Aurobindo Pharma Hiring Regulatory Affairs
- M.Pharm Regulatory Affairs Openings – Aurobindo Hyderabad
- Company Overview
- Job Role & Responsibilities
- Regulatory Affairs – 0 to 3 Years
- Eligibility / Qualifications
- Location & Salary
- Application Process
- FAQs
- Are freshers eligible?
- Is experience in M1 compulsory?
- What skills help in this role?
- Is this an onsite position?
- How do I apply?
- Summary Table
M.Pharm Regulatory Affairs Openings – Aurobindo Hyderabad
Aurobindo Pharma hiring M.Pharm Pharmacology freshers and RA professionals with 0–3 yrs experience at Bachupally, Hyderabad.
Aurobindo Pharma is hiring freshers and early-career Regulatory Affairs professionals for its APLRC1 facility in Bachupally, Hyderabad. The role is ideal for M.Pharm Pharmacology graduates who want to build a strong foundation in global regulatory submissions, dossier preparation and M1 documentation for EU and Canada markets.
Company Overview
Aurobindo Pharma is one of India’s largest pharmaceutical companies with a strong global footprint across formulations, APIs, biosimilars and specialty products. The organisation supports regulatory submissions to major global agencies, offering employees exposure to high-compliance processes, cross-functional coordination and end-to-end lifecycle management. Its regulatory centres in Hyderabad are known for structured training, mentorship and long-term career development.
Job Role & Responsibilities
Regulatory Affairs – 0 to 3 Years
- Support preparation and review of regulatory submissions as per EU and Canadian guidelines.
- Work on Module 1 (M1) activities including administrative documents, forms and compliance checks.
- Assist with dossier compilation, formatting, lifecycle updates and variation submissions.
- Coordinate with internal teams such as QA, QC, Formulation, Packaging and CMC groups to collect required data.
- Maintain regulatory trackers and ensure documentation accuracy.
- Review labels, artwork and country-specific regulatory requirements.
- Support responses to queries from regulatory authorities under supervision.
This role offers hands-on exposure to regulatory pathways, submission standards and global compliance expectations.
Eligibility / Qualifications
- Qualification: M.Pharm (Pharmacology).
- Experience: 0–3 years (freshers allowed).
- Preferred candidates include fresh M.Pharm Pharmacology graduates or RA professionals with experience in M1 for EU/Canada.
Relevant Courses (comma-separated): M.Pharm Pharmacology, M.Pharm Regulatory Affairs, PG Diploma in Drug Regulatory Affairs, CTD/eCTD certification, ICH guidelines training, Clinical Research certification.
Location & Salary
- Location: APLRC1, Bachupally, Hyderabad.
- Salary: Not disclosed; based on experience and internal grading.
Application Process
Interested candidates may apply by sending their resume to:
sreeja.yangam@aurobindopharma.com
Shortlisted candidates will be contacted for the next steps.
FAQs
Are freshers eligible?
Yes. M.Pharm Pharmacology freshers can apply.
Is experience in M1 compulsory?
Not mandatory, but preferred for EU and Canada submissions.
What skills help in this role?
Understanding of CTD/eCTD, dossier structure, regulatory documentation and pharmacology fundamentals.
Is this an onsite position?
Yes, based at APLRC1, Bachupally.
How do I apply?
Email your resume to sreeja.yangam@aurobindopharma.com.
Summary Table
| Category | Details |
|---|---|
| Company | Aurobindo Pharma |
| Vacancies | Regulatory Affairs – 0 to 3 Years |
| Required Education | M.Pharm (Pharmacology) |
| Experience | 0–3 years; M1 (EU/Canada) preferred |
To apply for this job email your details to sreeja.yangam@aurobindopharma.com
