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Katmai

Quality Assurance Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBrilliant, AL, USA$60k /yr

About the Job

Requirements

  • A minimum of three to five years of experience in the medical device or drug industry, including at least two years of direct experience in quality control/quality assurance or equivalent.
  • Proven understanding of FDA regulations.
  • Proven leadership experience.
  • Must have a clean driving record.
  • Must pass a drug test.
  • Must obtain and maintain any necessary security access and/or background checks.
  • Strong background and knowledge in Quality Systems and quality assurance/quality control principles and compliance.
  • Computer proficiency, including Microsoft Excel, Microsoft Word, and PowerPoint.
  • Must have or be able to attain a valid state driver's license and be insurable on the company's automobile insurance policy.
  • Driving, with or without accommodation, may be required when traveling for training and/or occasional local driving.
  • Frequent sitting, using hands and fingers, handling, reaching with hands and arms, talking, and hearing; occasional walking or standing; and occasional lifting of up to 10 pounds.

Responsibilities

  • Implement, monitor, and maintain the Quality System in accordance with FDA medical device and drug regulations.
  • Ensure Quality System regulations are understood by applicable company personnel and that the system functions effectively at all times.
  • Draft, review, maintain, distribute, and train personnel on facility documentation and procedures, including the Quality Manual and Quality System Procedures.
  • Ensure compliance with Document Control, Device History Records, and their management.
  • Maintain Quality System Manual Standard Operating Procedures and documentation control.
  • Prepare documentation and systems for compliance with FDA requirements.
  • Conduct and participate in quality inspections, internal and external audits, and FDA inspections.
  • Participate in CAPA systems and prepare reports and corrective actions.
  • Maintain and update the Quality Manual and QA Procedures, and introduce Quality Plan improvements as applicable.
  • Assist in analyzing and evaluating information concerning manufacturing problems, customer complaints, non-conformances, and the quality system.
  • Trend customer complaints and/or non-conformances.
  • Assist with and/or perform training activities in Quality Management system processes and product quality.
  • Confer with Operations about quality assurance and regulatory issues of products to ensure compliance with the quality system.
  • Maintain regular and punctual attendance.
  • Perform other duties as assigned.
  • May provide technical guidance and/or supervision to personnel.
  • Work Monday through Friday on the day shift; no weekends. Additional hours may be required to complete an assignment or project.
  • Travel less than 25% of the time; driving is expected to be less than 10% of the time.

Desired Qualifications

  • A bachelor's degree is preferred.
  • Strong communication skills, including verbal, written, and interpersonal communication.
  • Good organizational skills.
  • Ability to problem-solve, make decisions, and participate effectively on cross-functional teams.
  • Ability to work independently and manage multiple tasks.
  • Ability to collaborate across functions.
  • Professionalism, energy, high integrity, results orientation, and a solutions-driven approach.

About the Company

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