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Scientist, Quality Control (Microbiology) Days

2-3 years
Not Disclosed
10 June 16, 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

 

Job Summary:

Novo Nordisk is seeking a Scientist, Quality Control (Microbiology) for its cutting-edge Bloomington, Indiana site. This on-site role focuses on performing microbiological testing of process samples, raw materials, and finished pharmaceutical products in a cGMP-compliant environment. This is an excellent opportunity to grow within a global pharmaceutical leader committed to innovation, quality, and patient care.


Key Responsibilities:

  • Independently perform and document cGMP-compliant Quality Control microbiological testing.

  • Operate and troubleshoot basic and moderately complex QC lab equipment.

  • Assist in drafting and updating technical SOPs and reports.

  • Coordinate with supervisors to prioritize daily laboratory activities.

  • Support continuous improvement and training initiatives.

  • Review and ensure accuracy of laboratory data and documentation.

  • Enter test results into LIMS and prepare laboratory reports.

  • Maintain laboratory 5S housekeeping and equipment upkeep.

  • Participate actively in deviation investigations using TrackWise.

  • Apply problem-solving tools to identify root causes and CAPA.

  • Present findings to Deviation Review Board and drive quality improvements.

  • Assist in data collection for KPIs and quality reports.


Required Skills & Qualifications:

  • Education:

    • Bachelor’s degree in a scientific field with 3–5 years (1 year GMP) OR

    • Master’s degree in science with 0–2 years (1 year GMP preferred) OR

    • PhD in science with 0–2 years (GMP preferred).

  • Technical Expertise:

    • Knowledge of cGMP, GDP, GLP, SOPs.

    • Experience with general laboratory equipment, including micropipettes.

    • LIMS and TrackWise familiarity.

    • Understanding of cleanroom procedures and aseptic techniques.

    • Strong troubleshooting and preventive maintenance skills.

  • Behavioral Competencies:

    • Detail-oriented, problem-solving mindset.

    • Excellent written and verbal English communication.

    • Ability to multitask in a fast-paced, deadline-driven environment.

    • Positive, team-oriented attitude with adaptability to change.


Perks & Benefits:

  • Industry-leading pay with an annual performance bonus.

  • 14 paid holidays plus generous PTO.

  • Comprehensive health, dental, vision insurance (Day 1 coverage).

  • 8% guaranteed 401(k) contribution with additional company match.

  • Paid parental (14 weeks) and family medical leave (6 weeks).

  • Free access to Novo Nordisk-marketed pharmaceutical products.

  • Tuition Assistance Program.

  • Life & Disability Insurance.

  • Employee Referral Awards.


Company Description:

Novo Nordisk is a global leader in diabetes care, obesity management, and rare disease treatments. At its advanced Bloomington, Indiana facility, Novo Nordisk offers end-to-end pharmaceutical manufacturing services, committed to improving the lives of patients worldwide with innovative therapies and products.


Work Mode:

On-site – Bloomington, Indiana, USA


Call-to-Action:

Take your career to the next level with Novo Nordisk’s world-class Quality Control team. Apply today to contribute to life-changing pharmaceutical innovations!