We are seeking a highly skilled and innovative AI & MLTechnology Specialist to drive AI initiatives within our HR function. Theideal candidate will explore and implement advanced AI and machine learningsolutions to enhance HR processes, leveraging cutting-edge technologies such as data lakes, AI/ML bots, predictive analytics, and automation frameworks . Key Responsibilities: Develop AI-driven HR Solutions : Identify and implement AI and ML applications to optimize recruitment, onboarding, employee engagement, performance management, and workforce planning. Data Management & Analytics : Design and manage high-end HR data lakes , ensuring data integrity, security, and accessibility for advanced analytics. AI/ML Bot Development : Work on intelligent HR chatbots for employee queries, HR service automation, and improving user experience. Predictive Workforce Analytics : Utilize machine learning models to analyze workforce trends, predict attrition, assess employee satisfaction, and optimize talent management strategies. Collaborate with HR & IT Teams : Partner with cross-functional teams to understand business needs, develop AI-driven HR solutions, and ensure seamless integration with existing HR systems. Research & Continuous Innovation : Stay up-to-date with emerging AI/ML trends, tools, and frameworks, recommending best practices for HR transformation. Qualifications & Skills: Bachelor's/Masters degree in Computer Science, Data Science, Artificial Intelligence, or a related field . Proven experience in AI & ML technologies , with a focus on HR applications. Strong knowledge of data lakes, predictive analytics, NLP, chatbot development, and automation . Proficiency in programming languages such as Python, R, TensorFlow, or PyTorch . Experience with HR tech platforms, cloud-based AI solutions, and big data analytics is a plus. Excellent problem-solving skills, analytical mindset, and ability to communicate technical concepts to non-technical stakeholders.

Knowledge of various type of instrument Calibration & maintenance like a D.P transmitter, pressure, level, flow transmitter, magnatic flow transmitter, mass flow mitter ( yokogawa, Abb, Rosemount), RTD, thermocouple ,Vibration probe, VFD etc. Configuration through HART communicator Knowledge of various type of instrument like pressure switch, temp switch, level switch, pneumatic switch, vega magnetic strip etc. Troubleshooting, Calibration & maintenance of control valve, SOV, ON off valve, weigh scale of coal plant, etc.

Literature survey for assigned projects. Analysis of innovator samples as and when provided. Preparation of test report against the Test request form received and compilation of results if necessary. Analytical method development of drug substances and drug products. Validation of drug products and verifications on activities for drug substances. To act as instrument in-charge for the allotted instruments and responsible for calibration and maintenance of the same. Carry out basic trouble shooting for instrument related issue, whenever required. ll Impart training with respect to instrument handling to junior colleagues. Preparation and checking ofMDR, MVR and MOA. Maintain GLP Activity in Laboratories. To participate in method transfer, critical analysis activity at plant or outside testing laboratories Analysis of development batches and stability batches. Writing of experiments online in Laboratory Notebooks (LNB) with all details. Processing of raw data and calculations after completion of each analysis.

Education: BPharm/ BTech; Preferred: MBA (SCM) 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.

Qualification should be M.Sc. Organic chemistry/ PhD with organic chemistry. Person shall be 3-5 year experience in PD Lab/R&D/QA Key Job Responsibilities Handling of the deviation, OOS, OOT, Marketcomplaint, Lab incident, CAPA. Handling of audits and compliance. Shop floor investigation to identify the rootcause. To form CFT for investigation and lead theinvestigation. To review an investigation plan. To provide necessary information and data forthe investigation. To ensure investigation is completed within timeline. If investigation is not completed in time, toensure Interim Report is prepared, reviewed and request for extension isapproved by QA head. To prepare and review investigation report andcause or probable cause for finding cause of failure. Discuss the findings and improvement areas basedon trend analysis in Quality Review Meetings. Preparation, review and approvalof trend analysis reports. Identification of improvement areas based ontrend analysis report and providing feedback to the site management. To propose an investigation plan and evaluationof the impact of failure on already distributed batches, batches undermanufacturing or in staging/ Process area. To find out root cause or contributory factorfor most probable root cause. To carry out impact assessment and riskassessment. To notify the other functional head to carry outinvestigation.

