IQVIA Regulatory Affairs Job
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IQVIA Regulatory Affairs Job For Life Sciences – Apply Online

Life sciences candidates are encouraged to apply for a Regulatory Affairs position that is vacant and available at IQVIA. IQVIA Regulatory Affairs Job For Life Sciences – Apply Online. For more details on the Job description, responsibilities and such, check out all the details posted below.

Job Title: Reg Affairs Officer 2

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Job ID: R1154308

Location: Bangalore, India

Job Overview:

An individual contributor who is fully proficient in applying subject matter knowledge for a professional discipline. Works under limited supervision.

Essential Functions:

  • Acts as a Regulatory Team Leader on more complex projects, which may include technical writing;
  • Prepares and/or reviews regulatory documentation in area of expertise, as appropriate;
  • Establishes relationships with many customers; may meet face to face without the rest of the team to discuss regulatory issues, present lessons learned and discuss customer comments;
  • Acts as an SME/ expert in Regulatory knowledge in Chemistry, Manufacturing and Controls/ Lifecycle Maintenance/ Marketing Authorization Transfers/ Labeling/ Publishing as applicable;
  • Understands the Scope of Work, deliverables and management of the budget for any given project and manages workload as appropriate;
  • May give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development;
  • May present to clients on complex regulatory processes at large full-service bid defence meetings by phone or in-person;
  • May act as a reviewer for regulatory standard operating procedures, as assigned and appropriate;
  • May prepare and deliver regulatory training to IQVIA small groups or individuals;
  • Performs other tasks or assignments, as delegated by Regulatory management;
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  • Bachelor’s Degree Degree in Lifescience or related discipline Req Or
  • Master’s Degree Degree in Lifescience or related discipline Req
  • At least 3-4 years of relevant experience
  • Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls, Preclinical and Clinical), laws and related guidelines, as appropriate;
  • Possesses a specific regulatory or technical expertise;
  • Good, solid interpersonal communication (oral and written) and organisation skills;
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients;
  • Strong software and computer skills, including Microsoft Office, publishing applications and tools, as applicable;
  • Demonstrates self-motivation and enthusiasm;
  • Ability to work on several projects, with direction from senior staff as appropriate;
  • Ability to follow standard operating procedures consistently; provides independent thought to assist in process improvements;
  • Ability to make decisions on discrete tasks under senior supervision;
  • Requires advanced knowledge within a specific discipline typically gained through extensive work experience and/or education;
  • Makes adjustments or recommended enhancements in systems and processes to solve problems or improve the effectiveness of job area;
  • Problems faced are general and may require an understanding of a broader set of issues, but typically are not complex;
  • Ability to adapt quickly to a rapidly changing environment;
  • Applicable certifications and licenses as required by the country, state, and/or other regulatory bodies
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