Penumbra

QA Manager, Training Services

Penumbra$137K — $194K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 8+ years in Quality Assurance, Biotechnology, or related field
  • 5+ years of direct people management experience
  • Proficiency with Training Systems (e.g., MasterControl, SAP Litmos)
  • Strong communication skills in oral, written, and interpersonal contexts
  • Knowledge of FDA QSR, ISO 13485, and MDD/MDR regulations
  • Solid problem-solving and decision-making capabilities
  • High degree of accuracy and detail orientation

Responsibilities

  • Select, manage, and develop staff while providing performance feedback
  • Align group activities with corporate goals and regulatory requirements
  • Coordinate global training compliance activities
  • Analyze and implement process improvements proactively
  • Serve as a subject matter expert during compliance inspections
  • Drive Non-Conformance Reports (NCRs) and Corrective and Preventive Actions (CAPAs)
  • Design and develop Training System curriculum collaboratively with leadership

Benefits

  • Collaborative learning environment with performance rewards
  • Opportunity to be involved in groundbreaking medical treatments
  • Generous benefits package including medical, dental, and vision insurance
  • 401(k) plan with employer matching contribution
  • Paid parental leave and paid sick time in compliance with applicable laws
  • Minimum of fifteen days of accrued vacation per year, increasing with tenure
  • Eleven paid company holidays annually
Full Job Description
As a Quality Assurance Manager of Training Services, you will play a pivotal role in maintaining the integrity of our Quality System and processes. You will be responsible for overseeing the direction and supervision of the Quality Training System, Training Services, and leading projects to ensure compliance with Penumbra procedures and regulatory requirements.

What You'll Work On
• Select, manage, train, and develop staff. Establish objectives and assignments and provide ongoing feedback through performance reviews and development plans.
• Ensure the structure of all group activities is in alignment with corporate goals and initiatives.
• Coordinate global training activities to ensure compliance with regulatory requirements, ensuring that all team members are appropriately trained.
• Provide additional analysis of situations, reviewing various factors to solve problems, and proactively seek and implement improvements.
• Evaluate procedures and work instructions for process improvements, recommend changes to policies and procedures, and implement changes, as necessary.
• Act as subject matter expert for Training and participate in cGMP compliance inspections by the FDA, customers, and/or other regulatory bodies. This includes retrieval of quality documents/records/trend data and any other documentation requested during these inspections as well as defending Quality System processes.
• Own and drive any NCR's and CAPA's related to the Training System.
• Communicate and train internal customers when processes are changed.
• Responsible for providing Quality and MasterControl Orientation training.
• Resolve and respond to quality system training issues and questions from throughout the organization. Recommend, implement, and document solutions for systemic training related issues.
• Analyze regulatory, business, and customer requirements, as well as current industry best practices; propose and implement any required changes or improvements to the Training System.
• Design, develop and implement Training System curriculum in conjunction with functional leadership.
• Promote a safe, positive, and inclusive work environment.

What You Contribute
• A Bachelor's degree with 8+ years of experience in Quality Assurance, Quality Control, biotechnology, document control, or related field, or equivalent combination of education and experience
• 5+ year of experience in a position with direct management of people
• Proficiency with Training Systems (such as MasterControl, SAP Litmos),
• Ability to manage multiple, complex priorities within demanding timeframes with attention to detail
• Proficiency with Microsoft Office Professional Suite (Word, Excel, Access, PowerPoint)
• Knowledge of the FDA QSR, ISO13485, and the MDD/MDR
• Experience with MDSAP preferred
• Demonstrated strong supervisory experience and performance required
• Solid problem solving, decision-making, and leadership skills are required
• Strong oral, written and interpersonal communication skills
• High degree of accuracy and attention to detail
• Exercises judgment based on policies and management guidance to determine appropriate action

Working Conditions

General office environment. Willingness and ability to work on site. Business travel from 0% - 10%. Requires some lifting and moving of up to 25 pounds. Must be able to move between buildings and floors. Must be able to remain stationary and use a computer or other standard office equipment, such as a printer or copy machine, for an extensive period of time each day. Must be able to read, prepare emails, and produce documents and spreadsheets. Must be able to move within the office and access file cabinets or supplies, as needed. Must be able to communicate and exchange accurate information with employees at all levels on a daily basis.

Annual Base Salary Range: $137,000 - $194,000 / year

We offer a competitive compensation package plus a benefits and equity program, when applicable.

Individual total compensation will vary based on factors such as qualifications, skill level, competencies, and work location.

What We Offer
• A collaborative teamwork environment where learning is constant, and performance is rewarded.
• The opportunity to be part of the team that is revolutionizing the treatment of some of the world's most devastating diseases.
• A generous benefits package for eligible employees that includes medical, dental, vision, life, AD&D, short and long-term disability insurance, 401(k) with employer match, paid parental leave, eleven paid company holidays per year, a minimum of fifteen days of accrued vacation per year, which increases with tenure, and paid sick time in compliance with applicable law(s).

About Penumbra

Penumbra is a global healthcare company that designs, develops, manufactures, and markets innovative medical devices for the diagnosis and treatment of neurological and vascular diseases. The company's products include clot retrieval devices, neurovascular stents, and more. Penumbra serves a variety of markets including hospitals, clinics, and ambulatory surgery centers. With a commitment to improving patient outcomes, Penumbra is dedicated to advancing the field of interventional medicine through innovation and collaboration.
Learn more about Penumbra
Size
3,800 employees
Market Cap
$8.4 billion
Industry
Net Income
-$15.7 million
Founded
2004
5 Year Trend
+23.2%
Revenue
$560.4 million
NASDAQ

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