103 Jobs in Gajraula - Page 4

Note:- Prefer dairy and Milk and FMCG background candidate Transportation Management: Inventory Management: Compliance: Process Improvement: Staff Management: Teamwork:

Responsibilities: * Collaborate with marketing team on promotions & events * Oversee inventory control & merchandising strategies * Ensure customer satisfaction through exceptional service Assistive technologies

•Knowledge of CNC turning & Mazak Control machine. •Maintain accuracy & precision in production. •Interpret technical drawings & job instructions. •CNC Operation experience. •Must have experience in Manufacturing Industry

Maintenance Head, Distillery/Brewery, Delhi/NCR Btech-Mech/Electrical, 15+yrs exp of Distillery/Brewery unit - a must, Salary; -20-25lpa Role to manage entire plant maintenance operations - mechanical and electrical for both Distillery & Brewery

Role & responsibilities Responsible for processing and oversight of changes through the generation, justification, impact assessment, modification, review, approval, and implementation workflow. This includes but is not limited to SOPs, production records, test methods, specifications, protocols, reports, equipment, processes, material suppliers, facilities, computer systems etc. Responsible for review and approval of all continual improvement projects affecting quality at a site Responsible for processing of documents through the generation, modification, review, and approval workflow. This includes but is not limited to SOPs, production records, test methods, protocols, reports, labeling, etc. also, archival of records Responsible for Review of regulatory and quality compliance requirements and divisional policy, performance of gap assessments, and establishment or improvement of SOPs covering all areas of applicability. Development and monitoring of corrective action plans where needed Ensuring quality support to regulatory affairs as it relates to updates/changes to market authorizations Review of all documentation (i.e. LIR, OOS, Change Controls, etc.) Ensuring quality interface with internal and external customers when dealing with activities such as service requests, issue resolution, complaints, product information, or for movement of materials, products, or process from site to site Responsible for management of regulatory authority and other external compliance audits (e.g. Customer audits) including communication, tracking and resolution of observations. Management of communications with regulatory agencies including required reporting and resolution of any actions required by the agencies Responsible for Performing, reporting of observations and verification of compliance reports of internal audit

Responsibilities: * Maintain machines: press, electrical panel & EOT cranes 15 ton 5 ton, cnc plasma ect Perform preventative maintenance on equipment Follow safety protocols at all times Collaborate with production team for machine optimization Over time allowance

Apply now » Team Leader Production - TAPI Date: May 30, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62198 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 Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team. Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision 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. 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. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR) Coordination of production tasks to meet assigned schedule Your experience and qualifications Requires a B.Tech Chemical / Msc -Chemistry. or equivalent Requires a minimum of 3 - 5 years of relevant experience in a regulated industry Prefer previous experience in a leadership role 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 »

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 Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team. Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision 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. 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. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR) Coordination of production tasks to meet assigned schedule Your Experience And Qualifications Requires a B.Tech Chemical / Msc -Chemistry. or equivalent Requires a minimum of 3 - 5 years of relevant experience in a regulated industry Prefer previous experience in a leadership role 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. Show more Show less

Roles and Responsibilities Sales, Portfolio Management, Business Development, Cross selling of bank products, Current Account, CASA, LI, GI, Demat accounts, Portfolio handling, HNI Client handling. Customer engagement, new client on-boarding, sales for classic portfolio customers Desired Candidate Profile More than 3 years of experience in Retail branch banking Sales. Hiring for Personal Banker/CCE and CEE Local candidates shall be preferred Minimum 3 years of experience in Sales, Banking, full time graduation, knowledge of basic banking functions and the economy

Apply now » Team Leader Production - TAPI Date: May 29, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62165 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 Qualified in Production Tech and Senior Production Technician duties: Assigning daily tasks to production technicians pertaining to manufacturing of encapsulated products, while completing manufacturing documentation per approved procedures. Includes reviewing documentation for completeness and accuracy per established timelines Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team. Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision 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. 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. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards, and the current Code of Federal Regulations (CFR) Coordination of production tasks to meet assigned schedule Your experience and qualifications Requires a B.Tech Chemical / Msc -Chemistry. or equivalent Requires a minimum of 3 - 5 years of relevant experience in a regulated industry Prefer previous experience in a leadership role 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: * steel structures using fabrication drawings. * Ensure quality control during fabrication process. * Collaborate with project team on structural designs. *Fabrication of steel structure , pre fabricated steel building, sheeting , Health insurance

