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Biopharmaceutical Manufacturing Associate Jobs in Florida

Production Associate I

Saint Petersburg, FL

$14.25 - $18/hr

... manufacturing, and supply solutions for pharmaceutical and biopharmaceutical products in St ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Posted today

Facilities Maintenance Tech II

Davie, FL · On-site

$17.75 - $24.25/hr

We Are Teva We're Teva, a leading innovative biopharmaceutical company, enabled by a world-class ... Associate Degree with 8 years' experience within pharmaceutical or related manufacturing facility ...

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Biopharmaceutical Manufacturing Associate information

See Florida salary details

$13

$20

$29

How much do biopharmaceutical manufacturing associate jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for biopharmaceutical manufacturing associate in Florida is $20.27, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $23.70 per hour, depending on experience, location, and employer.

What is a biopharmaceutical manufacturing associate?

As a biopharmaceutical manufacturing associate, your primary responsibilities are to prepare equipment and materials for the production of biopharmaceutical products. Your duties include moving the product, supplies, and inventory to support the manufacturing process and operating devices like autoclaves and washers. You monitor the production and operations, make adjustments to increase efficiency, and ensure that you are meeting all safety regulations. You work with downstream and upstream processes to control quality. You are also in charge of preparing reports and reviewing GMP documents to ensure compliance with laws and industry regulations.

What does a biopharmaceutical manufacturing associate do?

A Biopharmaceutical Manufacturing Associate is responsible for producing biopharmaceutical products such as vaccines, antibodies, or therapeutic proteins under strict regulatory guidelines. Their tasks typically include preparing equipment, monitoring production processes, maintaining sterile environments, and ensuring that all procedures adhere to Good Manufacturing Practices (GMP). They may also be involved in quality control, documentation, and troubleshooting equipment issues. This role is crucial for ensuring the safety, efficacy, and quality of biopharmaceutical products.

What are the key skills and qualifications needed to thrive as a biopharmaceutical manufacturing associate?

To thrive as a Biopharmaceutical Manufacturing Associate, you need a solid background in life sciences or engineering, with knowledge of GMP (Good Manufacturing Practices) and often a relevant bachelor’s degree or associate’s certification. Familiarity with bioprocessing equipment, automation systems like SCADA, and quality control tools is essential. Attention to detail, teamwork, and strong communication skills are crucial soft skills for this role. These competencies ensure the safe, accurate, and compliant production of high-quality biopharmaceutical products.

What are some common challenges faced by biopharmaceutical manufacturing associates, and how can they be addressed?

Biopharmaceutical Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP) and troubleshooting equipment malfunctions under tight production schedules. To address these challenges, associates are trained extensively on standard operating procedures and cross-functional communication to quickly resolve issues. Teamwork and attention to detail are essential, as the role frequently involves collaborating with quality assurance, engineering, and process development teams to ensure product safety and compliance. Continuous learning and proactive problem-solving are key to success in this dynamic environment.

What is the difference between Biopharmaceutical Manufacturing Associate vs Quality Control Technician?

AspectBiopharmaceutical Manufacturing AssociateQuality Control Technician
Primary RoleSupports production processes, prepares materials, and ensures manufacturing runs smoothlyPerforms testing and inspection of products to ensure quality standards
Required SkillsKnowledge of GMP, aseptic techniques, and manufacturing proceduresLaboratory skills, attention to detail, knowledge of testing methods
Work EnvironmentCleanrooms, manufacturing floors, production facilitiesLaboratories, testing labs, quality control areas
CertificationsGMP training, sometimes cGMP certificationLab safety, GMP, and quality assurance training

The Biopharmaceutical Manufacturing Associate focuses on supporting the production process in manufacturing environments, while the Quality Control Technician specializes in testing and verifying product quality. Both roles require GMP knowledge and work in regulated settings, but their daily tasks and skill sets differ significantly.

What are the most commonly searched types of Biopharmaceutical Manufacturing jobs in Florida?

The most popular types of Biopharmaceutical Manufacturing jobs in Florida are:

What are popular job titles related to Biopharmaceutical Manufacturing Associate jobs in Florida?

For Biopharmaceutical Manufacturing Associate jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Biopharmaceutical Manufacturing Associate jobs in Florida look for?

The top searched job categories for Biopharmaceutical Manufacturing Associate jobs in Florida are:

What cities in Florida are hiring for Biopharmaceutical Manufacturing Associate jobs?

Cities in Florida with the most Biopharmaceutical Manufacturing Associate job openings:

Infographic showing various Biopharmaceutical Manufacturing Associate job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 26% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $42,156 per year, or $20.3 per hour.