1. Review compliance against 21 CFR Part 11requirements for electronic data generating systems. 2. Review SOPs, Checklists, Test procedures,Formats, Master batch records and Laboratory testing worksheets foridentification of complex procedures/formats. 3. Review controls on computerized systemsto ensure data generated from these systems is meeting the data reliabilityrequirements. Review paper data, electronic data and audit trail of GMPactivities at the site to check adherence and compliance level with respect todata reliability. 4. Perform walkthrough on the shop floor toidentify the complexities in the processes which may lead to deviation fromALCOA+, and to take CAPAs as needed. Provide training to employees on thedifferent topics related to data reliability and data security aspects. 5. Review several trends (but not limitedto) like GDP error, OOS, deviation and lab incident and identify CAPAs asappropriate to prevent the departure from ALCOA+. 6. Perform periodic surveys (related toALCOA+) from employees, analyze feedback received from survey, and to takeCAPAs as needed. Review of investigations related to data reliability at site. Qualification : M.Sc./M.Pharm. Experience / Exposure in. (2 points) : Musthave knowledge and experience in injectable plant. Candidates with QC backgroundwould be preferred.

Qualification - Msc Chemistry - 3- 6 Yrs Experience Experience of GC / HPLC Preferred . Experience in Zydus : Min.12 months Job Responsibilities o Handling of HPLC system /GC o Up-keep of all Instrument Usage Log,Inward Register, Training Records etc. o Usage of SOPs, Specifications and STPfor Inprocess, Intermediate, FiniAsh Product, Recovered Solvents, and CleaningSample. o Handling of LIMS for Receiving ofsample along with Intimation Slip for Inprocess, Intermediate, Finish Product,Recovered Solvents, Cleaning Sample and outside sample etc. and testing as pertheir Specification and STP. o To follow the GMP, Safety norms andadhere to companys policy. o Attending Training classes i.e.Internal and External program as per schedule. Usage of SOPs, Specificationsand STP for Inprocess, Intermediate, Finish Product, Recovered Solvents, andCleaning Sample. o Receiving of sample along withIntimation Slip for Inprocess, Intermediate, Finish Product, RecoveredSolvents, Cleaning Sample and outside sample etc. and testing as per theirSpecification and STP. o After analysing and writinganalytical data, hander over the raw data to senior person for review. o Timely reporting of results andinvestigation of any deviation, OOS, incident. Maintain house-keeping and GLPin working area. o Additional Job activities endorsed bySuperior.

Zydus Healthcare is looking for Operator QC to join our dynamic team and embark on a rewarding career journey Inspect and test products for quality standards. Document and report quality issues and findings. Collaborate with production teams to address defects. Implement and monitor quality control processes. Conduct audits and ensure compliance with regulations. Provide training on quality standards and procedures. ITI with 1 to 5Years of relevant experience in handling of samples, chemicals, reagents and SAP for procurement.

Responsible to prepare analytical method development, development validation, method transfer protocol and reports. Perform F&D Trial sample analysis, Wet analysis and stability sample analysis with proper data complication. Operation of machine and instrument like HPLC(Make = Shimadzu,Thermo Software =Chromeleon, Lab solution,LC Solution), UV spectrometer (Make = Shimadzu, Software = Lab Solution), IR (Make = Shimadzu, Software = Lab Solution) Dissolution apparatuses, Liquid partical counter and Karl fischer for water content. Perform instrument calibration as per respective SOP daily pH meter calibration and balance verification.

Department: Analytical Development Injectables / Complex Injectables US Market Job Description: Method Development of Drug Product and Method verification of Raw Materials using HPLC, UHPLC with sound knowledge of Chromeleon & Lab solution software. To perform analysis of Drug Product and Drug Substances for various test parameters and as per the product development requirement. Compilation of analytical results and preparation Method Development Report. Literature survey to support method development of Drug product and characterization activity of Drug product. Compilation and monitoring of routine and stability analysis data. Support to formulation team to develop the drug product.

