97 Jobs in Gajraula

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

Key Responsibilities:- Machine Operation, Material Handling, Quality Control, Machine Maintenance, Safety Compliance, Documentation Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹25,000.00 per month Shift availability: Day Shift (Preferred) Overnight Shift (Preferred) Work Location: Remote

*Ensuring the reliable operation of electrical systems at telecom sites, including power systems, backup power, and related infrastructure. *Performing preventive and corrective maintenance on electrical equipment. *Resolving any electrical faults. Required Candidate profile If you are interested in this job profile. Kindly contact me. HR Department Akanksha Tiwari Contact No: 7065061621 Email ID: akanksha.tiwari@bhardwajservices.com

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Ingrevia Limited JubilantIngreviaisnowamemberoftheeliteGlobalLighthouseNetwork(GLN) oftheWorldEconomicForum(WEF) Celebrating our Culture and People. We are proud to be aGreat Place to Work certified! Jubilant Ingrevia history goes back to 1978 with the incorporation of VAM Organics Limited, which later became Jubilant Organosys and then Jubilant Life Sciences and now demerged to an independent entity as Jubilant Ingrevia Limited, which is listed in both the stock exchanges of India. Over the years, company has developed global capacities and leadership in chosen business segments. Ingrevia is born out of a union of ‘Ingredients’ and ‘Life’ (‘Vie’ in French). Jubilant Ingrevia Limited is committed to offering high-quality and innovative life science ingredients to enrich all forms of life. Jubilant Ingrevia, a global integrated Life Science products and Innovative Solutions provider serving, Pharmaceutical, Nutrition, Agrochemical, Consumer and Industrial customers with our customised products and solutions that are innovative, cost-effective and conforming to excellent quality standards. Jubilant Ingrevia Limited offers a broad portfolio of high-quality ingredients that find application in a wide range of industries. Jubilant Ingrevia’s portfolio also extends to custom development and manufacturing for pharmaceutical and agrochemical customers on an exclusive basis. Ourbusinessissplitacross3businessverticals,withgloballeadership acrossourkeyproductlines. Speciality Chemicals : The Specialty Chemical business of Jubilant Ingrevia manufactures Pyridine, Picolines and its forward integration derivatives, which finds application in agrochemicals, pharmaceuticals, dyes, solvents, metal finishes, fine chemicals, semiconductors etc. We have also launched new platform of Diketene & its value-added derivatives for multiple industry use. We are an established ‘partner of choice’ in CDMO, with more investment plans in GMP & Non-GMP multi-product facilities for Pharma, Agro and Semi-conductor customers. Chemical Intermediates: The Chemical Intermediates business has acetic anhydride and value added anhydrides and aldehydes catering to various industries. Nutrition & Health Solutions: The Nutrition & Heath Solutions business unit offers B3 & Picolinates (Chromium & Zinc) which are fully backward integrated. Our ingredients find application in animal nutrition, human nutrition, personal care, etc. We provide high-quality feed & food additives having application in poultry, dairy, aqua & pet food industry. In Human Nutrition & Health Solutions, we offer food ingredients & premix solutions to nutrition. Jubilant Ingrevia Limited is supported by five state-of-the-art manufacturing facilities in India. We practice world-class manufacturing processes in our day-to-day operations, assuring our customers with unmatched quality and timely delivery of products through innovations and cutting-edge technology. Transforming Manufacturing for Operational Excellence & Sustainability with “zero tolerance to any non-compliance” is the core focus of Jubilant Ingrevia Manufacturing. We have 5 world-class manufacturing