Aurobindo Pharma Hiring Regulatory Affairs – Formulation R&D
- Career Opportunity: Regulatory Affairs – EU Markets (Formulation R&D) at Aurobindo Pharma
- Why Join Aurobindo Pharma?
- Job Role: Regulatory Affairs Executive – EU Market (Formulation R&D)
- Desired Candidate Profile:
- How to Apply:
- Educational Backgrounds That Apply:
- Job Summary Table
M.Pharm Regulatory Affairs Jobs – Formulation R&D Openings at Aurobindo Pharma, Hyderabad
Aurobindo Pharma is hiring M.Pharm professionals with 2–5 years experience in Regulatory Affairs – Formulation R&D for EU markets in Hyderabad. Apply now!
Career Opportunity: Regulatory Affairs – EU Markets (Formulation R&D) at Aurobindo Pharma
Aurobindo Pharma, one of India’s leading pharmaceutical companies with a strong global presence, is inviting skilled professionals to join its Regulatory Affairs team in the Formulation R&D division. This role focuses on EU market filings, offering a fantastic opportunity for individuals passionate about regulatory sciences and formulation development.
Why Join Aurobindo Pharma?
- Global Exposure: Work on regulatory filings for highly regulated markets including Europe.
- Career Advancement: Opportunities for continuous learning and growth within a well-established R&D setup.
- Supportive Environment: Collaborate with industry experts and make impactful contributions to global healthcare.
Job Role: Regulatory Affairs Executive – EU Market (Formulation R&D)
Location:
Hyderabad, Telangana
Qualification:
M.Pharm in Pharmaceutics or Pharmaceutical Analysis
Experience:
2 to 5 years of hands-on experience in regulatory affairs, specifically in formulation (OSD) for EU submissions
Key Responsibilities:
- Compile and review Modules 2 & 3 as per EU-filing requirements.
- Independently assess and review technical documents related to the Quality Module.
- Interpret and implement ICH and EMEA guidelines in regulatory filings.
- Ensure compliance with EU post-approval variation standards.
- Liaise with QA teams to ensure accurate review of plant-related documentation.
Desired Candidate Profile:
- In-depth understanding of EU regulatory processes and technical expectations.
- Proficiency in interpreting global regulatory guidelines.
- Basic knowledge of QA principles and pharmaceutical manufacturing documentation.
- Excellent communication and documentation skills.
How to Apply:
If you meet the eligibility criteria and are eager to contribute to impactful regulatory projects:
- Email your resume to: Pooja.Uppalapati@aurobindo.com or hrrc1@aurobindo.com
- Subject Line: Application for EU Market – Regulatory Affairs
Referrals are also encouraged. Share this opportunity within your network!
Educational Backgrounds That Apply:
Courses accepted for this opportunity include:
- M.Pharm in Pharmaceutics
- M.Pharm in Pharmaceutical Analysis
Job Summary Table
| Company Name | Aurobindo Pharma |
|---|---|
| Department | Regulatory Affairs – Formulation R&D |
| Required Education | M.Pharm (Pharmaceutics/Pharmaceutical Analysis) |
| Experience Required | 2–5 Years |
| Location | Hyderabad, Telangana |
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