Department LIVA PHARMA Job posted on May 06, 2025 Employment type T-T8-Trainee-HO Executive INVITING CANDIDATES FOR ZYDUS LIFESCIENCES LTD. VADODARA We are hiring for Injectable Manufacturing plant Production Apprentice: Fresher Education : 10th /12th / ITI / D.Pharm / Diploma in Engineering Passout Year : 2022,2023,2024 ,2025 Packing Apprentice: Fresher Education : 10th /12th / ITI Passout Year : 2022,2023,2024 ,2025 Engineering Apprentice: Fresher Education : 10th /12th / ITI / Diploma in Engineering Passout Year : 2022,2023,2024 , 2025 Job Location: Jarod , Vadodara To apply , Share your updated resume on Prem.Kumar2@zyduslife.com

Department DESIGN STUDIO Job posted on May 06, 2025 Employment type P-P7-Probationer-HO Staff JOB DESCRIPTION for DTP/Graphic Design Expert – Multilingual (Gujarati, Hindi & English) Department: Zydus Design Studio Qualifications Required : Diploma/Certificate from a reputed Institute or equivalent. Reporting: HOD, Zydus Design Studio Location: Zydus Corporate Office, Ahmedabad, Gujarat. Type: Full Time Experience: 4-7 Years Job Description: We are looking for a skilled and detail-oriented DTP (Desktop Publishing) Expert with strong proficiency in Gujarati, Hindi, and English languages. The ideal candidate will be responsible for creating high-quality publication and communication materials in multilingual formats. This role requires a strong eye for layout, language-specific typesetting, and brand consistency across formats. Key Responsibilities: Design and format documents, design templates, reports, brochures, communication materials, and other publications in Gujarati, Hindi, and English. Ensure language accuracy and proper formatting in all vernacular design outputs. Work closely with the design and content teams to translate concepts into visually compelling layouts. Maintain brand consistency across all materials and adhere to style guidelines. Prepare print-ready files and coordinate with printers/vendors as needed. Support the development of templates and design assets for recurring publications. Stay updated with the latest DTP tools, fonts, and layout trends, especially in multilingual publishing. Required Skills & Qualifications: Proven experience in DTP and multilingual design work, preferably in a corporate or agency environment. Proficiency in design and publishing software (Adobe InDesign, Illustrator, Photoshop and the most recent social media apps like Canva, Adobe Express etc.). Strong command of Gujarati, Hindi, and English for accurate typesetting and layout. Experience in designing materials for print and digital mediums. Attention to detail and excellent typographic skills. Ability to manage multiple projects with tight deadlines. Preferred Qualifications: Diploma in Graphic Design, DTP, Visual Arts, or a related field. Familiarity with working in a regulated or corporate environment (pharmaceutical or healthcare sector experience is a plus). Basic understanding of content localization and regional design sensibilities. Why Join Us? Be part of a collaborative and creative in-house design studio. Opportunity to work on meaningful communication that impacts thousands across the organization. Room for growth, learning, and working on diverse projects. - About the Design Studio The Zydus Design Studio is a vital part of Zydus Lifesciences Limited, comprising a team of multidisciplinary design professionals. We specialize in delivering innovative and visually compelling design solutions across multimedia platforms. Our strength lies in combining artistic finesse with strategic execution, enabling seamless integration across print, digital, and tech-based mediums. Committed to creative excellence, the studio continues to push boundaries to craft design narratives that leave a lasting impact.

