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Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Quality Assurance Manager - Training Services

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeAlameda, CA, USA

About the Job

Requirements

  • A Bachelor's degree with 8+ years of experience in Quality Assurance, Quality Control, biotechnology, document control, or a related field, or an equivalent combination of education and experience.
  • At least 5 years of experience in a position with direct management of people.
  • Proficiency with training systems such as MasterControl and SAP Litmos.
  • Ability to manage multiple complex priorities within demanding timeframes while maintaining attention to detail.
  • Proficiency with Microsoft Office Professional Suite, including Word, Excel, Access, and PowerPoint.
  • Knowledge of FDA Quality System Regulation (QSR), ISO 13485, and the Medical Device Directive/Medical Device Regulation (MDD/MDR).
  • Demonstrated strong supervisory experience and performance.
  • Strong problem-solving, decision-making, and leadership skills.
  • Strong oral, written, and interpersonal communication skills.
  • High degree of accuracy and attention to detail.
  • Ability to exercise judgment based on policies and management guidance to determine appropriate action.
  • Willingness and ability to work onsite.
  • Ability to lift and move up to 25 pounds, move between buildings and floors, remain stationary and use standard office equipment for extended periods, move within the office and access file cabinets or supplies, and communicate and exchange accurate information with employees at all levels.

Responsibilities

  • Oversee the direction and supervision of the Quality Training System and Training Services, and lead projects to ensure compliance with company procedures and regulatory requirements.
  • Select, manage, train, and develop staff; establish objectives and assignments; and provide ongoing feedback through performance reviews and development plans.
  • Ensure the structure of group activities aligns with corporate goals and initiatives.
  • Coordinate global training activities to ensure regulatory compliance and appropriate training for all team members.
  • Analyze situations, review relevant factors to solve problems, and proactively seek and implement improvements.
  • Evaluate procedures and work instructions for process improvements, recommend policy and procedure changes, and implement changes as needed.
  • Act as the subject matter expert for Training and participate in cGMP compliance inspections by the FDA, customers, and other regulatory bodies, including retrieving requested quality documents, records, and trend data and defending Quality System processes.
  • Own and drive nonconformance reports (NCRs) and corrective and preventive actions (CAPAs) related to the Training System.
  • Communicate process changes to internal customers and train them as needed.
  • Provide Quality and MasterControl Orientation training.
  • Resolve and respond to organization-wide quality system training issues and questions; recommend, implement, and document solutions for systemic training issues.
  • Analyze regulatory, business, and customer requirements and industry best practices, and propose and implement required Training System changes or improvements.
  • Design, develop, and implement Training System curriculum in conjunction with functional leadership.
  • Promote a safe, positive, and inclusive work environment.

Desired Qualifications

  • Experience with Medical Device Single Audit Program (MDSAP) is preferred.

About the Company

Penumbra Inc

Neurovascular and peripheral medical devices manufacturer

Penumbra Inc. designs, develops, and sells medical devices for neurovascular and peripheral vascular conditions. Its products are used by doctors in hospitals and clinics and work by being inserted into blood vessels to remove clots, support catheter-based procedures, or help reconstruct vessels. The company differentiates itself with a broad, integrated portfolio across neurovascular and peripheral interventions and a global sales network that serves Europe and the Americas. Its goal is to improve patient outcomes through high-quality tools and ongoing research and development to expand capabilities.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Alameda, CA
Founded
2004

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