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Medreich Pharma Hiring for AR&D, FR&D & Regulatory Affairs Jobs

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Medreich Pharma, a Meiji Group Company, has announced exciting career opportunities for experienced pharmaceutical professionals across multiple departments. The company is looking for talented candidates in Analytical Research & Development, Impurities Synthesis, Regulatory Affairs, and Formulation Research & Development. If you have relevant experience and are looking to grow your career in the pharmaceutical industry, this is an excellent opportunity.

Job Overview

Company Name: Medreich Pharma (A Meiji Group Company)

Job Type: Full-Time

Departments:

  • Analytical Research & Development (AR&D)
  • Impurities Synthesis
  • Regulatory Affairs
  • Formulation Research & Development (FR&D)

Available Positions

1. Analytical Research & Development (Solid Orals)

Experience Required: 5–7 Years

Key Skills:

  • Analytical Method Validation
  • Analytical Method Transfer
  • Working Standard Qualification
  • Stability Studies
  • Calibration
  • Dissolution
  • Compendia Evaluation
  • Method Equivalency
  • AD/ADL/QC Validation for OSD Formulations

2. Impurities Synthesis – Analytical Research & Development

Experience Required: 2–5 Years

Qualification:

  • M.Pharm (Pharmaceutical Analysis)
  • M.Sc. (Analytical Chemistry / General Chemistry / Applied Chemistry)

3. Regulatory Affairs – Formulation

Experience Required: 8–15 Years

Requirement:

  • Core Regulatory Affairs experience
  • Formulation background is mandatory

4. Formulation Research & Development (FR&D – Solid Orals)

Experience Required: 5–7 Years

Roles & Responsibilities

Depending on the department, selected candidates will be responsible for:

  • Performing analytical method validation and method transfer.
  • Conducting stability studies and dissolution analysis.
  • Supporting working standard qualification and calibration activities.
  • Carrying out impurity synthesis and analytical investigations.
  • Preparing and reviewing regulatory documentation for formulation products.
  • Developing and optimizing solid oral dosage formulations.
  • Ensuring compliance with quality systems and regulatory requirements.
  • Collaborating with cross-functional teams to support product development.

Required Qualifications

  • M.Pharm (Pharmaceutical Analysis)
  • M.Sc. (Analytical Chemistry / General Chemistry / Applied Chemistry)

Candidates must possess the relevant educational qualification and required experience for the respective position.

Salary & Benefits

Expected Salary: ₹6 LPA – ₹22 LPA (Approximate, based on experience and role)

Benefits may include:

  • Competitive salary package
  • Career growth opportunities
  • Learning and development programs
  • Professional work environment
  • Opportunity to work with a leading pharmaceutical organization

How to Apply

Interested and eligible candidates can send their updated resume to any of the following email addresses:

Applicants are advised to mention the position they are applying for in the email subject line.

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