Process Development & Manufacturing Specialist I

Maravai LifeSciences

Jupiter, FL • On-site

Other

Medical, Retirement, PTO

Re-posted yesterday


Job description

Process Development & Manufacturing Specialist I

Jupiter, FL

Maravai LifeSciences translates extraordinary science into everyday miracles, helping biotech, biopharma, and life sciences companies everywhere deliver novel vaccines, therapeutics, and diagnostics. We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.

At Maravai, we believe that diverse perspectives are the foundation of innovation. Through an inclusive and equitable culture where every team member is inspired to bring their best selves to work, we cultivate an environment in which we can lead together, providing differentiated value to our customers, and enabling the miracles of science. For over 35 years, Maravai's portfolio companies have served as a catalyst for innovative, lifesaving technology for humanity. Pioneering nucleotide research since its inception, we are now leading the way in the rapidly expanding mRNA market.

Your Next Role as a Miracle Maker

Maravai LifeSciences is seeking a Miracle Maker to join our Manufacturing team as a Process Development & Manufacturing Specialist I. The Process Development & Manufacturing Specialist I supports enzyme production and process development activities by executing established laboratory and manufacturing protocols. This role contributes to product manufacturing, process characterization, and production readiness while ensuring compliance with quality and safety standards. The Specialist I works under supervision to support process scalability, documentation, and continuous improvement initiatives within Alphazyme's manufacturing operations.

How You Will Make an Impact
  • Execute enzyme production and manufacturing processes, including fermentation, enzymatic reactions, filtration, and chromatography, following established protocols.
  • Prepare materials, equipment, and production areas to support manufacturing activities and ensure readiness for scheduled operations.
  • Accurately document production and experimental activities in batch records, logs, and reports in accordance with Good Documentation Practices (GDP).
  • Operate and maintain laboratory and manufacturing equipment, performing basic troubleshooting and routine maintenance.
  • Support process characterization and development activities under supervision to improve product quality and consistency.
  • Collaborate with Manufacturing, Quality, and Supply Chain teams to support production schedules and material flow.
  • Maintain compliance with cGMP (as applicable), ISO standards, and safety requirements.
  • Perform other duties as assigned to support production and process development objectives.
The Skills and Experience That You Will Bring
  • High school diploma with 2+ years of relevant industry experience, or Associate's/Bachelor's degree in Biochemistry, Biology, or related scientific discipline preferred.
  • Hands-on experience or exposure to enzyme production/manufacturing processes such as fermentation, filtration, chromatography, or enzymatic reactions preferred.
  • Basic understanding of GMP, ISO, or regulated manufacturing environments and documentation practices (GDP).
  • Ability to follow SOPs and execute protocols with attention to detail and data accuracy.
  • Strong organizational and problem-solving skills with the ability to manage multiple tasks in a dynamic environment.
  • Effective communication and teamwork skills; proficiency with Microsoft Office and familiarity with ERP or document control systems is a plus.
The Benefits of Being a Miracle Maker
  • You have the potential to change, improve, and save lives around the world.
  • You have the opportunity to be a part owner in Maravai through RSU grants and optional employee stock purchase plans.
  • We offer comprehensive medical plans and HSA/FSA options.
  • Fertility & family planning assistance.
  • A variety of additional optional benefits and insurance options, including pet insurance.
  • Retirement contributions.
  • Holidays & Paid Time Off.

Benefits may vary by region and employment type and do not apply to temporary employees or contractors. See a comprehensive list of benefits at our Benefits & growth site at https://www.maravai.com/careers/benefits-and-growth/

To view more opportunities to become a Miracle Maker, visit our career site at https://www.maravai.com/careers/

Maravai LifeSciences is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation, and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.

Click here to view Maravai LifeSciences Privacy Notice

Hiring Scam Alert

Recently, individuals impersonating Maravai LifeSciences Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that:

  • Maravai LifeSciences will never interview a candidate over RingCentral, similar messaging apps or social media (e.g. Telegram, Google Hangouts, WhatsApp, Facebook Messenger, etc.)
  • Maravai LifeSciences will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment.
  • Maravai LifeSciences will never provide excess money to an applicant and ask the applicant to write a check for repayment.

If you have any doubt about a job offer or any other communication purporting to come from Maravai LifeSciences, please reach out to us directly at taops@maravai.com. If you believe you have been a victim of fraud, you can report this activity at: www.iC3.gov or www.stopfraud.gov.