Pharma, Clinical Research & Healthcare Jobs in India

Quality Analyst Trainee

Desirous

A full-time Quality Analyst Trainee opening based in Chennai for candidates with zero to one year of experience. The role focuses on examining laboratory data, documenting testing protocols, and supporting quality control initiatives.

Regulatory Affairs – Executive / Trainee

Axxelent Pharma Science Private Limited

Axxelent Pharma Science Private Limited is recruiting entry-level candidates for a Regulatory Affairs Executive / Trainee position based in Tharamani, Chennai. The role involves preparing dossier packages, formatting CTD / eCTD documents, and handling regulatory compliance workflows.

QA Documentation Intern – Smart Document System (SDS)

Pfizer

Pfizer's Chennai site is executing a Smart Document System (SDS) rollout that replaces paper-based laboratory logbooks and controlled forms with validated digital templates — a foundational step in the company's paperless-lab, documentation-control and data-integrity strategy. This 6–8 month internship places a science, pharmacy or engineering student directly inside that transformation, working alongside Quality, Engineering, Validation, Laboratory and Digital functions. Rather than merely shadowing, the intern owns template creation, field configuration, verification and qualification tracking for records that regulators routinely inspect. For a B.Pharm, M.Pharm, MSc or engineering graduate, this is rare early exposure to Good Documentation Practices, electronic records and GMP change control at a global pharmaceutical major — a credential that accelerates entry into QA, validation or regulatory documentation careers.

TMF Specialist (all levels)

ICON Strategic Solutions

TMF Specialist role supporting sponsor-dedicated clinical research projects through research, data collection, analysis, reporting, administrative support and workflow improvement.

Associate, Associate Database Analyst, Clinical Database Management

Pfizer

Associate-level Clinical Database Management role supporting data monitoring, query management, database design, clinical data systems, documentation quality, and process improvement.

Associate I– Reg CMC Strategy (LEC Team)

Pfizer

Associate I supporting Regulatory CMC Strategy activities for Legal Entity Change variations across global markets, including regulatory assessments, document coordination, CMC authoring, submission planning, and regulatory database activities.

Associate I – Reg CMC Strategy (LEC Team)

Pfizer

Support Regulatory CMC Strategy activities for Legal Entity Change variations across US, EU and ROW markets, coordinating global regulatory inputs, authoring impacted Module 3 sections and maintaining submission timelines under manager supervision.

Associate I-Reg CMC Strategy

Pfizer

Provide regulatory CMC strategy and documentation support for product license renewals and annual reports across global markets, with a focus on post-approval regulatory requirements.

HCE

Pfizer

Drive territory-level pharmaceutical sales and customer engagement while promoting Pfizer products to healthcare professionals, managing key accounts, supporting product availability, and maintaining strict compliance with company policies and procedures.

TMF Specialist (All Levels)

ICON