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Sun Pharmaceuticals, Inc Senior Officer in India

Regulatory submission of new products, variations, response to queries, Life cycle management for Brazil including other LATAM countries through preparation of quality dossiers enabling timely approvals.

Area Of Responsibility

  1. New submissions:

a. Review & prepare CMC (Chemistry, Manufacturing and Controls) dossiers for fresh submissions.

b. Review documents (Development report, scale up report, specification, stability protocol), artworks etc.

before initiation of Exhibit batches for adequacy.

  1. Approval :

Review & prepare response to deficiency enabling approval of products filed to regulatory agency.

  1. Lifecycle management for drug formulations:

a. Prepare and review variations as per the country requirements to support approval of changes such as API

vendor changes/changes in ROS/test parameters; DF site changes; harmonization of products etc.

b. Prepare and review re-registration/PCH dossiers & submit the same to regional office/ regulatory agencies

  1. Regulatory compliance:

a. Prepare, Review and circulate approval package to stake holders upon receipt of approval and update the

same based on queries and variations.

b. Ensure reposition of comprehensive product information into central repository

C. Review regulatory filing impact of variations, change controls, etc.

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.