Medifodil Hiring Regulatory Affairs

Regulatory Affairs Jobs in India – Medifodil Pharma 4–6 Yrs

Medifodil Smart Pharma Solutions hiring Regulatory Affairs Specialist. 1 vacancy, 4–6 yrs experience, salary up to 6 LPA.

Medifodil Smart Pharma Solutions has opened an exciting opportunity for experienced Regulatory Affairs professionals seeking stable growth in the pharmaceutical and life sciences domain. The company is currently hiring a Regulatory Affairs Specialist with strong hands-on experience in CTD and eCTD dossier preparation and regulatory publishing. This role is designed for professionals who want to work closely with global regulatory frameworks while contributing directly to compliant, high-quality pharmaceutical submissions.

With increasing global regulatory scrutiny and rising demand for compliant drug approvals, regulatory affairs professionals remain among the highest-paid and most in-demand roles in the pharma industry. Medifodil offers a structured, compliance-driven environment where regulatory expertise directly supports patient safety, product approvals, and long-term healthcare impact.

Company Overview

Medifodil Smart Pharma Solutions is a specialized pharmaceutical services organization delivering regulatory, compliance, and life sciences support to pharmaceutical and biotech companies. The company focuses on providing smart, efficient regulatory solutions aligned with global standards such as USFDA, EMA, MHRA, and other international health authorities.

Known for its regulatory expertise and client-centric approach, Medifodil supports pharmaceutical companies across product lifecycle stages including development, submission, and post-approval compliance. Its regulatory teams work closely with evolving global guidelines, making Medifodil a strong workplace for professionals aiming to build deep regulatory expertise in high-value pharmaceutical careers.

Job Role & Responsibilities

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will play a critical role in dossier preparation, submission management, and regulatory documentation for pharmaceutical products.

Key Responsibilities:

• Preparation, review, and compilation of CTD and eCTD dossiers
• eCTD publishing and submission to global regulatory agencies
• Coordination with internal teams for technical documentation
• Ensuring regulatory compliance with current guidelines
• Managing variations, amendments, and lifecycle submissions
• Maintaining regulatory documentation and submission archives
• Supporting regulatory queries and deficiency responses

This role is ideal for professionals targeting regulatory affairs jobs in pharma companies with exposure to global submissions.

Eligibility / Qualifications

Educational Qualifications

• B.Pharmacy
• M.Pharmacy
• M.Sc. (Life Sciences, Chemistry, Biotechnology)

(Relevant courses accepted: BPharm, MPharm – Regulatory Affairs, Pharmaceutics, Pharmaceutical Analysis, MSc Life Sciences, MSc Biotechnology)

Experience Requirements

• 4 to 6 years of experience in Regulatory Affairs (Pharma / Life Sciences)
• Mandatory hands-on experience in CTD and eCTD dossier compilation and publishing

Required Skills

• Strong understanding of global regulatory guidelines
• Practical experience with eCTD publishing tools
• High attention to detail and documentation accuracy
• Ability to work with cross-functional technical teams
• Clear communication and regulatory interpretation skills

These skills align with high-CPC regulatory affairs pharma jobs and compliance-focused career searches.

Location & Salary

Job Location: India (Exact location will be communicated during the interview process)

CTC Offered: ₹4.5 – 6 LPA

The salary range is competitive for mid-level regulatory affairs roles and aligns with current market demand for experienced regulatory professionals.

Application Process

Interested and eligible candidates can apply by sending their updated resume to the official company email ID.

Apply Now: careers@medifodil.com

Candidates are advised to mention “Regulatory Affairs Specialist” in the email subject line for faster shortlisting.

Early applications are encouraged due to limited vacancies and high demand for regulatory affairs professionals.

Why Choose Medifodil Smart Pharma Solutions

• Specialized focus on regulatory affairs and compliance
• Exposure to global regulatory submissions
• High-demand skill development in CTD and eCTD publishing
• Competitive salary for experienced professionals
• Direct contribution to safe and compliant healthcare products

These factors make this role highly attractive for professionals searching for regulatory affairs specialist jobs, pharma compliance careers, and CTD eCTD regulatory roles.

FAQs

Who can apply for this Regulatory Affairs role?

Candidates with 4–6 years of regulatory affairs experience in pharma or life sciences can apply.

Is CTD/eCTD experience mandatory?

Yes. Hands-on experience in CTD and eCTD dossier compilation and publishing is mandatory.

Is this role suitable for freshers?

No. This position requires prior regulatory affairs experience.

What is the salary range?

The offered CTC ranges from ₹4.5 to 6 LPA based on experience and skill level.

Is there any application fee?

No. Medifodil Smart Pharma Solutions does not charge any recruitment fees.

Summary Table

Company	Medifodil Smart Pharma Solutions
Vacancies	Regulatory Affairs Specialist
Required Education	B.Pharmacy, M.Pharmacy, M.Sc.
Experience	4–6 years