Sr Microbiologist

Actalent; Town of Florida (NY); On-site; USD 7,285,000 - 7,947,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability coverage

HSA option

PTO / Vacation or Sick Leave

Job summary

Actalent is seeking a Sr QC Microbiologist to provide technical leadership for a growing analytical microbiology laboratory. This role supports GMP-compliant operations for product release, API batch release, and stability studies, and is based in Jupiter, FL with a hybrid work arrangement.

The ideal candidate brings 7+ years of GMP pharmaceutical microbiology experience, strong technical writing, and expertise in IQ/OQ/PQ, environmental monitoring, and regulatory inspections.

Qualifications

• Bachelor's degree in Microbiology or a related scientific discipline.
• At least seven years of GMP pharmaceutical microbiology experience.
• Strong experience with technical writing, equipment qualification, and laboratory validation.
• Previous experience supporting regulatory inspections and client audits.
• Demonstrated knowledge of pharmaceutical microbiology and cGMP laboratory operations.
• Excellent communication, organization, leadership, and project-management skills.
• Ability to manage multiple laboratory priorities in a growing operational environment.

Responsibilities

• Provide technical leadership for the analytical microbiology laboratory.
• Support the design, startup, and expansion of GMP-compliant laboratory operations.
• Lead the selection, qualification, and implementation of analytical instrumentation, including IQ, OQ, and PQ activities.
• Develop and maintain standard operating procedures, laboratory protocols, technical reports, and training programs.
• Perform and oversee method suitability, process verification, and microbiological testing activities.
• Establish and maintain environmental monitoring programs for cleanrooms and separative devices.
• Partner with Quality Assurance to support investigations, corrective and preventive actions, and overall cGMP compliance.
• Serve as the microbiology subject-matter expert during client interactions, regulatory inspections, and audits.
• Support laboratory accreditation activities, including alignment with ISO/IEC requirements.
• Establish programs for procurement, qualification, handling, storage, inventory control, traceability, and routine use of reference standard and challenge organisms.
• Ensure microbiological reference materials and laboratory practices comply with applicable USP requirements and recognized industry standards.
• Supervise, train, and professionally develop QC laboratory analysts as laboratory operations expand.
• Manage sample schedules, testing priorities, and laboratory workflow.
• Improve laboratory efficiency, throughput, and testing capacity.
• Oversee microbiological media, reference organisms, and related inventory.
• Coordinate activities with QC Chemistry and Quality Assurance.
• Support laboratory investigations and stability studies.
• Expand the laboratorys testing capabilities to meet operational and client needs.

Skills

Microbiology

Environmental monitoring

Aseptic technique

Bioburden testing

Quality control

Plating

Microbial testing

Laboratory leadership

Education

Bachelor's degree in Microbiology or related discipline

Master's degree preferred

Job description

Actalent is Hiring a Sr Microbiologist / Growth Opportunity within a Company!!

Job Description

We are seeking an experienced Sr QC Microbiologist to provide technical leadership for a growing analytical microbiology laboratory. This role is pivotal in building and scaling GMP-compliant laboratory operations that support pharmaceutical product release, API batch release, and stability studies.

Responsibilities

• Provide technical leadership for the analytical microbiology laboratory.
• Support the design, startup, and expansion of GMP-compliant laboratory operations.
• Lead the selection, qualification, and implementation of analytical instrumentation, including IQ, OQ, and PQ activities.
• Develop and maintain standard operating procedures, laboratory protocols, technical reports, and training programs.
• Perform and oversee method suitability, process verification, and microbiological testing activities.
• Establish and maintain environmental monitoring programs for cleanrooms and separative devices.
• Partner with Quality Assurance to support investigations, corrective and preventive actions, and overall cGMP compliance.
• Serve as the microbiology subject-matter expert during client interactions, regulatory inspections, and audits.
• Support laboratory accreditation activities, including alignment with ISO/IEC requirements.
• Establish programs for procurement, qualification, handling, storage, inventory control, traceability, and routine use of reference standard and challenge organisms.
• Ensure microbiological reference materials and laboratory practices comply with applicable USP requirements and recognized industry standards.
• Supervise, train, and professionally develop QC laboratory analysts as laboratory operations expand.
• Manage sample schedules, testing priorities, and laboratory workflow.
• Improve laboratory efficiency, throughput, and testing capacity.
• Oversee microbiological media, reference organisms, and related inventory.
• Coordinate activities with QC Chemistry and Quality Assurance.
• Support laboratory investigations and stability studies.
• Expand the laboratorys testing capabilities to meet operational and client needs.

Essential Skills

• Microbiology
• Environmental monitoring
• Aseptic technique
• Bioburden testing
• Sterilization
• Endotoxin testing
• Sterility testing
• Biology
• Quality control
• Plating
• Microbial testing
• Microbiology laboratory operations

Additional Skills & Qualifications

• Bachelors degree in Microbiology or a related scientific discipline; Masters degree preferred.
• At least seven years of GMP pharmaceutical microbiology experience.
• Strong experience with technical writing, equipment qualification, and laboratory validation.
• Previous experience supporting regulatory inspections and client audits.
• Demonstrated knowledge of pharmaceutical microbiology and cGMP laboratory operations.
• Excellent communication, organization, leadership, and project-management skills.
• Ability to manage multiple laboratory priorities in a growing operational environment.

Work Environment

The role is based in a clean room environment, offering a competitive salary, performance-based bonus eligibility, comprehensive benefits, continuing-education support, and opportunities for advancement into microbiology laboratory management or QC leadership. The position is in a startup environment with room for growth and expansion.

Job Type & Location

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

Pay and Benefits

• The pay range for this position is $52.88 - $57.69/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)

Workplace Type

This is a hybrid position in Jupiter,FL.

Application Deadline

This position is anticipated to close on Oct 15, 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 [e-mail] 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.