Microbiologist Manager Jobs in Florida (NOW HIRING)

Job Description

This role supports microbiological testing and environmental monitoring activities within a sterile injectable pharmaceutical manufacturing environment. The Microbiologist ensures product quality, sterility assurance, and compliance with FDA cGMP regulations by performing environmental monitoring, water system testing, sterility testing, microbial identification, contamination investigations, and accurate laboratory documentation. The position works closely with cross-functional teams to maintain robust contamination control programs, sustain inspection readiness, and uphold the highest standards of data integrity and good documentation practices.

Responsibilities

• Perform routine and non-routine environmental monitoring of cleanrooms and controlled areas to ensure compliance with regulatory and internal quality standards.
• Conduct testing of pharmaceutical water systems, including purified water (PW) and water for injection (WFI), to verify microbiological quality and system control.
• Execute sterility testing, bioburden testing, microbial identification, and bacterial endotoxin testing (BET) in support of sterile injectable products.
• Investigate microbial contamination events by collecting data, performing root cause analysis, and supporting the implementation of corrective and preventive actions (CAPA).
• Trend and interpret microbiological data to identify patterns, support contamination control strategies, and strengthen sterility assurance programs.
• Perform microbiological method validations and verifications, ensuring methods are suitable, robust, and compliant with applicable guidelines.
• Support equipment qualification activities for microbiology laboratory instruments, including installation, operational, and performance qualifications.
• Maintain microbiology laboratory instrumentation by coordinating and performing routine calibration, preventive maintenance, and troubleshooting to ensure reliable operation.
• Support quality systems activities such as deviations, change controls, out-of-specification (OOS) and out-of-trend (OOT) investigations, CAPAs, complaints, and quality risk assessments.
• Ensure all laboratory work complies with FDA cGMP regulations, USP and ICH guidelines, and internal procedures for aseptic processing and contamination control.
• Prepare, review, and maintain accurate laboratory documentation in accordance with ALCOA+ principles and good documentation practices to ensure data integrity.
• Collaborate closely with Quality, Manufacturing, Engineering, and Validation teams to support operational excellence, process improvements, and inspection readiness.
• Participate in or support regulatory inspections and internal or external audits by providing data, documentation, and subject matter expertise in microbiology.
• Support media preparation, plating, aseptic techniques, and sterilization activities required for microbiology laboratory operations.
• Contribute to continuous improvement initiatives to enhance microbiological control, laboratory efficiency, and overall compliance.

Essential Skills

• Bachelor's degree in Microbiology, Biotechnology, Biological Sciences, Pharmacy, or a related scientific discipline.
• 5+ years of pharmaceutical microbiology experience.
• Hands-on experience working within a sterile injectable pharmaceutical manufacturing environment.
• Proficiency in environmental monitoring of cleanrooms and controlled environments.
• Experience with pharmaceutical water systems, including purified water (PW) and water for injection (WFI).
• Demonstrated ability to perform sterility testing, bioburden testing, and microbial identification.
• Hands-on experience performing bacterial endotoxin testing (BET).
• Strong understanding of FDA cGMP regulations and their application to microbiology and sterile manufacturing.
• Solid knowledge of aseptic processing, aseptic technique, and contamination control principles.
• Experience working in a microbiology laboratory, including media preparation, plating, and sterilization.
• Familiarity with environmental monitoring and microbiological testing in a cGMP setting.
• Ability to support quality systems, including CAPA, deviations, OOS/OOT investigations, change control, and quality risk management.
• Strong commitment to data integrity and good documentation practices, including adherence to ALCOA+ principles.

Work Environment

The role operates in a cGMP-regulated sterile injectable pharmaceutical manufacturing environment, including microbiology laboratories and clean room areas. Work is performed in controlled environments that follow strict aseptic techniques, environmental monitoring programs, and contamination control procedures. The position involves routine work with microbiological media, plating, sterilization processes, and testing of water systems and sterile products. Standard working hours are generally 8:30 a.m. to 5:00 p.m., with the flexibility to adjust hours if operational demands change. Personnel follow cleanroom gowning procedures and adhere to all applicable safety, cleanliness, and compliance requirements while working in GMP facilities.

This is a Contract to Hire position based out of Delray Beach, FL.

The pay range for this position is $40.87 - $55.29/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

This is a fully onsite position in Delray Beach,FL.

This position is anticipated to close on Aug 28, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.