HYDERABAD · FULLTIME
Documentation Management Executive
Ang Lifesciences
Hyderabad · onsite · Posted 25d ago
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Section · 01
About this role
Role & responsibilities
- Act as the Document Management Executive for QA, BD, and Grants; the single point of contact for how documents are received, reviewed, and tracked across all three areas
- Review documents received from external partners, clients, and funding organizations to ensure accuracy, completeness, and adherence to quality standards. Maintain a clean, organized document management system/ Trackers so QA records are always easy to locate and audit-ready. Seek clarity if needed from external partners, clients, and funding organizations
- Verify documentation for compliance with GMP, GDP, and data integrity (ALCOA+) principles. Coordinate with different departments for document preparation, review, approval, and implementation. Maintain document history logs, master lists, and tracking records.
- Coordinate with internal teams to collect the documents to be sent to external partners, clients, and funding organizations who need them from the company on time and from time to time.
- Send the right and appropriate documents to external partners, clients, and funding organizations on time, and track their status until closure
- Maintain tracking sheet of every document- pending, sent, received
- Support the preparation and submission of grant proposals, manage post-submission and approval correspondence, and maintain comprehensive documentation from initial draft through final submission. Coordinate with internal teams and external partners to ensure grant documentation comes together accurately and on schedule
- Flag missing, outdated, or incorrect documents and taking corrective actions for the same along with stakeholders before it causes avoidable issues
- Build and maintain a reliable/ retrievable / available in a suitable medium for filing and tracking system that any team member can use to find what they need, when they need it
Who We're Looking For
- M.Sc./ M Pharm graduate, ideally with a background in QA or Pharmacovigilance
- 15 years of experience in QA, RA and associated Document Management
- Ability to assimilate new processes quickly
- Strong organizational skills and attention to intricate detail
- High level of fluency in written and verbal communication in English
- Reasoning skills
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Section · 02
Skills
Section · Company
About Ang Lifesciences

Ang Lifesciences
Pharma
175
employees
2006
20 years old
Amritsar,Punjab
India
₹3.4L PA avg
Avg at Ang Lifesciences
About
At Aodh Lifesciences, we are building a next-generation deep science drug development company focused on redefining respiratory drug delivery through a regulatory-driven approach. Our work integrates translational biology, microbiology, advanced formulation and device engineering, PBPK modelling, IVIVC modelling, and regulatory-grade data generation to develop targeted therapies designed to improve local efficacy while minimizing systemic exposure and addressing antimicrobial resistance. We are looking for driven individuals who are curious, think deeply about the science, and are excited to take ownership in a zero-to-one environment, building not just products but a globally relevant, regulatory-grade R&D ecosystem from the ground up.
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Culture
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Career growth
3.3
Work-life
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