facilities i.e. One in UP at Gajraula, Two in Gujarat at Bharuch and Savli, Two in Maharashtra at Nira and Ambernath. Environment Sustainability The company is committed to environmental sustainability and supports green chemistry by prioritising the use of bio inputs in manufacturing. Jubilant is one of the world’s largest producers of Acetaldehyde from the bio route. Find out more about us at www.jubilantingrevia.com The Position Organization : - Jubilant Ingrevia Limited Designation & Level: - Deputy Manager- Project Management Location : - Gajraula Reporting Manager: - Associate Director, Project Construction Job Summary The person will be responsible for overseeing the projects from concept to completion. This role requires ensuring that projects are delivered on time, within scope, and within budget, while coordinating with cross-functional teams to ensure seamless project execution. Key Responsibilities Project Management : Co-ordination, monitor & manage capital projects from concept to closer. Ensure projects are delivered on time, within scope, and within budget. Coordinate with cross-functional teams to ensure seamless project execution. Risk Management: Identifying, assessing and mitigating risks that could impact the project. Critical Thinking & Identify the risks early in the project lifecycle & take proactive steps to mitigate or avoid. Procurement Management: Procurement of resources such as services, materials, or equipment. Vendor & Contractor selection & Evaluates based on their ability to meet project needs, reliability, and financial stability. Budget & Cost Management: Preparation of Cost review reports, Invoicing plans & Cost book plans on Monthly basis. Constantly tracking expenses and ensure cost-effective solutions are implemented or cutting unnecessary costs to stay within the budget. Forecast future financial needs and ensure stakeholders/Management are informed of budgetary changes or risks. Stakeholder Management: Communicate project status, risk & issues to stakeholders including clients, senior Management Coordinates with internal & External stake holders. Scheduling, Monitoring & Control: Prepare Overall schedule of the projects based on Milestones. Ensure all design and engineering activities comply with relevant regulations and standards. Obtain necessary permits and approvals for projects. Reporting & Documentation: Prepare regular project reports including progress updates, financial status & Risk assessment. Maintain comprehensive project documents. Construction Management: Resource Mapping & augmentation. Assist site Construction team to deliver the project on time. The Person Educational Background: Mechanical/Chemical Engineer with 6-10 years of experience in chemical plants. Graduated from reputed university. Knowledge Levels: General Awareness: Fundamental understanding of concepts. Working Knowledge: Broad job knowledge, capable of applying a full range of concepts and practices in day-to-day activities. Functional Expert: Certified expert with strong knowledge of concepts. Mastery: Subject matter expert with command over the subject/concepts. Personal Characteristics: Excellent interpersonal and people management skills. Proficient in verbal and written communication. Strategic thinker and result-driven doer, capable of understanding business needs, providing strategic support, finding solutions, and implementing good ideas. Ability to work effectively in a matrix organization. Exceptional people manager and leader, skilled in recruiting, developing, and retaining a high-calibre team across diverse departments What’s on Offer: Opportunity to work with the only Indian company in Global Lighthouse Network under World Economic Forum in the chemical sector. Competitive salary and benefits package. Career growth opportunities in a rapidly evolving industry Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, please visit our LinkedIn page: https://www.linkedin.com/company/jubilant-bhartia-group/