Zydus Healthcare is looking for COE - Operator to join our dynamic team and embark on a rewarding career journey Team Leadership: Leading and managing a team within the Center of Excellence. Strategy and Planning: Contributing to the development and execution of strategies and plans related to the area of expertise covered by the COE. Process Improvement: Identifying and implementing process improvements to enhance efficiency and effectiveness within the COE. Collaboration: Working closely with other teams and departments to ensure alignment with overall organizational goals. Training and Development: Supporting the training and development of team members to enhance their skills and knowledge. Project Management: Overseeing projects within the COE, ensuring they are completed on time and within budget.

To review Raw Material, PackagingMaterial, In-process, Finished product, shelf life specification and itsrelevant Method of analysis and authorize the Testing work sheet. To review andapproved analytical data of Raw material, Packaging material, In-process,Finished product, Stability study and Consumable materials in LIMS. To ensure the compliance and routinechecks of current Good Laboratory Practices in the Quality Control department. Toreview chemical and microbiological analytical method validation, methodtransfer and Verification protocol and report. Handling, storage, withdrawal andreconciliation of stability samples in LIMS or out of LIMS. To reviewanalytical data and trend summary reports of stability studies. To verify theoutside laboratory samples and its reports. To ensure and review Change control,Deviation, LIR, OOS, OOT, OOC, CAPA, Trends and other investigations of qualitycontrol and quality assurance department. To initiate the departmental changecontrol, deviation, CAPA, BDIF and investigation report. To review thequalification and calibration documents of QC instruments/equipments. Toreview stability protocol and approved the schedule related to quality controldepartment. To prepare and review, stabilityschedule, other study protocol and their reports as per requirements. Toprepare and review the qualification/validation documents related to qualityassurance. To review the audit trial of the QCinstrument or equipment, Stability chambers/incubators. Temperature andhumidity data recording, review and approved for stability chambers/incubatorsand respective rooms. To participate in regulatory audit andits compliance. Notify event of QMS to customer andcompliance team, response to their query/comments. Handling and trending ofOversight observation and its compliance. To provide the Quality index andQuality Management review data. To ensure calibration, Qualification andPreventive maintenance of incubators and chambers as per schedule. To ensureand review the Alarm logs, alarm acknowledgement, alarm trending and alarmassessment. To review Critical Quality Attributes trend data. To review the protocol, analytical dataand report for in vitro Bioequivalence studies. To receive, store, control,reconcile, retain and destroy Investigational products for in vitroBioequivalence studies. Review and approved the data in LIMS (LaboratoryInformation Management System). Requirements: Qualification : B.Sc./M.Sc./B.Pharm/M.Pharm Experience / Exposure in (2 points) : Must have knowledge and experience in injectable plant.

Qualification : B.sc/M.sc Microbiology Key Job Description Responsible forOperation of Steam sterilizer. Media Preparationand Growth promotion test. BET by Gel clotmethod. Maintenance ofIn-house and ready to use Standard Cultures. Handling andCalibration of instruments (TOC, pH/conductivity, Balance, Biosafety cabinet,Steam sterilizer, water bath, Heating Block, Microbial Air sampler etc). Monitoring ofIncubators and Temp and RH of respective area . Responsible forFollowing cGMP, GDP, GLP and approved SOP procedures as applicable whileperforming the assigned task. Responsible forEnsure the cleanliness of area and upkeep the workbench, glassware instrumentsand accessories essential for performing analytical/microbial activities. Maintaining stockof auxiliary materials required for micro department. Sampling andTesting of Water samples (Purified water/Process water, Potable water and RinseSamples) and maintaining the records of all types of testing. Sampling andtesting of MLT for API. Disinfectantefficacy testing. Environmentalmonitoring of PPA and Microlab. Preparation oftrend for water and EM. Sampling andTesting of Nitrogen gases and compressed Air gases. Performingoperation and calibration of pH meter, Conductivity meter, TOC analyzer, andAnalytical Balance. Sampling and Testingof all packaging material and maintain retention samples records. Preparationand Review of Protocol and reports

Literature survey for assigned projects. Analysis of innovator samples as and when provided. Analysis of development batches. Analysis of stability batches. Writing of experiments online in Laboratory Notebooks (LNB) with all details. Processing of raw data and calculations after completion of each analysis. Analytical method development of drug products. Analytical method verifications for drug substances. Preparation of Specifications-STP for Raw materials and finished products.

