168 Jobs in Gajraula - Page 3

Integrate New Technologies : Receive and integrate new process technologies from R&D. Assess Feasibility : Ensure process feasibility on an industrial scale. Observe and Analyze : Observe lab demos to understand processes and generate pilot trial data. Test Deviations : Suggest and test deviation parameters for industrial-scale processes. Identify Hazards : Identify process hazards and define safeguards for catastrophic risks. Generate Balances : Create material and energy balances. Define Performance : Establish lab-scale process performance norms. Map Processes : Map process steps in pilot systems with the operations team. Monitor Trials : Oversee pilot plant trials and generate process parameters. Lead Troubleshooting : Address issues with the pilot plant and R&D teams. Demonstrate Performance : Validate and define process performance at pilot scale. Conduct Studies : Perform engineering lab studies for scale-up data. Develop Designs : Create and share conceptual designs for plant-scale operations. Implement Modifications : Review and implement necessary engineering modifications. Commission Processes : Lead process commissioning activities with cross-functional teams

Responsible to maintaining 5-S on shop floor.Analysis of rejection & find root cause for corrective & preventive action.Responsible for Operating, setting and programming on CMM. Inspection of part through DVC, Micrometer, Height Gauge. Required Candidate profile Knowledge of tools, operating, setting and programing of CMM.Should be from auto manufacturing industry only.

