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:
- ๐๐จ๐ฌ๐ข๐ญ๐ข๐จ๐ง: Quality Control (GMP / GC / LCMS / HPLC)/ Regulatory Affairs team within Research & Development
- Qualification: Msc,B.Pharm,Mparm
- ๐๐จ๐๐๐ญ๐ข๐จ๐ง: Naidupet
- ๐๐ฑ๐ฉ๐๐ซ๐ข๐๐ง๐๐: 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 & responsibilitiesย APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh)
Open Functions: Quality Control (GMP / GC / LCMS / HPLC)
Experience Required:ย 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 :ย naidupetahr@aurobindo.com
Exciting opportunity awaits you at Aurobindo. We’re looking for passionate and driven individuals to join our team
๐ We’re Hiring โ Regulatory Affairs Professionals (Formulation R&D) | EU Markets๐
We are looking for passionate individuals to join our Regulatory Affairs team within Research & Development, specifically supporting Formulation projects for global markets.
๐ M. Pharm in Pharmaceutics/ Pharmaceutical Analysis
๐งช 2โ5 years of experience in Regulatory Affairs with a focus on formulation, OSD
๐นCurrent Openings:
๐ EU Market โ hands in experience in Module 2 & 3 is essential
๐นKey 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 youโre ready to contribute to high-impact regulatory projects and grow in a dynamic R&D environment, weโd love to hear from you!
๐ฉ Please share your resume to Pooja.Uppalapati@aurobindo.com or hrrc1@aurobindo.com
Kindly share the resumes with the Subject line : โApplication for EU marketโ
Referrals are welcome!
