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Pharmazone Hiring for Regulatory Affairs, Pharmacovigilance, GCP & GMP Compliance , Business Development Roles

Join Pharmazone: Walk-In Interview Drive for Pharmaceutical and Life Sciences Professionals

Summary: Pharmazone, a leading global consulting partner specializing in Regulatory Affairs, Pharmacovigilance, GCP, and GMP Compliance, is hosting a walk-in interview drive to fill multiple open positions across various departments. We are seeking talented and motivated individuals to join our growing team and contribute to impactful projects in regulated markets such as the US, EU, and ROW regions. If you are passionate about the pharmaceutical and life sciences industry and seeking a challenging and rewarding career, we encourage you to attend our walk-in interview.

About Pharmazone:

Pharmazone is a trusted consulting partner for pharmaceutical and life sciences companies worldwide. We provide comprehensive solutions in Regulatory Affairs, Pharmacovigilance, GCP, and GMP Compliance, helping our clients navigate the complexities of global regulations and achieve their business goals. Our team of experienced professionals brings deep industry knowledge and a commitment to excellence, ensuring the highest quality service and support.

Walk-In Interview Details:

  • Date: December 7th, 2025
  • Time: 9:30 AM – 2:30 PM
  • Location: Pharmazone, Ahmedabad Office
  • Registration Email: [email protected]

Available Job Openings:

We are currently seeking qualified candidates for the following positions:

Department Position Code Eligibility Experience
Business Development Executive PZBD010 B.Sc/B.Pharm/M.Pharm/MBA Freshers – 2 Yrs
GCP Clinical Research Associate PZCRA010 B.Pharm/M.Pharm/M.Sc 1–2 Years
GMP GMP Auditor PZGMP020 B.Pharm/M.Pharm/M.Sc 4–6 Years
GMP Production Expert PZGMP018 B.Pharm/M.Pharm 10–14 Years
Pharmacovigilance Sr. Executive (Aggregate Reports) PZPV033 B.Pharm/M.Pharm/BDS 3–6 Years
Pharmacovigilance MICC Specialist PZPV0013 Life Science Degree 0–2 Years
Regulatory Affairs Senior Executive PZRA008 M.Pharm/M.Sc 2–6 Years (US/EU/ROW)

Responsibilities (Role-Dependent):

Depending on the specific role, responsibilities may include:

  • Supporting regulatory submissions across global markets
  • Conducting and supporting GCP/GMP audits and compliance checks
  • Executing PV reporting, RMP preparation, and case processing
  • Managing MICC calls and supporting scientific communication
  • Leading production activities and maintaining compliance in OSD environments
  • Driving business engagement and client coordination in consulting services

Required Qualifications:

  • B.Pharm / M.Pharm / B.Sc / M.Sc / MBA (Pharma) / BDS depending on role
  • Experience range: Fresher to 14 years based on position
  • Knowledge of ICH GCP, GxP, EMA, USFDA, PV Guidelines, Regulatory Submissions preferred

Skills & Competencies:

We are looking for individuals who possess the following skills and competencies:

  • Strong analytical & documentation skills
  • Knowledge of pharma compliance and guidelines
  • Excellent communication and teamwork ability
  • Willingness to work in a fast-paced consulting environment

Benefits of Working at Pharmazone:

We offer a comprehensive benefits package, including:

  • Competitive salary and performance benefits
  • Opportunity to work on global pharma and biotech projects
  • Career development programs and certifications
  • Collaborative and learning-oriented work culture

How to Apply:

There are two ways to apply:

  1. Email Your CV: Send your updated CV to [email protected].

  2. Attend the Walk-In Interview: Please bring the following documents:

    • Resume
    • Photo ID
    • Photocopies of certificates

We encourage all qualified candidates to apply. We look forward to meeting you!