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Quality Systems Specialist

Quality Systems Specialist

Almac GroupDurham, NC, US
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Overview

Almac Group is seeking a Quality Systems Specialist for our Durham, NC location. The Quality Systems Specialist I will be responsible for ensuring compliance with CLIA / CAP, ISO15189, ISO13485, GCP, GLP and GCLP requirements within Almac Diagnostic Services, and for ensuring that Quality Management System activities are implemented and maintained. This includes document control, KPI reporting, LMS management, hosting audits, maintaining laboratory licenses / accreditations and QMS reviews are adequately planned, performed, and implemented on a continual basis as required by the company\'s quality policy and regulatory agencies.

Responsibilities

  • Maintain the Quality Helpdesk and manage document requests in a timely manner.
  • Initial triage of incoming documents and quality systems review of documentation.
  • Provide feedback to unit SMEs and update KPIs.
  • Serve as System SME for the respective business unit and administer Q-Track (LMS).
  • Generate Weekly Q-Track KPIs and report trends to team leaders / managers.
  • Advise leadership on system updates / improvements and generate weekly SPC charts for discussion.
  • Manage Trackwise (LMS) system and reporting; generate reports including KPIs.
  • Provide training and maintain laboratory licenses and accreditations globally, including gap analyses against updated standards.
  • Review calibration and maintenance data for compliance with approved methods and procedures.
  • Ensure all necessary quality records are completed and reviewed / approved by responsible personnel.
  • Create, review, and approve policies, procedures, work instructions, protocols, and reports to ensure regulatory compliance (CLIA / CAP, ISO15189, ISO13485, GCP, GLP, GCLP).
  • Make recommendations for improvements where appropriate.

Qualifications

Required Experience / Education :

  • Bachelor\'s degree in biological or clinical laboratory science, or related field
  • Minimum of 1 year in a high complexity CLIA laboratory
  • Working knowledge of local, state and federal laboratory regulations
  • Working knowledge of high throughput genomic technologies
  • Preferred Experience / Education :

  • Master's degree in biological or clinical laboratory science, or related field
  • Minimum of 3 years in a high complexity laboratory and additional experience in an IVD environment
  • Minimum of 1 year managing quality system activities across multiple requirements (CLIA / CAP, ISO15189, ISO13485, GCP, GLP and GCLP)
  • What can Almac Group offer you?

  • Medical, Vision & Dental benefits from the 1st of the month following start date
  • 20 days PTO per year , accrued monthly following start date
  • 12 holidays per year plus one day for Annual Diversity Day
  • Company paid long and short-term disability along with Life Insurance
  • 401k company contribution
  • Professional development programs / continuous learning opportunities
  • Want to see our latest job opportunities? Follow us on LinkedIn

    Almac Group, Inc. is an Equal Opportunity Employer - Minorities / Women / Protected Veterans / Disabled - Proudly embracing diversity in all of its expressions.

    EEO is the Law

    EEO is the Law GINA Supplement

    Almac provides reasonable accommodations to people with disabilities who need assistance completing the application process. Please email us at ADARequest@almacgroup.com to request assistance.

    Seniority level

  • Entry level
  • Employment type

  • Full-time
  • Job function

  • Science, Administrative, and Quality Assurance
  • Industries

  • Pharmaceutical Manufacturing and Biotechnology Research
  • J-18808-Ljbffr

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