Aurobindo Pharma Hiring Immediate Joiner -Send Resume To HR mail

Aurobindo Pharma Walk-in Interview. Aurobindo Pharma Limited Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.

Vacancy details:

• 𝐏𝐨𝐬𝐢𝐭𝐢𝐨𝐧: Quality Control (GMP / GC / LCMS / HPLC)/ Regulatory Affairs team within Research & Development
• Qualification: Msc,B.Pharm,Mparm
• 𝐋𝐨𝐜𝐚𝐭𝐢𝐨𝐧: Naidupet
• 𝐄𝐱𝐩𝐞𝐫𝐢𝐞𝐧𝐜𝐞: 1 – 6 years

Important Details :

• Selection Process: The selection will be on the basis of Interview.
• Mode of Interview: Face to face
• Interview Rounds of Interview: HR

Job Description

Greetings From Aurobindo Pharma Limited..!

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh)

Open Functions: Quality Control (GMP / GC / LCMS / HPLC)

Experience Required: 1 – 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control

Job Titles & Grades: Executive / Sr. Executive (based on experience)

Job Description:

• Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc.
• Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ)
• Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry
• Investigate OOS/OOT results and implement effective CAPA
• Support regulatory, customer and internal audits

Common Requirements:

• Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry or related)
• Sound knowledge of current GMP guidelines (US-FDA, MHRA, EU, WHO)
• Good documentation, investigation and communication skills
• Willingness to work in shifts and collaborate with cross-functional teams

How to Apply

• Subject Line: Immediate Joiner
• Send you updated resume : naidupetahr@aurobindo.com

Exciting opportunity awaits you at Aurobindo. We’re looking for passionate and driven individuals to join our team

🌍 We’re Hiring – Regulatory Affairs Professionals (Formulation R&D) | EU Markets🚀

We are looking for passionate individuals to join our Regulatory Affairs team within Research & Development, specifically supporting Formulation projects for global markets.

🎓 M. Pharm in Pharmaceutics/ Pharmaceutical Analysis

🧪 2–5 years of experience in Regulatory Affairs with a focus on formulation, OSD

🔹Current Openings:

📌 EU Market – hands in experience in Module 2 & 3 is essential

🔹Key Responsibilities:

1.Component with EU-Filing requirements with respect to Module 2 & 3 ability to independently and correctly review technical documents related to Quality Module

2.Well versed with EU- Regulatory guidance and Processes (i.e., Ability to understand and interpret technical expectations as per applicable ICH & EMEA guidelines)

3.Should be aware of post approval variation requirements in EU markets. Should have basic QA knowledge to enable correct review of plant related documents

If you’re ready to contribute to high-impact regulatory projects and grow in a dynamic R&D environment, we’d love to hear from you!

📩 Please share your resume to Pooja.Uppalapati@aurobindo.com or hrrc1@aurobindo.com

Kindly share the resumes with the Subject line : “Application for EU market”

Referrals are welcome!