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Main Responsibilities: Improve the yield, efficiency, and cost-effectiveness of developed APIs by introducing new technologies and optimizing processes Preparation of various impurities required for quality control department with their characterization data as per CQA guidelines. Involved in new process scale-up, validation, and commercialization activities, adhering to TAPI Technology Transfer policies and regulatory requirements Evaluation and signoff Protocols received from manufacturing. User trial of raw material, intermediates and solvents required to verify new vendors as per the quality assurance guidelines. Establishing the solvent recover and reusability in lab and issue the reports. Generation of safety reports as and when required. Trouble shooting for the plant related problems, to overcome the process related difficulties for smooth production. Support to answer quarries related from customers. To maintain GMP in Lab. Coordinate with other departments from smooth functioning. Develop own skill by way of regarding / attending seminars etc. To maintain discipline and dignity of the organization. Contribute novel ideas by way of participation during technical discussion with superiors/ colleagues. Ensure that local and global EHS KPIs are met without any delay. Conduct Safety GEMBA walks to identify and mitigate workplace hazards. Prepare Nitrosamines Risk Assessments in line with regulatory expectations. Key Attributes Excellent communication skills to interact internally with project teams and externally with customers Retrosynthesis Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. Experience in working to GMP. Experience in the application of Process Safety to the design of chemical processes Key Skills Good understanding of Mole eq. calculations Technology Transfer Responsible for End-to-End Life cycle Management Cost reduction Continuous improvement Solvent recovery/recycle Qualifications Experience: 4 to 8 Years Qualification: M.Sc. (Organic Chemistry) Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Main Responsibilities: Improve the yield, efficiency, and cost-effectiveness of developed APIs by introducing new technologies and optimizing processes Preparation of various impurities required for quality control department with their characterization data as per CQA guidelines. Involved in new process scale-up, validation, and commercialization activities, adhering to TAPI Technology Transfer policies and regulatory requirements Evaluation and signoff Protocols received from manufacturing. User trial of raw material, intermediates and solvents required to verify new vendors as per the quality assurance guidelines. Establishing the solvent recover and reusability in lab and issue the reports. Generation of safety reports as and when required. Trouble shooting for the plant related problems, to overcome the process related difficulties for smooth production. Support to answer quarries related from customers. To maintain GMP in Lab. Coordinate with other departments from smooth functioning. Develop own skill by way of regarding / attending seminars etc. To maintain discipline and dignity of the organization. Contribute novel ideas by way of participation during technical discussion with superiors/ colleagues. Ensure that local and global EHS KPIs are met without any delay. Conduct Safety GEMBA walks to identify and mitigate workplace hazards. Prepare Nitrosamines Risk Assessments in line with regulatory expectations. Key Attributes: Excellent communication skills to interact internally with project teams and externally with customers Retrosynthesis Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. Experience in working to GMP. Experience in the application of Process Safety to the design of chemical processes Key Skills: Good understanding of Mole eq. calculations Technology Transfer Responsible for End-to-End Life cycle Management Cost reduction Continuous improvement Solvent recovery/recycle Qualifications Experience: 4 to 8 Years Qualification: M.Sc. (Organic Chemistry) Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) prior to disposition (release or rejection) of batch Review of executed document like batch record etc., and also to ensure on time compliance of errors/deviations identified (if any) & review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and resolution of any errors/deviations identified Monitoring and follow-up of corrective and preventive actions (review, approval, and on time closure of the CAPA) in order to resolve an event & review Process/documentation (i.e. Protocol/report) of reviewing effectiveness to determine the effectiveness of a corrective or preventive action. Involving in investigation and ensuring on time closure of the investigation and event with resolution including corrective and preventive actions along with effectiveness determination Initiating NTM to Senior Quality Unit Management, Operations, and other applicable functions for the purpose of expedited communication of critical quality/compliance related issues & ensuring Quality interface with internal and external customers when dealing with activities such as issue resolution, product information, or for movement of materials, products, or process from site to site Developing Process for observing, reviewing, and auditing operations activities in order to facilitate batch review and to assure compliance. Also, ensure self-availability on shop floor as per requirement i.e. support to investigation etc. Responsible for assuring/coordinating for timely shipment, delivery, and/or receipt to assure compliance with regulatory requirements. In addition, responsible to assure appropriate shipping instructions, coordinate/approve route validation and investigation of temperature excursions as required for materials, components, drug substance, and drug product Responsible for oversight and review of R&D product development & product tech transfer at the site and batch manufacture in GMP areas including resolution of deviations. Provide and ensuring support to Regulatory Affairs for Market Authorization (MA) application and maintenance Responsible for Collection, compilation, analysis, and review of all data (i.e. manufacturing, packaging, testing, sourcing, deviations, stability, and changes etc.) and information supporting to validation status of a product Responsible for Review of all documentation associated with the validation of the procedure(s) used to clean the equipment train for a product’s manufacturing and packaging process and cleaning verifications. This includes cleaning to remove active ingredients and cleaning agents Responsible for Review of all documentation including protocols and reports associated with the validation of a product’s manufacturing (and packaging process, if required) and continuous process verification (CPV). Assessment of stability requirements based on the type of validation Your Experience And Qualifications 7-12 years’ experience in API only M.Sc. chemistry, B. Pharm, M. Pharm and B. tech chemical Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Preparation of Instrumentation engineering deliverables including Specifications, Instrument Datasheets, URS, BOQ, control philosophy, PLC I/O’s detailing, Logic Diagrams, calibration schedules, PM schedules etc. Provide inputs and review of engineering drawings including Instrument Location Plans, Cable & JB Schedules, Cable Routing Layouts, Instrument Installation Details, Process / Pneumatic Hook-Ups, Interconnection Diagrams, Loop Diagrams, Instrument Loop Diagrams Hands on experience of detail engineering of field Instrumentation in modification nature project & experience of calibration of field instrument (i.e. Temperature, Pressure) with master instruments and shall review calibration executed by technician Execute, supervise & support to technician team in day-to-day instrumentation maintenance activity. Prepare of spare need identification plan and support to Instrumentation Manager for spare management & fix repeated service call with route cause analysis and ensure maintenance activity right in first time with fast response Hands on experience of HART protocol based Instruments & transmitters & experience on working with DCS/PLC based SCADA System, HMI, DAS-Rockwell/Siemens/Emerson (i.e. loop testing, fault identification, data backup & migration activity etc.) Hands on experience on safety sensor or leak detection system (i.e. Hydrogen/Ammonia/VOC) etc., and execute time-to-time calibration/bump test with experience on EHS critical instrument/system working & maintenance Execute scheduled in house PM calls and Coordination with external Service Engineer for scheduled AMC PM calls or breakdown calls Having good knowledge of pharma documentation shall arrange to execute related documentation (i.e. CCM initiation, validation, qualification, testing, calibration etc.) Understanding and ensuring quality compliance with cGMP, GDP, GEP, GAMP, 21 CFR part 11 & EHS compliances i.e. IP rating, Intrinsic safe instrumentation, FLP, hazardous area classification, zone classification, FLP rating. Related operational PPEs. Work permit system System, Job safety analysis, Risk assessment. LOTTO procedure Good in computer skills and preparation of daily/monthly excel reports, work power point presentation and using of industrial software i.e. Priority/SAP/EAM etc. Your Experience And Qualifications BE/B.Tech - Electronics & Instrumentation/Electronics/Instrumentation Experience - 5+ year required Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Knowledge of automatic sheeting machine operation and c and z machine profiling machine knowledge required Oprator for working in Gajraula, only those candidates working on this machine can apply The CNC Plazo Machine Operator is responsible for operating and maintaining CNC plasma cutting machines to produce precision metal parts as per technical drawings and specifications. The role requires attention to detail, understanding of machine parameters, and adherence to quality and safety standards. Key Responsibilities:Operate CNC plasma cutting machines (Plazo) to cut metal sheets as per given specifications. Read and interpret technical drawings, blueprints, and job orders. Load and unload raw materials and finished components. Set up machine parameters such as speed, feed, and cutting path. Inspect and measure finished parts to ensure accuracy and quality standards. Perform routine machine maintenance and report any malfunctions or repair needs. Ensure safe operation by following all workplace safety standards and procedures. Maintain production records and documentation as required.

