Scope of Function: The Bioprocess Specialist position reports to the Upstream Manufacturing ... Associate degree in science or engineering, or related field and minimum of 3 years of experience ...
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Scope of Function: The Bioprocess Specialist position reports to the Upstream Manufacturing ... Associate degree in science or engineering, or related field and minimum of 3 years of experience ...
Bioprocess Associate information
See Florida salary details
$11.68 - $13.21
9% of jobs
$13.21 - $14.74
0% of jobs
$14.74 - $16.28
0% of jobs
$16.28 - $17.81
0% of jobs
$17.81 - $19.34
0% of jobs
$19.34 - $20.87
7% of jobs
$22.10 is the 25th percentile. Wages below this are outliers.
$20.87 - $22.40
10% of jobs
$22.40 - $23.94
18% of jobs
The median wage is $24.23 / hr.
$23.94 - $25.47
27% of jobs
$25.66 is the 75th percentile. Wages above this are outliers.
$25.47 - $27
25% of jobs
$27 - $28.53
3% of jobs
$11
$23
$28
How much do bioprocess associate jobs pay per hour?
As of Aug 11, 2026, the average hourly pay for bioprocess associate in Florida is $23.45, according to ZipRecruiter salary data. Most workers in this role earn between $22.21 and $25.66 per hour, depending on experience, location, and employer.
What is a bioprocess associate?
A Bioprocess Associate is responsible for supporting the manufacturing of biopharmaceutical products by operating and monitoring bioprocessing equipment, following standard operating procedures, and ensuring compliance with Good Manufacturing Practices (GMP). They assist in cell culture, fermentation, purification, and other production processes. This role requires strong attention to detail, problem-solving skills, and the ability to work in a regulated laboratory or production environment.
What skills and qualifications are needed to be a bioprocess associate?
To thrive as a Bioprocess Associate, you need foundational knowledge in biology, chemistry, or a related field, attention to detail, and experience with standard operating procedures (SOPs). Familiarity with bioreactors, filtration systems, aseptic techniques, and commonly used software like LIMS is often required; certifications such as GMP (Good Manufacturing Practice) training can be advantageous. Strong teamwork, communication, and problem-solving skills help you excel in dynamic, collaborative environments. These skills and qualifications are critical to maintaining product quality, ensuring regulatory compliance, and supporting efficient bioprocessing operations.
What does a bioprocess associate do?
A typical day for a Bioprocess Associate involves preparing and operating bioprocessing equipment, monitoring production batches, and performing quality control checks to ensure processes remain compliant with regulatory standards. You’ll work closely with scientists, engineers, and quality assurance teams to troubleshoot any process deviations and uphold safety protocols in a cleanroom or laboratory setting. The role often includes detailed record-keeping and reporting, which are essential for maintaining traceability and supporting process improvements. Collaboration and adaptability are important, as daily priorities can shift based on production needs or urgent issues.
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Full-time
Re-posted 16 days ago
Job description
Description:
Scope of Function:
The Bioprocess Specialist position reports to the Upstream Manufacturing, Manager. Prior experience in GMP manufacturing, operation of GMP process equipment and aseptic technique are prerequisites. This role is responsible for supporting the overall Upstream GMP process, 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 microbial and cell culture systems for Phase 1/11/111 and commercial GMP manufacturing.
Specific Duties:
• 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.
• Performs and monitors critical processes, execute manufacturing batch records (MBR) for specific projects to manufacture cell-derived biopharmaceuticals in compliance with cGMP guidelines and regulations.
• Supports 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.
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:
• BS degree in Science or Engineering.
• Associate degree in science or engineering, or related field and minimum of 3 years of experience with biologic production processes under GMP compliance. Downstream experience preferred.
• Minimum of High School Diploma or equivalent and 3 years of experience with biologic production processes under GMP compliance. Upstream experience preferred.
• Excellent documentation skills including comprehension and review & establishing batch production records.