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. The opportunity This role is responsible for leading the Indirect Procurement team of TAPI India. Responsibility includes management of 2 Procurement Managers who support all TAPI Indirect Procurement activities in India. This includes working with the relevant TAPI stakeholders to identify and optimize all Indirect Procurement needs in India, implementation of the global Indirect category strategies, supplier sourcing and management, contract negotiations, risk management, stakeholder engagement and ongoing continuous improvement activities. This role strives to generate and deliver ongoing value through year-over-year savings, to maintain excellent customer satisfaction and to ensure the supply of required Indirect goods & services for TAPI. How You’ll Spend Your Day Manage a team of 2 Procurement Managers. Support Head of Indirect Procurement in development and implementation of global and regional Procurement strategies, goals and objectives. Execute Indirect category strategies for all spend under its responsibility. Establish and maintain collaborative relationships with the relevant TAPI stakehoders. Manage supplier relationships (SRM) for all suppliers under its responsibility. Accountable to achieve Indirect categories objectives – most notably for savings generation, supplier risk management and uninterrupted plant operations and services. Conduct supply market research to provide category intelligence and benchmarks on industry dynamics, trends and best practices. Source the right suppliers to support and deliver business needs. Lead supplier negotiations and contracting, including management of tender and bids Your Experience And Qualifications Education Required: Bachelor’s Degree Degree in Engineering, Business, Logistics, Law is an advantage but not mandatory. Understanding of Industrial manufacturing environment is highly desirable. Experience Required: at least 7 years of indirect procurement management experience preferably in a large industrial company. Functional Skills: Strong leadership skills. A team player with capability to influence stakeholders while working in cross functional teams. Excellent communication and presentation skills, both written and verbal – the ability to gain senior leadership support. Strong Interpersonal/Relationship Management Skills. Ability to work in a dynamic and demanding work environment. Strategic mindset with demonstrable capabilities of executing assignments in Indirect Procurement. Excellent command of ERP systems like SAP / ARIBA etc. is a must. Language requirements: Proficiency with spoken and written English Travel Requirements – Once every quarter to TAPI sites in India. 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. Show more Show less

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) 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: - Sr. Research Scientist/Group Leader-Biochemical Research Location: - Gajraula Reporting Manager: - Dr. Samir Singh. VP- Chemical Research Direct Reports (Optional): - 01 Team Size (Optional): - NA Matrix Relationship (Optional): - ….. Key Responsibilities Carrying and implementing all microbiological studies for projects related to R&D Microbiological Control Solution formulation products for personal care, food application, and exterior & interior paints application and used as disinfectants. Understanding of fermentation, biological/enzymatic conversion processes. Maintenance of ‘Microbial Culturing/Clean room facility’ so that required microorganisms can be cultured in-house and studies can be done on time. Carrying out all microbiological studies of formulated products for biocides and ANU/HNU business. Responsible and executing all analytical activities related to effluent, water and wastewater treatment/management. Providing resolutions to customer queries/complaints received from Business, Quality control, Quality assurance and manufacturing plants for Ethanol and biocides business. Supervising all QC related Microbiological testing of Raw & finished products and water quality. Responsible and Maintaining Microbiological clean room lab and bio-analytical lab facilities for R&D MCS & ANU business, QC and Plants related microbiological analysis. Responsible of bio-analytical and microbiological support for R&D functions, Plant and QC. Responsible for biological effluent treatment methodologies & provide the solution for effluent treatment for all R&D functions The Person Qualifications: Ph.D. or M.Sc. in Microbiology/Biochemistry from one of the top institutes in the state or country. 5+ years of experience in the field. Working experience in effluent treatment will be preferred. Professional Skills: Proven track record in the field with extensive knowledge of Microbiology/Bio Chemistry. Knowledge on various effluent treatment methodologies will be preferred. Strong command over recent developments in the relevant field. 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/ Show more Show less

Role & responsibilities •To prepare review, approve and distribution the instruction for the production of intermediates and /or APIs according to written procedure. • Ensures that all work carried out is in compliance with the required standards conforming to company e.g. cGMP, SOP, Health and Safety and Environmental requirements • Responsible for training and qualification of plant personnel and ensures that the required training is carried out and adapted according to need; • 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. • Extensive Knowledge of Documentation in the Pharmaceutical industry related to process & cleaning validation, DHT, CHT , Cleaning Verification etc. • Extensive Knowledge to carried out investigation of any OOS/OOT/ Deviation with proper tools. • Coordination with the cross functional teams including Global teams(EHS, RA, R&D, SCM etc.) to provide accurate approach for the Implementation • Estimate base line performance and implementation of OPEX in respective area to achieve the targeted continuous improvement in cost, quality , compliances and EHS. • Extensive Knowledge about the dry powder processing Equipment and technology of Particle size distribution . • Must understand the concept of Particle Size Distribution (PSD), which refers to the relative proportions of particles of different sizes within a sample. They need to grasp how PSDs impact various properties, such as flow, reactivity, stability, and dissolution & able to identify and solve problems related to particle size and distribution.