Role Description This is a full-time on-site role based out in Gajraula, District Amroha, Uttar Pradesh. The Assistant Manager Payroll will be responsible for overseeing and managing payroll administration, ensuring the accurate and timely processing of payroll and managing employee benefits and statutory compliances. Qualifications Candidate must have work minimum 05 years experience in HR Payroll process of University or Medical College only. Hands on experience of Saral Payroll ERP and proficient in MS excel Experience with Employee Benefits management Excellent attention to detail and organizational skills Strong communication and interpersonal skill. Salary:- Best in industry

Udupiwala Restaurants is looking for following staff - Steward/Waiter-4 Post Minimum Qualification-12th or Diploma in Hotel Management. Skill- Oral/Written Communication Computer and any software friendly Problem Solving Skill The flexibility to work shifts. Multi-tasking Minimum Experience- 3-5 years in reputed restaurants. Location- Kathgodam and Rajabpur Job Type: Full-time Pay: ₹120,000.00 - ₹180,000.00 per year Benefits: Food provided Work Location: In person

Apply now » Operator II - TAPI Date: Jul 29, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62850 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills Your experience and qualifications 2 to 3 years – Msc. ( Chemical) 0 to 2 years - B.Tech / B.E / Diploma(Chemical) Make a difference with Teva Pharmaceuticals Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Responsibilities: * Provide patient care under supervision * Assist with nursing procedures and medication administration * Collaborate with healthcare team on treatment plans * Maintain confidentiality at all times Free meal Work from home Food allowance Over time allowance Travel allowance House rent allowance Annual bonus Joining bonus Sales incentives

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description At the heart of seamless operations and efficient customer delivery, the Associate Director – Supply Chain plays a pivotal role in driving performance across business-critical functions. This position blends strategic thinking, leadership, and operational excellence, touching every facet of the supply chain including production planning, inventory control and warehouse management. Key Responsibilities: Strategic Leadership Lead functional planning and policy development to address complex challenges. Drive performance and resource optimization across the site and function. Production Planning Translate customer orders into strategic production plans. Manage open order planning and enforce timely fulfillment systems. Warehouse Management Supervise warehouse operations and safety standards. Monitor equipment usage and ensure compliant stacking/storage. Inventory Control Conduct age-wise inventory reviews and strategize liquidations. Schedule raw and packaging materials in line with LBE & AOP. Customer Relationship Management Champion reliability and satisfaction across internal and external stakeholders. ✅ Compliance & Governance Maintain SOP/cGMP documentation with ethical rigor. Cultivate awareness around compliance practices. Monitoring & Coordination Daily oversight of production, volume, and dispatch metrics. Collaborate cross-functionally to ensure delivery precision. MIS & Analytics Provide actionable insights for budgeting and planning. Support long-term forecasting using sales simulations. Financial Stewardship Manage departmental budgets with cost-center discipline. Team Leadership & Training Lead and mentor multi-level staff. Promote efficiency via tools, skill enhancement, and safety programs. Distribution & Logistics Oversee global product pickup, delivery, and routing coordination. Ensure timely and accurate shipment execution beyond borders. Qualifications We’re looking for candidates with a strong supply chain site background. The ideal candidate will have: Education: B.E. / B.Tech. in Chemical / Mechanical Engineering + M.Sc. / MBA (preferred). Experience: Minimum 15 years of experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description At the heart of seamless operations and efficient customer delivery, the Associate Director – Supply Chain plays a pivotal role in driving performance across business-critical functions. This position blends strategic thinking, leadership, and operational excellence, touching every facet of the supply chain including production planning, inventory control and warehouse management. Key Responsibilities 🔧 Strategic Leadership Lead functional planning and policy development to address complex challenges. Drive performance and resource optimization across the site and function. 📅 Production Planning Translate customer orders into strategic production plans. Manage open order planning and enforce timely fulfillment systems. 📦 Warehouse Management Supervise warehouse operations and safety standards. Monitor equipment usage and ensure compliant stacking/storage. 📊 Inventory Control Conduct age-wise inventory reviews and strategize liquidations. Schedule raw and packaging materials in line with LBE & AOP. 💬 Customer Relationship Management Champion reliability and satisfaction across internal and external stakeholders. ✅ Compliance & Governance Maintain SOP/cGMP documentation with ethical rigor. Cultivate awareness around compliance practices. 📈 Monitoring & Coordination Daily oversight of production, volume, and dispatch metrics. Collaborate cross-functionally to ensure delivery precision. 📉 MIS & Analytics Provide actionable insights for budgeting and planning. Support long-term forecasting using sales simulations. 💸 Financial Stewardship Manage departmental budgets with cost-center discipline. 👥 Team Leadership & Training Lead and mentor multi-level staff. Promote efficiency via tools, skill enhancement, and safety programs. 🚚 Distribution & Logistics Oversee global product pickup, delivery, and routing coordination. Ensure timely and accurate shipment execution beyond borders. Qualifications We’re looking for candidates with a strong supply chain site background. The ideal candidate will have: Education: B.E. / B.Tech. in Chemical / Mechanical Engineering + M.Sc. / MBA (preferred). Experience: Minimum 15 years of experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Knowledge of automatic sheeting machine operation and c and z machine profiling machine knowledge required Oprator for working in Gajraula, only those candidates working on this machine can apply

