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Principal Scientist, Qc

4-7 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

 

Principal Scientist – Quality Control (QC) | Bloomington, USA

Job Summary:
Novo Nordisk is hiring a Principal Scientist – QC at its cutting-edge Bloomington, Indiana site. This senior-level quality control role is pivotal in supporting GMP compliance, managing QC investigations, driving analytical testing, and mentoring team members. Ideal for candidates with strong GMP experience and a background in analytical chemistry or biotech QC, this role offers career growth and the opportunity to make a global impact on patient outcomes.


Key Responsibilities:

  • Independently perform cGMP-compliant QC testing of raw materials, process samples, and finished products.

  • Lead and document QC investigations (TrackWise), perform root cause analyses, and support CAPA development.

  • Mentor junior QC scientists and support their training in analytical techniques and compliance.

  • Execute process improvement projects and drive lab efficiency initiatives.

  • Conduct self-review and data entry into LIMS and associated systems.

  • Perform general and preventive lab equipment maintenance.

  • Collaborate cross-functionally and participate in DRB presentations.

  • Author technical documents including SOPs and QC reports.

  • Serve as subject matter expert and technical consultant internally and externally.


Required Skills & Qualifications:

  • PhD in a science field with 0–4 years of experience, or

  • Master’s degree with 4–6 years (including 4+ years GMP/regulated industry), or

  • Bachelor’s degree with 7–9 years (including 4+ years GMP experience).

  • Strong understanding of GMP, GLP, GDP, and cleanroom procedures.

  • Proficiency in analytical chemistry, QC instrumentation, and LIMS usage.

  • Prior experience in investigations, SOP compliance, and CAPA development.

  • Effective written and verbal communication in English.

  • Ability to multitask and manage multiple priorities in a fast-paced lab setting.


Perks & Benefits:

  • Competitive base pay plus annual performance bonus

  • Health, dental, and vision insurance from day one

  • 14 paid holidays, paid parental & family medical leave

  • Guaranteed 8% 401(k) contribution plus match option

  • Tuition reimbursement and free access to Novo Nordisk products

  • Life and disability insurance, employee referral awards

  • Inclusive culture with strong career development support


Company Description:

Novo Nordisk is a global healthcare leader in diabetes, chronic disease management, and pharmaceutical innovation. The Bloomington, IN site specializes in end-to-end biomanufacturing and QC services, supporting life-saving drug delivery worldwide. With cutting-edge technology and a people-centric culture, Novo Nordisk empowers employees to transform global health.


Work Mode: On-site – Bloomington, Indiana
Experience Required: 4–9 years (depending on degree) in GMP QC or related regulated industry
Salary Range: Not explicitly stated (competitive with performance bonus)
Application Deadline: Open until filled


Call to Action:

Are you ready to lead QC excellence and make a global impact? Apply today to join Novo Nordisk as a Principal Scientist and help shape the future of pharmaceutical quality.