Pharma Regulatory Analyst Vacancy @ Accenture - Apply Online

Pharma Regulatory Analyst Vacancy @ Accenture – Apply Online

Accenture announces job opening for pharma candidates. B Pharma job opening 2023. B Pharma job vacancy 2023. Pharma Analyst-Regulatory job opening 2022. Analyst-Regulatory job opening 2023. Candidates with a bachelor’s degree in pharma may apply for the job opening at Accenture

Job Title: Analyst

Job Location: Bengaluru

Qualifications: Bachelor of Pharmacy/Master of Pharmacy

Years of Experience: 3-5 years

Skill required: Regulatory – Life Sciences Regulatory Operations

What are we looking for?

They are looking for individuals who have the following skillset:

  • Ability to perform under pressure
  • Ability to establish strong client relationship
  • Commitment to quality
  • Written and verbal communication
  • Collaboration and interpersonal skills

Roles and Responsibilities

  • In this role, you are required to analyze and solve lower-complexity problems
  • Your day-to-day interaction is with peers within Accenture before updating
  • supervisors you may have limited exposure with clients and/or Accenture management
  • You will be given moderate-level instructions on daily work tasks and detailed instructions on new assignments
  • You will need to be well versed with basic statistics and terms involved in the day to day business and use it while discussing with stakeholders
  • You will be expected to constantly be on the lookout for ways to enhance value for your respective stakeholders/clients
  • The decisions you make impact your work and may impact the work of others
  • You will be an individual contributor as a part of a team, with a focused scope of work.

What would you do?

  • The Healthcare Operations vertical helps our clients drive breakthrough growth by combining deep healthcare delivery experience and subject matter expertise with analytics, automation, artificial intelligence and innovative talent. We help payers, providers and government agencies increase provider, member and group satisfaction, improve health outcomes and reduce costs.
  • You will be working as a part of the Labeling, Artwork review and Product Registrations team which is responsible for preparation & review of the data in the Regulatory database as well as ensuring Product Registrations with the local Health Authorities. In addition you will also be working with raw material Suppliers for ingredient information. You may also be required to do Case processing of customer complaints. Additionally, manage end to end Product Core and Country Labelling and its respective repository.
  • You will be expected to coordinate the essential documentation and resources required for the filing of global applications. Understand, manage & process electronic submissions that include original application filings, Life Cycle Management submissions such as CMC, Ad-promos, amendments, annual reports, SPL submissions, etc.

Apply Online

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