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives. Your Experience And Qualifications 2-4 Years - Diploma (Chemical)3-5 Years – M.SC 0.5 to 3 years - B.Tech / B.E (Chemical) 24/7 Shifts Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Responsible for conducting the qualification of microbiology lab To conduct environmental monitoring, water sampling and testing, product testing and other microbial analysis as per monograph and SOP's Responsible to follow of quality management system documents Raising the purchase requisition for arranging the items related to microbiology To execute the protocol and report to perform the validation/study activities To perform the calibration and verification of microbiological instruments Perform the trend and summary report Follow GMP and GLP and maintain the compliance in microbiology lab & the site safety procedure To perform the analysis of API and final products based on the requirement within the timeframe Responsible for Media preparation, sterilization, GPT and reconciliation and for handling and storage of BIO-ball culture Your Experience And Qualifications Minimum experience 3-4 years required Qualification M.Sc. Microbiology Reports To Manager Quality Control Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives Your Experience And Qualifications 2 to 3 years – Msc. ( Chemical) 0 to 2 years - B.Tech / B.E / Diploma(Chemical) Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Apply now » Operator II Date: Jul 25, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62923 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives Your experience and qualifications 2 to 3 years – Msc. ( Chemical) 0 to 2 years - B.Tech / B.E / Diploma(Chemical) Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Apply now » Operator III - TAPI Date: Jul 25, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62925 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Ensure housekeeping of plant and cleanliness of the equipments, update the equipment Report accidents and irregularities at the work station to the Shift Officer. Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives. Your experience and qualifications 2-4 Years - Diploma (Chemical)3-5 Years – M.SC 0.5 to 3 years - B.Tech / B.E (Chemical) 24/7 Shifts Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Role & responsibilities : Responsible for issuance of raw material from warehouse as per production requirement. Storage and labeling as per applicable procedure. Assisting the Team leader in ensuring proper storage of raw materials, intermediates and finished goods in designated areas and labeling as per applicable procedures. Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /APIs according to the approved batch cards. Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card. Ensure verification of weigh balances and all daily documents as per applicable procedures. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. Follow Standard operating procedure (SOP), Safety and cGMP guideline. Ensure housekeeping of plant and cleanliness of the equipments/ area, update the equipment status board, use log book, other documents as per applicable procedure. Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements. Expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others. Batch details put in ERP system. Preparation of batch card, qualification protocol, report & other GMP related documents. Preparation of safety work permits to carry out maintenance activities in shift. Report accidents and irregularities at the work station to the Shift Officer. Preferred candidate profile An individual must have experience into API industry. Expertise in Powder Processing. If you're interested in exploring opportunities with us, please share your updated profile at jasleen.kaur@tapi.com or connect via phone at 8076954558 . Alternatively, if you know someone who might be suitable, feel free to share their referencewe’d love to reach out.

