Bayer Pharmacy & Pharmaceutical Science Job - 1 Year Experience Required

Bayer Pharmacy & Pharmaceutical Science Job – Apply Online

Bayer Regulatory affairs job opening 2022. Pharmacy job opening 2022. Pharmaceutical Science job opening 2022. Candidates with bachelor’s and master’s degree in pharmacy and pharmaceutical science may apply for the job opening at Bayer. Intrested and eligible candidates may check out all the details on the same below:

Job Title: Liaisoning Specialist – Regulatory Affairs

Elibgility Criteria & Experience:

  • Bachelor’s degree in Science (B Sc/MSc) / Pharmacy/Pharmaceutical Sciences or other Life Sciences/ technical subjects or related discipline with 1-2 years of regulatory affairs experience in the pharmaceutical industry
  • Have experience liaising with the Govt bodies /Institutions
  • Ability to work independently and with diverse stakeholders
  • Have basic communication skills, both oral and written to interact with stakeholders based in various locations and diverse local stakeholders
  • Ability to multi-task and work to competing, tight deadlines. Ability to prioritize workload to deliver on pre-agreed KPIs
  • Computer literacy with MS Office. SharePoint is highly desired. Willingness to learn new systems and processes as required
  • Motivated self-starter with good interpersonal, organization, and problem-solving skills

Responsibilties: 

  • Act as the one-point contact for DCGI/ FDA and other govt bodies
  • Receiving the documents for DCGI/FDA/Govt Bodie’s submission and doing the submission
  • Keeping track on the applications and the query response submitted to the DCGI /FDA /Govt Bodies
  • Giving an heads up of any anticipated questions /feedback from DCGI/FDA/Govt bodies
  • Facilitating meetings and cooperation among people, agencies and Bayer colleagues during the visit to these govt institutions
  • Keeping a track on the new regulations and giving an update on the same
    identifying issues in communication and coordination within the company or organization and creating solutions for overcoming these challenges
  • Prepare documents to support licensing activities (eg. submissions, testing and import licenses, tenders, safety reporting, post-approval commitments) to the India health authority and other government institutions
  • Support process improvements and implementation of best practices within RA India
  • Database maintenance: timely and accurate maintenance and updating of tracking sheets, contact reports, and regulatory information as defined by RA India KPI
  • Support for follow-up in CDL/IPC/NIBL and another govt lab

Click Here To Apply Online

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