Acme Generics Regulatory Affairs Executive Recruitment 2026 | B.Pharm M.Pharm Jobs in Ahmedabad for EU Regulatory Affairs Professionals

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Acme Generics Regulatory Affairs Executive / Senior Executive Jobs 2026 (Acme Generics Regulatory Affairs Executive Recruitment 2026) Introduction Acme Generics has announced new recruitment opportunities for Regulatory Affairs Executive and Senior Executive positions at its Ahmedabad facility. This latest pharmaceutical job opening is ideal for professionals with experience in EU Regulatory Affairs, eCTD dossier preparation, lifecycle management, pharmaceutical compliance, and regulatory submissions. Candidates looking for Regulatory Affairs jobs in Ahmedabad, EU market pharmaceutical jobs, eCTD submission careers, or international regulatory affairs opportunities can explore this opening. The company is seeking qualified professionals who can support European regulatory operations and ensure compliance with global pharmaceutical standards. About Acme Generics Acme Generics is a well-established pharmaceutical company engaged in the development, manufacturing, and marketin...

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"Join ICON as a Due Diligence Specialist in Bangalore & Chennai – Clinical Research Career Opportunity"

"Career Opportunity: Due Diligence Specialist I/II at ICON plc – Bangalore & Chennai"


Are you passionate about clinical research, regulatory compliance, and making a global impact in healthcare? ICON plc, a worldwide leader in healthcare intelligence and clinical research, is offering an exciting opportunity for the position of Due Diligence Specialist I/II in its Bangalore and Chennai offices.

This is a full-time, office-based role with flexible working options, designed for professionals who are eager to contribute to cutting-edge clinical trials and shape the future of healthcare innovation.


Key Responsibilities:-

As a Due Diligence Specialist, your role will be vital in driving success across ICON's clinical trial projects. Responsibilities include:

  • Performing due diligence assessments for clinical sites, investigators, and vendors.
  • Reviewing regulatory documentation and study protocols to ensure compliance and identify risks.
  • Supporting development of effective risk mitigation plans.
  • Coordinating with cross-functional teams to ensure timely and accurate project execution.
  • Maintaining audit-ready documentation of all due diligence processes and outcomes.

Eligibility & Required Skills:-

Educational Background:

  • Bachelor’s degree in Life Sciences, Regulatory Affairs, or related field.

Experience:

  • 1 to 4 years of experience in clinical research, regulatory affairs, or relevant pharmaceutical domains.

Skill Set:

  • Strong attention to detail and analytical thinking.
  • Excellent time management and ability to prioritize tasks under tight deadlines.
  • Effective communication and collaboration skills.
  • Familiarity with global clinical trial regulations is a plus.

Benefits of Joining ICON:-

ICON is known for its dynamic, inclusive culture and commitment to employee well-being. Perks include:

  • Attractive Salary: INR 6–10 LPA, depending on experience.
  • Health Coverage: Comprehensive health insurance for you and your family.
  • Retirement Plans: Long-term savings options to secure your future.
  • Wellness Support: 24/7 mental and emotional support via TELUS Health.
  • Employee Perks: Country-specific benefits like travel discounts, gym memberships, and childcare support.
  • Flexible Work-Life Balance: Generous leave and hybrid work setup.

Job Location:-

  • Bangalore or Chennai, India

How to Apply:-

Interested candidates can apply directly via the official portal:
👉 Apply Here


ICON is an equal opportunity employer and encourages candidates from diverse backgrounds to apply. Take this step forward in your pharma career and be a part of global healthcare transformation!

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