Lead Technician, Quality Assurance - IntePros : Job Details

Lead Technician, Quality Assurance

IntePros

Job Location : Ventura,CA, USA

Posted on : 2025-09-09T23:52:51Z

Job Description :
Quality Control (QC) Specialist/Associate - Expertise Calibration Associate About the Company Our client is a leading global medical device company committed to advancing healthcare through innovative solutions and uncompromising quality. They are seeking a detail-oriented and motivated individual to join their team as a Quality Control Specialist/Associate (Expertise Calibration Associate). Role Overview In this entry-level role, you will play a key part in ensuring the highest standards of quality and compliance across multiple functions. You will support the development and refinement of evaluation standards by calibrating and aligning subject-matter expertise across teams. This position is ideal for candidates who want to build experience in quality assurance, training, or data evaluation within the medical device industry. Key Responsibilities
  • Support the development and calibration of evaluation standards to align expertise across teams.
  • Implement quality standards and ensure compliance at every stage of the process.
  • Assess potential risks, provide recommendations, and execute corrective actions when needed.
  • Take responsibility for quality control across laboratory studies, clinical research, testing, operations, raw materials, production, and finished products.
  • Facilitate audits and regulatory inspections to ensure adherence to company and regulatory requirements.
  • Prepare and maintain accurate documentation in support of quality assurance activities.
  • Collaborate with cross-functional teams to strengthen compliance and continuous improvement initiatives.
Qualifications
  • Bachelor's degree in a scientific, engineering, or related field (preferred).
  • Minimum of 5+ years of experience in quality control, quality assurance, or a related function within life sciences, medical devices, or pharma.
  • Strong knowledge of quality systems, compliance requirements, and regulatory standards.
  • Familiarity with laboratory practices, clinical operations, or manufacturing processes.
  • Excellent attention to detail with the ability to identify risks and propose solutions.
  • Strong communication and organizational skills with the ability to collaborate effectively across teams.
What We Offer
  • Opportunity to gain hands-on experience in quality assurance and compliance within a global leader in the medical device industry.
  • Exposure to audits, regulatory inspections, and compliance systems in a highly regulated environment.
  • Professional growth and career development through structured processes, mentorship, and on-the-job learning.
Apply Now!

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