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Scientist, Quality Control (Microbiology)

0-3 years
Not Disclosed
10 July 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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

 

Scientist, Quality Control (Microbiology) – Days

Location: Bloomington, Indiana, United States
Work Mode: On-site | Schedule: Typical business hours


Job Summary:

Novo Nordisk is hiring a Scientist, Quality Control (Microbiology) at its state-of-the-art biomanufacturing site in Bloomington, Indiana. This position offers the opportunity to work in a regulated cGMP environment, performing microbiological testing on raw materials, in-process samples, finished products, and stability samples. Ideal for professionals with a strong microbiology background, this role supports global quality and compliance while advancing your scientific career in the pharmaceutical industry.


Key Responsibilities:

  • Perform routine microbiology testing on process samples and pharmaceutical products in a cGMP lab.

  • Operate and maintain microbiology lab instruments and software systems.

  • Document all test results accurately and in compliance with SOPs and regulatory standards.

  • Participate in investigations, CAPAs, and deviations using TrackWise.

  • Author and review technical documents including SOPs and laboratory reports.

  • Provide technical support for cleanroom procedures, aseptic techniques, and data review.

  • Support equipment maintenance, LIMS data entry, and laboratory housekeeping per 5S standards.

  • Engage in process improvement initiatives and team collaboration sessions.


Required Skills & Qualifications:

  • Education:

    • Bachelor’s in science with 3–5 years’ experience (1+ year in GMP preferred)

    • Master’s or PhD in science with 0–2 years’ experience (GMP experience preferred)

  • Technical Expertise:

    • Hands-on experience with microbiology lab equipment and aseptic techniques

    • Knowledge of cGMP, GLP, GDP, and SOPs in a regulated pharma environment

    • Experience with deviation handling, CAPA systems (e.g., TrackWise), and LIMS

    • Excellent analytical, documentation, and communication skills

    • Ability to perform root cause analysis and risk mitigation

  • Behavioral Competencies:

    • Strong multitasking and time management skills

    • Adaptability to fast-paced, high-pressure environments

    • Detail-oriented and team-focused with a positive mindset


Perks & Benefits:

  • Competitive salary with annual performance bonus

  • 14 paid holidays and generous PTO

  • Health, Dental, Vision Insurance (starts Day 1)

  • 8% guaranteed 401K contribution + company match

  • Parental leave: 14 weeks + 6 weeks family medical leave

  • Tuition assistance for professional development

  • Life & disability insurance

  • Employee referral rewards

  • Complimentary access to Novo Nordisk pharmaceuticals


Company Description:

Novo Nordisk, a global healthcare leader in diabetes care, operates its Bloomington, Indiana site as a major biomanufacturing and quality control hub. The facility integrates formulation, fill/finish, and packaging capabilities for clinical and commercial pharmaceutical production, offering cutting-edge infrastructure and a collaborative work culture focused on innovation, compliance, and patient care.


Salary/Compensation:

Not specified – Competitive pay structure with leading benefits and performance bonuses.


Call to Action:

If you’re ready to advance your microbiology career in a global pharmaceutical leader, apply today to join Novo Nordisk’s QC team and make a real impact in global healthcare quality.