Department PTC - CHANGODAR Job posted on May 06, 2025 Employment type P-P6-Probationer-R&D Executive Formulation development of topical dosage form and oral liquid dosage form for regulatory markets. Additional e xperience on solid dosage form is advantageous. Literature search for assigned projects Planning and organizing day-to-day research activities along with group leader for timely completion of projects Preparation of various documents like PDR, MFC, BMR, scale-up protocol and other technology transfer and regulatory documents Support in Manufacturing of clinical, scale-up and exhibit batches whenever required

Department FILL AND FINISH Job posted on May 11, 2025 Employment type P-P6-Probationer-R&D Executive Perform all Application Administration for QC and MFG Departments. Implementation of desktop policy and its adherence. Execution and Verification of backup and restoration and documentation of this activity. Prepare and/or Review software qualification for activity including challenge test with documentation. Liaison with Service Engineer. Maintain the Instrument Applications Inventory. Training record of user shall be available for applicable SOPs. Training and Support to End User and Service Engineers. Responsible to explain internal, external auditor / regulator. Follow Site QMS procedure. Responsible for preparation, review and adherence of SOP & its attachments at all locations. Monthly Review of Site Annexures and its reporting. Project Management for New Validation Projects. Preparation and Presentation of Monthly Report.

Department ALIDAC QA Job posted on May 12, 2025 Employment type P-P7-Probationer-HO Staff ZTMP – REQUEST FORMAT Name : Garima Jha BU : Quality Place : ZLL-SEZ Oncology Injectable, SEZ, Matoda, Ahmedabad. Contact # : 9173639189 Email Id : Garima.G.Jha@ZydusLife.com Basic Details: Position : Senior Executive Designation : Senior Executive Reports to : Deputy Manager Department : Quality Assurance Location : ZLL-SEZ Oncology Injectable (Alidac) No of Posts : 1 Role : Critical Neev Level : 1 Details : Replacement Position code : 60056568 Position Name : Senior Executive Key Job Description: (Not more than 5 points in 6 lines) Lab QA Role - To review Raw Material, Packaging Material, In-process, Finished product, shelf life specification and its relevant Method of analysis and authorize the Testing work sheet. To review and approved analytical data of Raw material, Packaging material, In-process, Finished product, Stability study and Consumable materials in LIMS. To ensure the compliance and routine checks of current Good Laboratory Practices in the Quality Control department. To review chemical and microbiological analytical method validation, method transfer and Verification protocol and report. Handling, storage, withdrawal and reconciliation of stability samples in LIMS or out of LIMS. To review analytical data and trend summary reports of stability studies. To verify the outside laboratory samples and it’s reports. To ensure and review Change control, Deviation, LIR, OOS, OOT, OOC, CAPA, Trends and other investigations of quality control and quality assurance department. To initiate the departmental change control, deviation, CAPA, BDIF and investigation report. To review the qualification and calibration documents of QC instruments/equipment’s. To review stability protocol and approved the schedule related to quality control department. To prepare and review, stability schedule, other study protocol and their reports as per requirements. To prepare and review the qualification/validation documents related to quality assurance. To review the audit trial of the QC instrument or equipment, Stability chambers/incubators. Temperature and humidity data recording, review and approved for stability chambers/incubators and respective rooms. To participate in regulatory audit and its compliance. Notify event of QMS to customer and compliance team, response to their query/comments. Handling and trending of Oversight observation and its compliance. To provide the Quality index and Quality Management review data. To ensure calibration, Qualification and Preventive maintenance of incubators and chambers as per schedule. To ensure and review the Alarm logs, alarm acknowledgement, alarm trending and alarm assessment. To review Critical Quality Attributes trend data. To review the protocol, analytical data and report for in vitro Bioequivalence studies. To receive, store, control, reconcile, retain and destroy Investigational products for in vitro Bioequivalence studies. Review and approved the data in LIMS (Laboratory Information Management System). Requirements: Qualification : B.Sc./M.Sc./B.Pharm/M.Pharm Years of Experience : 5 to 10 years Experience in Zydus : 2 years Experience / Exposure in (2 points) : Must have knowledge and experience in injectable plant. Mail your CVs to: Garima.G.Jha@ZydusLife.com/HardikA.Bhatt@ZydusLife.com

