We are looking for an experienced Assistant Manager for R2R, general accounting and month end closure activities in our internal Global Shared Services (GSS) which serves our US based pharma company. You will closely work with the GSS Head and the business controllers and ensure that accounting/ reporting is efficient and as per the given timelines. You must have a solid Shared Services background and consistently keep up-to-date with advancements in the field of automation/ service delivery. Role & responsibilities Responsible for monthly and quarterly closing and reporting of the entities as per Ind AS Review B/S and P&L GL accounts and recommend corrective/ provision entries Reconciliations- B/S accounts, Intercompany, Fixed Assets Create and post required Journal Entries and/ or purchase orders Audit support and provide required information and schedules for Audit and consolidation team Variance Analysis and profitability analysis MIS as per management requirements Consolidation and HFM experience are added advantage Preferred candidate profile CA/CWA with 2-6 years of relevant experience Good Communication skills and working knowledge of MS office applications specifically excel. Knowledge of ERP and consolidation software preferably Oracle/SAP/Peoplesoft. Prior experience in Month End closing and Reporting. Hand-on on systems and internal controls, knowledge of Ind-AS Shift Timings 1pm to 10pm- Monday to Friday.

We are looking for a highly capable reporting Analyst to own and scale the reporting, analytics, and data exchange systems within our Europe operations. This position is central to ensuring visibility into manufacturing performance, process traceability and enterprise data exchange. Role & responsibilities Data Gathering and Preparation Data Analysis and Interpretation Report and Presentation Development Business Process Improvement Collaboration and Communication Cross-functional communication Continuous Improvement mindset Preferred candidate profile Strong analytical and problem-solving skills. Proficiency in data analysis tools and techniques (e.g., SQL, Advance Excel, Python, R). Data visualization skills (e.g., Tableau, Power BI). Ability to communicate technical information clearly and concisely. Strong understanding of business processes and industry trends. Experience with databases and data warehousing Postgraduate/Graduate (Preferable MBA)

Role & responsibilities To support assigned Regions businesses with robust marketing support across multiple therapy areas like Anti-infectives, Urology, CVS, CNS & Oncology to facilitate the sales team across countries to achieve their budgets. Devise promotional strategies & marketing plans for branding of core products Plan & develop printed, electronic & other promotional materials throughout the year as per the approved promotional budget. Liaise with Regional & Country Heads, Marketing teams to assess the response to and suitability of current promotional materials. Enable effective planning & execution of the CMES for the important products across countries & support with necessary inputs like slide deck, CME Kits. etc To enhance prescription and prescriber base Conduct Quarterly Cycle meetings (Online & offline) in the core countries of the assigned region. training and Development of field force in the core countries of the assigned region. Drive identification, planning & launches of the new products across various therapies & countries for the assigned region. Enhancing In-clinic effectiveness of Sales Team Preferred candidate profile - Preferably B. Pharma, MBA - 10-16 years experience in domestic (India) Brand Management with renowned Indian Pharma companies. - Creative & strong marketing skills - Preferred exposure to Anti-infectives/ Urology/ CVS/ CNS brands/ therapy marketing - Experience of launching new products - Experience of handling multiple & diverse products’ portfolio - Credible and confident communicator - Proficiency in Excel & PowerPoint.

Key Accountabilities Process/ Operational: 1. Basic knowledge for Review of Pharmaceutical Development Report. 2. Basic knowledge / hands on experience of review of manufacturing documents like batch formula, batch manufacturing records, batch packaging records, yield and reconciliation, manufacturing summaries, in-process controls data, etc. 3. Basic knowledge / hands on experience of review of analytical documents like specifications, test procedures, method equivalency reports, method validation/verification reports and method transfer reports, dissolution protocols, stability protocols, extractable & leachable study reports, etc. 4. Basic knowledge / hands on experience for preparation, review and compilation of assigned ANDAs for submission. 5. Basic knowledge / hands on experience for preparation, review and compilation of Annual Reports (ANDAs/NDAs). Strategic: 1. Basic knowledge of ICH guidelines, FDA guidelines. 2. Knowledge of CTD modules 1,2 and 3.

