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Proclinical

QA Specialists

Proclinical Waterford
32 - 40 hour


Show Recently closed jobs

    Proclinical

    QA Specialists

    Proclinical Waterford
    32 - 40 hour
    Status Open
    Apply now

    Apply on the employer's website


    What we ask

    Education

    No minimum education required

    What we offer

    Hours
    32 to 40 hours per week
    Employment type
    contract

    Job description

    Are you ready to safeguard quality, ensure compliance, and make a real impact in a GMP-driven environment?

    Proclinical is seeking a QA Specialist to join a dynamic team in ROI. In this role, you will play a key part in ensuring that products are manufactured, stored, and packaged in compliance with cGMP standards. This position involves supporting quality systems, conducting audits, and contributing to continuous improvement initiatives.

    Responsibilities:

    Support the development and delivery of GMP training packages.
    Prepare and review procedures and batch documentation.
    Conduct audits across departments according to an agreed schedule.
    Ensure the quality system is effectively implemented and maintained.
    Act as a quality point of contact for systems and processes, providing guidance on quality issues.
    Review documentation, investigations, and reports in a timely manner, addressing concerns based on risk.
    Collaborate with departments to ensure timely closure of quality actions and findings.
    Contribute to continuous improvement initiatives and report Right First Time (RFT) data trends.
    Participate in internal, supplier, and regulatory audits.
    Perform critical reviews of procedures and practices.
    Investigate deviations and ensure all product deviations are resolved before release.
    Maintain compliance with cGMP requirements at all times.
    Adhere to safety protocols and maintain good housekeeping standards.

    Key Skills and Requirements:

    A degree in science or a related discipline is preferred.
    Experience in a similar role, ideally within a GMP-regulated environment.
    Strong knowledge of cGMP and regulatory standards.
    Excellent accuracy, attention to detail, and interpersonal skills.
    Proficiency in computer applications and good presentation skills.
    A flexible approach and ability to adapt to ongoing changes.
    Self-motivated, results-driven, and able to work with minimal supervision.
    If you are having difficulty in applying or if you have any questions, please contact Dean Fisher at (url removed).

    Apply Now:

    If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

    Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

    By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data
    Apply now

    Apply on the employer's website

    Apply now

    Apply on the employer's website


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