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Biotech Manufacturing Associate Jobs in Boca Raton, FL

Unicon Pharma Inc.

MS&T Specialist I

Davie, FL · On-site

The Microbiology & Cleaning Validation Associate supports MS&T activities related to ... and Manufacturing teams. Education Master's degree in Microbiology, Biology, Biotechnology.

Compunnel, Inc.

Maintenance Technician

Davie, FL · On-site

$32/hr

... or Associate degree with 8+ years of experience in pharmaceutical or related manufacturing. 1-3 ... Preferred Qualifications GMP experience (pharmaceutical, biotechnology, medical devices, vitamins ...

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All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Boca Raton, FL

Biotech Manufacturing Associate information

See Boca Raton, FL salary details

$11

$19

$31

How much do biotech manufacturing associate jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for biotech manufacturing associate in Boca Raton, FL is $19.77, according to ZipRecruiter salary data. Most workers in this role earn between $15.53 and $22.12 per hour, depending on experience, location, and employer.

What are Biotech Manufacturing Associates?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What jobs can I get with an associate's degree in biotechnology?

Biotech Manufacturing Associates are common roles for those with an associate's degree in biotechnology, involving tasks such as preparing and operating laboratory equipment, following strict safety protocols, and documenting processes. Other positions include quality control technician, laboratory technician, and production operator, often requiring knowledge of GMP standards and familiarity with lab tools and procedures.

What does a biotech associate do?

A biotech manufacturing associate is responsible for performing tasks related to the production of biotechnological products, such as preparing equipment, following manufacturing protocols, and ensuring quality control. They often work in laboratory or cleanroom environments, using tools like bioreactors and adhering to safety and regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing, processing, and packaging biological products in a manufacturing environment. They operate equipment, follow strict safety and quality protocols, and document production activities to ensure compliance with regulatory standards. The role often requires attention to detail, knowledge of GMP practices, and the ability to work in a team setting.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by Biotech Manufacturing Associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

How much does a manufacturing associate make at KBI Biopharma?

A Biotech Manufacturing Associate at KBI Biopharma typically earns between $50,000 and $70,000 annually, depending on experience and location. The role involves working in a regulated environment, often requiring knowledge of GMP protocols and bioprocessing equipment.

What are the key skills and qualifications needed to thrive as a Biotech Manufacturing Associate, and why are they important?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.
What job categories do people searching Biotech Manufacturing Associate jobs in Boca Raton, FL look for? The top searched job categories for Biotech Manufacturing Associate jobs in Boca Raton, FL are:
What cities near Boca Raton, FL are hiring for Biotech Manufacturing Associate jobs? Cities near Boca Raton, FL with the most Biotech Manufacturing Associate job openings:
Biotech Manufacturing Associate jobs near you

Manufacturing Biotech Maintenance Technician

AKRON BIOPRODUCTS LLC

Boca Raton, FL • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 9 days ago

Job description

Description

Akron Biotech is hiring a Manufacturing Biotech Maintenance Technician to support cleanroom operations, laboratory readiness, and GMP-compliant manufacturing activities within a growing biotechnology organization advancing cell and gene therapy solutions.

This is a great opportunity for a detail-oriented, hands-on professional with experience in laboratory, manufacturing, cleanroom, or regulated environments who is comfortable supporting equipment maintenance, environmental monitoring, documentation, cleaning procedures, and day-to-day operational readiness.

In this role, you will help maintain cleanroom and laboratory environments, support manufacturing and process development teams, perform equipment and facility support activities, and ensure accurate documentation in accordance with SOPs, safety standards, and regulatory requirements.

Akron Biotech manufactures and distributes components and raw materials that support cell therapy discovery, development, and commercialization worldwide. This is an opportunity to contribute to a growing organization delivering high-quality, industrial-scale solutions for advanced therapy development.

General Responsibilities

  • Maintain cleanroom and laboratory readiness through routine cleaning, disinfecting, and facility upkeep in accordance with SOPs, safety standards, and regulatory requirements.
  • Conduct environmental monitoring for ISO 7/8 cleanrooms and ISO 5 environments using viable air samplers, contact plates, and particle counters.
  • Support manufacturing and process development teams with equipment cleaning, glassware preparation, preventive maintenance, calibration support, qualification activities, tubing assembly, sterilization preparation, and autoclaving.
  • Follow cGMP, safety, PPE, gowning, and documentation requirements while working with biohazards, chemicals, temperature-controlled materials, pressure systems, and cleanroom processes.
  • Maintain accurate records, including logbooks, batch records, SOPs, work instructions, forms, reports, CAPAs, change controls, and other manufacturing or operations documentation.
  • Assist with buffer and media formulation, fill-finish activities, aseptic processing, in-process testing, validation, equipment qualification, product labeling, raw material preparation, kitting, packaging, shipping verification, and inventory support.
  • Use critical thinking, troubleshooting, and teamwork to support daily operations and meet business needs in a fast-paced biotech manufacturing environment.

Akron provides its associates with the following general benefits:

  • 401K plan with employer monthly match
  • PPO and EPO medical insurance plan availability
  • Company paid dental and vision insurance
  • Company paid short-and long-term disability
  • Company paid life insurance
  • Company paid holidays
  • Generous paid time off allowances
  • Employee referral bonus
  • Employee gym reimbursement program

EOE/DFW

Requirements

Qualifications

Minimum of 1 year of relevant experience in a biotech, manufacturing, laboratory, cleanroom, or regulated environment.

High school diploma required; associate degree in life sciences or a related field preferred.

Strong attention to detail with solid organizational, time management, and prioritization skills.

Ability to work independently, manage multiple priorities, and perform effectively in a fast-paced environment.

Clear verbal communication skills with a collaborative, customer-focused approach.

Basic proficiency with Microsoft Outlook, Word, Excel, and related software programs.

Commitment to following cGMP, regulatory, safety, SOP, SDS, and equipment manual requirements.

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