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Biotech Operations Jobs in Florida (NOW HIRING)

Established professional network within clinical operations, biometrics, data management, or regulatory affairs functions at pharma and/or biotech organizations. * Proficiency with CRM platforms ...

Established professional network within clinical operations, biometrics, data management, or regulatory affairs functions at pharma and/or biotech organizations. * Proficiency with CRM platforms ...

Packaging Operator I

Tampa, FL · On-site

$20 - $24/hr

Experience with primary and secondary packaging operations * Familiarity with automated packaging equipment * Experience working in regulated manufacturing environments (pharmaceutical, biotech, or ...

Maintenance Mechanic

Tampa, FL · On-site

$23.50 - $30.25/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Repairs and maintains, in accordance with diagrams, sketches, operation manuals, and manufacturer ...

Packaging Operator I

Tampa, FL · On-site

$15 - $20/hr

Experience with primary and secondary packaging operations * Familiarity with automated packaging equipment * Experience working in regulated manufacturing environments (pharmaceutical, biotech, or ...

Maintenance Mechanic

Tampa, FL · On-site

$25 - $35/hr

Our client is a leading biotechnology company that combines technological insight with world-class ... Repairs and maintains, in accordance with diagrams, sketches, operation manuals, and manufacturer ...

Laboratory Technician

Sunrise, FL · On-site

$18 - $30/hr

As a rapidly expanding biotech company, we offer a dynamic and purpose-driven environment where ... Operations, and Administrative teams while serving as a key liaison with our lab team. This role ...

... biotech products. You will be responsible for performing sterility and particulate testing ... Participate in clean lab operations, preventive actions, and continuous improvement programs to ...

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Biotech Operations information

See Florida salary details

$8

$19

$39

How much do biotech operations jobs pay per hour?

As of Jun 23, 2026, the average hourly pay for biotech operations in Florida is $19.61, according to ZipRecruiter salary data. Most workers in this role earn between $13.27 and $22.64 per hour, depending on experience, location, and employer.

What is the difference between Biotech Operations vs Laboratory Technician?

AspectBiotech OperationsLaboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; sometimes certifications in GMP or quality assuranceAssociate's or bachelor's degree in biology, chemistry, or related field; lab safety certifications often preferred
Work EnvironmentManufacturing facilities, quality control labs, production linesResearch labs, clinical labs, testing facilities
Employer & Industry UsageBiotech companies, pharmaceutical manufacturers, biotech startupsResearch institutions, hospitals, biotech and pharma labs

Biotech Operations roles focus on managing production processes, quality assurance, and ensuring compliance in manufacturing settings. Laboratory Technicians primarily perform experiments, testing, and data collection in research or clinical labs. While both roles require scientific knowledge, Biotech Operations emphasizes process management and compliance, whereas Laboratory Technicians focus on hands-on lab work and data analysis.

What are some common challenges faced in Biotech Operations, and how can new team members effectively navigate them?

Biotech Operations professionals often encounter challenges such as stringent regulatory compliance, maintaining production timelines, and managing cross-functional communication between research, quality, and manufacturing teams. New team members can navigate these challenges by proactively seeking mentorship, staying organized with project management tools, and maintaining open communication channels with colleagues in related departments. Embracing a mindset of continuous learning and adaptability is also crucial, as processes and technologies in biotech are constantly evolving.

What are biotech operations?

Biotech operations refer to the management and coordination of processes involved in developing, manufacturing, and distributing biotechnology products. This includes overseeing laboratory research, quality control, regulatory compliance, production scaling, and supply chain logistics. Professionals in biotech operations ensure that products such as pharmaceuticals, vaccines, or genetically engineered organisms are produced safely, efficiently, and in compliance with industry standards. Their work is critical in bringing scientific discoveries from the lab to market and ultimately to patients or consumers.

What are the key skills and qualifications needed to thrive in Biotech Operations, and why are they important?

Thriving in Biotech Operations requires a solid background in life sciences or engineering, experience with regulatory compliance, and a relevant degree such as a B.S. or M.S. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and certifications like Six Sigma or GMP training are highly valuable. Excellent problem-solving abilities, attention to detail, and strong collaboration skills help individuals excel and adapt in dynamic environments. These competencies are essential for ensuring operational efficiency, regulatory adherence, and successful product development in the biotech industry.
What are popular job titles related to Biotech Operations jobs in Florida? For Biotech Operations jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Biotech Operations jobs in Florida look for? The top searched job categories for Biotech Operations jobs in Florida are:
Manager, QA Operations

Other

Posted 27 days ago


Job description

Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Manager, QA Operations. The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485:2016 Quality Management System.  The Quality Assurance Manager is expected to ensure compliance with operational, statutory, and regulatory requirements in support of the Company's business objectives. 

How you will make an impact: 

  • Manage Quality Assurance department day to day operations, including implementing training and performance management activities for direct reports 
  • Implement and periodically evaluate documentation and policies to ensure continuous compliance to the quality, integrity, and efficiency standards set by the organization, the ISO 13485:2016 standard, and other statutory and regulatory requirements.  
  • Collaborate with management to identify and fill documentation and process gaps required to maintain QMS compliance and address CAPAs, NCs, and audit findings 
  • Author and maintain quality documentation, oversee timely reviews of all work instructions associated with production and quality control activities 
  • Support Quality Control with customer complaints and Out of Specification (OOS) investigations 
  • Actively participate on core teams and provide deliverables from QA on quality processes and required documentation practices from production through testing and shipment  
  • Implement and track metrics to monitor performance associated with Quality management 
  • Identify and implement efficiency improvement initiatives in support of Continuous Improvement 
  • Facilitate proactive solutions by collecting and analyzing quality data 
  • Manage Internal Audit Program 
  • Perform other functions and duties as required  

 The skills and experience that you will bring: 

  • Bachelor's Degree in Life Science, Biology, Chemistry or Pharmaceutical or related discipline 
  • 3-5 years of managerial experience in non-academic biotechnology related industry 
  • 1-3 years of supervisory experience 
  • Proven experience with: ISO 13485 certification, federal regulations 21 CFR 820 and 21 CFR Part 11 
  • Industry experience in a Good Manufacturing Practice (GMP) environment is preferred 
  • Thorough knowledge of analytical testing industry standards and quality assurance methodologies 
  • Excellent communication and presentation skills are required 
  • Demonstrated scientific "problem solving" skills, translated into consultative selling process where the "win" is for both the client and the company 
  • Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance success of project and maintain strong relationships within all parts of company  
  • Proven ability to thrive in a start-up/change oriented environment 
  • Great attention to detail and results driven approach 
  • Self-starter with ability to organize and prioritize a diverse set of responsibilities to ensure that focus on growth and success of company is achieved 
  • Proven coaching, mentoring, team building and leadership skills 

#LI-Onsite