Table of Contents
Freshers Chemistry DRA Jobs at Synthimed Labs Private Limited
Trainee – Drug Regulatory Affairs (DRA)
Company: Synthimed Labs Private Limited
Industry: Pharmaceutical Research & Regulatory Support
Job Type: Full-Time (Trainee)
Experience Level: Freshers / Early-Career Candidates
Job Location: Chandigarh | Mohali | Derabassi
About the Company
Synthimed Labs Private Limited is a pharmaceutical research and regulatory support
organisation offering end-to-end regulatory solutions aligned with global regulatory
frameworks such as ICH, WHO, and CDSCO. The company specialises in regulatory
documentation, product dossier preparation, submissions, data evaluation, and lifecycle
management for regulated and semi-regulated markets. Synthimed provides an excellent
learning environment for candidates aspiring to build a long-term career in Drug Regulatory
Affairs.
Job Description
Synthimed is hiring fresh graduates for the position of Trainee – Drug Regulatory Affairs
(DRA). The selected candidates will work closely with the regulatory team to support
documentation, submissions, and compliance activities. This role offers hands-on
exposure to real-time regulatory processes and international compliance standards.
Roles & Responsibilities
- Assist in the preparation, compilation, and review of regulatory documents and product
dossiers - Support regulatory submissions in accordance with ICH, WHO, and CDSCO guidelines
- Perform literature reviews and verify regulatory and technical data
- Maintain accurate and compliant regulatory documentation
- Support lifecycle management activities including variations, amendments, and updates
- Coordinate with internal teams to collect regulatory data and meet submission timelines
- Learn and apply global and regional regulatory requirements and compliance processes
Eligibility & Qualifications
Candidates must have one of the following qualifications:
M.Sc. in Organic Chemistry (preferred)
M.Sc. in Analytical Chemistry / Pharmaceutical Chemistry
PG Diploma or Certificate in Drug Regulatory Affairs
M.Pharm in Regulatory Affairs
Required Skills & Competencies
• Strong understanding of organic chemistry concepts and reaction mechanisms
• Basic knowledge of regulatory guidelines and pharmaceutical documentation
• Good analytical, organizational, and documentation skills
• High attention to detail and accuracy
• Willingness to learn regulatory frameworks and compliance processes
• Good written and verbal communication skills
Experience
• Freshers and early-career candidates are eligible to apply
Salary & Benefits
• Salary: ₹18,000 – ₹25,000 per month (as per industry standards)
• Structured regulatory training and professional mentorship
• Exposure to global regulatory frameworks (ICH, WHO, CDSCO)
• Hands-on experience in dossier preparation and regulatory compliance
• Excellent opportunity for long-term career growth in Drug Regulatory Affairs
