Fresher Drug Regulatory Affairs (DRA) Hiring at Rivpra Formulation

Rivpra Formulation Pvt. Ltd.; Ghaziabad District; Presencial; INR 240.000 - 300.000; Jornada completa

Descripción de la vacante

Rivpra Formulation Pvt. Ltd. in Ghaziabad seeks M.Pharm freshers to join the Drug Regulatory Affairs team.

You will learn end-to-end regulatory processes, dossier compilation, submission, and product registration under experienced mentors. This role offers exposure to regulatory guidelines across global markets and practical insights into product documentation, labeling, and data management. Be part of a learning-centric setup in Kaushambi with a clear path to a career in DRA and regulatory

Formación

• M.Pharm fresh graduate in Pharmaceutics, Pharmaceutical Chemistry, or Regulatory Affairs.
• Fresher (0 years) with eagerness to learn in regulatory affairs.
• Male candidates preferred as per advertisement.
• Strong communication, analytical, and documentation skills.
• Proficient with MS Office, Excel, and PDF handling.

Responsabilidades

• Assist in preparation and submission of regulatory dossiers for domestic and international markets.
• Support labeling, artwork, and product registration activities.
• Maintain regulatory databases and product files.
• Coordinate with internal teams for regulatory documents.
• Stay updated with guidelines (USFDA, EMA, CDSCO, WHO, MHRA).

Descripción del empleo

DRA (Drug Regulatory Affairs) Fresher – M.Pharm | Ghaziabad

If you’re an M.Pharm fresher looking to build a strong foundation in the pharmaceutical regulatory field, this is your chance to join one of the most promising pharma organizations - Rivpra Formulation, located in Kaushambi, Ghaziabad.
This role offers exposure to Drug Regulatory Affairs, a vital area in ensuring the safety, efficacy, and compliance of pharmaceutical products across global markets.

Starting your career here means working alongside seasoned experts, learning end-to-end regulatory processes, and gaining practical insights into dossier compilation, submission, and product registration - the core of pharma compliance.

Rivpra Formulation Pvt. Ltd. is a reputed pharmaceutical manufacturing and formulation company, known for its commitment to quality, innovation, and global regulatory compliance.
With a strong presence in domestic and international markets, Rivpra adheres to GMP, WHO, and ICH guidelines and maintains a diverse product portfolio across multiple therapeutic segments.

By joining Rivpra, you’ll be part of a company that emphasizes research-driven manufacturing and continuous learning - ideal for professionals eager to grow in Drug Regulatory Affairs (DRA).

Job Role & Responsibilities

As a DRA Fresher, you will be trained and guided by the Regulatory Affairs team to understand pharmaceutical documentation, regulatory guidelines, and compliance processes.
Your core responsibilities will include:

• Assisting in preparation and submission of regulatory dossiers for domestic and international markets

• Supporting labeling, artwork, and product registration activities

• Maintaining and updating regulatory databases and product files

• Coordinating with internal teams for product information and compliance documents

• Staying updated with current regulatory guidelines (USFDA, EMA, CDSCO, WHO, MHRA)

This is a learning-centric position ideal for candidates aiming to specialize in pharma regulatory operations, drug licensing, or global dossier management.

Eligibility / Qualifications

• Qualification: M.Pharm (Master of Pharmacy) - preferably in Pharmaceutics, Pharmaceutical Chemistry, or Regulatory Affairs

• Experience: Fresher (0 years)

• Gender Preference: Male candidates preferred

• Essential Skills:

  • Strong communication and analytical ability

  • Understanding of basic pharmaceutical regulatory concepts

  • Attention to detail and willingness to learn documentation practices

  • Computer proficiency (MS Office, Excel, and PDF handling)

Relevant courses: M.Pharm in Pharmaceutics, M.Pharm in Pharmaceutical Chemistry, M.Pharm in Regulatory Affairs, M.Pharm in Industrial Pharmacy

Location & Salary

• Location: Kaushambi, Ghaziabad (Near Kaushambi Metro Station) - easily accessible via Delhi Metro

• Work Environment: Office-based, full-time position in a structured regulatory team setup

• Salary: As per company standards and candidate potential

This is a great opportunity for fresh M.Pharm graduates looking to begin their journey in a professional pharma regulatory environment.

FAQs

1. Who can apply for this position?
Only M.Pharm freshers (preferably male candidates) who are eager to start a career in Drug Regulatory Affairs may apply.

2. Is prior experience required?
No, this position is open to fresh graduates. Training and mentoring will be provided.

3. Where is the job located?
The role is based in Kaushambi, Ghaziabad, near the Kaushambi Metro Station - easily commutable from Delhi NCR.

4. What is the salary range for a DRA fresher?
Salary will be as per company norms, with performance-based growth opportunities in the regulatory domain.