Regulatory Affairs Executives Fresher Hiring – Elevatia Solutions

Elevatia Solutions Hiring Regulatory Affairs Executive in New Delhi

Elevatia Solutions has announced a new hiring opportunity for the position of Regulatory Affairs Executive at its Sarojini Nagar, New Delhi location. The company is inviting applications from pharmacy and life sciences candidates interested in building careers in regulatory affairs, clinical research, pharmaceutical compliance, and CRO operations.

This recruitment drive is attracting candidates searching for regulatory affairs jobs in Delhi, clinical research vacancies, CRO jobs for freshers, pharmaceutical regulatory executive openings, CTD and eCTD submission careers, drug regulatory affairs jobs, and healthcare compliance opportunities.

Candidates with strong documentation skills, regulatory understanding, communication abilities, and interest in pharmaceutical compliance operations can apply for this opportunity.

Company Overview

Elevatia Solutions operates in the pharmaceutical and clinical research sector with focus areas including regulatory affairs operations, clinical research support, pharmaceutical compliance, healthcare documentation, and regulatory coordination activities.

The organization supports regulatory submissions, product registration processes, clinical documentation management, and pharmaceutical compliance functions aligned with healthcare industry standards.

Regulatory affairs and clinical research sectors continue to generate high demand for skilled professionals due to increasing pharmaceutical product approvals, healthcare compliance requirements, global submission standards, and drug safety regulations.

New Delhi remains one of India’s major hubs for pharmaceutical consulting, healthcare operations, regulatory services, and CRO activities, creating strong career opportunities for pharmacy and life sciences professionals.

Job Role & Responsibilities

Regulatory Affairs Executive Responsibilities

Candidates selected for this role will support regulatory operations and pharmaceutical compliance activities.

Key responsibilities include:

• Preparing and reviewing regulatory applications and dossiers
• Supporting regulatory submissions and technical documentation activities
• Preparing CTD and eCTD documentation
• Assisting ethics submissions to regulatory authorities
• Supporting product registration and approval processes
• Maintaining compliance with regulatory guidelines and SOPs
• Responding to regulatory queries and follow-up activities
• Assisting license and documentation management processes
• Supporting regulatory audits and inspection activities
• Assisting SAE and safety reporting operations
• Coordinating with regulatory offices and compliance teams
• Maintaining accurate documentation and reporting systems

Skills Required

Candidates should possess:

• Regulatory documentation skills
• Good communication abilities
• Coordination and follow-up skills
• Attention to detail
• Knowledge of CTD/eCTD submissions
• Understanding of regulatory guidelines
• Documentation management capabilities
• Time management and organizational skills
• Professional communication skills
• Ability to work in pharmaceutical and CRO environments

Candidates with exposure to pharmaceutical compliance systems, clinical research documentation, healthcare regulations, and CRO operations will have an advantage.

Eligibility / Qualifications

Educational Qualification

Candidates with pharmacy and life sciences educational backgrounds are eligible.

Relevant educational qualifications include:

B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, Microbiology, Clinical Research, Pharmaceutical Sciences.

Experience Requirement

• 0–2 years of experience
• Experience in Regulatory Affairs preferred
• Clinical Research or CRO experience preferred
• Pharmaceutical industry exposure preferred

These openings are suitable for:

• Regulatory affairs freshers
• Clinical research candidates
• CRO professionals
• Pharmacy graduates
• Pharmaceutical documentation specialists
• Healthcare compliance professionals
• Life sciences candidates seeking pharma careers

Location & Salary

Location

Sarojini Nagar, New Delhi

Estimated Salary

₹3.0 LPA – ₹5.8 LPA approximately

Salary may vary depending on regulatory affairs knowledge, CRO exposure, CTD/eCTD understanding, and communication skills.

Application Process

Interested candidates can apply by sending their updated CV through email.

Apply Through Email

• Reachus@ElevatiaSolutions.com

Frequently Asked Questions (FAQs)

1. What role is Elevatia Solutions hiring for?

Elevatia Solutions is hiring for the position of Regulatory Affairs Executive.

2. Which qualifications are eligible for this role?

Candidates with B.Pharm, M.Pharm, Pharm.D, Life Sciences, Biotechnology, and Clinical Research qualifications can apply.

3. Are freshers eligible for this regulatory affairs job?

Yes. Candidates with 0–2 years of experience are eligible.

4. What skills are preferred for this pharmaceutical role?

Knowledge of CTD/eCTD submissions, regulatory documentation, clinical research, and pharmaceutical compliance is preferred.

5. What is the estimated salary for Regulatory Affairs Executive roles?

The expected salary range is approximately ₹3.0 LPA to ₹5.8 LPA.

6. What is the work location for this opportunity?

The work location is Sarojini Nagar, New Delhi.

Summary Table

Company	Elevatia Solutions
Department Vacancies	Regulatory Affairs Executive
Qualification	B.Pharm, M.Pharm, Pharm.D, Biotechnology, Clinical Research, Life Sciences
Experience	0–2 Years
Location	Sarojini Nagar, New Delhi

Tagged as: Pharma Jobs in Delhi