Division ALIDAC QA Job posted on May 12, 2025 Employee Type P-P7-Probationer-HO Staff Experience range (Years) 5 years - 10 years ZTMP – REQUEST FORMAT Name : Garima Jha BU : Quality Place : ZLL-SEZ Oncology Injectable, SEZ, Matoda, Ahmedabad. Contact # : 9173639189 Email Id : Garima.G.Jha@ZydusLife.com Basic Details: Position : Senior Executive Designation : Senior Executive Reports to : Associate Manager Department : Quality Assurance Location : ZLL-SEZ Oncology Injectable (Alidac) No of Posts : 1 Role : Critical Neev Level : 1 Details : Replacement Position code : 60055060 Position Name : Senior Executive Key Job Description: (Not more than 5 points in 6 lines) QA-QMS Role - To perform investigation of Deviation, Market complaint, Adverse Drug Events, Alert notification and product failures as per approved procedure. To ensure proper justification for the change proposed with its impact analysis, risk assessment and effectiveness check with its acceptance criteria. To complete the preliminary investigation and final investigation report within stipulated time. To do document historical check with inference by examining relevant data sources with respect to the nature of the event. To use appropriate investigation tool for investigation. To collect circumstantial evidence and considering for investigation. To interview personnel involved if needed in such a way that its relevant and adequate to identify cause. To review batch records & relevant records and identify the indicators of an event. To identify the root cause based on investigation outcome. To perform vertical and horizontal impact assessment based on the root cause. To coordinate with cross functional team for immediate action which may be deemed necessary to isolate the event, to limit any adverse effect on production, materials, equipment, areas, processes, procedures including discontinuation of processing or quarantine. To coordinate with contract givers for alert notification filing to the Agency, if applicable. To derive on appropriate CAPA in consultation with CFT for the event with a justifiable target completion date. To determine appropriate CAPA effectiveness plan. To Handle the Change control and check the effectiveness of the proposed change. To prepare, execute and review of Process Validation and Cleaning Validation. To prepare and review SOP’s in documentum software against current regulatory guidance. To do trend analysis of QMS (Change control, deviations, CAPA, market complaints, FAR, and Product recall ). To participate in Regulatory audit/ Customer audit and its compliance. To do trend analysis of repetitive issues. To discuss outcomes of trend analysis with the QA head and suggest appropriate CAPA. To have a focus on the investigation to get the consistency for improving the quality of investigation. To evaluate the change for its impact and recommend actions based on the change, to identify any additional members required for evaluation based on the change proposed. To maintain online entries in ZyQMS. To maintain APQR calendar/ schedule. To prepare and review the APQR. To monitor and prepare CPP report of product through validator and Minitab software. To prepare and review the visual inspection rejection trend in Minitab software. Requirements: Qualification : M.Pharm Years of Experience : 5 to 10 years Experience in Zydus : 2 years Experience / Exposure in (2 points) : Must have knowledge and experience in injectable plant. Mail your CVs to: Garima.G.Jha@ZydusLife.com/HardikA.Bhatt@ZydusLife.com

Division ZRC BIOTECH Job posted on May 13, 2025 Employee Type P-P6-Probationer-R&D Executive Experience range (Years) 6 years - 10 years Prepare and review continued process verification reports for ongoing commercial products & communicate risks for taking appropriate measures for mitigation. Maintain timeline for completion of the reports along with approval. Ensure identification of CQAs and CPPs & assess the risks in the on-going products and processes. Prepare & analyse trend analysis of critical material attributes, critical process parameters, and critical quality attributes by using Minitab software and interpret same for identifying opportunities and solutions. Review & compute Process capability to understand the health of product and identify the batches which are contributing towards Poor capability index. Communicate the early risks identified by poor capability to concern Head Escalate Issues related to the Process, Product, Quality, Cleaning process or documentation related activities to his/her immediate supervisor and take the appropriate action related to it. Escalate any failures and overdue activity that can have a potential impact on product quality to his/her immediate reporting authority. Venue : Begumpet Rd, Leelanagar, Begumpet, Hyderabad, Telangana 500016 Date and Time : 18/05/2025 (Sunday) @ 09.00 am to 05.00 pm.

