Cencora, through its affiliate PharmaLex India Private Limited, has announced two exciting trainee-level career opportunities in Noida, India. These roles are ideal for Life Sciences, Pharmacy, and Biomedical graduates seeking to enter Global Medical Writing or Regulatory Affairs with a reputed multinational organization.

Cencora is a global healthcare leader committed to creating healthier futures by supporting pharmaceutical, biotech, and medical device companies worldwide. If you are looking to build a long-term career in medical writing jobs in India or regulatory affairs trainee roles, this is a strong opportunity to begin your professional journey.

📌 Open Positions at Cencora

1️⃣ Trainee Specialist – CLS Global Medical Writing

Location: Noida, India
Employment Type: Full Time
Application Deadline: 27 February 2026

Key Responsibilities

• Perform systematic literature searches for regulatory and scientific documents
• Assist in preparation of pre-clinical and clinical sections of marketing authorization dossiers
• Support development of toxicology assessments such as PDE, OEL, and related documents
• Contribute to medical-scientific documents including publications, product rationales, and medico-marketing materials
• Collaborate with managers and cross-functional teams on global projects

Required Skills & Knowledge

• Strong command of English (written and verbal)
• Basic understanding of EU marketing authorization procedures
• Familiarity with toxicology and regulatory documentation
• Excellent MS Office and literature research skills
• High attention to detail and team-oriented mindset

2️⃣ Trainee – Regulatory Affairs

Location: Noida, India
Employment Type: Full Time
Application Deadline: 30 January 2026

Key Responsibilities

• Support regulatory submissions including applications, renewals, and variations
• Assist in documentation for pharmaceuticals, medical devices, cosmetics, herbal products, and food supplements
• Participate in regulatory intelligence and knowledge-sharing activities
• Support project planning and execution aligned with KPIs
• Work closely with regulatory leads and client teams

Qualifications & Skills

• University degree in Life Sciences / Pharmacy / Biotechnology
• Basic experience or strong willingness to learn regulatory processes
• Excellent organizational and time management skills
• Business-fluent English communication
• Strong service orientation and attention to detail

🎁 Benefits of Working at Cencora

• Exposure to global regulatory and medical writing projects
• Structured learning and on-the-job training
• Inclusive, diverse, and equal-opportunity workplace
• Competitive salary aligned with Indian market standards
• Long-term career growth within Cencora / PharmaLex global network

📝 How to Apply

Application Link for Trainee Specialist – CLS Global Medical Writing

Application Link for Trainee – Regulatory Affairs