Role & responsibilities To prepare review, approve and distribution the instruction for the production of intermediates and /or APIs according to written procedure. • To Ensure that all production deviation are reported and evaluated on time, critical deviation are investigated and the conclusion are recorded as per the standard procedure. • Ensures that all work carried out is in compliance with the required standards conforming to company e.g. cGMP, SOP, Health and Safety and Environmental requirements. • Responsible for training and qualification of plant personnel and ensures that the required training is carried out and adapted according to need; • Leads, staffs, and develops a motivated, skilled and optimally resourced team to ensure that performance levels and professional development achieve or exceed business objectives; • Act as qualified trainer of those with less experience. Conduct in-direct supervision of others in the team • Provides input into annual performance evaluations of production technicians as applicable. Investigate and resolve problems. Clear and concise communication to Process Lead and Supervision • 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 organizations objectives. • As an Opex champion, identification of improvements projects in respective area and supporting functional head to implement the project • Extensive Knowledge of Documentation in the Pharmaceutical industry related to process & cleaning validation, DHT, CHT , Cleaning Verification etc. • Extensive Knowledge to carried out investigation of any OOS/OOT/ Deviation with proper tools. • Coordination with the cross functional teams including Global teams(EHS, RA, R&D, SCM etc.) to provide accurate approach for the Implementation • Estimate base line performance and implementation of OPEX in respective area to achieve the targeted continuous improvement in cost, quality , compliances and EHS. • Oversee the daily operations of the solvent recovery plant, ensuring smooth and efficient solvent recovery processes • Monitor and optimize solvent extraction and distillation processes to maximize recovery yields and minimize waste. • Identify and implement process improvements to enhance efficiency, safety, and cost-effectiveness &Implement strategies to reduce solvent consumption, energy usage, and overall costs associated with the solvent recovery process.

#9315768794# Anatomy,Biochemistry,Forensic,Community Medicine @ Medical College Location- Rajasthan, Uttar Pradesh Qualification- DNB / DM Anatomy,Biochemistry,Forensic,Community Medicine Salary- Open for discussion Contact / WhatsApp -#9315768794 ( Kritya ) Email - hr22pathfinders@gmail.com Kindly share the same with your friends and colleagues. Also share your spouse CV if he/she is a doctor. Regards, Kritya

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) 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: - Senior Executive-Draughtsman Band / Grade / Level: - A4 Location : - Gajraula Reporting To: Senior Manager- Design & Engineering Key Responsibilities P&ID & Layout Design : Proficient in developing P&IDs from PFDs using AutoCAD and Smart Plant P&ID experienced in plant and piping layout design (plan, elevation, isometric). 3D Modelling & BOQ Extraction : Skilled in 3D model development and extracting BOQs for piping, valves, fittings, and cable trays from 2D/3D layouts. Plot Planning & Equipment Coordination : Knowledge of master planning, plot plan development, and coordination with equipment GA and nozzle orientation. Electrical Layouts : Experience in cable tray and lighting layout design aligned with piping systems. Documentation & Compliance : Strong control over drawing revisions, as-built documentation, and adherence to statutory and engineering standards. Collaboration : Effective coordination with detail engineering consultants to ensure design accuracy and compliance. The Person Qualifications & Experience: - Diploma /BE in Mechanical / ITI 3-6 years of exp. Chemical Industry experience Personal Characteristics: - Good communication. Knowledge of statutory compliance and best engineering practice for plant layout. 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/ Show more Show less

Role & responsibilities 24 7 audit readiness. Exposure in Wet Chemistry. Responsible to works in different shifts. Perform the raw material analysis & wet lab activity by using the technique (KF, pH, KFC, UV, FTIR, SOR, Oven, Auto titrator, Polari meter & TLC) etc. Sampling of Raw material / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. Perform analytical test according to the monograph and SOP. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Participation in internal, external, regulatory audits. Ensure 100% participation in trainings against CAPAs. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader /Manger. Responsible for calibration and verification of instruments. Maintaining of reserved samples room and chambers. Must be ensured sampled, approved, and rejected labels timely as required. Responsible to maintain the stock record of chemicals and reconciliation of standards. Any other job assigned by the Manger -QC Manger or group leader-QC

Role & responsibilities Skills : Candidates should have thorough exposure and proficient knowledge in the following areas at a minimum: Cleaning validations Process validations and continuous process verification Investigations of Out-of-Specifications (OOS)/deviations 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 products. Responsible for Review of all documentation associated with the validation of the procedure(s) used to clean the equipment train for a products 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 products manufacturing (and packaging process, if required) and continuous process verification (CPV). Assessment of stability requirements based on the type of validation. Additional responsibilities assigned by the Manger QA (Quality Assurance) / Site quality head.