Role & responsibilities Order Processing: Order Receipt, creation of Sales Order Check sheet, working with the CROM team to ensure the SOs are raised on time and as per procedure. Rolling Sales Forecast: Collaborating with Country Managers, receiving 24 months rolling Forecasts, take Region Head approval and upload the same on Disha and ERP for the region. Invoicing and Shipment Dispatches: Working closely with the FG warehouses for timely invoicing as per the committed billing plan for the region, coordinating with the logistics team to ensure the dispatch planning. Supporting the country teams with required shipment documents, follow up for required MOH import permits and timely shipments. Logistics Documentation: support the country teams with all required logistics documents for smooth clearances of the stocks. Proforma Invoices and Payment follow up: support country heads in timely payment receipts by creating proforma invoices as per the payment terms, take region head approvals for processing the same AMT material dispatches : Timely support to UAE to supply required AMT material by coordinating with tech support teams of various manufacturing sites. MIS and report generation: Working under the guidance of Region Head to create various reports for the region like maintaining order book, creating monthly billing plan, MIS report for the region, Spill over reports, RFD vs invoice reports.

Roles and Responsibilities Perform secondary operations such as HICART packaging. Operate blister packing machine, compression machine, coating machine, granulation machine, formulation machine (FBD), OSD machines. Ensure quality control measures are in place to maintain high-quality products. Monitor production processes to identify areas for improvement. Collaborate with team members to achieve production targets.

Responsibilities: Analytical method development/ verification & optimisation Analytical developmental support Analytical method transfer

Responsibilities: Review IP landscape reports, non-infringement& FTO analysis Devise strategies for patent non infringement and invalidations Collaborate with R & D Scientist to explore design around strategies for P-IV & NCE products Conduct IP due diligence for product selection/ new opportunity identification. Support RA for patent certification, PIL clearances and declaration Monitor, review and manage ANDA litigations Conduct patentability searches, draft and file patent applications and manage prosecutions Ensure timely and effective task delivery through strategic planning prioritisation and execution.

General Job Description Interact with cross functional teams (BD / CROM / Supply Planning / Material Planning Team) to provide and process information in response to inquiries, concerns and requests about pharmaceutical products and related services. Main Job Role and Responsibilities deal directly with CFT either by telephone, electronically or face to face respond promptly to inquiries, concerns & requests and communicate / coordinate with internal departments obtain and evaluate all relevant information to handle product and supply related inquiries Facilitate order acceptance direct requests and unresolved issues to the designated resource record details of inquiries, comments and complaints record details of actions taken Education and Experience PG in Pharmaceuticals or equivalent. MBAs would be preferred basic pharmaceuticals knowledge knowledge of relevant computer applications knowledge of administrative procedures numeric, oral and written language applications Expected work experience: 1-2 years in pharmaceutical or similar field(s) Key Competencies PG in Pharmaceuticals or equivalent to MBAs would be preferred basic pharmaceuticals knowledge knowledge of relevant computer applications knowledge of administrative procedures numeric, oral and written language applications Expected work experience: 1-2 years in pharmaceutical or similar field(s) interpersonal skills communication skills - verbal and written listening skills problem analysis and problem-solving attention to detail and accuracy data collection and management adaptability ability to take initiatives stress tolerance Designation will be decided after considering candidate's existing designation, experience and knowledge.

Work Location: Naidupeta, Tirupati District, Andhra Pradesh Experience Required: 8-12 years (OSD Process Maintenance) Qualification: • B.E. / B.Tech. in Mechanical, Electrical, Instrumentation or allied discipline. Key Responsibilities: • Plan, schedule and execute preventive, predictive and breakdown maintenance for OSD production and packing equipment (RMG, FBD, FBP, Fette/Sejong presses, auto coaters, capsule fillers, blister / bottle lines, etc.). • Lead troubleshooting and root-cause analysis to minimise downtime and improve Overall Equipment Effectiveness (OEE). • Prepare and control spare-parts inventory, maintenance budgets and AMCs. • Drive equipment qualification, calibration, re-validation and change-control activities in alignment with QA/Validation teams. How to Apply: Send your updated CV to: Ganesh.janne@aurobindo.com or WhatsApp: 8096888868 (Subject: AM/DM Process Maintenance OSD – ”)

