Eurofins Scientific logo

Microbiologist (2nd Shift)

Eurofins Scientific

Rahway, NJFull-time$27–34/hrPosted 2 days agoVerified open today

Get personalized insights for this job

Sign in to access AI-powered tools that help you stand out:

Resume evaluation
Tailored coaching
Mock interviews
Sign In to Get Started

At a glance

Compensation
$27–34/hr
Location
Rahway, NJ
Schedule
Full-time
Work Authorization
US work authorization required

Requirements

Credentials this posting asks for.

Master's degree

Job overview

Eurofins Scientific is hiring a Microbiologist (2nd Shift). The Scientist will be a critical part of the Analytical Research and Development Microbiology team, leading the rapidly growing pipeline through collaboration with stakeholders. Responsibilities include delivering critical data in a GMP microbiology laboratory, focusing on finished products testing, utilities, and environmental monitoring.

Key focus areas include Perform routine viable and non-viable Environmental Monitoring of classified cleanroom areas., Conduct active air, passive air, and surface sampling in accordance with site EM programs., and Operate and maintain EM instruments such as viable air samplers and particle counters..

Successful candidates bring MS Degree In Microbiology Or Related Biological Sciences, 2 Years Pharmaceutical Industry Experience With MS Degree, and 3 Years Pharmaceutical Industry Experience With BS Degree. Important skills include Environmental Monitoring, GMP Requirements, Viable Air Samplers, Particle Counters, RODAC Plates, and Isolator/BSC Environmental Sampling Tools. Preferred (not required): Testing In Clean Room Environments, Sterile Manufacturing, Nonsterile Manufacturing, and GMP Product Testing.

Skills & qualifications

RequiredNice to have

Skills

Environmental MonitoringGMP RequirementsViable Air SamplersParticle CountersRODAC PlatesIsolator/BSC Environmental Sampling ToolsAseptic Sampling TechniquesUtility Sampling/TestingWater System MonitoringBioburden TestingMicrobial IdentificationEndotoxin TestingEM Data AnalysisDeviation InvestigationsRoot Cause AssessmentsCAPA DevelopmentALCOAData Integrity PrinciplesInventory ManagementMicrobiology Finished Goods TestingBiological Indicator TestingSterility TestingMethod Suitability TestingMicrobial EnumerationMedia/Reagent Quality Control TestingMicrobiology Laboratory ExperienceCommunicationOral CommunicationInterpersonal SkillsAseptic ManufacturingUtilities TestingCurrent Microbiology Industry GuidelinesCompendia KnowledgeTesting in Clean Room EnvironmentsSterile ManufacturingNonsterile ManufacturingGMP Product TestingQuality Investigations in MicrobiologyMODASAPVeevaLIMS

Qualifications

MS Degree in Microbiology or Related Biological Sciences2 Years Pharmaceutical Industry Experience With MS Degree3 Years Pharmaceutical Industry Experience With BS DegreeDirect Microbiological Testing GMP ExperienceAuthorization to Work in the United States Indefinitely Without Restrictions

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
401(k) Match
Paid Time Off

Full job description

In your role as Scientist, you will be a critical part of the Analytical Research and Development Microbiology team with responsibilities including leading the rapidly growing pipeline via collaboration with stakeholders to deliver on critical data in a good manufacturing practices (GMP) microbiology laboratory, including finished products testing, utilities, and environmental monitoring.

Primary Responsibilities

  • Perform routine viable and non‑viable Environmental Monitoring of classified cleanroom areas (Grad A-D), including surfaces, air, and equipment.

  • Conduct active air, passive air (settle plates), surface sampling, in accordance with site EM programs and GMP requirements.

  • Operate and maintain EM instruments (e.g., viable air samplers, particle counters, RODAC plates, isolator/BSC environmental sampling tools).

  • Execute aseptic sampling techniques to ensure data integrity and contamination‑free sample collection.

  • Perform utility sampling/testing (WFI, purified water, clean steam) and support routine water system monitoring.

  • Perform microbiology laboratory testing associated with EM samples, including bioburden, microbial identification, and endotoxin testing.

  • Trend, analyze, and interpret EM data; escalate atypical or out‑of‑trend (OOT) results and support investigations.

  • Participate in deviation investigations, root cause assessments, and CAPA development related to environmental or microbiological events.

  • Maintain accurate documentation of sampling activities in compliance with ALCOA and data‑integrity principles. Inventory management.

  • Conduct microbiology finished goods testing and biological indicator (BIs) testing

  • Support of sterile operations within the quality control department including utilizing isolator for  sterility testing, conduct method suitability testing, endotoxin, microbial enumeration, media / reagent quality control testing, Experience with testing in clean room environments preferred

  • Conduct the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA and data integrity principles

  • Partner with internal stakeholders and partners, including Quality, Pipeline, and Operations.

  • Perform second scientist review microbiology experiments in line with GMP expectations

  • Support internal and external compliance audit activities.

  • May need to be flexible with weekday work hours and weekend support as needed Minimum Requirements:

  • Minimum 2 years of pharmaceutical industry experience for applicants with a MS degree or  3 years of experiences for BS degree in Microbiology or related Biological Sciences, or equivalent with direct microbiological testing GMP experience

  • A proven record of microbiology laboratory experience.

  • Excellent written and oral communication skills, as well as interpersonal skills, are necessary to qualify for this role.

  • Knowledge and experience of microbiology testing in context of, environmental monitoring, aseptic manufacturing, and utilities testing in a GMP environment

  • Knowledge of current microbiology industry guidelines and compendia

  • Authorization to work in the United States indefinitely without restrictions Preferred Experience

    • Knowledge in sterile, nonsterile and aseptic manufacturing and associated GMP product testing
    • Experience in supporting quality investigations in the microbiology discipline
    • Experience with MODA, SAP, Veeva, LIMS is a plus Position is full-time, Mon-Fri 3pm-11pm  Candidates currently living within a commutable distance of Rahway, NJ  are encouraged to apply. Base compensation is between $27-34/hr based on experience. 2nd shift has a 10% shift differential.  
  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options

  • Life and disability insurance

  • 401(k) with company match

  • Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Ready to take the next step in your career?