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    Project Leadership - United Kingdom - Cagents

    Cagents
    Cagents United Kingdom

    3 weeks ago

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    Description
    We use cookies to enhance your browsing experience, serve personalized ads or content, and analyze our traffic. Use Website In a Screen-Reader Mode Accessibility Screen-Reader Guide, Feedback, and Issue Reporting Skip to Content ↵ ENTER CQV Project Manger
    United Kingdom, UK / United Kingdom / Full Time

    About


    CAI:

    CAI is a 100% employee-owned company established in 1996, that has grown year over year to nearly 700 people worldwide.

    We provide commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.

    As part of our company culture, we invest in YOUR future, and commit to hands on certifications as well as professional training.

    We are now seeking a Project Manager to join our growing operations in the UK.

    Managing mid-sized to large projects related to process equipment and clean utilities including start-up and commissioning - Lead design review, site acceptance and installation of equipment - Write, Review and Approve CQV documents following established 21 CFR standards, both internally and externally.

    Standard Operating Procedures, Impact Assessments, Risk Assessments, Specifications (URS/FRS/DDS), FATs, SATs, IOQ/PQs, Validation Protocols and Commissioning Test Plans - Support onsite and offsite activities, such as: FATs, SATs, Executions and System Walkdowns - Management of any aspect of C & Q, verification as requested i.e., Change Controls, Management of Contractors and Vendors, document control, punch list management.

    - Allocate project resources for efficient execution of project deliverables. - Coordinate support during C&Q execution

    Position Requirements:

    • BS or MS in a relevant science or engineering field, or equivalent
    • 8 + years of Commissioning, Qualification, Validation and Compliance experience in the Life Sciences or Regulated Industries; Sound technical knowledge of UK, EU and global regulatory requirements. Experience in collaborating and managing Commissioning, Qualification and Validation deliverables for one or Multiple Projects
    • Skilled at planning and tracking project activities and schedules
    • Excellent interpersonal skills to form strong relationships with internal and external clients
    • Excellent oral and written communication skills
    • Excellent problem-solving skills
    • Customer-service focused.
    • Able to travel domestically and internationally if required. 24 Days PTO/5 Sick days per year + Additional Holidays depending on Country
    ~ Medical / Dental / Vision (In accordance with each countries' applicable regulations)
    ~ Professional Development (Approximately $5,000 paid career-related, continuing education)
    ~ Company Paid Long-Term Disability
    ~ Company Paid Life Insurance
    ~ Company Paid Parental Leave (In accordance with each countries' applicable regulations)
    ~ For screen-reader mode - click the first button of the website
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