To review site responses to CAC audit foradequacy & supporting exhibits in ZyACTM. Tracking and review of regulatory/ Corporatecommitments. To organize compliance meeting, follow upmeetings / communication with site and CQ Leads to discuss unresolvedobservations or findings. To Present the progress in monthly reports forthe site (include ZyACTM Response of audit reports) and participation indepartmental meetings. To ensure SOP on Corporate Audit andCompliance is followed effectively. To participate in need based corporate auditsand compliance verification as per schedule. To support site for compliance duringpreparedness and follow up for updates compliance. assignedby management) for adequacy and appropriateness. To identify and escalate specific issue tomanagement for compliance & support. To maintain all portals updated (ZyACTM, CQACalendar, Regulatory commitment) Participation in development of new initiatives Preparation of monthly reports and participationin departmental meetings. Any other task assigned by reporting authoritytime to time for enhancement of compliance. System harmonization-Identification of need,escalation & Tracking for resolution. Travel to multiple sites as per requirement foraudit purpose. Candidate Requirements: Candidate Must have rich experience in API auditand compliances. Must have Excellent Communication, Drafting andInterpersonal skills. Must have experience of audit andcompliances of API. Must be ready to travel on multiple sites foraudit purpose.

To Maintain the machine and work place clean in all respect. Carry out all activities in area with required status labelling procedure as per SOP. To maintain overall cGMP and GDP in department. To impart training and evaluation of company employees. Preparation of SOP, BPR and Validation Protocol. Handling of deviation, incident, change control and CAPA. Responsible for all activities carried out in shift. To ensure availability of secondary packing material for packing activities. Responsible to ensure dispensing, equipment cleaning, visual inspection, vial labelling, cartonator machine,online Responsible for in process Packing activities and Finished good activities as per SOP. Planning and participation in validation of equipment. Report to Department head regarding any process or operation related problem. Manpower planning and allocation of work according to their skill.

Zydus Healthcare is looking for Executive / Sr. Executive - Manufacturing QMS to join our dynamic team and embark on a rewarding career journey Implement and maintain Quality Management System (QMS) procedures and documentation related to production processes. Conduct regular audits and assessments to ensure compliance with quality standards, regulations, and industry best practices. Identify areas for process improvement and lead initiatives to enhance quality, efficiency, and productivity in production operations. Develop and deliver training programs to educate production staff on quality standards, procedures, and compliance requirements. Investigate and resolve quality-related issues, non-conformances, and customer complaints in a timely manner. Collaborate with cross-functional teams including production, engineering, and quality assurance to drive corrective and preventive actions. Analyze data and performance metrics to monitor quality trends, identify root causes of quality issues, and implement effective solutions. Participate in the design and implementation of new production processes or equipment to ensure compliance with quality standards and regulatory requirements. Support internal and external audits, inspections, and regulatory assessments related to production activities. Stay updated on industry trends, regulatory changes, and emerging best practices in quality management to continuously improve the QMS for production. 1- Having experience in Biotech/Vaccine/Complex Injectable mfg processes. 2. Overall experience in QMS 3 to 5 years. 3. Well expertise in Track wise, Investigation, CAPA, CC, incident, OOS, OOT. 4. Having id

