Aurobindo Pharma Limited Walk-in Interview.Aurobindo Pharma Limited Limited Notification full details below. Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Location -Naidupeta, Tirupati
- Experience – 4 to 15 yearsย
- Education – M. Pharm/B. Pharm/Msc
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
We are looking for skilled QC professionals to join our Quality team at our Naidupeta unit.
ย Position: ๐๐/๐๐ – ๐๐ข๐๐ซ๐จ๐๐ข๐จ๐ฅ๐จ๐ ๐ฒ
ย Experience: 9 โ 15 Years.
ย Location: Naidupeta, Tirupati
๐๐๐ฒ ๐๐๐ช๐ฎ๐ข๐ซ๐๐ฆ๐๐ง๐ญ๐ฌ:
ย Operational Leadership: Manage day-to-day operations of the microbiology lab, ensuring all tests (Sterility, Bacterial Endotoxin Test (BET), and Microbial Limit Tests (MLT)) are performed according to SOPs.
Environmental Monitoring: Oversee and review environmental monitoring (EM) of cleanrooms and production areas to ensure sterile formulation environments are maintained.
Method Validation: Lead the development and validation of microbiological test methods for new formulation products, including Gowning and Disinfectant validation.
Compliance & Audits: Ensure the lab is “audit-ready” at all times. Participate in internal and external regulatory audits (e.g., NABL, WHO-GMP).
Investigations: Lead root-cause investigations for out-of-specification (OOS) results, deviations, and contamination incidents; implement corrective and preventive actions (CAPA).
Quality Management: Review and approve laboratory data, trending reports, and technical protocols. Manage the calibration and maintenance schedule for all lab equipment (LAF, Autoclaves, Incubators).
Required Qualifications
Education: Masterโs degree (M. Sc) or Bachelor’s in Microbiology or Biotechnology. M. Pharm is also highly valued for formulation-specific roles.
Experience: 6โ10 years of progressive experience in a pharmaceutical microbiology laboratory, with at least 2โ3 years in a supervisory or assistant management role.
Technical Skills:
Deep knowledge of GLP/GMP and pharmacopoeia standards (USP/BP/EP/IP).
Hands-on experience with water system validation and sterile manufacturing processes.
Proficiency in software like LIMS for data management.
ย ๐๐ฉ๐ฉ๐ฅ๐ฒ ๐๐จ๐ฐ:
Interested candidates, please share your updated CV to:
PraveenKumar.Gullipalli@aurobindo.com
Please repost 
ย to help connections find this opportunity! 
Assistant Manager in the Quality Management System (QMS) /Market complaints section, ๐
๐จ๐ซ๐ฆ๐ฎ๐ฅ๐๐ญ๐ข๐จ๐ง, APL Healthcare Ltd Unit IV, ๐๐๐ข๐๐ฎ๐ฉ๐๐ญ๐, ๐๐ข๐ซ๐ฎ๐ฉ๐๐ญ๐ข.
Job Title: Sr. Executive Assistant Manager – Quality Assurance (QMS)/MC
Job Summary
We are looking for a highly skilled QA professional to lead the implementation, monitoring, and continuous improvement of our site Quality Management System (QMS). The successful candidate will ensure all formulation manufacturing activities comply with current Good Manufacturing Practices (cGMP) and international regulatory standards (USFDA, MHRA, WHO-GMP).
Key Responsibilities
QMS Element Administration: Lead the management and timely closure of critical QMS elements, including Deviations, Change Controls, and CAPA (Corrective and Preventive Actions).
Investigation Leadership: Lead and approve root-cause investigations for Out of Specification (OOS), Out of Trend (OOT) results, and market complaints.
Risk Management: Conduct and review Quality Risk Assessments (QRA) to identify and mitigate potential quality risks in the formulation process.
Audit Preparedness: Act as a key member in preparing the site for external regulatory, third-party, and internal audits; manage post-audit CAPA implementation.
Documentation Control: Oversee the issuance, revision, and archival of controlled documents such as SOPs, Master Formula Records (MFR), and Batch Manufacturing Records (BMR).
Compliance Monitoring: Conduct routine GMP walkthroughs in manufacturing departments to ensure shop-floor adherence to protocols and data integrity policies.
Required Qualifications
Education: B.Pharm, M.Pharm, or M.Sc in Chemistry/Biotechnology.
Experience: 7โ12 years of experience in QA/QMS within a pharmaceutical formulation facility, with significant experience in a supervisory role.
Regulatory Knowledge: Deep understanding of cGMP, USFDA, MHRA, and ICH guidelines.
Technical Skills: Proficiency in QMS software (e.g., TrackWise) and Laboratory Information Management Systems (LIMS) is highly desirable.
ย ๐๐ฉ๐ฉ๐ฅ๐ฒ ๐๐จ๐ฐ:
Interested candidates, please share your updated CV to:
ganesh.janne@aurobindo.com
Please repost ย to help connections find this opportunity!
ABAC
