Corelex Solutions Hiring Freshers for Regulatory Affairs Roles in Delhi

Are you a recent graduate looking to build a rewarding career in the pharmaceutical industry? Do you aspire to work in regulatory affairs, compliance management, drug approvals, and healthcare documentation? If yes, then this opportunity could be the perfect launchpad for your professional journey.

M/s. Corelex Solutions Pvt Ltd has announced recruitment for the position of Regulatory Affairs Fresher at its Delhi office. This opening is ideal for B.Pharm, B.Sc Life Sciences, and M.Sc graduates who want to enter the growing field of pharmaceutical regulatory affairs.

The pharmaceutical and healthcare sectors are among the fastest-growing industries in India. As regulatory requirements become more complex across global markets, companies are actively seeking talented professionals who can help ensure compliance with national and international regulations.

This recruitment drive provides fresh graduates with an excellent opportunity to gain hands-on experience in dossier preparation, documentation management, regulatory submissions, and compliance-related activities.

In this article, you will find complete details regarding eligibility criteria, job responsibilities, required skills, benefits, application process, and career growth opportunities associated with this position.

🏢 About Corelex Solutions Pvt Ltd

Corelex Solutions Pvt Ltd is a regulatory consulting and compliance services company that supports pharmaceutical, biotechnology, medical device, cosmetics, and food businesses.

The organization assists manufacturers and healthcare companies in navigating complex regulatory frameworks established by authorities such as:

CDSCO (Central Drugs Standard Control Organisation)
FSSAI (Food Safety and Standards Authority of India)
State Drug Authorities
International Regulatory Bodies

Corelex provides end-to-end support for:

Drug licensing
Product registrations
Regulatory submissions
Import and export compliance
Documentation management
Market authorization applications
Technical dossier preparation

The company serves as a bridge between healthcare manufacturers and regulatory authorities, ensuring that products meet all required legal and quality standards before reaching consumers.

For freshers, joining Corelex Solutions offers valuable exposure to real-world pharmaceutical regulatory operations.

📋 Job Overview

Particulars	Details
Company Name	Corelex Solutions Pvt Ltd
Position	Regulatory Affairs Fresher
Location	Okhla Phase-II, South Delhi
Job Type	Full-Time
Employment Category	Permanent
Experience Required	0–1 Year
Qualification	B.Pharm, B.Sc, M.Sc
Industry	Pharmaceutical & Regulatory Affairs
Application Mode	Email

📍 Job Location

Selected candidates will work from the company’s office located in:

Okhla Phase-II Industrial Area, South Delhi, Delhi – 110020

Okhla is one of Delhi’s major industrial and business hubs and is well connected through:

Delhi Metro
Public Transport
Railway Connectivity
Road Networks

The location provides excellent accessibility for candidates residing in Delhi NCR.

🎯 Key Responsibilities

As a Regulatory Affairs Fresher, you will be trained to perform various compliance and documentation-related activities essential for pharmaceutical product approvals.

1️⃣ Dossier Preparation and Compilation

One of the primary responsibilities will involve preparing regulatory dossiers.

You may assist senior team members in:

Collecting technical data
Organizing product information
Formatting regulatory documents
Preparing CTD and ACTD dossiers
Reviewing submission packages

This work plays a crucial role in obtaining approvals from regulatory agencies.

2️⃣ Documentation Management

Regulatory affairs professionals deal with large volumes of technical documentation.

Responsibilities include:

Maintaining document databases
Tracking submissions
Organizing certificates
Managing product registration records
Updating compliance documents

Accurate documentation is critical because even small errors can delay approvals.

3️⃣ Regulatory Compliance Monitoring

The pharmaceutical industry is heavily regulated.

Candidates may help monitor:

CDSCO updates
Regulatory guidelines
Compliance requirements
Product registration changes
Industry standards

Keeping track of evolving regulations helps organizations remain compliant.

4️⃣ Query Response Support

Regulatory authorities often request additional information during product review processes.

Freshers may assist in:

Drafting responses
Collecting supporting documents
Coordinating with technical teams
Updating submission records

This activity develops communication and analytical skills.

5️⃣ Cross-Functional Coordination

Regulatory affairs teams interact with multiple departments.

You may collaborate with:

Quality Assurance
Production
Research & Development
Supply Chain
Legal Teams
Product Development Teams

This exposure provides a broader understanding of pharmaceutical business operations.

🎓 Educational Qualification

Candidates with the following educational backgrounds are eligible to apply:

✅ Bachelor of Pharmacy (B.Pharm)

Pharmacy graduates possess foundational knowledge of:

Drug formulations
Pharmaceutical sciences
Drug regulations
Quality systems

This makes them excellent candidates for regulatory affairs careers.

✅ Bachelor of Science (B.Sc)

Candidates from Life Sciences backgrounds can apply, including:

Biotechnology
Microbiology
Biochemistry
Zoology
Botany
Life Sciences

Their scientific understanding supports regulatory documentation activities.

