DDReg Pharma Hiring Regulatory Affairs Trainees | M.Pharm Freshers
- DDReg Pharma Hiring Regulatory Affairs Trainees in Gurgaon | M.Pharm Freshers Can Apply
- DDReg Pharma Pvt. Ltd. Company Overview
- Regulatory Affairs Trainee Vacancy Details
- Department
- Designation
- Job Type
- Job Location
- Experience Required
- Number of Vacancies
- Key Responsibilities of Regulatory Affairs Trainee
- Core Responsibilities
- Eligibility Criteria and Educational Qualification
- Required Qualification
- Relevant Courses Accepted
- Preferred Skills
- Preferred Certifications
- Application Process
- Apply Here
- Frequently Asked Questions
- Is this DDReg Pharma job open for freshers?
- What qualification is required for this regulatory affairs job?
- What is the job location for this role?
- Is Regulatory Affairs a good career option in the pharmaceutical industry?
- What is the expected salary for freshers?
- Is experience mandatory for this role?
- Where can candidates apply for this vacancy?
DDReg Pharma Hiring Regulatory Affairs Trainees in Gurgaon | M.Pharm Freshers Can Apply
Freshers looking to build a long-term career in pharmaceutical regulatory affairs now have an excellent opportunity with DDReg Pharma Pvt. Ltd. The company is hiring Regulatory Affairs Trainees for its Gurgaon office. This full-time pharma job is ideal for M.Pharm graduates who want hands-on exposure to global regulatory submissions, CTD/eCTD documentation, dossier preparation, and pharmaceutical compliance management.
DDReg Pharma currently has openings for the position of Regulatory Affairs Trainee in the Regulatory Affairs department. Candidates with a Pharmacy or Life Sciences background who are interested in clinical research, regulatory compliance, pharma documentation, pharmacovigilance support, and global healthcare operations can apply for this fresher pharma job opportunity in Haryana.
The role offers practical training in regulatory submission processes for US, EU, and emerging markets, making it one of the most valuable entry-level pharmaceutical industry jobs for freshers in India.
DDReg Pharma Pvt. Ltd. Company Overview
DDReg Pharma Pvt. Ltd is a growing pharmaceutical consulting and regulatory services company serving global pharma and biopharma organizations. The company specializes in Regulatory Affairs, Pharmacovigilance, GMP Compliance, Intellectual Property Rights, Toxicology, and Quality Assurance services.
With expertise in global pharmaceutical regulations and product lifecycle management, DDReg Pharma supports healthcare and life sciences companies in accelerating drug approvals and ensuring compliance with international regulatory standards. The company also uses AI-driven regulatory intelligence systems and advanced Regulatory Information Management Systems (RIMS) to improve submission efficiency and compliance management.
For freshers aiming to enter the pharmaceutical industry, DDReg Pharma provides strong learning exposure, regulatory documentation training, compliance management experience, and opportunities to work on global healthcare projects.
Regulatory Affairs Trainee Vacancy Details
Department
- Regulatory Affairs
Designation
- Regulatory Affairs Trainee
Job Type
- Full-Time
- Onsite
Job Location
- Gurgaon, Haryana, India
Experience Required
- Freshers
- Candidates with internship exposure in regulatory affairs or pharmaceutical documentation may have an added advantage
Number of Vacancies
- Multiple openings expected based on current hiring activity
Key Responsibilities of Regulatory Affairs Trainee
Candidates selected for this pharmaceutical regulatory affairs job will work closely with experienced regulatory professionals and gain exposure to global pharma compliance operations.
Core Responsibilities
- Assist in preparing and assembling regulatory dossiers for global submissions
- Support CTD and eCTD documentation activities
- Operate electronic publishing and submission validation tools
- Participate in pharmaceutical product lifecycle management activities
- Maintain regulatory product history logs and submission trackers
- Review pharmaceutical artwork and labeling documents for compliance
- Coordinate with internal regulatory teams and external stakeholders
- Support dossier compilation and submission processes for US, EU, and emerging markets
- Assist in drafting responses to regulatory authorities
- Ensure regulatory documentation follows international compliance standards
- Participate in project tracking and regulatory operations management
This role gives candidates valuable exposure to pharmaceutical compliance consulting, healthcare documentation management, medical regulatory writing, and global regulatory strategy operations.
Eligibility Criteria and Educational Qualification
Candidates applying for this pharma fresher job should meet the following eligibility requirements.
Required Qualification
- Bachelor’s Degree in Pharmacy
- Master’s Degree in Pharmacy (M.Pharm Preferred)
- Life Sciences graduates may also be considered
Relevant Courses Accepted
B.Pharm, M.Pharm, Pharmaceutics, Pharmaceutical Analysis, Pharmaceutical Chemistry, Pharmacology, Clinical Pharmacy, Regulatory Affairs, Pharmaceutical Biotechnology, Biotechnology, Microbiology, Biochemistry, Life Sciences
Preferred Skills
- Knowledge of pharmaceutical regulatory affairs processes
- Understanding of CTD/eCTD structure and submission workflows
- Familiarity with regulatory compliance standards
- Good written and verbal communication skills
- Strong attention to detail
- Knowledge of MS Office and regulatory documentation tools
- Ability to work in deadline-driven pharmaceutical environments
- Good coordination and project management skills
Preferred Certifications
- Regulatory Affairs Certification (Preferred but not mandatory)

Application Process
Interested and eligible candidates can apply directly through the official LinkedIn job posting.
Apply Here
🔗 https://www.linkedin.com/jobs/view/4409343531/
Candidates are advised to keep the following documents ready before applying:
- Updated Resume
- Educational Certificates
- Internship Certificates (if available)
- Government ID Proof
- Passport-size Photograph
Applicants should ensure their resume highlights pharmaceutical regulatory knowledge, project work, internships, software skills, and communication abilities
Frequently Asked Questions
Is this DDReg Pharma job open for freshers?
Yes. This Regulatory Affairs Trainee position is mainly targeted toward freshers and early-career candidates with M.Pharm or Pharmacy backgrounds.
What qualification is required for this regulatory affairs job?
Candidates with B.Pharm, M.Pharm, or relevant Life Sciences qualifications are eligible to apply.
What is the job location for this role?
The work location is Gurgaon, Haryana, India.
Is Regulatory Affairs a good career option in the pharmaceutical industry?
Yes. Regulatory Affairs is considered one of the most stable and high-growth career paths in the pharmaceutical and healthcare sector due to increasing global compliance requirements.
What is the expected salary for freshers?
Freshers may expect an approximate salary package between ₹2.8 LPA and ₹4.5 LPA based on skills and qualifications.
Is experience mandatory for this role?
No. Freshers can apply. Internship exposure in pharmaceutical documentation or regulatory affairs can be beneficial.
Where can candidates apply for this vacancy?
Candidates can apply through the official LinkedIn application link provided in the article.
| Category | Details |
|---|---|
| Company | DDReg Pharma Pvt. Ltd. |
| Vacancies | Regulatory Affairs Trainee |
| Required Education | B.Pharm, M.Pharm, Life Sciences |
| Experience | Freshers Eligible |
| Job Location | Gurgaon, Haryana, India |
| Employment Type | Full-Time, Onsite |
| Salary | ₹2.8 LPA – ₹4.5 LPA (Approx.) |
| Department | Regulatory Affairs |
| Application Mode | Online |
| Apply Link | https://www.linkedin.com/jobs/view/4409343531/ |
To apply for this job please visit www.linkedin.com.