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) 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: - Senior Research Associate (A4) Location : - Gajraula Reporting Manager: - Group Leader-Chemical Research Direct Reports (Optional): - NA Team Size (Optional): - NA Matrix Relationship (Optional): - NA Key Responsibilities Literature Search: Conduct literature searches through patents, journals, SciFinder, and other relevant sources to gather necessary information for projects. Laboratory Experiments: Perform laboratory experiments as per assignments, ensuring accuracy and adherence to protocols. Handling Hazardous Gases: Demonstrate knowledge and practical experience in handling hazardous gases such as chlorine, AHF, hydrogen, and nitrogen safely. Chemical Reactions: Apply practical knowledge of Halogenation, nitration, H igh pressure reac tion, reduction, and other basic reaction chemistries in experimental procedures. Plant Troubleshooting: Troubleshoot issues related to existing chlorinated products in the plant, providing effective solutions to maintain production efficiency. Basic Unit Processes: Understand and operate basic unit processes such as reaction, distillation, filtration, and drying. Material Safety Data Sheets (MSDS): Interpret and apply information from Material Safety Data Sheets to ensure safe handling and use of chemicals. Software Proficiency: Utilize software tools such as BAAN, ELN, and SAP for data management and process documentation. R&D Lab Indenting: Manage the indenting of R&D lab items, ensuring timely procurement and availability of necessary materials. ISO Documentation: Maintain and update ISO documentation to ensure compliance with quality standards. Team Coordination: Coordinate and cooperate effectively with subordinates and other team members to achieve project goals. Safety and Compliance: Adhere to safety rules and regulations, implementing good laboratory practices to maintain a safe working environment The Person Education Qualification: M.Sc. in Organic Chemistry Industrial Experience: 6-8 years of relevant experience. Desirable Experience: Proven work experience in organic synthesis, with a focus on chlorination, reduction, and oxidation reactions. Proficiency in interpreting and analysing chromatograms from GC (Gas Chromatography), GC-MS (Gas Chromatography-Mass Spectrometry), HPLC (High-Performance Liquid Chromatography), LC-MS (Liquid Chromatography-Mass Spectrometry), and KF (Karl Fischer) Apparatus. What’s on Offer: Opportunity to work with a leading company in the chemicals sector. 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/ Show more Show less

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: - Assistant Manager- Design & Engineering Location : - Gajraula Reporting Manager: - Senior Manager- Design & Engineering Job Summary As a Design & Engineering person, you will be responsible for managing design and engineering 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 Design & Engineering Plant MB, EB , Equipment design, process calculations D esign codes for Drawing approvals Plant commissioning support Plant Debottlenecking suppo rt. Knowledge of ASPEN, HYSYS & other eng ineering . Software will be additional advantage Project Management: Assist in managing projects from concept to completion. Ensure projects stay on schedule and within budget. Collaborate with cross-functional teams. Team Collaboration: Work closely with engineers and designers. Work closely with R&D, process , project & SCM team Contribute to a collaborative and innovative work environment. Participate in team meetings and provide input. Technical Support: Offer technical guidance and support. Stay updated with industry trends. Help troubleshoot technical issues. Client Interaction: Communicate with clients to understand their needs. Present design concepts and gather feedback. Assist in making necessary design adjustments The Person Educational Background: Chemical Engineer with Min. 4 3-5 years of Plant Design experience. Graduated from IIT/NIT /LIT . Knowledge Levels: General Awareness: Basic understanding of concepts. Working Knowledge: Broad job knowledge for daily activities. Functional Expert: Certified with strong conceptual knowledge. Mastery: Subject matter expert. Personal Characteristics: Excellent interpersonal and communication skills. Commitment to learn & grow Strategic thinker and result driven. Effective in a matrix organization. Skilled in recruiting, developing, and retaining high-caliber teams What’s on Offer: Opportunity to work with the only Indian company in Global Lighthouse Network under World Economic Forum in the chemical sector. 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/ Show more Show less