✅ Master of Science (M.Sc)

Postgraduates in Life Sciences disciplines are also encouraged to apply.

Advanced academic training often helps candidates understand technical data more effectively.

💡 Skills Required

To succeed in regulatory affairs, candidates should possess the following skills:

Communication Skills

Strong written communication is extremely important.

Professionals frequently prepare:

Emails
Compliance reports
Regulatory documents
Submission packages

Clear communication improves efficiency and accuracy.

Attention to Detail

Regulatory submissions require precision.

Candidates must carefully review:

Product information
Certificates
Technical documents
Compliance records

Even minor mistakes can impact approval timelines.

Organizational Skills

Managing multiple documents and projects simultaneously requires excellent organizational abilities.

Professionals should be comfortable handling:

Databases
Document trackers
Submission timelines
Compliance schedules

Computer Proficiency

Basic knowledge of:

Microsoft Word
Microsoft Excel
PowerPoint
Document Management Systems

is highly beneficial.

Learning Attitude

Since regulations continuously evolve, successful professionals remain committed to ongoing learning and development.

🌟 Why Choose a Career in Regulatory Affairs?

Many pharmacy and life science graduates are unfamiliar with the immense career potential offered by regulatory affairs.

Here are some reasons why regulatory affairs is becoming a preferred career option:

High Demand

Pharmaceutical companies must comply with strict regulations.

As a result, regulatory professionals remain in demand across:

Pharma companies
CROs
Medical device firms
Biotechnology organizations

Global Opportunities

Regulatory affairs professionals can work on projects involving:

India
United States
Europe
Middle East
Asia-Pacific Markets

This opens doors to international career growth.

Stable Career Path

Unlike certain functions that fluctuate with market conditions, compliance-related roles remain essential for business continuity.

Attractive Growth Prospects

Professionals can progress through roles such as:

Regulatory Affairs Associate
Regulatory Executive
Senior Executive
Regulatory Specialist
Regulatory Manager
Global Regulatory Lead

💎 Benefits of Joining Corelex Solutions

Practical Industry Exposure

Freshers gain hands-on experience instead of purely theoretical learning.

Mentorship Opportunities

Work alongside experienced regulatory professionals who can guide your career development.

Diverse Product Portfolio

Exposure to:

Pharmaceuticals
Medical Devices
Cosmetics
Nutraceuticals
Food Products

creates a versatile skill set.

Professional Growth

The role helps build a strong foundation for long-term career advancement.

📈 Career Growth After Regulatory Affairs Fresher Role

A regulatory affairs career can offer excellent long-term opportunities.

Year 1–2

Regulatory Affairs Associate
Documentation Executive

Year 3–5

Regulatory Executive
Submission Specialist

Year 5–8

Senior Regulatory Executive
Regulatory Affairs Specialist

Year 8+

Regulatory Manager
Global Regulatory Affairs Lead

With experience, professionals can also transition into:

Quality Assurance
Pharmacovigilance
Clinical Research
Medical Writing
Compliance Management

📝 Application Process

Interested candidates should apply via email.

Email Address

info@corelex.in

Documents Required

Updated Resume
Educational Certificates (if requested)
Internship Details (if applicable)

Recommended Subject Line

Application for Regulatory Affairs Fresher – Your Name

Using a professional subject line improves visibility and creates a positive first impression.

📌 Resume Tips for Freshers

Before applying, ensure your resume includes:

Personal Details

Full Name
Mobile Number
Email Address
Location

Education

Mention:

Degree
University
Year of Passing
Percentage/CGPA

Skills

Highlight:

MS Office
Documentation Skills
Communication Skills
Regulatory Knowledge

Projects

Include academic projects relevant to:

Pharmacy
Biotechnology
Microbiology
Drug Development

Certifications

Any certification related to:

Regulatory Affairs
Pharmaceutical Quality Systems
Clinical Research

can strengthen your profile.

🔥 Who Should Apply?

This opportunity is highly suitable for:

✅ B.Pharm Freshers

✅ B.Sc Life Sciences Graduates

✅ M.Sc Candidates

✅ Candidates Interested in Regulatory Affairs

✅ Freshers Seeking Pharma Industry Careers

✅ Individuals Looking for Compliance & Documentation Roles

📢 Final Words

The Corelex Solutions Recruitment 2026 drive presents an excellent opportunity for pharmacy and life sciences graduates seeking a strong entry point into the pharmaceutical industry.

Regulatory Affairs is one of the most promising career paths available today, offering stable employment, global opportunities, continuous learning, and long-term professional growth.

If you possess strong attention to detail, communication skills, and a willingness to learn, this position can provide the foundation needed to build a successful career in pharmaceutical compliance and regulatory management.

Interested candidates are encouraged to submit their updated resumes at the earliest and take advantage of this exciting opportunity.

📩 Apply Now

Email: info@corelex.in

Position: Regulatory Affairs Fresher

Location: Delhi

Qualification: B.Pharm, B.Sc, M.Sc

Experience: Freshers (0–1 Year)