UnimediCo Labs, a growing pharmaceutical manufacturing company, is currently hiring DRA Trainee / Chemist / Junior Officer – Drug Regulatory Affairs at its facility in Pharma City, Dehradun, Uttarakhand.
This Regulatory Affairs fresher job in Dehradun is ideal for candidates with B.Pharm, M.Pharm, or M.Sc in Pharmaceutical Sciences who are interested in regulatory documentation, pharmaceutical submissions, and global product registration processes.
The role provides hands-on exposure to ACTD, CTD dossiers, regulatory submissions, and pharmaceutical documentation, making it a strong entry-level opportunity in the pharmaceutical regulatory affairs sector.
Job Overview
- Position: DRA Trainee / Chemist / Jr. Officer – Drug Regulatory Affairs
- Company: UnimediCo Labs
- Location: Pharma City, Dehradun, Uttarakhand, India
- Experience: Fresher / 0–1 Year
- Qualification: B.Pharm / M.Pharm / M.Sc (Pharmaceutical Sciences)
- Industry: Pharmaceutical Manufacturing
- Department: Regulatory Affairs
Key Responsibilities
Candidates selected for this Regulatory Affairs fresher job in the pharmaceutical industry will be responsible for supporting regulatory documentation and submission processes.
Main responsibilities include:
- Assisting in preparation and compilation of regulatory dossiers such as ACTD, CTD, and country-specific submissions
- Supporting documentation required for pharmaceutical product registrations in regulated and semi-regulated markets
- Preparing regulatory documents including:
- Product Information (PI)
- Patient Information Leaflet (PIL)
- Summary of Product Characteristics (SmPC)
- Package Inserts
- Coordinating with Quality Assurance (QA), R&D, and Production teams for regulatory documentation
- Maintaining regulatory databases, submission records, and documentation archives
- Supporting internal regulatory compliance and submission readiness
This role helps fresh graduates gain real-world exposure to global regulatory submissions and pharmaceutical compliance requirements.
Required Qualifications
Candidates applying for this Drug Regulatory Affairs fresher job should meet the following requirements:
- B.Pharm, M.Pharm, or M.Sc in Pharmaceutical Sciences
- 0–1 year experience (freshers are welcome to apply)
- Strong interest in Regulatory Affairs in the pharmaceutical industry
- Good documentation and communication skills
- Basic understanding of pharmaceutical regulatory guidelines (preferred but not mandatory)
- Ability to collaborate with cross-functional teams
Skills That Will Be an Advantage
For candidates pursuing a career in pharmaceutical regulatory affairs, the following skills will be beneficial:
- Knowledge of CTD and ACTD dossier preparation
- Familiarity with drug registration processes
- Understanding of pharmaceutical documentation standards
- Strong attention to detail
- Regulatory compliance awareness
Why Start a Career in Regulatory Affairs?
Regulatory Affairs is one of the fast-growing career paths in the pharmaceutical industry. Professionals in this field ensure that pharmaceutical products meet global regulatory standards and compliance requirements.
Benefits of starting as a DRA trainee include:
- Exposure to global pharmaceutical regulatory submissions
- Career growth in international regulatory markets
- Opportunities to work with R&D, QA, and manufacturing teams
- Strong demand across pharma manufacturing and regulatory consulting companies
Salary & Benefits (Estimated)
For entry-level Regulatory Affairs fresher jobs in India, the typical salary range is:
- ₹2.5 LPA – ₹4.2 LPA (depending on skills and qualifications)
Additional benefits may include:
- Professional training in regulatory submissions
- Industry exposure to dossier preparation
- Career growth in regulatory affairs departments
How to Apply
Interested candidates can apply directly by sharing their updated CV.
📧 Email: hr@unimedicolabs.com