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    Job · 16244375

    HYDERABAD · FULLTIME

    Document Control Administrator

    Thermo Fisher Scientific logo

    Thermo Fisher Scientific

    Hyderabad · onsite · Posted 44d ago

    Sourced fromNaukri
    Undisclosed3–8 yrsfulltimeHyderabad

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    Section · 01

    About this role

    Work Schedule
    Standard (Mon-Fri)
    Environmental Conditions
    Office
    Job Description
    As part of the Thermo Fisher Scientific team, you ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
    Job Summary
    The Lead Document Control Administrator is responsible for coordinating and overseeing daily document control activities to ensure the accuracy, integrity, and compliance of controlled documentation. This role serves as the subject matter expert (SME) for document control processes and electronic document management systems (EDMS), provides technical guidance to team members, partners with cross-functional departments, and drives continuous improvement while supporting quality and regulatory compliance.
    Key Responsibilities
    • Coordinate daily document control activities to ensure timely processing of controlled documents.
    • Manage document creation, revision, approval, distribution, archival, and obsolescence.
    • Serve as the primary resource for document control procedures and EDMS functionality.
    • Maintain document accuracy, version control, and audit trails.
    • Provide technical guidance and mentorship to End Users.
    • Collaborate with Quality, Regulatory, Manufacturing, Engineering, and Operations.
    • Monitor document metrics and recommend process improvements.
    • Support internal, customer, and regulatory audits.
    • Ensure compliance with company policies and applicable regulations.
    • Participate in change control, CAPA, and quality system initiatives.
    • Support EDMS upgrades, testing, validation, and user training.
    • Generate reports and dashboards for document control performance.
    Qualifications
    • Bachelors degree in Business Administration, Life Sciences, Engineering, Quality, or related field.
    • 3 years or more of document control or quality systems experience in a regulated industry.
    • Experience with Electronic Document Management Systems (EDMS).
    Preferred Skills
    • Advanced knowledge of document control principles and document lifecycle management.
    • Experience with EDMS platforms such as MasterControl, Veeva, TrackWise Digital, SharePoint, or OpenText.
    • Strong understanding of Quality Management Systems (QMS).
    • Excellent organizational, communication, and problem-solving skills.
    • Proficiency with Microsoft Office Suite.
    Preferred Knowledge
    • FDA 21 CFR Part 11
    • 21 CFR Parts 820
    • ISO 9001 and/or ISO 13485
    • GMP, GDP, Change Control, CAPA, and Risk Management
    Leadership Responsibilities
    • Provide day-to-day technical leadership and guidance.
    • Mentor and train team members.
    • Coordinate workload and priorities.
    • Promote best practices and continuous improvement.
    Key Competencies
    • Technical Leadership
    • Attention to Detail
    • Quality Compliance Focus
    • Collaboration
    • Communication
    • Continuous Improvement
    • Accountability


    Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

    Sourced from naukri

    Section · 02

    Skills

    opentextDocument ManagementCfrISO 13485ISO 9001auditsCAPAChange ControlCancerMicrosoft Office SuiteQuality SystemsQuality ComplianceManufacturingoperationsAdministrationcomplianceLife Sciencesquality management

    Section · Company

    About Thermo Fisher Scientific

    Thermo Fisher Scientific logo

    Thermo Fisher Scientific

    Biotechnology

    4.8k+

    employees

    1956

    70 years old

    Waltham,Massachusetts

    United States

    About

    Thermo Fisher Scientific enables their customers to make the world healthier, cleaner and safer.

    Industries

    BiotechnologyBiotech & Life sciencesInternetAnalytics & KPOPharma

    Employee ratings

    1,052 reviews

    3.8/ 5

    Culture

    3.7

    Career growth

    3.0

    Work-life

    3.8

    Employees rate it well for

    Work Life Balance177Work Culture134Senior Management98Salary96Career Growth65

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