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    Job · 22148909

    Tetrahedron Manufacturing Services Pvt. Ltd. logo

    Consultant US FDA_FDA Compliance

    Tetrahedron Manufacturing Services Pvt. Ltd. · Noida · onsite · Posted 5d ago

    Not disclosed5–10 yrsfulltimeSourced fromFoundit

    About a minute. You'll make an account on the way through.

    About this role

    Hiring: US FDA / FDA Compliance Consultant

    Company: Tetrahedron Manufacturing Services Pvt. Ltd.

    Department: Consulting

    Experience: 5–10 Years

    Industry: Pharmaceutical, Food & FDA-Regulated Industries

    Location: Pan India | Willingness to travel required

    Employment Type: Full-Time

    Open Positions: 5–10

    Job Description

    We are looking for experienced US FDA / FDA Compliance Consultants with hands-on experience in the Pharmaceutical, Food, or other FDA-regulated industries.

    Key Requirements
    • 5–10 years of relevant industry or consulting experience.
    • Mandatory experience in US FDA-related projects.
    • Hands-on experience in GxP documentation development and implementation.
    • Knowledge of FDA regulations, GMP, quality management systems, and regulatory compliance.
    • Experience in validation activities, compliance assessments, gap analysis, CAPA, SOPs, and audit readiness.
    • Ability to coordinate with clients, conduct assessments, prepare reports, and implement compliance projects.
    • Strong communication, documentation, analytical, and presentation skills.
    • Willingness to travel to client locations across India.
    Preferred Candidate Profile
    • Pharmaceutical manufacturing and quality assurance professionals.
    • Food manufacturing and food safety compliance professionals.
    • FDA compliance consultants with experience in regulated manufacturing environments.
    • Professionals experienced in consulting assignments and regulatory implementation projects.

    Apply Now

    Email: [HIDDEN TEXT]

    WhatsApp: [phone removed]

    Website: www.tetrahedron.in

    Reporting Office: 204, Ground Floor, Block A, Udyog Kendra-I, Ecotech III, Greater Noida, Uttar Pradesh – 201306.

    Interested candidates may share their updated CV along with details of their FDA project experience, industry background, and current location.

    Sourced from foundit

    Skills

    GMP quality management systemsGxP documentation development and implementationUS FDA-related projectsAudit Readinesscompliance assessmentsgap analysisSOPsCAPAFDA regulationsvalidation activitiesRegulatory Compliance

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