Head Regulatory Affairs (india)

Year    Gurgaon, Haryana, India

Job Description

Reporting to: Sr. Vice President - Regulatory Affairs
Qualification: Master's Degree in Pharmacy, PhD in Pharmacology or Pharmaceutics (desirable).
Experience: 10+ years
Location: Baroda / Mumbai.
Responsibilities:

  • Work with various cross-functional teams within the organization to ensure that availability of a development, execution and submission pathway for submission of products for India market ensuring first time approval/first mover advantage.
  • Develop optimum regulatory pathway for product approval to ensure competitive advantage for new drugs/FDC/devices/neutraceuticals etc.
  • Participate and provide regulatory guidance to development and other teams during the development to ensure right data is generated and presented in the submission.
  • Provide regulatory guidance for protocol design for clinical studies that are cost efficient and productive.
  • Participate in SEC and other related discussions to represent regulatory view point.
  • Support manufacturing plants during inspections.
  • Provide support to life cycle management and business continuity for current products such as transfers.
  • Work with CROs/CMOs to support out sourcing by providing regulatory inputs.
  • Ensure procurement and renewal of Licenses of all locations for the outsourced products.
  • Ensure regulatory compliances at Company's warehouses and godowns.
  • Work with IP commission, NIB, Central and State Laboratories for company related issues.
  • Draft and submit appropriate justifications and representation to State and Zonal offices Central HQ in cases of NSQ issues reported in monthly drug alert.
Technical Skills
  • Thorough understanding of applicable rules and regulations including Indian Drugs & Cosmetics Act, Medical Device, NDCT Rules, Nutraceutical and other regulations.
  • Regulatory understanding of licensing requirements as applicable for development and commercialization of products in India.
  • Familiarity of Indian systems impacting regulatory workflows.
  • Familiarity with licensing authorities in India including CDSCO.
  • Understanding of different pharmaceutical dosage forms.
Personal Skills
  • Negotiation skills.
  • Communication & presentation - written and verbal.
  • Attention to detail.
  • Willingness to challenge the status quo and ask questions.
  • Curiosity.
  • The ability to listen and learn.
  • Able to view issues from a holistic perspective.
  • Passionate and proactive.
  • Time management.
  • Problem solving.
  • Ability to work in large teams and lead a team.

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Job Detail

  • Job Id
    JD3978307
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Gurgaon, Haryana, India
  • Education
    Not mentioned
  • Experience
    Year