Position Assistant Manager (BE & Six Sigma) Business Unit / Function JVL /Business Excellence Location Gajraula Reports to BE Site Head Summary Of Job (Purpose/ objective of the job Department organogram to be enclosed) Coordinating BE projects with plant and central function people to execute as per time lines, Support 5S, Six sigma and Lean. Drive cost reduction and value creation projects, Identifying new cost reduction opportunities, Facilitating project management involving all stakeholders Work closely with site team on data generation validation and analysis Key Responsibilities (Performance Indicators) Responsible for delivering business impact by improving business processes, solving problems and driving improvement projects/activities within the site. Execute cost reduction/Process improvement projects in plant using Process engineering, lean principles and Project management activities. Monitoring of OPE and analyzing the down time and action to reduce To prepare material & energy balance, scheme preparation, technical specification data sheet, TBE sheet preparation, float enquiry for quotation from vendors, creating baseline of Project YOY. Mentoring YB and GB projects of respective Business. Coordination with design & projects for investment and scheme validation, coordinating HAZOP study, prepare & raise capex for BE projects, follow-ups for approval Ordering coordination, follow-up with procurement & projects team Preparation & approval of savings, vetting with Accounts on quarterly basis, Project charter preparation and submission. Coordination with Execution team for the timely completion of the projects. Responsible for the End to End BE capex (Preparation and closure of the Projects). Preparation of Monthly MIS and PPT for the Monthly review. No. of Reportees NA Qualification & Experience B.E – Chemical Engg. 10-12 years within API/Chemical Industry with at least 3 years in Business Excellence/Operational Excellence/Process Engineering/Technical Services Key Competencies ( Technical, Functional & Behavioral) Sound Technical knowledge (chemical engineering) with excellent knowledge on cost reduction initiatives, Energy audits, utility improvements etc. Sound knowledge on data classification and analysis, analysis of operating expenses, project management. Lean six sigma green belt certified is preferred. Good inter personal and people management skills. Excellent in verbal and written communications. Person should have Adaptability, Flexibility, decision making and result oriented.

Role & responsibilities Work with the RSPs in the respective markets to ensure efficient order booking in accordance to MJP. Ensure achievement of sales and distribution objectives by RSPs Manage the primary and secondary sales of the identified stockist in direct towns. Monitor daily sales performance and provide regular feedback to the sales team. Submit daily /weekly / monthly sales reports to the regional manager. Develop and execute market - specific promotional plans to increase brand visibility.

Basic Knowledge of Computer Good Knowledge of Word, Excel, PPT Track of store inventory Good Communication skills

Apply now » Operator III - TAPI Date: Jul 23, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62854 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards . Coordination of production tasks to meet assigned schedule Knowledge of Liquide chromatography Operations. Your experience and qualifications 3-5 Years – M.SC 0.5 to 3 years - B.Tech / B.E (Chemical) 24/7 Shift Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Daily Work Planning: Develop and implement daily work schedules in alignment with project timelines and goals. Drawing Verification: Review and crosscheck HVAC system drawings against site conditions to ensure accuracy and feasibility. Material Management: Oversee material requisitions for HVAC components and ensure timely indenting based on project requirements. Coordinate with procurement for HVAC materials and track deliveries. Vendor Coordination & Quotation Management: Solicit quotations from labor contractors for HVAC installation tasks. Finalize the scope of work with HVAC contractors and ensure all agreements are documented. HVAC Work Execution: Implement HVAC system installation activities in accordance with the approved drawings and specifications. Ensure that HVAC installation follows best practices, standards, and compliance with safety regulations. Site Coordination: Collaborate with consultants, project management consultants (PMC), and clients to ensure smooth site operations and resolve any HVAC-related issues promptly. Coordinate with other site teams to ensure the HVAC systems are integrated with other building systems. Measurement and Documentation: Conduct regular site measurements for HVAC work completed. Prepare measurement sheets for HVAC systems and obtain necessary certifications from the client. Bill Preparation: Prepare and submit bill annexures related to HVAC work, ensuring accurate documentation and timely submission for approval. Material Reconciliation: Maintain accurate records of HVAC materials used, ensuring proper reconciliation between the actual materials used and materials ordered. HVAC Installation Support: Assist in the installation, testing, and commissioning of HVAC systems, ensuring adherence to project specifications. Perform inspections to verify the quality and integrity of HVAC installations. Job Types: Full-time, Permanent Pay: From ₹20,000.00 per month Benefits: Provident Fund Work Location: In person