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    Regulatory Affairs Jobs For Pharma at Thermo Fisher Scientific – Apply Online

    Build Your Future at Thermo Fisher Scientific: Quality & Regulatory Affairs Jobs| Apply Now

    Thermo Fisher Scientific continues to set global standards in quality and compliance, making it an ideal destination for professionals seeking Regulatory Affairs Jobs, Thermo Fisher Careers, and Pharma Jobs. With a mission-driven culture focused on accuracy, safety, and global impact, this role offers an exciting opportunity to contribute to life-improving innovations while growing your career in a collaborative environment.

    Job Details:

    • Job Position: RCR Specialist (Admin), Regulatory Compliance Review, Regulatory Affairs
    • Office Environment : Standard (Mon–Fri)

    About the Company

    Thermo Fisher Scientific is a global leader committed to quality and excellence. Their teams share a passion for getting it done right the first time and ensuring customer trust. Quality professionals at Thermo Fisher collaborate on global projects, expanding skills and discovering new career paths that make a real-world impact.

    Job Description: Regulatory Affairs Jobs at Thermo Fisher Careers

    • Perform global regulatory compliance review of essential documents supporting the customization of study-specific Essential Document Checklists.
    • Respond to project teams on queries regarding Essential Document Checklist requirements.
    • Facilitate discussion on deviations to the RCR process when applicable.
    • Ensure effective management and coordination of the Essential Document Checklist Process.
    • Maintain knowledge of PPD SOPs, Client SOPs/directives, and current regulatory guidelines.
    • Review, finalize, and post Essential Document Checklists.
    • Perform other duties as required.

    Key Responsibilities: Regulatory Affairs Jobs

    • Global regulatory compliance handling
    • Checklist approval and documentation accuracy
    • Query management and cross-functional collaboration
    • SOP compliance and regulatory guideline adherence
    • Process coordination for essential document management
    • Quality-driven support for regulatory operations

    Qualifications :Ideal for Pharma Jobs & Regulatory Affairs Jobs

    Education & Experience:

    • Bachelor’s degree or equivalent
    • 1–3 years of related experience

    Skills & Abilities:

    • Strong English communication skills
    • Good attention to detail and proofreading
    • Effective interpersonal and teamwork abilities
    • Proficiency in Word, Excel, PowerPoint; ability to learn new tools
    • Basic organizational, planning, and time-management skills
    • Understanding of global/regional/national regulatory affairs procedures
    • Analytical, investigative, and problem-solving skills
    • Ability to interpret data

    CLICK HERE TO APPLY ONLINE

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