Dear Aspirant ,Greetings From Eugia Pharma Specialties , Unit ..!We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit.Department - Production (Injectable)Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITIDesignation - Sr. Executive / Executive/ OperatorsExperience - 2Yrs to 8 yr.Skills - Vial Filling/ Sealing / Autoclave / Lyo and etcWalk In Details:Date : 23.03.2025Time : 10 AM - 02 PMVenue :Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202Google link : https://maps.app.goo.gl/TpvUmrAjTBXakHv77Contact : Mr Prabhakar / Ms Rama

Dear Aspirant ,Greetings From Eugia Pharma Specialties , Unit ..! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit.Department - Production (Injectable)Qualification - M. Pharmacy / B. Pharmacy / M. Sc /B Sc / Diploma / ITIDesignation - Sr. Executive / Executive/ OperatorsExperience - 2Yrs to 8 yr.Skills - Vial Filling/ Sealing / Autoclave / Lyo and etcWork Location : Eugia Unit -3, PashamylaramWalk In Details:Date : 23.03.2025Time : 10 AM - 02 PMVenue :Eugia SEZ (Aurobindo Pharma Limited-Unit 16), Balanagar, Ambatapur, Telangana 509202Google Maps: https://maps.app.goo.gl/KxN3JSa7wL8MoYpm6Contact : Mr Prabhakar / Ms Rama

Role & responsibilities:Outline the day-to-day responsibilities for this role.Preferred candidate profile:Specify required role expertise, previous job experience, or relevant certifications.Perks and benefits:Mention available facilities and benefits the company is offering with this job.

Role & responsibilities 1. Responsible for administrator activities (User ID creation for new employees and ID remove for resigned employees) related to all IPC/SCADA based system of process & packing equipments in Unit VII. 2. Responsible for carrying out Backups and Restorations of all IPC/SCADA based process and packing equipments. 3. Responsible to ensure periodic review of all archived back-ups related to process and packing equipments as per schedules. 4. Responsibility to ensure all Operating system Controls are implemented for all computer systems available in manufacturing, engineering and packing departments. 5. Responsible for creation of folders, files, users and configuring user roles in share point. 6. Responsible for DSRS, e-residue Pro administrator activities (User ID creation for new employees and ID remove for resigned employees and audit trail review) 7. Responsible to provide remote access to external OEM/service provider for maintenance and troubleshooting activities. 8. Responsible to participate/execute qualification & validation of computerized system wherever applicable. 9. Responsible to prepare SOPs and schedules related to user management, backup and restoration of all computerized systems at unit VII. 10. Responsible to provide necessary support during internal and external audits. 11. Responsible to provide necessary support during Remote Access Control for Standalone Computerized Systems in Production and Utilities. 12. To ensure computerized systems in manufacturing, engineering and packing are in compliance with the current approved procedures. 13. Responsible to review the SOPs and formats in Quality Management System Application.Preferred candidate profile 1. 15-20 Years of Experience from Pharmaceutical Industry2. Qualification : BE/B. Tech/MCA/IT /Computer ApplicationsPerks and benefits Best In The Industry

Role & responsibilities *Operate and maintain tablet compression machines, ensuring they run efficiently and produce tablets that meet quality standards. * Monitor the compression process to ensure tablets are produced according to specifications, conducting regular checks for weight, thickness, and hardness. * Identify and resolve any mechanical or process issues that arise during production to minimize downtime and maintain productivity. Preferred candidate profile ITI / Diploma or Graduate with 2-8 years of experiencePerks and benefits Relocation allowanceTravel allowanceInitial accommodationVirtual Interview (Online Interview)

Role & responsibilities Cross functional and within department co-ordination to ensure all the Change controls, Exceptions, Process non-conformance and Material non-conformance for the closure within due date.Responsible for all the change control coordination activities, Coordination with customers for approval of change controls in Quality management system moduleMonitor and to trace the Change controls, Exceptions, Process non-conformance and Material non-conformance in Quality management systemInitiate, review the Corrective action & preventive action and to coordinate with other departments for its closure within due date.Prepare and review the trends for Change controls, Process non-conformance and Material non-conformance, Exceptions and Corrective action & preventive actions Preferred candidate profile 02 to 07 years pharma formulations experience preferrable. Perks and benefits As per Industrial standards

Role & responsibilities 1. Prepare the validation schedules for new projects, revalidation schedules for existing equipment/utilities as per respective procedures2. Execute and review of all the qualification/re-qualification protocols and reports pertaining to equipment, utilities, instruments and facilities3. Responsible to update or review Qualification, Production and engineering related procedures which are compliant to current GXP regulatory norms4. Responsible for preparation of Validation master plan/Site master fileResponsible for reviewing and ensuring all the scheduled activities for Preventive maintenance, filter cleaning, filter replacements, calibrations, Alarm/audit trail reports etc are performed as per the respective procedures within specified time Preferred candidate profile B Pharmacy/Msc Education qualification with 03 to 09 years experiancePerks and benefits Best in industry

Work Location:Naidupet (Near TIrupati)Role & responsibilities 1. Handling of market complaints. 2. To acknowledge the complaints to the reporter3. conducting complaint Investigations4. Co-ordinate with functional investigators (Cross Functional Team/Subject Matter Experts) for timely completion of complaint investigations.5. Follow up for complaints closure letter from the Reporter and close the complaint in complaints closure form.6. Involve in root cause analysis, Failure Investigations and Risk assessment activities.7. Initiate, review of Corrective action & preventive action and To prepare trend of complaints.To Maintain all the Quality management system documentations. Preferred candidate profile B. Pharma/Msc Educational qualification with 03 to 08 years experiancePerks and benefits Best In industry

