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ProPharma Group

Regulatory sciences consultant for life sciences

Quality Record Investigation Consultant

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeChicago, IL, USANo salary listed

About the Job

Requirements

  • Strong investigation, documentation, and batch record review and closure experience.
  • Ability to work independently within the client environment.

Responsibilities

  • Review assigned records.
  • Perform investigations and documentation activities.
  • Complete record closure activities.
  • Escalate issues, exceptions, and support needs appropriately.
  • Assume responsibility for overall execution, milestone management, and delivery performance.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

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