Role & responsibilities Aurobindo Pharma Ltd. Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Assurance (Market Complaints / QMS / Validation / IPQA) Quality Control (GMP / GC / LCMS / HPLC) 3 Experience Required: 2 7 years (pharmaceutical manufacturing) Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Quality Assurance Key Scope • Handle Market Complaint investigations, trend analysis and regulatory responses • Maintain site QMS: Deviations, CAPA, Change Control, Audit readiness • Execute and review Equipment / Process / Cleaning Validation documentation • Perform IPQA activities: line clearance, in-process checks, batch record review • Conduct GMP & Data-Integrity training for shop-floor teams Quality Control Key Scope • Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. • Prepare/standardise 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 / B.Sc. / 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 • Send you updated resume : naidupetahr@aurobindo.com • WhatsApp : 9851444337

Job Title: Executive / Sr. Executive / Assistant Manager / Deputy Manager Production QMS (OSD) Work Location: Naidupeta, Tirupati District, Andhra Pradesh Experience Required: 3 15 years (must be from an OSD plant) Qualification • B.Pharm / M.Pharm Key Responsibilities • Own and update Production SOPs, BMR/BPRs, logbooks, and work instructions in line with cGMP and regulatory guidelines (US FDA, MHRA, EU, WHO, etc.) • Coordinate and investigate deviations, OOS/OOT, incidents, and execute effective CAPA & change-control activities • Perform risk assessments (FMEA/RA) for new processes, equipment, and layout changes • Conduct shop-floor audits, line clearance, and data-integrity checks; ensure readiness for all internal/external audits • Review and approve batch documentation; ensure timely batch release support in coordination with QA/QC How to Apply Email your updated CV to Ganesh.janne@aurobindo.com OR share via WhatsApp: 8096888868 (Subject/Message: Application – Production QMS (OSD) – ”) Join Aurobindo Pharma and be a key driver of world-class quality systems in our OSD operations!

Job Title : Capsule Filling Operator OSD (2-8 Yrs) Company : Aurobindo Pharma Ltd – Unit IV Location : Naidupeta, Tirupati (AP) Key Skills : Capsule Filling, Bosch/ACG Pam/IMA, BMR, cGMP, Hard-Gelatin Education : ITI / Diploma / B.Sc / B.Pharm Apply To : ganesh.janne@aurobindo.com | WhatsApp 8096888868

Role & responsibilities 1. Responsible for operation and maintenance of multi grade filter, softeners pre ultra-filtration, reverse osmosis, electro de ionization and post ultra-filtration feed and permit ,pressures, flows, voltage, and current in water system. 2. Responsible for operation and maintenance of purified water system, distribution systems and connected supervisory control data acquisition system. 3. Responsible to check the critical, non-critical alarms on daily basiss with respective to supervisory control data acquisition system reports as per the standard operating procedure. 4. Responsible to involve in the chemical preparations, chemical weighing and dosing as per the validated quantity as per the standard operating procedure. 5. Responsible for checking the regenerations and sanitization cycles as per the standard operating procedure. 6. Responsible to perform the preventive maintenance of purified water system as per the schedule and record in the log books. 7. Responsible to bring spares/items for any maintenance activities as per indent. 8. Responsible to involve in execution of qualification activities and follow the good engineering practices at work areas. 9 .Responsible to involve in the water system periodic validations in all areas. 10. To follow the laid down quality culture principles and behaviors. 11. To follow and ensure compliance on environmental management systems related procedures. 12. Shall follow any other departmental activity assigned by head of the department or designee. Qualifications: ITI/Diploma / Any Graduation Experience: 2 to 6Years How to Apply: Share your CV to naidupetahr@aurobindo.com Interview Mode : Virtual

Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh WERE HIRING | Aurobindo Pharma Ltd. Unit IV (Oral Solid Dosage) Work Location: Naidupeta, Tirupati District, Andhra Pradesh Tablet/Pellet Coating Operators (2-7 yrs) | Key Responsibilities • Run tablet / pellet coating machines (Glatt, Gansons, ACG, etc.). • Mix coating solution and load materials as per the batch sheet. • Set and watch basic machine settingspan speed, temperature, spray rate. • Do simple in-process checks (weight gain, colour, appearance) and note results. • Fix small issues like blocked spray guns or wrong settings; call maintenance if bigger problems arise. • Keep all records, logbooks and tags up-to-date, neat and accurate. • Clean the machine and area after every batch; get line-clearance before the next product. • Follow cGMP, safety and PPE rules at all times; report any deviations. • Work closely with QA, engineering and warehouse teams for smooth flow. • Share ideas to cut waste, improve yield and speed up the process; help train new helpers/operators. Have hands-on experience on Glatt, Gansons, Sejong or Bohle auto-coaters? US-FDA approved OSD facility and accelerate your pharma journey! ITI / Diploma / Any Graduation Exposure to cGMP & global audits How to Apply Email your CV (Subject: Coating Operator 2-7 Yrs) to: naidupetahr@aurobindo.com OR WhatsApp to: +91 80968 88868 Immediate / 30-day joiners preferred.

Job Description (Global Legal) 1. Drafting, reviewing, vetting of various cross border commercial agreements like: Confidentiality agreements; Service Agreements, In-Licensing and Out-Licensing agreements, Supply Agreements, Distribution Agreements, Agency Agreements, Consultancy Agreements, Clinical Trial Agreements, API supply and procurement Agreements, Shareholders Agreements, Share Purchase/Asset Purchase Agreements, MOUs, JV agreements, Contract Manufacturing Agreements, Customer Protection agreements in accordance with the regulatory requirements in Europe, USA, and other rest of the World countries. 2. Handling Due Diligence in Mergers & Acquisition Projects, JV Projects. 3. Drafting employment agreements for the employees of Aurobindos overseas subsidiaries in consultation with local law firms 4. Drafting and reviewing of all other agreements with respect Aurobindos overseas subsidiaries 5. Active participation in the negotiations with the customers for concluding the agreements. 6. Handling cross border disputes/litigationarbitration and courts 7. Maintaining central archive for all the agreements.

Job Title: Project Manager - New Product and Project Launches (Private Label OTC) Location: Aurohealth Corporate Office Department: Aurohealth Project Management Reports To: Senior Project Manager US GM Supply Chain Company Overview: We are a leading consumer products company specializing in private label over-the-counter (OTC) healthcare products . Our commitment to quality and innovation has made us a trusted partner for major retailers, including Walmart, CVS, and Walgreens. We pride ourselves on delivering high-quality products and maintaining strong relationships with our customers. As we continue to expand our portfolio, we are looking for a highly motivated Project Manager to join our team and oversee the successful launch of new products and projects. Position Summary: The Project Manager will be responsible for overseeing the planning, development, and execution of new product and project launches within the private label OTC sector . This role will focus on managing the lifecycle of product introductions for key customers such as Walmart, CVS, and Walgreens . The ideal candidate will possess strong project management skills , a solid understanding of the retail and OTC markets , and a proven ability to work collaboratively with cross-functional teams to meet customer expectations and timelines. Key Responsibilities: New Product Launches: Manage the end-to-end process for new product launches, from concept through production and delivery to customers like Walmart, CVS, and Walgreens. Project Coordination: Work closely with internal teams (PD, marketing, sourcing, logistics, quality control) to ensure smooth project execution and alignment with customer specifications. Customer Communication: Act as the primary point of contact for major retail customers, providing timely updates on product development progress, addressing customer needs, and resolving any issues that may arise. Timeline Management: Develop and maintain detailed project plans, ensuring that milestones, deadlines, and budgets are met for all product launches. Cross-functional Collaboration: Coordinate with departments such as supply chain, sourcing, and regulatory to ensure all necessary steps are completed for successful product launches. Retailer-Specific Requirements: Ensure that all products meet the specific standards and expectations of key retailers (Walmart, CVS, Walgreens) including packaging, labeling, and regulatory compliance. Risk Management: Proactively identify potential risks or delays to project timelines and work to resolve them before they impact product launch or customer satisfaction. Reporting & Documentation: Provide regular status updates to senior management and stakeholders on the progress of each project, including any changes to scope, timelines, or costs. Market Insights: Stay current on industry trends, customer preferences, and competitive products to ensure that our offerings are aligned with market demand. Required Skills & Qualifications: Bachelors degree in Business Administration, Marketing, Project Management, or related field (or equivalent experience). 3+ years of project management experience , preferably in the consumer products, private label, or OTC sectors. Experience working with major retailers such as Walmart, CVS, and Walgreens is highly preferred. Strong understanding of OTC products , including regulatory standards, packaging requirements, and retail-specific needs. Proven ability to manage multiple projects simultaneously and deliver results on time and within budget. Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders. Strong problem-solving and decision-making abilities. Proficiency in project management tools (e.g., Microsoft Project, Asana, Trello) and Microsoft Office Suite (Excel, PowerPoint, Word). Strong attention to detail and organizational skills. Ability to work in a fast-paced environment and handle competing priorities. Decent understanding of packaging & development Preferred Qualifications: PMP certification or equivalent project management training is a plus. Experience in private label development and OTC healthcare product regulations.