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Ingrevia Limited JubilantIngreviaisnowamemberoftheeliteGlobalLighthouseNetwork(GLN) oftheWorldEconomicForum(WEF) Celebrating our Culture and People. We are proud to be aGreat Place to Work certified! Jubilant Ingrevia history goes back to 1978 with the incorporation of VAM Organics Limited, which later became Jubilant Organosys and then Jubilant Life Sciences and now demerged to an independent entity as Jubilant Ingrevia Limited, which is listed in both the stock exchanges of India. Over the years, company has developed global capacities and leadership in chosen business segments. Ingrevia is born out of a union of ‘Ingredients’ and ‘Life’ (‘Vie’ in French). Jubilant Ingrevia Limited is committed to offering high-quality and innovative life science ingredients to enrich all forms of life. Jubilant Ingrevia, a global integrated Life Science products and Innovative Solutions provider serving, Pharmaceutical, Nutrition, Agrochemical, Consumer and Industrial customers with our customised products and solutions that are innovative, cost-effective and conforming to excellent quality standards. Jubilant Ingrevia Limited offers a broad portfolio of high-quality ingredients that find application in a wide range of industries. Jubilant Ingrevia’s portfolio also extends to custom development and manufacturing for pharmaceutical and agrochemical customers on an exclusive basis. Ourbusinessissplitacross3businessverticals,withgloballeadership acrossourkeyproductlines. Speciality Chemicals: The Specialty Chemical business of Jubilant Ingrevia manufactures Pyridine, Picolines and its forward integration derivatives, which finds application in agrochemicals, pharmaceuticals, dyes, solvents, metal finishes, fine chemicals, semiconductors etc. We have also launched new platform of Diketene & its value-added derivatives for multiple industry use. We are an established ‘partner of choice’ in CDMO, with more investment plans in GMP & Non-GMP multi-product facilities for Pharma, Agro and Semi-conductor customers. Chemical Intermediates: The Chemical Intermediates business has acetic anhydride and value added anhydrides and aldehydes catering to various industries. Nutrition & Health Solutions: The Nutrition & Heath Solutions business unit offers B3 & Picolinates (Chromium & Zinc) which are fully backward integrated. Our ingredients find application in animal nutrition, human nutrition, personal care, etc. We provide high-quality feed & food additives having application in poultry, dairy, aqua & pet food industry. In Human Nutrition & Health Solutions, we offer food ingredients & premix solutions to nutrition. Jubilant Ingrevia Limited is supported by five state-of-the-art manufacturing facilities in India. We practice world-class manufacturing processes in our day-to-day operations, assuring our customers with unmatched quality and timely delivery of products through innovations and cutting-edge technology. Transforming Manufacturing for Operational Excellence & Sustainability with “zero tolerance to any non-compliance” is the core focus of Jubilant Ingrevia Manufacturing. We have 5 world-class manufacturing facilities i.e. One in UP at Gajraula, Two in Gujarat at Bharuch and Savli, Two in Maharashtra at Nira and Ambernath. Environment Sustainability The company is committed to environmental sustainability and supports green chemistry by prioritising the use of bio inputs in manufacturing. Jubilant is one of the world’s largest producers of Acetaldehyde from the bio route. Find out more about us at www.jubilantingrevia.com The Position Organization : - Jubilant Ingrevia Limited Designation & Level: - Production Chemist Location : - Gajraula Reporting Manager: - Group Leader, Pilot Plant Job Summary Handles chemical process execution in a pilot plant, ensuring compliance with BPR, SOPs, and safety standards. Manages shift planning, utility readiness, documentation, and supports production targets through safe and efficient operations . Job Responsibilities Process & Compliance Ensure execution of operations as per approved BPR, WIs, SOPs, and safety guidelines, maintaining documentation in line with IMS, RC, cGMP standards. Shift & Resource Management Plan shift workloads, assign chemists, and ensure availability of required utilities (steam, DM water, nitrogen, etc.) before process startup. Production & Quality Execute production to meet targets for timely delivery, yield, and quality, while verifying BPR entries and maintaining logbooks. Safety & Training Ensure safety of personnel and equipment, and manage safety work permits The Person Qualifications & Skills BSC/MSC/ Diploma in chemical with 1-3 years of work experience. Knows the fundamental or general understanding of concepts. Has broad job knowledge; knows and applies the full range of concepts and practices. Candidate should use these concepts in day-to-day practices. Should know the basics of operation & chemistry. What’s on Offer: Opportunity to work with a leading company in the chemicals sector. Competitive salary and benefits package. Career growth opportunities in a rapidly evolving industry Jubilant is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, colour, gender identity or expression, genetic information, marital status, medical condition, national origin, political affiliation, race, ethnicity, religion or any other characteristic protected by applicable local laws, regulations and ordinances. To know more about us, please visit our LinkedIn page: https://www.linkedin.com/company/jubilant-bhartia-group/