Department GDSO Job posted on May 14, 2025 Employment type P-P8-Probationer-HO Executive Role: Demand Planner – EMB Market Designation: Deputy Manager Experience: 6 – 12 Years Education: BPharm/ BTech; Preferred: MBA (SCM) Location: Zydus Corporate Office Job Description: Demand Planning: Ensure finished goods (FG) availability at points of sale according to market requirements. Inventory Management: Oversee FG inventory at all levels in accordance with established norms. Manufacturing Plan: Prepare monthly manufacturing plans for Material Requirements Planning (MRP) runs. Production Prioritization: Review and prioritize production plans within SKUs across markets to maintain sales continuity. Cross-Functional Coordination: Collaborate with Marketing, Regulatory, Quality, Manufacturing, and P&D teams to ensure smooth supply chain operations. MIS Preparation: Develop various Management Information Systems (MIS) reports (MPRM, S&OP, etc.) for dynamic monitoring and control of business operations. S&OP Participation: Engage in Pre-S&OP and S&OP discussions for business cycles and escalate unresolved issues. Demand Management: Handle sudden changes in demand to seize sales opportunities and balance inventory levels. New SKU Launch: Coordinate activities related to the launch of new SKUs. Required Skills: Strong analytical and problem-solving skills. Excellent communication and coordination abilities. Proficiency in inventory management and forecasting tools. Ability to work collaboratively with cross-functional teams. Strong attention to detail and organizational skills.

Department INFOTECH Job posted on May 23, 2025 Employment type P-P8-Probationer-HO Executive Title: CSV - IT Location: Gujarat Qualification: BCA / MCA Experience: 4+ years Key Responsibilities: Perform all Administration activities as mentioned in the user management SOP. Responsible for Activation/Reset/Change/Deactivation of User Access (24x7). Review, configure, and manage the Privilege Right Matrix. Prepare, create, and deactivate/update User Access Matrix. Provide access to service engineer user accounts and review service engineer audit trials. Prepare and update application-wise process steps for user management. Prepare and update the list of applications. Prepare and implement site SOPs and ensure their periodic updates. Prepare/Review qualification protocols and participate in all instrument and software qualification activities, including challenge tests with documentation. Handle all IT-related QMS activities (e.g., Change Control, Deviation, CAPA, Incident, Qualification documents, SOPs, etc.). Responsible for Backup and Restoration activities. Provide support during software assessment and mitigation plans. Provide support during software maintenance and network-related problems. Participate and ensure compliance with periodic reviews. Conduct periodic verification of GLP and desktop policies. Conduct risk-based network failure tests periodically. Explain the IT role in analytical applications and user management to internal/external auditors and regulators. Communicate effectively with middle/senior management. Capable of handling a team.

Department FILL AND FINISH Job posted on May 27, 2025 Employment type P-P6-Probationer-R&D Executive 1. Quality Control Operator: ITI with 1 to 5Years of relevant experience in handling of samples, chemicals, reagents and SAP for procurement. Analyst- Chemical: B.Pharm/B.Sc/M.Sc. with 2 to 8 years of hands-on experience on HPLC, GC, Dissolution apparatus and UV –Visible Spectrometer. Should also have knowledge of weight analysis, stability studies, for Injectable dosage forms. 2. Warehouse Shift In charge - Any Graduate/ Postgraduate with 6 to 10 years in warehouse operation and activities maintenance of inventory. Should have exposure of SAP. Operator/Tech Assistant - DME/ITI/H.Sc. with 1 to 7 Years of relevant experience of Warehouse operations. Maintain inventory and accurate records of stock transactions. Exposure of ASRS. 3. Engineering Operator/ Tech Assistant - Engineering: Diploma/ITI with 2 to 8 Years of experience in the Process maintenance, Instrumentation, Water System and FMS/ BMS in Injectable Plant. 4. Production Shift In charge - B. Pharm / M. Pharm / B.E /B.Tech. with 2 to 6 years of experience supervising and controlling production areas like Aseptic Filling, Vial Washing, Autoclave and Lyophilizer. Exposure of machine qualification activity will be added advantage. Operator/Tech.Assistant (Autoclave, Filling, Compounding, Washing/Tunnel/Capping & Lyophilizer)D. Pharm/DME/ITI with 1 to 7 Years of relevant experience in operating production machines like Autoclave, Filling, Compounding, Washing/Tunnel/Capping, Lyophilizer. For all the positions, candidates should also have sound knowledge cGMP documentation and must be familiar with cGMP requirements. Interested candidates may “Walk-in-interview” for an interview along-with their updated CVs, latest passport sized photo, Salary Slip and relevant documents as per below schedule: Date: Sunday, 1st June 2025 Timings: 8.30 a.m. - 4.00 p.m. Venue: Hotel Fortune Park Galaxy National Highway Number 8, GIDC, Vapi, Gujarat 396195

