Zuche Pharma Hiring Regulatory Affairs Executive

M.Pharm/B.Pharm Regulatory Affairs Executive Vacancy | New Delhi

Apply for Executive Regulatory Affairs at Zuche Pharma, New Delhi. B.Pharm/M.Pharm with 1+ year experience in medical devices regulatory compliance.

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Looking to advance your career in Regulatory Affairs within the medical device and pharmaceutical industry? Zuche Pharma, a trusted and growing healthcare organization, invites talented professionals to join as Executive in Regulatory Affairs at its New Delhi office. This opportunity is ideal for candidates passionate about compliance, documentation, and ensuring product safety in line with global regulatory standards.

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Company Overview

Zuche Pharma is a reputed pharmaceutical company recognized for its commitment to delivering high-quality, affordable healthcare solutions. With a strong presence in medical devices, formulations, and global regulatory markets, Zuche Pharma operates with strict adherence to international cGMP, ISO, and WHO-GMP guidelines. The company’s regulatory team plays a key role in maintaining compliance and facilitating seamless product registration across multiple regions.

Zuche Pharma’s mission is to improve patient outcomes through continuous innovation, quality assurance, and ethical practices, making it an excellent place for professionals seeking career growth in pharma regulatory affairs.

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Job Role & Responsibilities

As an Executive in Regulatory Affairs, you will be responsible for managing and reviewing technical and compliance documentation related to medical devices and pharmaceutical products. Your role ensures the company meets both domestic and international regulatory standards.

Key Responsibilities:

• Prepare, compile, and review CTD (Common Technical Document), ACTD (ASEAN Common Technical Dossier), and TCF (Technical Construction File) dossiers.
• Review essential documents such as:
  • Process Validation Reports (PVR)
  • Specifications (SPEC)
  • Standard Testing Procedures (STP)
  • Certificates of Analysis (COA)
• Collaborate with cross-functional teams (Quality Control, R&D, Production) to ensure data accuracy and compliance.
• Support submission of regulatory filings for product approvals and renewals.
• Maintain current knowledge of evolving medical device and pharmaceutical regulations.
• Ensure timely completion and accuracy of all regulatory documentation as per company SOPs.

This position demands attention to detail, excellent documentation skills, and a proactive approach to solving compliance challenges in a fast-paced environment.

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Eligibility / Qualifications

To qualify for this role, candidates must meet the following educational and professional requirements:

Educational Qualification:

• B.Pharm (Bachelor of Pharmacy) or M.Pharm (Master of Pharmacy)

Preferred Courses/Streams:
Pharmaceutical Technology, Industrial Pharmacy, Regulatory Affairs, Pharmaceutical Chemistry, Pharmaceutics.

Experience Required:

• Minimum 1 year of experience in Regulatory Affairs for Medical Devices or Pharmaceuticals.
• Hands-on experience with CTD/ACTD dossier preparation, document review, and regulatory submissions.

Desired Skills:

• Strong understanding of ISO 13485, cGMP, and Indian Drug Regulatory Guidelines.
• Proficiency in document management and regulatory data compilation.
• Excellent communication and attention to detail.

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Location & Salary

Location: New Delhi, India
Work Type: Full-time, On-site
Salary: Competitive and based on experience (market-aligned package)

Zuche Pharma offers a competitive compensation structure, professional growth pathways, and exposure to international regulatory practices.

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Application Process

If you meet the qualifications and are eager to make an impact in the field of Regulatory Affairs, don’t miss this opportunity.

Apply Now: hrm@zuchepharma.in
Apply before: November 15, 2025

Candidates are encouraged to apply early to secure consideration for the role. Shortlisted applicants will be contacted for further rounds of evaluation.

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Why Join Zuche Pharma?

• Opportunity to work in a globally recognized pharmaceutical organization.
• Hands-on experience with medical device regulations and global dossier submissions.
• Exposure to a professional team dedicated to regulatory compliance and product safety.
• Competitive salary, learning opportunities, and a growth-oriented environment.

Zuche Pharma believes in empowering professionals who value precision, innovation, and excellence in compliance.

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FAQs

1. Who can apply for the Executive – Regulatory Affairs role at Zuche Pharma?
Candidates with a B.Pharm or M.Pharm degree and at least 1 year of experience in Regulatory Affairs (Medical Devices) can apply.

2. What are the key skills required for this role?
Knowledge of CTD/ACTD dossier preparation, document review, and familiarity with ISO 13485 and GMP guidelines are essential.

3. Is this position open for freshers?
Currently, the role requires a minimum of 1 year of experience. However, exceptional candidates with internship experience in regulatory documentation may also be considered.

4. What is the mode of application?
Interested candidates can send their resumes directly to hrm@zuchepharma.in.

5. What is the expected joining timeline?
Immediate joiners are preferred. Apply before November 15, 2025, to secure early consideration.

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Company	Zuche Pharma
Vacancies	Executive – Regulatory Affairs
Required Education	B.Pharm, M.Pharm (Pharmaceutics, Industrial Pharmacy, Regulatory Affairs)
Experience	Minimum 1 year in Regulatory Affairs (Medical Devices)