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Surmodics

Supplies IVD reagents and device coatings

Quality Associate 2

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeEden Prairie, MN, USAIn-person

About the Job

Requirements

  • A four-year technical degree and at least two years of experience in the medical device industry, or at least ten years of experience in a quality-related field in the medical device industry.
  • Proficiency with Microsoft Word, Access, and Excel.
  • Ability to read, follow, and generate detailed instructions.
  • Ability to prioritize activities amid competing demands from multiple sources.

Responsibilities

  • Lead or participate in corrective and preventive actions (CAPAs) and nonconformances.
  • Support supplier quality activities.
  • Assist Quality Engineering with assigned tasks supporting product and manufacturing operations.
  • Support release of intermediates and final product for internal and external distribution.
  • Assist with customer-requested documentation, including customer quality system surveys.
  • Participate in improvement and efficiency projects within Quality and cross-functionally.
  • Oversee the material and product retain management program.
  • Ensure quality procedures, processes, and systems are standardized throughout the business and correctly and consistently implemented to meet internal requirements and external regulations.
  • Write and revise documents to meet internal requirements and external regulations.
  • Support internal audits of quality system processes, manufacturing areas, and documentation, as assigned.
  • Support Quality leadership in managing external customer and regulatory audits.
  • Develop and present training material for new or changing processes as required to ensure compliance with procedures and regulations.
  • Serve as Quality Event Coordinator for nonconformances, CAPAs, and complaints, assisting with completion and reviewing investigations and records for content, accuracy, and completeness.
  • Assist in developing and maintaining quality system metrics.
  • Provide insight into statistical trends using quality system data and create system solutions for quality system issues.
  • Ensure quality system documentation and recordkeeping activities comply with established procedures and work instructions.
  • Perform document administration activities within the electronic quality management system (eQMS) software.
  • Coordinate and archive quality records.

About the Company

Surmodics

Supplies IVD reagents and device coatings

Surmodics provides essential components for in vitro diagnostics (IVD) and advanced coatings for medical devices. Its IVD offerings include ELISA reagents, antigens, antibodies, and microarray slides that help researchers develop sensitive, reproducible immunoassays. It also creates lubricious, hemocompatible, and drug-delivery coatings for medical devices, including coatings used on drug-eluting stents, and it offers design and production services for advanced balloon catheters in the U.S. and Ireland. The company collaborates closely with customers to move products from concept to market quickly with practical development support, aiming to help clients bring diagnostic tests and coated medical devices to market efficiently.

Company size
201-500
Company stage
IPO
Headquarters
Eden Prairie, MN
Founded
1979

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