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Job summary
A leading life sciences manufacturer is seeking a Data Management Specialist to support data management and compliance for medical device registrations. The role involves gathering regulatory data, maintaining the Product Data Management system, and developing Standard Operating Procedures. Candidates should possess a Bachelor's degree in a relevant field and ideally have 1–2 years of experience in the medical device industry. This position is remote within the Pacific Time zone.
Qualifications
1–2 years of experience in the medical device or IVD industry is highly preferred.
Responsibilities
Gather, consolidate, and verify regulatory data related to IVDR device registrations.
Enter, maintain, and validate data in the Product Data Management system.
Develop and document Standard Operating Procedures (SOPs) for data governance.
Collaborate with Regulatory Affairs, Quality, R&D, and Supply Chain teams.
Support system validation testing and continuous improvement initiatives.
Identify and escalate data inconsistencies or process gaps.
Skills
Proficiency in Microsoft Word
Proficiency in Microsoft Excel
Education
Bachelor’s degree in Life Sciences or related field
Job description
A leading life sciences manufacturer is seeking a Data Management Specialist to support data management and compliance for medical device registrations. The role involves gathering regulatory data, maintaining the Product Data Management system, and developing Standard Operating Procedures. Candidates should possess a Bachelor's degree in a relevant field and ideally have 1–2 years of experience in the medical device industry. This position is remote within the Pacific Time zone.