Synthimed Hiring Trainee DRA
- Company Overview
- Job Role & Responsibilities
- Trainee – Drug Regulatory Affairs (DRA)
- Eligibility / Qualifications
- Relevant Courses (for broader eligibility reach)
- Location & Salary
- Application Process
- FAQs
- Is this role suitable for freshers?
- Do I need prior regulatory experience?
- What skills will I develop here?
- Which backgrounds are preferred?
- Is relocation required?
- Summary Table
MSc Organic Chemistry Trainee DRA Vacancy | Chandigarh & Mohali
Synthimed hiring MSc Organic Chemistry candidates for Trainee DRA role in Chandigarh, Mohali, Derabassi. Apply now.
Drug Regulatory Affairs is a strong career path for candidates who want to build expertise in regulatory documentation, compliance, and dossier preparation. Synthimed is opening a trainee-level opportunity for fresh and early-career graduates with a solid understanding of organic chemistry and an interest in regulatory systems. This role suits candidates looking for structured learning, hands-on exposure to regulatory submissions, and long-term career growth in the pharmaceutical regulatory field.
Company Overview
Synthimed is involved in research, development, and regulatory support services for pharmaceutical products. The company works with global regulatory frameworks, documentation standards, and compliance systems that help streamline product submissions and lifecycle management. Joining the team gives candidates exposure to real-world regulatory documentation, structured review processes, and professional development within an established pharma environment.
Job Role & Responsibilities
Trainee – Drug Regulatory Affairs (DRA)
- Assist in preparing regulatory documents, technical files, and product dossiers
- Support compilation and review of data for regulatory submissions
- Learn regional and international regulatory guidelines (ICH, WHO, CDSCO)
- Maintain documentation accuracy and follow established workflow systems
- Perform literature searches, regulatory data checks, and basic analytical comparisons
- Work closely with the regulatory team to support ongoing submissions and updates
Eligibility / Qualifications
- M.Sc in Organic Chemistry
- Candidates with a Drug Regulatory Affairs study background are also eligible
- Strong fundamentals in organic chemistry, reaction mechanisms, and chemical analysis
- Good documentation, analytical thinking, and process-oriented mindset
Relevant Courses (for broader eligibility reach)
M.Sc Organic Chemistry, M.Sc Analytical Chemistry, M.Sc Pharmaceutical Chemistry, M.Sc Chemistry, PG Diploma in Regulatory Affairs, Certificate in DRA Documentation, M.Pharm Regulatory Affairs.
Location & Salary
- Locations: Chandigarh, Mohali, Derabassi
- Salary: As per company standards (competitive for trainee roles)
Application Process
Interested candidates can apply through:
- Email: astha.trivedi@synthimed.com
- Contact: +91 89683 74200
Ensure your email includes updated resume, contact details, and preferred location.
FAQs
Is this role suitable for freshers?
Yes. The trainee position is designed for fresh graduates with strong chemistry fundamentals.
Do I need prior regulatory experience?
No. Basic understanding of organic chemistry and willingness to learn regulatory concepts are sufficient.
What skills will I develop here?
You will gain hands-on exposure to regulatory documentation, dossier preparation, compliance review, and technical writing.
Which backgrounds are preferred?
M.Sc Organic Chemistry is the primary requirement, but candidates with DRA training or certificates can also apply.
Is relocation required?
Candidates must be willing to work at any of the listed locations: Chandigarh, Mohali, or Derabassi.
Summary Table
| Company | Synthimed |
|---|---|
| Vacancies | Trainee – Drug Regulatory Affairs |
| Required Education | M.Sc Organic Chemistry, DRA background |
| Experience | Freshers or early-career candidates |
To apply for this job email your details to astha.trivedi@synthimed.com
