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Stability Specialist – St. Louis, Missouri

2+ years
$64,400 – $104,900
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Stability Specialist – St. Louis, Missouri | Full-Time

Job ID: 293094
Employer: MilliporeSigma

Overview

MilliporeSigma is seeking a dedicated and detail-oriented Stability Specialist to support the development, execution, and analysis of stability studies for in-vitro diagnostic (IVD) products. This role ensures full compliance with regulatory standards, including IVDR and ISO 13485, and plays a critical part in product quality, performance assessment, and lifecycle management.

This position requires strong analytical capabilities, experience in stability or laboratory operations, and the ability to work within cross-functional teams to support regulatory submissions and internal quality systems.
Note: This role does not offer visa sponsorship. Applicants must be eligible to work in the United States.


Key Responsibilities

  • Develop and execute stability study protocols in accordance with internal SOPs and regulatory requirements.

  • Conduct stability sample testing with accuracy, precision, and adherence to quality standards.

  • Monitor, maintain, and troubleshoot stability chambers and related laboratory equipment.

  • Record data accurately in electronic systems and ensure proper documentation practices.

  • Analyze stability data, interpret trends, and prepare comprehensive stability reports.

  • Assess product shelf life, storage conditions, and long-term performance based on stability study results.

  • Investigate deviations or unexpected results and escalate findings when necessary.

  • Prepare documentation for internal quality systems and regulatory submissions.

  • Ensure full compliance with standards including IVDR and ISO 13485.


Experience Required

Minimum Qualifications

  • Bachelor's degree in a Life Science discipline (Biology, Chemistry, Biochemistry, or related field).

Preferred Qualifications

  • 2+ years of laboratory or quality experience.

  • Strong analytical, organizational, and troubleshooting skills.

  • Ability to collaborate effectively in cross-functional environments.

  • Excellent communication and documentation skills.

  • Ability to manage multiple projects concurrently with attention to detail.


Compensation

Pay Range: $64,400 – $104,900 annually
Actual compensation will depend on experience, education, skill level, and geographic considerations. This role may also be eligible for performance-based bonuses.
Benefits include health insurance, paid time off, retirement contributions, and additional company-provided perks.


Why Join MilliporeSigma?

MilliporeSigma is a global leader in life science innovation, committed to accelerating scientific progress and developing solutions that shape the future of healthcare and technology. Employees benefit from a diverse, inclusive culture with strong support for career development, continuous learning, and long-term growth.


How to Apply

Submit your application to join a collaborative organization dedicated to advancing science and delivering high-quality IVD solutions. Selected candidates will be contacted with further steps.


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