Medreich Pharma Hiring Regulatory Affairs

Regulatory Affairs Openings | Medreich Pharma Bengaluru
Apply for Regulatory Affairs positions at Medreich Bengaluru. Hiring professionals with 2–6 years experience for Europe, Canada, Australia & LatAm markets.

Medreich Limited, a trusted global pharmaceutical company, is expanding its Regulatory Affairs (RA) team in Bengaluru. With operations spanning across regulated markets such as Europe, Canada, Australia, and Latin America (LatAm), this is an excellent opportunity for skilled RA professionals to be part of a fast-growing organization committed to global healthcare.

If you have 2–6 years of experience in Regulatory Affairs and are looking to grow in a world-class pharmaceutical environment, this is the right career move for you.

Company Overview

Medreich Limited is a global pharmaceutical company with decades of experience in formulation development, contract manufacturing, and regulatory compliance. Known for its strong presence in regulated markets and collaborations with leading multinational pharma companies, Medreich continues to drive innovation while maintaining the highest standards of quality, safety, and compliance.

By joining Medreich, candidates gain exposure to international regulatory frameworks and the chance to contribute to the development and approval of medicines that make a difference worldwide.

Job Role & Responsibilities

As part of the Regulatory Affairs Department, you will be responsible for:

• Preparing and reviewing regulatory submissions for Europe, Canada, Australia, and LatAm markets.

• Handling dossier compilation, variation filing, and renewals in line with global regulatory requirements.

• Coordinating with cross-functional teams including Quality Assurance, R&D, and Manufacturing.

• Managing communication with regulatory agencies to resolve queries and ensure timely approvals.

• Maintaining compliance with evolving ICH, FDA, EMA, and regional guidelines.

• Supporting audits, inspections, and continuous improvements within the RA team.

Eligibility / Qualifications

• Education: B. Pharm / M. Pharm (Regulatory Affairs / Pharmaceutics / Pharmaceutical Chemistry preferred).

• Experience: Minimum 2 to 6 years of hands-on experience in Regulatory Affairs.

• Skills Required:

  • Strong knowledge of dossier preparation and submission.

  • Experience in regulated markets (Europe, Canada, Australia, LatAm).

  • Familiarity with CTD/eCTD formats, ICH guidelines, and regional regulatory frameworks.

  • Excellent communication, problem-solving, and coordination skills.

Location & Salary

• Location: Medreich Limited, Bengaluru (Office-based role).

• Salary: Attractive compensation package, aligned with industry standards and candidate experience.

Application Process

Interested candidates are invited to share their updated CV with the Medreich HR team:

• aravinda.p@medreich.com

• hr.ho@medreich.com

• padmanaban.d@medreich.com

Shortlisted candidates will be contacted for formal discussions and interviews.

Why Join Medreich?

• Opportunity to work with a global pharma leader in Regulatory Affairs.

• Exposure to multiple international markets (EU, Canada, Australia, LatAm).

• Career growth in a fast-expanding RA team.

• Collaborative work culture with industry experts.

FAQs

Q1. What experience is required?
Minimum 2–6 years in Regulatory Affairs handling submissions for regulated markets.

Q2. Is this role office-based or hybrid?
 The role is office-based at the Bengaluru corporate office.

Q3. Which markets will I work on?
 You will gain exposure to Europe, Canada, Australia, and Latin America (LatAm) regulatory submissions.

Q4. How can I apply?
Share your resume directly with HR at aravinda.p@medreich.com / hr.ho@medreich.com / padmanaban.d@medreich.com.

Summary Table