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: - Digital Lead (Translator)- Manufacturing -Manager Location: - Gajraula Reporting Manager: - Digital Tech Lead- Manufacturing Reporting Manager: - Yes Job Summary: As Digital Translator, you'll collaborate with key stakeholders to optimize processes, manage cutting-edge projects, and drive innovation. You'll prioritize high-impact use cases, evaluate state-of-the-art solutions, and ensure seamless implementation and value realization. Join us to transform the manufacturing landscape and make a tangible impact. Job Responsibilities: Deliver Digitalization Initiatives : Oversee digital projects across the manufacturing value chain. Collaborate with Stakeholders : Identify process and automation gaps, and optimization opportunities with business stakeholders. Cross-Functional Collaboration : Work with various functions to resolve issues and expedite execution. Project Management Office (PMO) : Manage all manufacturing projects in alignment with business partners. Use Case Prioritization : Prioritize use cases based on business value and agreed criteria. Value Discovery : Lead the discovery and definition of business cases for digital use cases with business teams. Techno-Functional Scoping : Translate digital opportunities into techno-functional scopes and map to best-in-class solutions. Implement innovation from opportunity to operationalization. Techno-Commercial Evaluation : Evaluate digital solutions and products for fit and purpose. Program Implementation : Lead and govern digital program implementation, ensuring change management, adoption, and benefit realization. Value Realization Tracking : Implement and track value realization through a defined framework The Person: Educational Qualifications: B. Tech (Chemical/ Instrument/Electrical/ Mechanical) MBA/ PGDBM preferred Six Sigma Green Belt preferred 3-5 years total experience with at least 2 years of relevant experience including successful delivery of at least 2 projects Technical Skills: (Preferred) MES, Data Historian, Golden Batch Analytics, AI/ML, Optimization, RPA/Bots Domain Experience : Manufacturing, Pharma, Nutrition, Industrial Automation Other Skills: Design Thinking Cost Benefit Analysis Data Analytics Project Management 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/ Show more Show less

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 on-Site product transfer & New Product transfer, scale-up, proposals, Capex evaluations & Process Engineering calculations Improvement in the yield, efficiency and cost effectiveness of developed API’s by introducing new Technologies and further development of process fine tuning Extensive experience in API manufacturing with a deep understanding on Scale-up. Troubleshooting the plant related problems, to overcome the process related difficulties for smooth production Contribute novel ideas by way of participation during technical discussion with superiors/ Colleagues Cycle time reduction, Capacity enhancement and making capacity increase proposals with the support of site CFT members/ leads. Ability to manage 4-5 Engineers coaching, career development and build high performing, engaged and effective teams through motivation and inspiration Person will be expected to support chemistry projects to develop the process engineering knowledge and lead the transfer from lab to scale-up lab and further to production scale Experience on handling CDMO products will be an advantage Person will have demonstrated expertise in the scale-up and process understanding of chemical process unit operations in the manufacture of APIs, intermediates and raw materials. Experience in Quality by Design, process safety, technology transfer and commercial production would be advantageous. Person will be responsible to execute trial and validation batches and support in related activities at plant in the time of scale up In-depth, hands-on expertise and up-to-date knowledge of a wide range of chemistry unit operations such as reactions, distillation, separation, filtration and drying. Strong scientific track record, ability to handle several projects in different stages of development at the same time. Person will be responsible to Investigate and troubleshoot in case of issues in scale up/validation and support troubleshooting activities in case of issues in scale up/validation batches Responsible to use process modelling tools like Dyno Chem, VISMIX for reaction, crystallization, filtration, solubility and mixing studies Good knowledge on solvent recovery & recycle by using latest technologies etc Your Experience And Qualifications B. Tech/ M. Tech Chemical (Regular from reputed Institute) 14-16 Years experience & 5 years in people management Excellent communication skills to interact internally with project teams and externally with customers Good project management and supervisory skills. Collaboration and influencing skills to build partnerships with the other disciplines, similar groups, Conscientious with a can-do attitude and thorough attention to detail. A team player & Competent in the use of key process engineering and modelling software packages Equivalent experience in a Process, Synthetic Chemistry or Manufacturing environment. Experience in working to GMP. Experience in the application of Process Safety to the design of chemical processes Reports To Associate Director, MS&T 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. Show more Show less

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.

Having own hand work experience of preventive and breakdown maintenance on following machines:- Gear Hobbing Gear shaping Bore Grinding machine VMC Having good knowledge of Hydraulic. Required Candidate profile Candidate background from Gear Industry Having knowledge of mechanical drawing and machine kinetic.