Senior SW Compliance Specialist – Regulatory Affairs, Design Assurance

🕒 June 20

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🚔 Compliance

👻 Ghost score 16%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Meridian Bioscience Inc.

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

💰 Grant on 2022-01

Healthcare • Consulting • Food & Beverage

Meridian Bioscience Inc. is a leading manufacturer of molecular and immunological reagents designed for diagnostic applications. The company specializes in providing innovative solutions to enhance point-of-care diagnostics and streamline assay development for various medical conditions, including infectious diseases and cancers. Meridian is dedicated to advancing medical diagnostics and improving patient outcomes through its high-quality products and services.

📋 Description

• Responsible for supporting Meridian’s regulatory and quality processes • Assist the regulatory department with product compliance throughout all stages of the product lifecycle • Provide support and guidance to quality and regulatory activities, including Design Control activities • Supports and helps draft sections of regulatory submissions for domestic, worldwide commercialization • Drafts, evaluates, and reviews technical protocols and data in support of clinical trials • Reviews software architecture, software requirements, traceability, verification and validation documentation • Provides direct support associated with adverse events, medical device reportable events and product recall activities • Supports cybersecurity compliance activities

🎯 Requirements

• Bachelor of Science degree in Biology, Biochemistry, Microbiology, Software Engineering, Computer Science, Computer Engineering, Biomedical Engineering, Electrical Engineering, or other related scientific, engineering, or technical discipline required • A minimum of 4–6 years of direct Regulatory Affairs, Design Assurance, Software Quality, or related regulated industry experience is required • Proven knowledge of FDA and ISO regulated environment • Experience with design, development, and clearance of medical devices • Knowledge of FDA software documentation requirements • Experience reviewing software lifecycle documentation • Working knowledge of cybersecurity requirements applicable to medical devices • Ability to assess software, firmware, cybersecurity, and connectivity changes for regulatory impact

🏖️ Benefits

• Health insurance • Flexible work arrangements • Professional development opportunities