responsible for setting up, operating, and maintaining purlin forming machines to produce high-quality sheet metal products. They ensure the machines run efficiently, meet production targets, and adhere to safety protocols and quality standards. Key duties include machine setup, monitoring performance, conducting quality checks, and performing routine maintenance. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹22,000.00 per month Work Location: Remote

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 🚀 We’re seeking a hands-on production expert with deep GMP knowledge, ISO Class 8 compliance, ERP proficiency, and operational expertise in powder processing equipment, documentation, safety. 🔧 Key Responsibilities Expertise in operating powder processing equipments involved in API process (micronizer, sifter, fitz mill and others). Execute batch manufacturing as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Complete knowledge of clean area standards, specifically adhering to ISO class 8 requirements. Handle raw materials, intermediates, and finished products safely and efficiently Maintain accurate documentation of process parameters, deviations, and cleaning records Ensure compliance with cGMP, EHS, and regulatory standards during operations Coordinate with maintenance and quality teams for equipment troubleshooting and process deviations Participate in training programs and continuous improvement initiatives Preparation of batch card, qualification protocol, report & other GMP related documents. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. 🧪 Skills & Competencies Good understanding of Production procedures. Fam Understating of GMP & Safety Good communication and teamwork skills. ✅ Preferred Experience Prior experience in regulated environments (USFDA, WHO-GMP, etc.) Exposure to API manufacturing in pharma. 💼 What We Offer Competitive salary. Opportunity to work in a world-class API facility Training and career development programs Safe and inclusive work environment Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.Sc./ M.Sc./ Diploma (Chemical) or B.E. / B.Tech. in Chemical Engineering. Experience: 1 to 3 years of experience. 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 We’re seeking a hands-on production expert with deep GMP knowledge, ISO Class 8 compliance, ERP proficiency, and operational expertise in powder processing equipment, documentation, safety. Key Responsibilities: Expertise in operating powder processing equipments involved in API process (micronizer, sifter, fitz mill and others). Execute batch manufacturing as per Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOPs). Complete knowledge of clean area standards, specifically adhering to ISO class 8 requirements . Handle raw materials, intermediates, and finished products safely and efficiently Maintain accurate documentation of process parameters, deviations, and cleaning records Ensure compliance with cGMP, EHS, and regulatory standards during operations Coordinate with maintenance and quality teams for equipment troubleshooting and process deviations Participate in training programs and continuous improvement initiatives Preparation of batch card, qualification protocol, report & other GMP related documents. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. Skills & Competencies: Good understanding of Production procedures . Fam Understating of GMP & Safety Good communication and teamwork skills. ✅ Preferred Experience: Prior experience in regulated environments (USFDA, WHO-GMP, etc.) Exposure to API manufacturing in pharma. What We Offer: Competitive salary. Opportunity to work in a world-class API facility Training and career development programs Safe and inclusive work environment Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.Sc./ M.Sc./ Diploma (Chemical) or B.E. / B.Tech. in Chemical Engineering . Experience: 1 to 3 years of experience. 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!

Job Title : .NET Developer Experience : 3+ Years Location: Shri Venkateshwara University, Gajraula, Uttar Pradesh Salary : Maximum 5.50 LPA Education Qualification: Bachelors or Masters Degree in Computer Science, IT. Industry Preference : Experience in University or Medical College setting preferred Job Summary We are seeking a skilled .NET Developer with 3+ years of hands-on experience to join our IT team at SVU, Gajraula . The ideal candidate should have a strong background in .NET technologies and experience working in educational or healthcare institutions. You will be responsible for developing, maintaining and supporting web-based applications that support academic and administrative functions. Key Responsibilities Design, develop, test, and deploy web applications using .NET (C#, ASP.NET, MVC) Maintain and enhance existing applications and systems Work with SQL Server for database design, queries, and stored procedures Collaborate with academic and administrative departments to gather and define software requirements Ensure application performance, scalability, and security standards Troubleshoot and resolve application issues and bugs Prepare technical documentation and user guides Required Skills Proficiency in C#, ASP.NET, MVC, and .NET Framework/Core Strong experience with SQL Server, including stored procedures and database optimization Knowledge of front-end technologies (HTML, CSS, JavaScript, jQuery, etc.) Experience with version control tools like Git Ability to write clean, maintainable, and well-documented code Excellent problem-solving and debugging skills Preferred Qualifications Experience working in a University, Medical College, or educational institution environment Familiarity with ERP or academic management systems Understanding of IT workflows in academic or healthcare settings How to Apply Interested candidates may send their CV to svuhr@svu.edu.in

Lead full plant operations, including production, quality, maintenance & supply chain. Drive efficiency, cost control, and safety. Ensure compliance and implement Lean/Six Sigma for continuous improvement.

