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Gmp Manager Jobs in Florida (NOW HIRING)

Lonza

Manager, Product Development GMP Operations

Tampa, FL · On-site

$108K - $135K/yr

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

Lonza

Manager, Product Development GMP Operations

Tampa, FL

$108K - $135K/yr

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

Strive Pharmacy

GMP Systems Administrator

Alachua, FL · On-site +1

Manage the periodic review program for all validated computerized systems, ensuring scheduled ... GMP Cybersecurity & Data Integrity * Implement and maintain cybersecurity controls aligned with FDA ...

The Mint Dispensary

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 ...

ABM

GMP/CLEANROOM CLEANER

Tampa, FL

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 ...

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Gmp Manager information

See Florida salary details

$18.3K

$44.5K

$86.7K

How much do gmp manager jobs pay per year?

As of Aug 12, 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 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 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 are popular job titles related to Gmp Manager jobs in Florida? For Gmp Manager jobs in Florida, the most frequently searched job titles are:
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:
Gmp Manager jobs near you
Infographic showing various Gmp Manager job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $44,483 per year, or $21.4 per hour.

GMP Assistant Manager (Devens, MA)

CSI International

Tampa, FL • On-site

$90K/yr

Full-time

Posted 20 days ago

Job description

Who We Are

CSI International Inc, founded in 1989, provides integrated building services to clients in real estate, property management, pharmaceuticals, telecommunications, higher education, manufacturing, and insurance. Throughout CSI International Inc.’s constant growth and evolution, our primary goal – exceeding our clients’ expectations – has remained unchanged. Because of this, we enjoy an incomparable reputation for cost-effective solutions with responsive services with uncompromising quality.

What You Will Be Doing

The GMP Assistant Manager is responsible for supporting the day-to-day operations of GMP cleaning and sanitization programs within regulated and critical environments. This role provides frontline leadership through operational supervision, shift coordination, labor deployment, schedule execution, and field oversight. The GMP Assistant Manager works closely with site leadership to ensure staffing levels, service delivery, GMP compliance, and customer expectations are consistently achieved.

The successful candidate will play a critical role in maintaining operational excellence, supporting team development, and ensuring quality standards are met across all assigned shifts and work areas.

This position is located in Devens, MA.

GMP Assistant Manager Duties and Responsibilities

  • Provide daily supervision and direction to GMP cleaning personnel and lead staff.
  • Coordinate shift activities to ensure schedules are executed efficiently and service commitments are met.
  • Monitor staffing levels and deploy labor resources based on operational requirements and priorities.
  • Conduct routine field inspections to verify cleaning quality, GMP compliance, and adherence to standard operating procedures.
  • Support the implementation of technical cleaning and sanitization programs within GMP-regulated environments.
  • Assist with training, onboarding, coaching, and development of team members.
  • Ensure employees follow company policies, safety procedures, and GMP requirements.
  • Address operational issues in real time and escalate significant concerns to management as appropriate.
  • Monitor attendance, timekeeping, and workforce productivity.
  • Support investigations, corrective actions, and continuous improvement initiatives.
  • Maintain accurate operational records, shift reports, and documentation.
  • Partner with the GMP Operations Manager to achieve customer satisfaction, quality objectives, and operational performance goals.
  • Participate in customer meetings, audits, and site inspections as required.
  • Foster a positive, team-oriented work environment focused on accountability and continuous improvement.

GMP Assistant Manager Requirements and Qualifications

  • 2+ years of supervisory or leadership experience within janitorial, facilities services, GMP, pharmaceutical, biotechnology, healthcare, cleanroom, or other regulated environments.
  • Experience coordinating labor, schedules, and daily operations in a fast-paced environment.
  • Knowledge of GMP, GxP, cleanroom, or quality-controlled environments preferred.
  • Strong leadership, organizational, and problem-solving skills.
  • Ability to communicate effectively in English, both verbally and in writing.
  • Working knowledge of safety procedures and compliance requirements.
  • Proficiency with Microsoft Office applications and web-based systems.
  • Ability to work flexible schedules, including evenings, weekends, or holidays as business needs require.
  • Ability to walk, stand, inspect work areas, and perform field oversight for extended periods.
  • High School Diploma or GED required; Associate's or Bachelor's degree preferred.
  • Authorized to Work in the US – We Use Everify.

CSI International, Inc. is committed to fostering, cultivating, and preserving a culture of diversity and inclusion. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Our commitment extends beyond preventing discrimination and harassment; it’s about creating an environment where diverse backgrounds and perspectives are valued. We believe in the power of our people, the ideas they bring, and what we can accomplish together.

Consistent with the Americans with Disabilities Act (ADA), all state & federal requirements, it is the policy of CSI International, Inc. to provide reasonable accommodation when requested by a qualified applicant or employee with a disability, unless such accommodation would cause an undue hardship. CSI International, Inc. also provides reasonable accommodations as required under the Pregnant Workers Fairness Act (PWFA) for limitations related to pregnancy, childbirth, or related medical conditions. The policy regarding requests for reasonable accommodation applies to all aspects of employment, including the application process. If reasonable accommodation is needed, please contact the Recruitment Team at 813-425-1985.


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