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Gmp Manager Jobs in Florida (NOW HIRING)

Product Development Manager GMP Operations

Tampa, FL · On-site

$108K - $135K/yr

Product Development Manager GMP Operations Tampa, FL, USA The actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.

Product Development Manager GMP Operations

Tampa, FL · On-site

$108K - $135K/yr

Product Development Manager GMP Operations Tampa, FL, USA The actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.

Be Seen First

Pack products following GMP standards * Comply with PPE requirements at all times * Prepare ... Inventory management skills * Strong attention to detail * Effective teamwork and communication

Veteran-friendly

Urgent

Be Seen First

Pack products following GMP standards * Comply with PPE requirements at all times * Prepare ... Inventory management skills * Strong attention to detail * Effective teamwork and communication

Veteran-friendly

Urgent

GMP Compliance Specialist

Murdock, FL · On-site

$55K - $60K/yr

This role supports the company's Compliance team by overseeing GMP adherence, managing supplier quality documentation, and assisting with BioTrack reporting. The ideal candidate is detail-oriented ...

Must be 18 years of age or older Previous experience in cleaning within a GMP-regulated environment ... Manager concerning the need for minor or major repairs or additions to building operating systems ...

GMP/CLEANROOM CLEANER (H)

Saint Petersburg, FL · On-site

$13.25 - $15.50/hr

Must be 18 years of age or older Previous experience in cleaning within a GMP-regulated environment ... Manager concerning the need for minor or major repairs or additions to building operating systems ...

GMP/CLEANROOM LEAD CLEANER

Pompano Beach, FL

$15.25 - $18.25/hr

Must be 18 years of age or older Previous experience in cleaning within a GMP-regulated environment ... Manager concerning the need for minor or major repairs or additions to building operating systems ...

GMP/CLEANROOM LEAD CLEANER

Davie, FL · On-site

$15 - $17.75/hr

... • Notify Manager concerning the need for minor or major repairs or additions to building ... GMP-regulated environment, preferably in the pharmaceutical or healthcare industry • No high ...

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Showing results 1-20

Gmp Manager information

See Florida salary details

$18.3K

$44.5K

$86.7K

How much do gmp manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for gmp manager in Florida is $44,483.00, according to ZipRecruiter salary data. Most workers in this role earn between $31,400.00 and $51,200.00 per year, depending on experience, location, and employer.

What is a GMP manager?

GMP Managers are professionals responsible for ensuring that manufacturing processes in industries such as pharmaceuticals, biotechnology, and food production comply with Good Manufacturing Practice (GMP) regulations. They oversee quality control, develop and implement standard operating procedures, and conduct internal audits to maintain regulatory standards. Their role is crucial for ensuring that products are consistently produced and controlled according to quality standards, thereby safeguarding consumer health and safety.

What are some common challenges faced by a GMP manager in maintaining regulatory compliance, and how are they typically addressed?

A GMP Manager often encounters challenges such as keeping up with evolving regulatory standards, ensuring consistent staff training, and managing thorough documentation. To address these, managers implement regular training programs, conduct internal audits to identify gaps, and foster a culture of quality across teams. Staying proactive about changes in regulations and collaborating with cross-functional teams helps ensure ongoing compliance and smooth inspections.

What are the key skills and qualifications needed to thrive as a GMP manager, and why are they important?

To thrive as a GMP Manager, you need in-depth knowledge of Good Manufacturing Practices, quality assurance, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with quality management systems (QMS), audit tools, and relevant certifications such as Six Sigma or ISO standards is typically required. Strong leadership, problem-solving abilities, and effective communication are vital soft skills for managing teams and ensuring adherence to regulations. These skills and qualifications ensure product safety, regulatory compliance, and continuous improvement within manufacturing processes.

What is the difference between Gmp Manager vs Quality Assurance Manager?

AspectGmp ManagerQuality Assurance Manager
CertificationsGMP certifications, Quality Management certificationsISO 9001, Quality Management certifications
Work EnvironmentPharmaceutical, biotech, or medical device manufacturingVarious industries including manufacturing, healthcare, and food
Employer & Industry UsageRegulated industries with strict compliance standardsBroadly used across multiple industries for quality oversight
Primary FocusEnsuring compliance with Good Manufacturing PracticesOverseeing overall quality assurance processes

The Gmp Manager primarily focuses on ensuring compliance with Good Manufacturing Practices in regulated industries like pharmaceuticals and biotech. In contrast, the Quality Assurance Manager oversees broader quality assurance processes across various industries. Both roles require similar certifications and work environments but differ in their specific compliance and quality scope.

What job categories do people searching Gmp Manager jobs in Florida look for?

The top searched job categories for Gmp Manager jobs in Florida are:

What cities in Florida are hiring for Gmp Manager jobs?

Cities in Florida with the most Gmp Manager job openings:

Infographic showing various Gmp Manager job openings in Florida as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $44,483 per year, or $21.4 per hour.

Product Development Manager GMP Operations

Lonza

Tampa, FL • On-site

$108K - $135K/yr

Full-time

Medical, Dental, Vision

Re-posted 17 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical


Job description

Product Development Manager GMP Operations
Tampa, FL, USA
The actual location of this job is in Tampa, FL. Relocation assistance is available for eligible candidates and their families, if needed.
The Manager, Product Development GMP Operations is a site-based leadership role supporting early-phase clinical trial drug product manufacturing and packaging. This position offers the opportunity to design and lead GMP capabilities, guide multidisciplinary teams, and directly contribute to bringing innovative therapies into the clinic.
What you will get
  • An agile career with opportunities for growth in a dynamic Product Development environment
  • A collaborative, inclusive, and ethical workplace culture
  • Compensation programs that recognize high performance and leadership impact
  • Competitive medical, dental, and vision insurance coverage
  • Access to Lonza's learning, development, and leadership programs

What you will do:
  • Lead and develop Product Development GMP manufacturing operations supporting early-phase clinical trial drug products
  • Design, oversee, and maintain PD GMP spaces, including equipment selection, engineering build-outs, and approval of engineering drawings
  • Serve as the technical and operational SME for PD GMP activities, supporting projects, new technologies, and strategic growth initiatives
  • Provide leadership and administrative management for a diverse technical team, including performance reviews, coaching, training, and career development
  • Ensure compliance with cGMPs, SOPs, safety standards, and regulatory requirements, maintaining inspection readiness at all times
  • Act as a key internal and external stakeholder, participating in regulatory audits, client meetings, and on-site visits
  • Coordinate closely with engineering, quality, manufacturing, and project teams to ensure timely, compliant, and cost-effective delivery of work

What we are looking for:
  • M.S. or Ph.D. in science or concentrated studies that meets or exceeds minimum years of experience requirement
  • 10+ years of experience early-phase GMP drug product manufacturing within a pharmaceutical or life sciences environment
  • OSD (Oral Solid Dosage) experience in early-phase GMP drug product manufacturing within a pharmaceutical or life sciences environment
  • Strong understanding of cGMP regulations, quality systems, regulatory inspections, and audit readiness
  • Proven ability to lead technical teams, manage resources, resolve complex issues, and deliver results through others
  • Experience designing or supporting GMP facilities, including collaboration with engineering and oversight of build-out activities
  • Effective communication and stakeholder management skills, including customer-facing and cross-functional collaboration
  • A scientific degree or similar field required, with an emphasis on applying knowledge to advance drug product development

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

What Lonza employees say

Pay

Benefits

Hours and flexibility

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US