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    Document Control Specialist - Taguig, Pilipinas - John Clements Consultants Inc

    John Clements Consultants Inc
    John Clements Consultants Inc Taguig, Pilipinas

    3 araw ang nakalipas

    John Clements Consultants Inc background
    Buong oras
    Paglalarawan
    Job Title : Document Control Specialist Responsibilities :
    • Responsible for coordination of controlled documents within global Document Control system
    • Maintain and improve processes associated with an electronic document control system within the eQMS.
    • Work cross-functionally to ensure change orders are executed in a complaint and timely manner.
    • Responsible for the accuracy of documentation per approved Standard Operating Procedures, GMP and internal change control.
    • Supports the request from users for documents and reports in the eQMS
    • Supports internal and external audits in backrooms and helps with the coordination of document requests.
    • Aids in the responses to internal and external audits as they related to the Document Control process.
    • Maintains quality records per applicable SOPs.
    • Responsible for coordinating document change orders (packets), collaboration, approval, release, archival and retention.
    • Closely work with Training coordinator to ensure change orders are triggering training as required
    • Other duties may be assigned as deemed necessary by management.
    Required Qualifications :
    • Must have strong communication (verbal and written) and interpersonal skills
    • Attention to detail and timeliness are critical
    • Computer Skills: software proficiency in Microsoft Office Suite is required
    • Previous Master Control experience is highly desirable
    • Must build rapport across functional teams within the organization
    • Bachelor's Degree or equivalent experience
    • Minimum of 5 years of experience in Document Management System or 2 years in Document Control and 3 years in applicable quality discipline
    • Understanding of the regulations and regulatory processes for document control/ management
    • Must operate through collaboration and transparency
    • Experience in cGMP/GDP/GCP environments and FDA-regulated industries is preferred
    • Night shift schedule / 1x month onsite.

    Salary – 50,000-56,000
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