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Data Management Specialist

Job in Lee's Summit, Lees Summit, Jackson County, Missouri, 64002, USA
Listing for: Tucker Parker Smith Group (TPS Group)
Contract position
Listed on 2026-07-08
Job specializations:
  • Healthcare
    Data Scientist
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 30 - 40 USD Hourly USD 30.00 40.00 HOUR
Job Description & How to Apply Below
Location: Lee's Summit

Overview

Tucker Parker Smith Group (TPS Group) provided pay range. Base pay range: $30.00/hr - $40.00/hr location:
California (Remote) - Pacific Time, 8:00 AM – 5:00 PM. Duration: 6 month assignment (potential to extend / convert). Pay Range: $30 – $40/hour.

Role

Data Management Specialist – IVDR (EUDAMED)

On behalf of our client, a leading manufacturer of life science research and clinical diagnostic products, we are seeking a Data Management Specialist to join the Regulatory Affairs and Quality teams in support of the EU In Vitro Diagnostic Regulation (IVDR).

About the Role

This role focuses on the collection, organization, and entry of regulatory data related to medical device registrations and associated attributes into the company’s Product Data Management (PDM) system. The specialist will also assist with system validation testing and the development of Standard Operating Procedures (SOPs) to ensure long-term data accuracy and compliance.

Key Responsibilities
  • Gather, consolidate, and verify regulatory data related to IVDR device registrations from internal and external sources.
  • Enter, maintain, and validate data in the Product Data Management system, ensuring accuracy, completeness, and compliance with internal standards.
  • Develop and document Standard Operating Procedures (SOPs) and work instructions to support data governance and integrity.
  • Collaborate with Regulatory Affairs, Quality, R&D, and Supply Chain teams to align and maintain traceable data across functions.
  • Support system validation testing and continuous improvement initiatives related to data quality and process efficiency.
  • Identify and escalate data inconsistencies or process gaps to relevant stakeholders.
Qualifications
  • Bachelor’s degree (or equivalent) in Life Sciences, Quality Management, Regulatory Affairs, or a related field.
  • 1–2 years of experience in the medical device or in vitro diagnostics (IVD) industry is highly preferred.
  • Proficiency in Microsoft Word and Excel.

Please submit your resume in Word or PDF format to be considered.

Note

Referrals increase your chances of interviewing at Tucker Parker Smith Group (TPS Group) by 2x.

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