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    Clinical Quality Specialist - Boise, United States - Idaho State Job Bank

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    Description


    Clinical Quality Specialist at Bausch Health in Boise, Idaho, United States Job Description Bausch Health is a global company that develops, manufactures, and markets a differentiated product portfolio across multiple high-growth therapeutic areas including Gastroenterology, Generics, Neurology, Ortho Dermatologics, Medical Aesthetics and Dentistry.

    We are delivering on our commitments as we build an innovative company dedicated to advancing global health. Each day, Bausch Health products are used by over 150 million people around the world. Our approximately 7,000 employees are united around our mission of improving peoples lives with our health care products.

    Are you passionate about elevating quality standards in clinical research? Join our team as a Clinical Quality Specialist within the Research & Development Quality function, where you'll play a pivotal role in managing Quality Management Systems (QMS), ensuring compliance, and fostering a culture of continuous improvement.

    This role offers an opportunity to impact our clinical quality initiatives, grow professionally, and contribute to a vibrant team.


    Your Responsibilities:
    + Strategic QMS Management:
    Lead our QMS strategy to uphold impeccable quality standards

    + Nonconformance Handling:

    Manage CQA-related nonconformance processes, supporting effective corrective actions.


    • Performance Metrics & Risk Management:
    Develop performance metrics, analyze data for trends, and mitigate emerging quality issues proactively.


    • Process Improvement & Change Control:
    Contribute to process improvement initiatives and oversee CQA-related Controlled Document processes

    + Collaborative Auditing:

    Possibility to engage in audits as part of process improvement initiatives


    Your Qualifications & Experience:
    + 2+ years of quality experience in Clinical Operations, Quality, or Consulting. + BA/BS in a related field, with a focus on GCP regulations and guidelines. + Excellent verbal and written communication skills, ability to work effectively in team dynamics. + Strong computer skills, including proficiency in Microsoft Office Suite, especially Excel. + Experience in electronic quality systems, auditing, and clinical operations. + Background in risk management and process improvement. + Experience in clinical monitoring or project management. + Ability to drive process improvements and apply critical thinking.

    #LI-Remote This position may be available in the following location(s):
    [[location_obj]] We thank you in advance for your interest in gro To view full details and how to apply, please login or create a Job Seeker account

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