Preparation, review and compilation of assigned ANDA/NDA [505 b (2)]/projects for filing and knowledge of eCTD, Module 2 and 3. Hands on experience in reviewing CMC documents of Solid and Liquid Oral Dosage forms. Preparation, review and compilation of Supplements and Amendments. Review of Pharmaceutical Development Reports Review of manufacturing documents like batch manufacturing records, batch packaging records, yield and reconciliation, manufacturing summaries, hold time study reports, master formula cards, master packaging cards etc. Review of analytical documents like specifications, test procedures, method equivalency reports, method validation/verification reports and method transfer reports, dissolution protocols (multi point, multimedia and alcohol dose dumping etc), stability protocols and stability data

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 - Engineering - Injectables Qualification - Diploma / B Tech Designation - Sr. Executive / Executive/ Technical Assistants Experience - 4Yrs to 12 Yrs. Skills - BMS / Calibration / Process Maintenance Job Description: BMS: Hands on experience in BMS,IBMS,UMS,CCTV, (Software &Hardware), HVAC controls and door interlock system. Calibration : Hands on experience in calibration to verify the calibration activity related to all the sterile instruments/ equipments and verify/review the raw data, calibration reports, schedule verification, compliance towards QMS and Spares managements, . Having hands of experience in trouble shooting of calibration instruments/ equipments Process Maintenance: Hands on experience in shift maintenance, breakdowns and preventive maintenance of washing, tunnel, filling, capping machine and Autoclave, terminal sterilization (TS) compounding vessels, CIP& SIP skids , Lyophilisation (Lyo) and other process equipment's Work Location : Eugia Unit -3, Pashamylaram. Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090. Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama

Dear Aspirant , Greetings From Eugia Pharma Specialties Limited (Aurobindo Group)!!!! We glad to inform you all that we planned Walk In Interviews for below vacancies in our Manufacturing unit. Department : Quality Assurance (IPQA) No. of Vacancies : 30 Education Qualification : B. Pharmacy / M Pharmacy Experience : 2-5 Years Designation : Executive Required Skills : Aseptic Area Monitoring / Environmental Monitoring / Aseptic behavior / Media Fill / Gowning Practices / Sterility Assurance/ In Process checks in Injectable Work Location : Eugia Unit -3, Pashamylaram Walk In Details: Date : 29.06.2025 Time : 09 AM - 02 PM Venue : Aurobindo Pharma Limited - Unit - 3 Sy. No. 313, Bachupally, Hyderabad, Telangana 500090 Google Map : https://maps.app.goo.gl/qoL8vZ6EwDm5GcWb8 Contact : Mr Prabhakar / Ms Rama