Bristol Myers Squibb Hiring B Pharma & M Pharma Candidates

Bristol Myers Squibb Hiring B Pharma & M Pharma Candidates - Apply Now

Bristol Myers Squibb Hiring B Pharma & M Pharma Candidates

Bristol Myers Squibb announces job opening for pharma candidates, B Pharma & M Pharma job opening 2022. Pharmacy job opening 2022. Bristol Myers Squibb job vacancy for pharma candidates. B Pharma job, M Pharma job opening 2022. Candidates with bachelor’s and master’s degree in pharma may apply for the job vacancy. Check out all the details on the same below:

Job Title: Manager, Regulatory Affairs India

Location: Mumbai, India

Department: Medical and Regulatory Affairs

Id: R1559270

Eligibility Criteria:

  • Required degrees, certifications, and/or licensure relevant to role- Bachelor’s degree or Master’s degree in science or equivalent or BPharm or MPharm
  • Professional experience with 5-10 years of relevant regulatory experience

Required Knowledge: Up-to-date regulatory knowledge required to do the job as described above, and experience with new drug development work for India registration

Required Skills: Excellent communication skill & fluency in English, good presentation skills, excellent strategic thinking ability, good negotiation skills, excellent leadership skills, excellent problem-solving ability, excellent coaching skills, and good facilitation skills.

Key Responsibilities

  • Coordinate, compile, and review all marketing and import registration applications and Clinical Trial applications, and maintenance applications.
  • Responsible for complying with the regulatory processes in line with business/R&D objectives to ensure timely registration of new products/line extensions and variation applications of BMS products.
  • Ensure the local labeling requirement are developed in alignment with local regulatory requirements and BMS standards
  • Responsible for assuring that approved labeling (PIL, PI, pack) is implemented in production in accordance with local legislation.
  • Responsible for filing clinical trial applications to the competent regulatory authorities in the country, and all following interactions, in line with BMS company policies and practices where applicable.
  • Responsible for interactions with Country Regulatory Authorities and feedback to BMS regarding product registrations.
  • Drives and supports local projects and department-related assignments.
  • Responsible for the identification of opportunities to improve departmental functions/processes.
  • Responsible for keeping up to date with the regulatory environment within the industry.
  • Responsible for archiving of regulatory files and documentation and maintenance of regulatory databases.
  • Work closely with key partners, global regulatory team and country business function, medical function, Clinical Operations function, Market Access function and Logistics function.
  • Creates and updates local procedural documents.

Editors Note: Bristol Myers Squibb Hiring Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.

Source link

Leave a Reply

Your email address will not be published. Required fields are marked *