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8 - 12 years

5 - 15 Lacs

Posted:21 hours ago| Platform: Naukri logo

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Job Type

Full Time

Job Description

Position:

About Us:

Industry:

About the Role:

Key Responsibilities:

  • Independently design, conduct, and interpret

    in vivo repeated dose toxicity studies

    for regulatory submissions across the globe (FDA, OECD, EU, REACH, etc.)
  • Select appropriate doses and determine

    PoDs (NOEL, NOAEL, STD10)

    based on preclinical toxicology results
  • Ensure all preclinical research and reports comply with

    GLP

    ,

    OECD

    ,

    ICH

    ,

    Indian Schedule Y

    , and other global regulatory guidelines
  • Contribute to

    pre-clinical/non-clinical development plans

    , including study design, data interpretation, and strategy support for pharmaceuticals, agrochemicals, biotechnology products, and medical devices
  • Provide

    risk assessment

    and regulatory support to ongoing

    R&D projects

  • Lead and mentor a

    team of 510 toxicology professionals

    , providing guidance and support throughout the study lifecycle
  • Resolve study-related, regulatory, and client-related issues in a timely and compliant manner
  • Collaborate effectively with

    cross-functional teams

    including Sponsors/Clients, Business Development, Project Management, and Technical Teams
  • Participate in on-site and telecon meetings to support client interactions and study updates

Preferred Qualifications:

  • M.sc / Ph.D. in Toxicology, Pharmacology, or related life sciences field
  • DABT Certification

    (preferred)
  • Proven expertise in

    preclinical toxicology

    ,

    risk assessment

    , and regulatory submissions
  • Strong knowledge of

    GLP

    ,

    OECD

    ,

    FDA

    ,

    EU

    ,

    REACH

    , and

    IND

    requirements
  • Excellent communication, leadership, and problem-solving skills
  • Willingness to

    relocate to Mysore

Desired Qualities:

  • Problem-Solving:

    Strong problem-solving skills with a proactive approach to addressing technical challenges.
  • Innovative Thinking:

    Ability to think critically and creatively to develop and implement new methodologies.
  • Time Management:

    Effective time management skills to balance multiple projects and meet deadlines.
  • Adaptability:

    Flexibility to adapt to changing priorities and project requirements.

What We Offer:

  • Competitive salary and benefits package
  • Opportunities for professional development and career advancement
  • A dynamic and inclusive work environment
  • Access to state-of-the-art research facilities and technology

Application Process:

hr@vipragen.com

Vipragen is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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