Role & responsibilities: : 1. Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements. 2. Expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others. 3. Batch details put in ERP system. 4. Preparation of batch card, qualification protocol, report & other GMP related documents. 5. Preparation of safety work permits to carry out maintenance activities in shift. 6. Report accidents and irregularities at the work station to the Shift Officer. 7. Carrying out process and sampling activities during the production of Intermediate /APIs according to the approved batch cards. 8. Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card. 9. Ensure verification of weigh balances and all daily documents as per applicable procedures. 10. Carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures. 11. Follow Standard operating procedure (SOP), Safety and cGMP guideline. 12. Ensure housekeeping of plant and cleanliness of the equipment/ area, update the equipment status board, use log book, other documents as per applicable procedure. Requirement - *API experience is required* Interested candidate can share their resume on jasleen.kaur@tapi.com or connect on 8076954558.

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. Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills Coordination of production tasks to meet assigned schedule 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.

Ensure plaining and scheduling for annual preventive maintenance of all mechanical and utility installations in the plant. Attend and timely response for all emergency breakdowns of mechanical and utility installations in the plant. Implement GMP requirements in function. Aligning SOP corporate SOP and guideline. Ensure spare part inventory of the mechanical and utility equipment items in Engineering Stores. Evaluate new equipment/facility proposals for Capex & modification and its procurement with timely execution. Support site project team for evaluation and timely completion of project. Renewal of registrations and licenses related to Utility & Mechanical equipment for concerned Government Department as per standards. Ensure the safety of persons, plant & Equipment while carrying out the maintenance job. Work procedure update and training. Critically analyze the expenditure on procurement of items and overall equipment and utility maintenance expenditure periodically and find out ways and means to control the same at optimum level. Review the planning and implementation of energy conversion schemes and maintenance excellence schemes. Timely closely of permanent change Control, temporary change control, deviation, CAPA and service calls. Is accountable for the performance and results of a team with own disciplined & Function. Defines Team operating standard and ensures essential procedure are followed based on knowledge of own disciplined, to ensure completion of assigned the training of self & Team members. Excretive limited management authority, sets employee performance objectives, conducts performance reviews and recommends pay actions. To ensure all the activities perform in own discipline for self and team should follow the compliance requirements

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 🚀 We’re looking for a proactive engineering leader with a passion for capital project execution and GMP excellence—if you thrive in high-impact environments, this opportunity is for you. 📋 Key Responsibilities 🧩 Project Management & Execution Lead end-to-end execution of capital projects, ensuring they are delivered on time, within budget, and in line with business objectives Own and track the annual capital spending plan for the site Drive cost optimization and execution excellence through industry best practices Align projects with Global Engineering policies, procedures, and governance frameworks Provide design oversight for new processes, equipment, and facilities to ensure FDA and internal compliance Contribute to long-term planning for strategic product and manufacturing initiatives 👥 Talent & Procurement Collaboration Identify gaps in the project team’s expertise and support skill enhancement or hiring Collaborate with procurement to finalize capital equipment orders, including techno-commercial bid analysis Monitor and report Capex cash flow, forecasts, and monthly budget utilization Develop and maintain Capex governance tracking Prepare and analyze Annual Operating Plans (AOP) and Long Range Plans (LRP) for capital investment Finalize Capital Expenditure Requests (CERs) and manage global approval workflows ⚠️ Safety, Compliance & EHS Oversight Ensure full implementation of safety and HR compliance protocols for internal and contractor teams Meet local and global EHS KPIs consistently Conduct regular Safety GEMBA walks and lead risk assessments Ensure availability of Emergency Response Team (ERT) and first aid-trained personnel across all shifts 🔄 Miscellaneous Perform any additional tasks as assigned by the Department Head. Must Have Good understanding of Project procedures. Understanding of GMP. Qualifications We’re looking for candidates with a strong engineering site project management background. The ideal candidate will have: Education: B.E. / B.Tech. in Mechanical or Chemical Engineering. Experience: Minimum 12 years of experience in Engineering Site Project management. 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!