality, and cost-effectiveness. It typically involves taking a concept or product from the laboratory or pilot stage to full-scale production, ensuring that the process is robust, reproducible, and compliant with industry standards. Professionals in process development work closely with research, engineering, and production teams to identify improvements and troubleshoot issues during scale-up.

What is the difference between Process Development vs Process Engineering?

AspectProcess DevelopmentProcess Engineering
FocusDesigning and optimizing new processes for products or manufacturingImplementing, maintaining, and improving existing processes
Work StageEarly-stage process creation and testingScaling up, troubleshooting, and sustaining processes
Skills & CertificationsChemical/biochemical engineering, lab skills, process modelingProcess optimization, quality control, engineering principles

Process Development primarily focuses on creating and refining new processes, while Process Engineering emphasizes implementing and maintaining those processes in production. Both roles require similar technical backgrounds but differ in their stage of involvement within the product lifecycle.

What are the most commonly searched types of Process Development jobs in Florida? The most popular types of Process Development jobs in Florida are:
Infographic showing various Process Development job openings in Florida as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $52,356 per year, or $25.2 per hour.

Process Engineer II, Process Development

ADMA BIOMANUFACTURING LLC

Boca Raton, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago


Job description

Job Description Header:
ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Process Engineer II, Process Development in Boca Raton, FL!
Job Title: Process Engineer II, Process Development
Job Description:
Position Summary
The Process Engineer II provides process development and transfer expertise for IgG Immunotherapy Production. Provide updates to Process Development (PD) Management team on a regular basis to ensure compliance issues are being met. Responsible for maintaining compliance in PD laboratory and executing process development/evaluation studies as well as process validations using a scale down model. As a key member of the PD group, provide support for Manufacturing, Quality Control/Quality Assurance, and Regulatory departments.
Essential Functions (ES) and Responsibilities
The standard schedule for this position is 8:00 AM to 5:00 PM, but employees may occasionally be required to work 12-hour rotating shifts during operational campaigns and manufacturing model runs.
  • Provide support for technical issues related to the manufacturing process and product quality.
  • Develop new processes as required for production of plasma derived therapies.
  • Be familiar with regulatory guidelines to process development/validation as well as implementing manufacturing process changes.
  • Optimize and maintain compliance in PD laboratory by ensuring all equipment calibration/IQ/OQ/PM status are current.
  • Design and plan scientific experiments to achieve corporate goals for existing projects. Write protocols and reports in support of PD studies.
  • Review and/or approve cGMP documentation generated by other PD group members as necessary.
  • Lead execution of process development/evaluation studies as well as process validations using a qualified scale down model.
  • Be responsible for transferring process changes and/or new processes from PD to Manufacturing.
  • Act as a liaison between PD and Manufacturing for supporting deviations and investigations as well as when transferring new and/or optimized processes.
  • Maintain and review process development Batch Records for scale down process models.
  • Perform other activities as assigned by the PD Managers.
  • Support Manufacturing, Engineering, and Quality Management departments with the development and implementation of new process/technology.
  • Assist manufacturing personnel in the execution of process development and process validation studies in cGMP production environment as necessary.

Job Responsibilities or Job Requirements
Competencies
Ability to follow the cGMP's and procedures with great attention to detail
Able to work in high-pressure, deadline-driven environment
Demonstrated ability to achieve goals, overcome obstacles, and meet deadlines
Possess time management skills and be able to balance multiple job assignments at once
Possesses excellent oral and written communication skills with close attention to detail and accuracy to collaborate effectively with cross-functional teams and communicate findings and recommendations
Experience Requirements
Education Requirements:
  • Bachelor's degree in Science or Engineering required.

Experience Requirements:
  • A minimum of five (5) years of experience in a cGMP, Pharmaceutical/Biological manufacturing environment is required.
  • Familiarity with many aspects of process development is expected.
  • Knowledge of FDA cGMP requirements is required.

Preferred Experience
Compliance Requirements (ES)
The minimum compliance expectation for this role entails strict adherence to FDA regulations and company policies governing sales and marketing activities. This includes completion of required compliance training, accurate documentation of sales interactions, and adherence to data privacy regulations. Additionally, the role requires proactive participation in compliance reviews, prompt reporting of any potential issues, and ongoing education to stay updated on relevant FDA regulations.
Job Description Footer:
In addition to competitive compensation, we offer a comprehensive benefits package including:
  • 401K plan with employer match and immediate vesting
  • Medical, Vision, Life and Dental Insurance
  • Pet Insurance
  • Company paid STD and LTD
  • Company Paid Holidays
  • 3 Weeks' Paid Time Off (within the first year)
  • Tuition Assistance (after the first year)
  • Easily accessible to Tri-Rail
  • Free shuttle to the Boca Tri-Rail station

ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit www.dhs.gov/E-Verify.
ADMA Biologics is an Equal Opportunity Employer.