Apprentice - Business Strategy

Zydus Lifesciences
πŸ‘œ 0 - 2 years
πŸ“ Ahmedabad, Gujarat
πŸ’Ό Full-Time
πŸ’° Not Disclosed
Posted on May 09, 2026

Job Description:

πŸš€ WE’RE HIRING – APPRENTICE BUSINESS STRATEGY (REGULATORY AFFAIRS) πŸš€

Looking to start your career in Regulatory Affairs and pharmaceutical compliance? Zydus Lifesciences is hiring freshers and early-career pharmacy professionals for the role of Apprentice – Business Strategy in Ahmedabad.

This is an excellent opportunity for B.Pharm and M.Pharm graduates specializing in Regulatory Affairs, Pharmaceutics, or Quality Assurance to gain hands-on exposure to CDSCO submissions, CTD/eCTD documentation, regulatory compliance, and pharmaceutical business strategy operations.

Candidates interested in Regulatory Affairs jobs, CDSCO documentation careers, and pharmaceutical compliance roles should definitely explore this opportunity.

🏒 Company: Zydus Lifesciences 
🌐 Website: https://www.zyduslife.com ;

πŸ‘‰ Role: Apprentice – Business Strategy 
πŸ‘‰ Department: Legal & Regulatory 
πŸ‘‰ Experience: 0–2 Years 
πŸ“ Location: Ahmedabad, Gujarat 
🧾 Job Type: Full-Time, Temporary/Contractual 
🏒 Industry: Pharmaceutical & Life Sciences 

🧾 Role Overview:
The selected candidate will support regulatory and business strategy operations related to pharmaceutical regulatory submissions, CDSCO documentation, and compliance activities. This role provides practical exposure to regulatory dossier preparation, CTD/eCTD documentation, CMC review processes, and coordination with cross-functional pharmaceutical teams.

πŸ”§ Key Responsibilities:
β€’ Support applications submitted to CDSCO, New Delhi 
β€’ Assist in obtaining marketing authorization for new drugs 
β€’ Handle import and registration documentation for APIs, finished formulations, medical devices, IVDs, and cosmetics 
β€’ Review dossiers related to CMC documentation 
β€’ Support API characterization and impurity documentation review 
β€’ Review stability studies, degradation products, and process validation documents 
β€’ Assist with QA controls and manufacturing documentation review 
β€’ Prepare and review CTD/eCTD documentation 
β€’ Coordinate with internal cross-functional teams 
β€’ Support regulatory compliance activities under: 
β€’ New Drugs and Clinical Trial Rules, 2019 
β€’ Drugs and Cosmetics Act & Rules, 1945 

πŸ›  Required Skills:
β€’ Knowledge of CDSCO regulatory processes 
β€’ Understanding of CTD/eCTD documentation 
β€’ Basic understanding of CMC dossier review 
β€’ Familiarity with Indian pharmaceutical regulatory guidelines 
β€’ Strong coordination and communication skills 
β€’ Ability to manage documentation and compliance activities 
β€’ Good analytical and organizational abilities 

πŸŽ“ Required Qualifications:
β€’ B.Pharm or M.Pharm in: 
β€’ Regulatory Affairs 
β€’ Pharmaceutics 
β€’ Quality Assurance 

πŸ’‘ Preferred Skills / Requirements:
β€’ Interest in pharmaceutical regulatory affairs and compliance 
β€’ Understanding of pharmaceutical documentation standards 
β€’ Knowledge of regulatory submission workflows 
β€’ Strong willingness to learn regulatory operations and business strategy 

✨ Why Join Zydus Lifesciences?
β€’ Excellent entry-level opportunity in Regulatory Affairs 
β€’ Exposure to CDSCO submissions and pharmaceutical compliance 
β€’ Hands-on experience with CTD/eCTD documentation 
β€’ Opportunity to work with experienced regulatory professionals 
β€’ Strong long-term career growth in pharmaceutical regulatory affairs 
β€’ Opportunity to work with one of India’s leading pharmaceutical companies 

🌟 About Zydus Lifesciences:
Zydus Lifesciences is one of India’s leading pharmaceutical organizations known for innovation, regulatory excellence, research-driven healthcare solutions, and strong global presence in pharmaceutical manufacturing and development.

πŸ’¬ Join WhatsApp Group: 
Join Now

⚑ If you are a pharmacy graduate looking to build a successful career in Regulatory Affairs, CDSCO submissions, and pharmaceutical compliance, this opportunity at Zydus Lifesciences could be the perfect starting point.

Required Skills:

Knowledge of CDSCO regulatory processes, Understanding of CTD/eCTD documentation, Basic understanding of CMC dossier review, Familiarity with Indian pharmaceutical regulatory guidelines, Strong coo...

About Zydus Lifesciences

βœ” Verified