Role & responsibilities: 1. To organize / co-ordinate the internal / external trainings2. To co-ordinate and execute the training programme for all personnel in co-ordination with respective Stakeholder for new and existing employees through EPIQ Learn IQ3. To prepare the training schedule to all personnel in plant. 4. To initiate the refresher training to plat personnel as per training schedule 5. To prepare training content/documents as per requirements. 6. To track the training practical effectiveness of employees 7. To prepare and maintain Training need identification matrixs to all the plant personnel Preferred candidate profile :Candidate with 02 to 07 years of experience in Training & Documentation . Perks and benefits As per Company Norms

Greetings from Aurobindo Healthcare Limited..! We are looking for Quality Control - ( Executives/ Senior Executives) Plant Location :Aurobindo Pharma , APL Healthcare Limited- Unit 4 , SEZ Menakur , Naidupeta, Andhra Pradesh.(50 KMS from Thirupathi, 60 KMS from Nellore) Handling of OOS and OOT Investigations, Change controls, Planned and un-planned deviations.Handling of Microbiology method suitability and other validations.Knowledge about the Antimicrobial Efficacy test Hands on Experience in Antibiotic assay Handling of cultures and Environmental isolates.Desired Candidate Profile Quality Control (MSc - Microbiology) with minimum 4 - 8 years experience only preferably Pharma Formulations.Preference will be given only to candidates who are Formulations - OSD background.Perks and Benefits Salary will be best and based on candidate caliber and competency.

Preferred candidate profile Passionate Pharma Recruiter with hands-on experience in bulk hiring.Demonstrated hunger for achieving set targets.Ability to influence and persuade.

Responsibilities:Manage preparation, review, and timely revision of SOPs, GTPs, and guidelines.Oversee DMS applications and ELN systems. Review and approve analytical protocols, reports (e.g., Method Validation, Verification, Regulatory Queries, Equivalency, PDR, MFC, AMT), and instrument qualifications.Conduct internal audits, lab monitoring, and ensure compliance with GDP and GLP standards.Provide training, review QMS documents (Incidents, Deviations, Change Control), verify electronic data, perform audit trail reviews, and assess Computer System Validation reports

Experience in pharmaceutical research, experimentation, and data interpretation based on the analytical results . Proficiency in laboratory techniques, handling of equipment’s and GMP knowledge. Good knowledge on the scale-up factors from R D to EB scale. Good formulation development knowledge and passion to become scientist. Knowledge on the pharmacokinetics of drugs is mandatory and proficiency in BE studies is required. Knowledge of regulatory requirements and quality standards in the pharmaceutical industry. Excellent problem-solving, critical thinking, and communication skills

Role & responsibilities Post ApprovalPre ApprovalDossier CompilationLife Cycle ManagementPreferred candidate profile Europe Market

Role & responsibilities Collaborate with department managers to forecast future hiring needs.Proficient in HR databases and Applicant Tracking Systems Work closely with managers to gain a comprehensive understanding of the organization hiring needs for every role, and to meet competitive hiring goals and expectationsFoster high-touch relationships using a database of qualified candidates to choose from when positions become openUtilize knowledge of multiple recruiting sources and execute innovative strategies to find quality candidates and prospect for new businessScreen resumes and CVs and manage job candidates throughout hiring process, from interview preparation to final-offer negotiationReviewing resumes and screening candidatesScheduling interviews by coordinating with candidates and hiring managersNegotiating job offers and compensation packages with candidatesStaying updated about hiring trends and best practices.Preferred candidate profile For Senior Executive 5+ years of experience in recruitment Excellent oral and written communication skillsAbility to manage and handle multiple tasks Perks and benefits Work Location : Jadcherla-Mahbubnagar- Telangana

Role & responsibilities Lead,OPEX,Purchase,InjectablePreferred candidate profile Perks and benefits

Role & responsibilities Good work experience in Business development & Portfolio management of Pharmaceutical (Generic) products.Identify, pursue New Business Opportunities (new suppliers)Manage Strategic partnerships, AlliancesCustomer/ Vendor Relationship management (Third-party)Contract management, negotiations & life cycle managementDrive revenue growth & improve margins through engaging alternate suppliers Stake-holder coordination (Sales & marketing, Business dev Regulatory, Supply Chain, R&D, Manufacturing, Commercial operations team)Preferred candidate profile Perks and benefits

Roles and ResponsibilitiesConduct analytical testing using various instruments such as GC, HPLC, XRD, LIMS, Empower3, and other relevant equipment.Develop and validate new methods for biochemistry tests to ensure accuracy and reliability.Collaborate with cross-functional teams to resolve issues related to test results or instrument malfunctions.Maintain accurate records of test data, instrument calibration, and maintenance schedules.Participate in continuous improvement initiatives to optimize laboratory processes.Desired Candidate Profile2-7 years of experience in a similar role within the pharmaceutical industry.MSC or B. pharm or M pharmStrong understanding of biochemistry principles and techniques including chromatography (HPLC), spectroscopy (GC), microscopy (XRD), mass spectrometry (LIMS).Proficiency with analytical instruments such as LIMS software for data management. API Experience will not be considered