Department Ambernath Mfg. Job posted on Jun 02, 2025 Employment type C-C8-Confirmed-HO Executive Person required for Indirect Procurement at Zydus Lifesciences, Ambernath, Maharashtra Summary Statement: The incumbent will be responsible for the timely procurement of Machines & Engineering spares, consumables & services, QC consumables and equipment, Admin Services and IT services. Qualification: BE in Mechanical Designation: Asst. Manager./ Sr. Executive Experience: 6 to 8 year of experience in Indirect purchasing. Experience in Pharma will be preferred. Major Responsibilities (KRA) : Candidate will be responsible for following: Understanding of user requirement for Purchasing of Spares, Machines, services, consumables, QC Chemical & consumables etc. Prepares & develops bid documents to obtain competitive quotations. Preparation of techno -commercial comparison. Converting PR to PO as per Techno –Commercial recommendation. Ensuring timely delivery of goods. Vendor evaluation as per performance. Preparation & maintain records & documentation of all solicitation, Communications, contracts & related follow ups. Competencies : To conform above job, Following are expected competencies: Technical : Technical understanding of Pharma Machines, Pharma consumables/Chemicals, Utility machineries i.e. HVAC, Boiler, Water treatment, BMS, Pharma QC equipment, Power distribution, LT,HT, DG etc. Analytical : Collecting, comparing & relating data from different sources, identifying issues, anticipating problems Commercial Skills : Negotiation skills & Knowledge of applicable taxes for purchasing goods & services. Computer Skills : SAP (MM module), Excel, Word, Power Point & good typing skill. Team Skills : Being able to work collaboratively with others in participative way; working independently as well as working on a team.

Department GOA QC Job posted on Feb 12, 2025 Employment type P-P8-Probationer-HO Executive Please enter job description : The review includes verifications and approved of test reports of Raw materials, In-process Samples, finished, Stability, Calibration & Validation, Environmental monitoring reports of production & microbiology lab, Identification of microorganism (Vitek 2 compact), Biological indicator, BET, sterility, water reports etc. Review of analytical documents and approval through LIMS. Protocol and summary report preparation of method validation of MLT, BET, STERILITY and other miscellaneous study protocols, summary reports etc. Qualification and validation documents reviewed. Handling & Investigation of Microbiological Non-conformances like OOAC, OOAL, OOS and other errors related to microbiological incidences, transcription errors etc. Software handlings like LIMS, SAP, Ample logic, DMS etc. Ensure adherence of cGMP & cGLP regulatory requirement as per standard operating procedure & assurance of the same by means of regular monitoring.

Department SIKKIM QA II Job posted on Jun 25, 2025 Employment type C-C7-Confirmed-HO Staff Candidate must be able to monitoring of entire production operations and confirm quality conformance to specifications in shift. Candidate is able to handle IPQA production and packing area. Candidate must be able to review online documents. Candidate must be aware about SAP. Candidate must be aware about GMP, GDP, Alcoa Candidate must be able to review different floor test.

