Manager / Assistant Manager - Regulatory Affairs

JOB DESCRIPTION:MAIN PURPOSE OF THE ROLEExperienced professional individual contributor that works under limited supervision.Applies subject matter knowledge in the area of Regulatory Affairs.Requires capacity to apply skills/knowledge within the context of specific needs or requirements.MAIN RESPONSIBILITIES• As the Experienced professional in the Regulatory Affairs Sub-Function, possesses well developed skills in directing development of product registration submission, progress reports, supplements, amendments, or periodic experience reports.• Interacts with regulatory agency to expedite approval of pending registration.• Serves as regulatory liaison throughout product lifecycle.• Participates in some of the following: product plan development and implementation, regulatory strategy, risk management, chemistry manufacturing control (CMC).• Ensures timely approval of new drugs, biologics or medical devices and continued approval of marketed products.• Serves as regulatory representative to marketing, research teams and regulatory agencies.• Advises development and/or marketing teams on manufacturing changes, line extensions, technical labeling, appropriate regulations and interpretations.QUALIFICATIONSEducationEducation Level    Major/Field of Study    or    EquivalentAssociates Degree (± 13 years)            Experience/BackgroundExperience    Experience DetailsMinimum 1 year    Licenses and CertificationsLanguage ProficiencyLanguage    Proficiency      The base pay for this position is N/AIn specific locations, the pay range may vary from the range posted.     JOB FAMILY:Regulatory Operations     DIVISION:EPD Established Pharma        LOCATION:India > Mumbai : BKC Building     ADDITIONAL LOCATIONS:     WORK SHIFT:Standard     TRAVEL:Not specified     MEDICAL SURVEILLANCE:Not Applicable     SIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)