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Quality Control Microbiology Technician

0-1 years
USD 23.19 - 30.92
10 Oct. 28, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🧫 Job Title: Quality Control Microbiology Technician

📍 Location: Swiftwater, Pennsylvania, USA
💰 Salary Range: USD 23.19 – 30.92 per hour
🕒 Shift: 2nd Shift (Monday – Friday, 2:00 PM – 10:30 PM)
🏢 Company: Sanofi
🔗 Application: [Apply Now]


🧭 About the Company

Sanofi is a global healthcare innovator committed to improving people’s lives through the miracles of science.
Our Manufacturing & Supply teams produce and deliver over 4 billion units of medicines and vaccines annually.
With AI-driven smart factories and cutting-edge automation, Sanofi ensures faster, safer, and more sustainable access to healthcare solutions worldwide.


💼 About the Role

The Quality Control Microbiology Technician supports execution of routine microbiological testing in compliance with cGMP, FDA, and Sanofi Pasteur standards.
You will perform laboratory tests to support production, validation, and stability studies, ensuring accuracy, documentation, and regulatory compliance.


⚙️ Key Responsibilities

Testing & Analysis

  • Perform routine microbiological tests on production and validation samples.

  • Support sterility, bioburden, and environmental monitoring programs.

  • Conduct visual evaluations of vials, syringes, plates, and containers.

Laboratory Operations

  • Maintain laboratory safety, cleanliness, and equipment readiness.

  • Participate in cleaning, waste disposal, and setup/breakdown of testing equipment.

  • Execute testing per cGMP and site Standard Operating Procedures (SOPs).

Documentation & Compliance

  • Complete accurate documentation in systems such as SAP, TrackWise, LIMS, MASTER, and eDoc.

  • Demonstrate understanding of change controls, CAPAs, and QA deviation systems.

  • Participate in initial deviation investigations through analyst interviews.

Team Collaboration & Training

  • Attend and contribute to team and safety meetings.

  • Participate in professional training programs and provide training to others.

  • Assist in developing or revising training materials and lab procedures.

Continuous Improvement

  • Identify and report trends or issues that may impact quality or process integrity.

  • Develop a working knowledge of regulatory guidance and pharmacopoeial standards (USP, EP, JP, etc.).


🎓 Qualifications & Experience

Required:

  • Bachelor’s degree (preferably in Life Sciences such as Microbiology, Biotechnology, or Biochemistry).

  • 0–1 year experience in a laboratory or pharmaceutical manufacturing environment.

  • Knowledge of cGMP regulations and microbiological testing techniques.

  • Strong written communication and attention to detail.

Preferred:

  • Prior Quality Control experience.

  • Experience with environmental monitoring, sterility testing, or bioburden assays.

  • Proficiency in SAP, LIMS, TrackWise, or eDoc systems.

Other Requirements:

  • Must pass an eye exam and receive required vaccinations.

  • Must be able to work off-shift schedules (evenings/weekends).

  • Strong teamwork, organization, and multitasking skills.


🌍 Why Join Sanofi

  • Be part of a future-focused and supportive team shaping the future of global health.

  • Access to career growth opportunities (promotions or cross-functional moves globally).

  • Enjoy a comprehensive rewards and benefits package, including:

    • High-quality healthcare and wellness programs

    • Prevention and safety initiatives

    • 14 weeks of gender-neutral parental leave


⚖️ Equal Opportunity Statement

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a diverse and inclusive workforce.
All qualified applicants will be considered without regard to race, color, religion, sex, national origin, age, sexual orientation, disability, or veteran status.


🔖 Job Category:

Quality Control (QC) – Microbiology / Pharmaceutical Manufacturing