Department SIKKIM FORMULATION Job posted on Jun 25, 2025 Employment type P-P2-Probationer-Operator Name of the Company – Zydus Healthcare Limited Industry – Pharmaceuticals Website of the company - https://www.zyduslife.com/zyduslife/ Location –Sikkim Unit II Position - Technical Assistant / Plant Operator Qualification – Diploma / ITI / BA Experience Required – Between 3 - 8 Years Of Experience Role – Machine Operator Area – Granulation / Compression / Capsule / Coating Job Summary Responsible for manufacturing drug products as per BMR and SOPs, maintaining GMP standards, equipment operation, and documentation. Key Responsibilities Doer Role (Operator): Operate, clean, and changeover equipment as per SOP. Manufacture products as per BMR and conduct in-process checks. Maintain area hygiene and follow gowning/PPE procedures. Monitor environmental parameters (Temp, RH, DP). Handle process materials and equipment qualification. Report quality issues and unsafe conditions. Maintain accurate documentation (e.g., PLC printouts). Requirements Good understanding of manufacturing processes and equipment. Strong documentation skills (ALCOA compliance). Adherence to cGMP and internal policies (including PRM). Attention to detail and readiness to support validation activities.

Department SIKKIM FORMULATION Job posted on Jun 25, 2025 Employment type P-P2-Probationer-Operator Name of the Company – Zydus Healthcare Limited Industry – Pharmaceuticals Website of the company - https://www.zyduslife.com/zyduslife/ Location –Sikkim Unit I Position - Technical Assistant / Plant Operator Qualification – Diploma / ITI / BA Experience Required – Between 3 - 8 Years Of Experience Role – Machine Operator Area – Granulation / Compression / Capsule / Coating Job Summary Responsible for manufacturing drug products as per BMR and SOPs, maintaining GMP standards, equipment operation, and documentation. Key Responsibilities Doer Role (Operator): Operate, clean, and changeover equipment as per SOP. Manufacture products as per BMR and conduct in-process checks. Maintain area hygiene and follow gowning/PPE procedures. Monitor environmental parameters (Temp, RH, DP). Handle process materials and equipment qualification. Report quality issues and unsafe conditions. Maintain accurate documentation (e.g., PLC printouts). Requirements Good understanding of manufacturing processes and equipment. Strong documentation skills (ALCOA compliance). Adherence to cGMP and internal policies (including PRM). Attention to detail and readiness to support validation activities.

Department SIKKIM FORMULATION II Job posted on Jun 30, 2025 Employment type C-C7-Confirmed-HO Staff Candidate must be qualified B. Tech/ Diploma ( instrumental or electrical background ) Candidate must be sound knowledge of PLC, HMI, Scada, CSV Candidate is able to handle Production and packing machine (OSD, MDI, Topical) engineering aspects. Candidate is proficient to handle troubleshoot.

Division SIKKIM FORMULATION II Job posted on Jul 01, 2025 Employee Type C-C7-Confirmed-HO Staff Experience range (Years) 3 years - 7 years candidate must be sound knowledge of PLC, Scada, HMI. Candidate is able to handle Production and packing machine breakdown. Candidate must be sound knowledge of QMS and CSV. Candidate must be proficient to handle troubleshot

Department SIKKIM FORMULATION II Job posted on Jul 14, 2025 Employment type P-P2-Probationer-Operator Name of the Company – Zydus Healthcare Limited Industry – Pharmaceuticals Website of the company - https://www.zyduslife.com/zyduslife/ Location –Sikkim Unit II Position – Plant Operator / Technical Assistant Qualification – Diploma / ITI Experience Required – Between 02 to 08 Years of Experience Role – Electrical Process Operator(Electrical) 1. Attending day-to-day electrical breakdown related to the equipment of production area. 2. Responsible for smooth and efficient operation of the plant. 3. Carrying out the predictive & preventive maintenance of all the equipment related to production area 4.To check the equipment sequential log & to fill the breakdown in log if any. 5. Responsible for the other areas electrical breakdown in absence of technician 6. Responsible for developmental jobs, modification, alternation where ever necessary 7. Other responsibilities assigned by the seniors as and when required. 8. Responsible for taking all necessary and corrective actions against the Faults and Breakdown related issues in Production and Packing Area. 9. Inspection and supervision of all the machines for its smooth operation and also engage manpower in different maintenance related tasks that come up in the Area.