Roles and Responsibilities
Review regulatory, BD, and Grants documents for accuracy, language, and formatting errors
Flag deviations from required compliance or technical format for review by the concerned function
Maintain version control and track approval status across all documents
Maintain traceability between source information and the documents in which it is subsequently used
Maintain a centralized repository of trackers, templates, and reference documents
Act as a coordination point for Business Development documentation, including proposals, presentations, and vendor communications
Act as a coordination point for Grants-related documentation, including applications and reports
Liaise with internal stakeholders to gather inputs and ensure timely submission of documents
Support consistency of scientific and regulatory information across submissions, reports,
and BD materials
Coordinate with vendors and external parties for BD-related documentation and follow-ups
Learn and follow the company's documentation and coordination processes under guidance from the regulatory and BD teams
This role focuses on coordination and documentation of data, and business decisions are made by the relevant experts.
Educational Qualification
B.Pharm / M.Pharm / M.Sc. in Pharmaceutical Sciences, Biotechnology, Life Sciences or a related discipline.
M.Pharm in Pharmaceutical Quality Assurance, Pharmaceutics or Pharmacology would be preferred but is not mandatory.
An MBA in any specialization will be preferred but not mandatory.
Fresh graduates with solid documentation, coordination and communication capabilities are encouraged to apply