Reportsto : Deputy General Manager Department : TPM (Total Productive Maintenance) Total Productive Maintenance Develop and execute a comprehensive TPM program, including autonomous, preventive, and predictive maintenance strategies. Monitor and improve Overall Equipment Effectiveness (OEE) by reducing downtime and enhancing machine performance. Lead initiatives like 5S, Kaizen, and root cause analysis to drive operational excellence. Train operators and maintenance teams on TPM methodologies and tools. Track and analyze maintenance metrics, such as Mean Time Between Failures (MTBF) and Mean Time to Repair (MTTR), to identify improvement opportunities. Work closely with production, engineering, and quality teams to ensure seamless operations. Should bring TPM culture within facility where employees work on the principle of I operate, and I maintain. Reduction of equipment related issues at site. Drafting, Customizing, Establishing industry specific Excellence roadmap/framework with focused outcomes like - Efficiency improvement Cost Reduction Value StreamLosses Reduction Capacity Release Manufacturing Footprint Optimization. Augmenting profitability across manufacturing processes, while attaining manufacturing excellence through streamlined operations. Enhancement of plant productivity levels and systematically minimizing value stream losses. Creating excellence by structuring & shaping quality engagements, solving complex manufacturing challenges, while building innovative & pragmatic solutions. Implementing & cultivating a culture of change management through Total Employee Involvement and deployment of relevant quality tools & management concepts. Effectively managing multiple organizational improvement programs, optimizing various business verticals and functional stakeholders and delivering desired business results. Effective communication skills with strong relationship management ability and capability to relate to people at all hierarchical levels. Should have experience of establishing end to end Quality systems & practices. Experience / Exposure in (2 points) : Must have experience of FMCG industry.

Provide supply planning support for filing batches across markets and manufacturing locations Create Work Orders for issuance to BMR & BPR, including batch splits where required, and coordinate with the manufacturing team for execution calendar Coordinate with the PTC team for requirements, material planning, and document planning Coordinate with warehouse & QC for timely release of materials as per production plan requirements, and for FG, coordinate with QC, QA, and Manufacturing Track batches, share weekly status updates, and escalate issues promptly Responsible for long-range planning for filing requirements Manage RM, PM, SFG & FG (having issues) inventory and stock transfer orders Handle MIS and SNOP for business. Skill Set: Proficient in SAP & MS Office Strong understanding of processes and excellent communication skills Good presentation skills and ability to multitask Go-getter attitude, ready to accept challenges and resilient under pressure

To perform investigation of Deviation,Market complaint, Adverse Drug Events, Alert notification and product failuresas per approved procedure. To ensure proper justification for thechange proposed with its impact analysis, risk assessment and effectivenesscheck with its acceptance criteria. To complete the preliminary investigationand final investigation report within stipulated time. To do document historical check withinference by examining relevant data sources with respect to the nature of theevent. To use appropriate investigation tool for investigation. To collectcircumstantial evidence and considering for investigation. To interviewpersonnel involved if needed in such a way that its relevant and adequate toidentify cause. To review batch records & relevant records and identify theindicators of an event. To identify the root cause based oninvestigation outcome. To perform vertical and horizontal impact assessmentbased on the root cause. To coordinate with cross functional teamfor immediate action which may be deemed necessary to isolate the event, tolimit any adverse effect on production, materials, equipment, areas, processes,procedures including discontinuation of processing or quarantine. To coordinate with contract givers foralert notification filing to the Agency, if applicable. To derive on appropriate CAPA inconsultation with CFT for the event with a justifiable target completion date. Todetermine appropriate CAPA effectiveness plan. To Handle the Change control andcheck the effectiveness of the proposed change. To prepare, execute and reviewof Process Validation and Cleaning Validation. To prepare and review SOPs in documentumsoftware 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 repetitiveissues. To discuss outcomes of trend analysis with the QA head and suggestappropriate CAPA. To have a focus on the investigation to get the consistencyfor improving the quality of investigation. To evaluate the change for itsimpact and recommend actions based on the change, to identify any additionalmembers required for evaluation based on the change proposed. To maintain online entries in ZyQMS. Tomaintain APQR calendar/ schedule. To prepare and review the APQR. To monitorand prepare CPP report of product through validator and Minitab software. To prepare and review the visual inspection rejection trend in Minitab software. Qualification : M.Pharm Experience / Exposure : Must have knowledge and experience in injectableplant.