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    Quality Specialist 2024-05-28 - Calgary, Canada - Fluid Biomed Inc.

    Fluid Biomed Inc.
    Fluid Biomed Inc. Calgary, Canada

    4 days ago

    Default job background
    Upper Management / Consulting
    Description

    This is a unique opportunity to join a early-stage company to advance the development of a novel implantable medical device, ensuring its readiness for human use.

    Fluid Biomed is an innovative medical device startup focused on developing a cutting-edge neurovascular stent to treat brain aneurysms and enhance patient outcomes worldwide.

    We are seeking a highly flexible and motivated person for the role of Quality Specialist to join our talented team.

    Reporting to the Quality Engineer, the Quality Specialist will act as management representative in administrating the elements of the Quality Management System (QMS), lead the quality inspection and supplier quality activities, manage overall inventory, training, and calibration programs, and support the Engineering and Operations team.

    The role will work within the Quality Department in a fast paced and dynamic environment where attention to detail, ability to multi-task, taking initiatives and collaborating cross-functionally are critical for success.


    Key Responsibilities include:

    • Own and maintain effective QMS processes and procedures in accordance with ISO 13485 standards
    • Manage company document control activities including revision controls, SOP/document review and approval, document retention and archiving, electronic and hardcopy filing, etc.
    • Maintain Technical documents (Engineering Specifications & Drawings) library
    • Complete receiving documentation for incoming parts, components, or equipment
    • Prepare and lead annual QMS Management Review meetings and present to the team and executives
    • Act as Management Representative in coordinating regulatory compliance activities/audits with external regulatory affair bodies to obtain and maintain necessary ISO certifications and approvals
    • Under ISO 13485 requirements, maintain and execute the internal audit process to assess compliance with QMS requirements and identify areas for improvements
    • Establish and maintain key performance indicators (KPIs) to monitor product quality and process effectiveness
    • Lead and improve product inspection activities, including the development of standard inspection reports, and communicating with internal and external stakeholders
    • Initiate, investigate, and resolve nonconformance reports (NCRs), by implementing corrective and preventive actions (CAPAs) to address root causes of product and process quality issues, and prevent recurrence in a timely manner
    • Own and maintain Approved Supplier List (ASL) including qualification, approval, development of quality agreements, and performance evaluation of suppliers in coordination with Engineering team
    • Assist in the procurement and installation of necessary quality and operational equipment by preparing request for quotes (RFQs), shipping documentation, technical qualification documentation, etc. as required
    • Maintain supplier quality documentation including Certificate of Analysis, inspection reports, etc.
    • Execute Non-Disclosure Agreements (NDAs) for external service providers, as required
    • Manage overall equipment calibration process including maintenance of calibration/maintenance reports, and coordinate ongoing equipment service or testing, in coordination with the Engineering team
    • Manage overall inventory control process including physical and electronic inventory of conforming/nonconforming product, delivery components, and supporting equipment
    • Manage overall training program and maintain training KPI reports, matrix, files, and records for all staff
    • Provide training and education to staff on quality processes, procedures, and regulations as required
    • Lead and support continuous improvement project activities across the organization
    • Support other Quality Department activities as required

    Education and Experience Requirements:

    • Bachelor's degree and a minimum of 2 years' experience with QA/document control in industry required
    • Experience working in ISO 9001 or 13485 certified organization required
    • Demonstrated experience with Quality Management System, and audit activities required
    • Experience or knowledge with root cause analysis techniques required
    • General understanding of the training, calibration and inventory processes required
    • Demonstrated attention to detail and excellence in written communication

    Additional Skills:

    • Experience as lead resource with document control software preferred
    • Certification as Internal Auditor preferred
    • Previous R&D/technical industry exposure, able to understand company technology at a practical level
    • Excellent documentation, communication, and interpersonal relationship skills
    • Strong problemsolving, organizational, analytical, and critical thinking skills
    • Ability to navigate uncertainty/fluidity in role scope, priorities, and timelines
    • Ability to manage competing priorities in a fastpaced and dynamic environment
    • Proven expertise in usage of MS Office Suite
    Role is on-site in Calgary, AB and candidates must be legally entitled to work full time in Canada.
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