What Jobs are available for Manufacturing in Chennai?

**Req ID:**
NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now.
We are currently seeking a Oracle Manufacturing Consultant to join our team in Chennai, Tamil Nādu (IN-TN), India (IN).
7 + years experience in Oracle SCM (industrial machinery or automotive referred)
+ At least 1 full cycle implementation of Oracle SCM module - WIP, BOM, inventory, quality
+ Knowledge and skillset of Oracle reports and form personalization
+ This position requires the resource to be present in the Client office (Guindy area) or the plant (mainly Gummudipoondi) and several trip to Bengaluru (PP plant) will be expected.
+ preferred to speak Tamil along with English for more detail understanding with Business.
+ Additional Details
+ Analyze business processes and identify opportunities for improvement with Oracle SCM solutions.
+ Implement and configure Oracle SCM modules to meet business requirements.
+ Provide support and maintenance for Oracle SCM applications.
+ Conduct testing and validation to ensure systems meet performance expectations.
+ Develop and deliver training sessions for users and stakeholders.
+ Work collaboratively with cross-functional teams to ensure seamless integration across departments.
+ Create detailed documentation of configurations, processes, and user guides.
+ Perform regular audits and assessments of the Oracle SCM environments.
**About NTT DATA**
NTT DATA is a $30+ billion business and technology services leader, serving 75% of the Fortune Global 100. We are committed to accelerating client success and positively impacting society through responsible innovation. We are one of the world's leading AI and digital infrastructure providers, with unmatched capabilities in enterprise-scale AI, cloud, security, connectivity, data centers and application services. Our consulting and industry solutions help organizations and society move confidently and sustainably into the digital future. As a Global Top Employer, we have experts in more than 50 countries. We also offer clients access to a robust ecosystem of innovation centers as well as established and start-up partners. NTT DATA is part of NTT Group, which invests over $3 billion each year in R&D. . Visit us at us.nttdata.com ( possible, we hire locally to NTT DATA offices or client sites. This ensures we can provide timely and effective support tailored to each client's needs. While many positions offer remote or hybrid work options, these arrangements are subject to change based on client requirements. For employees near an NTT DATA office or client site, in-office attendance may be required for meetings or events, depending on business needs. At NTT DATA, we are committed to staying flexible and meeting the evolving needs of both our clients and employees. NTT DATA recruiters will never ask for payment or banking information and will only use @nttdata.com and @talent.nttdataservices.com email addresses. If you are requested to provide payment or disclose banking information, please submit a contact us form, .
**_NTT DATA endeavors to make_** **_ **_accessible to any and all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact us at_** **_ **_._** **_This contact information is for accommodation requests only and cannot be used to inquire about the status of applications. NTT DATA is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. For our EEO Policy Statement, please click here ( . If you'd like more information on your EEO rights under the law, please click here ( . For Pay Transparency information, please click here ( ._**

**Job Description Summary**
1. Responsible & accountable as a lead for compliance.
2. To review and approval of all master document like standard operating procedures, batch manufacturing, incidents/events, process validation, annual product reviews, master datas, protocols and qualification documents.
3. To review the Production planning, weekly / monthly / yearly as per the forecast /market requirement and complete within timelines.
4. Utilization of resources as per the work demand and target timelines.
5. Effective coordination with CFT teams for smooth flow of Manufacturing and Packaging activities.
6. Responsible for QMS compliance & investigation of event , market complaint & effective CAPA closer.
7. Responsible for change control approval, execution and closure cycle.
8. Provide motivation, support and guidance to the team to build a quality working culture.
**Job Description**
**Safety:**
To ensure 100% safe operation in production area. Ensure all the necessary PPE's are available in production facility and monitor proper PPE's are worn by the personnel's during operation. Reporting the near misses and ensure their compliance. To follow the procedure pertaining to the environmental management system (ISO14001 & ISO45001). To support in implementation new procedure related to environment management system. To follow and maintain 5S in workplace.
**Quality and Compliance:**
No Critical/Major observations in GMP regulatory audit i.e. internal/external. cGMP compliance in entire manufacturing and packaging area and SOP compliance on all aspects. Upgradation of system consistently to deliver the quality production, improvement to plan. Ensure all area logbooks, BMR entries and all documents calibration records area online and updated. Area up keeping hygiene, cleanliness, all areas are in good condition for 24x7. Ensure proper people, material, scrap, SFG movement to avoid cross contamination. Ensure proper Status labeling of each area, item, equipment, accessories, and scrap movement. Ensure proper gowning in the production area, PPE, Personal hygiene. Ensure review and acknowledgement of the EMS alarm, power failure, tooling etc., To ensure 100% adherence to the SOP/Batch instructions, specifications, and control parameters. Follow ALCOA+ and ready for ant time inspection. To ensure Zero overdue on training assigned.
**Head count and manpower handling:**
People to follow shifts. Only required head count to plan. 100% utilization of head count. Share a trusting relationship with the work group. Provide motivation, support and guidance to the team to build a quality working culture.
**Facility/Area management:**
Check production facility building carvings, corners, ceiling, walls, wall guard etc., Ensure each and every item to be placed in its designated area with proper labelling. Developing down line people so that work should not get affect. Focus on continuous improvements on all means (Safety, quality, and delivery). Monthly reviews to perform Quality, yield, simplification, documentation, QMS, and take proper action.
**Teamwork and Coaching**
Ensure efficient collaboration and co-ordination with cross functional departments. Coach team members to solve increasing problems. Mentor team/subordinates in developing documentation. Regulatory interacts with senior management on matters concerning several functional areas, divisions and or customers. Work team COOSST to work efficiently. Involve on culture of excellence implementation and activities.
**Key Responsibilities:**
Responsible & accountable as a lead for compliance. To review and approval of all master document like standard operating procedures, batch manufacturing, incidents/events, process validation, annual product reviews, master datas, protocols and qualification documents. To review the Production planning, weekly / monthly / yearly as per the forecast /market requirement and complete within timelines. Utilization of resources as per the work demand and target timelines. Effective coordination with CFT teams for smooth flow of Manufacturing and Packaging activities. Responsible for QMS compliance & investigation of event , market complaint & effective CAPA closer. Responsible for change control approval, execution and closure cycle. Provide motivation, support and guidance to the team to build a quality working culture. Regularly to interact with senior management on packaging improvisations and continuous improvement projects. Timely issue resolution through daily/weekly meetings. Day today interactions with the team and building up the co-ordination and effective communications. Troubleshooting the projects with assessment and handling continuous improvement project. Developing a systematic and smooth working environment for the team. Involve on culture of excellence implementation and activities. Review and approval of all master document like standard operating procedures, batch packing, events, process validation, qualification documents and other quality documents. Supporting to the Cross functional team during Audit. Site responsible for SAP training and control on the system. Ensure the Process capability studies and Risk Assessment. Responsible for continuous improvement projects.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

**Job Description Summary**
Technician required for Compression operation
**Job Description**
Safety: 1. To follow and ensure 100% safe operation in manufacturing area. 2. Ensure all the necessary PPEs are available in production facility and were the proper PPEs during manufacturing. 3. Reporting the near miss and ensure their compliances. 4. Follow ISO 14001 & 45001 practices. 5. To follow and maintain 5s in workplace.
Quality and Compliance:
1. cGMP Compliance in entire manufacturing area and SOP compliance on all aspects. 2. To ensure zero overdue on trainings. 3. Follow ALCOA+ and ready for any time inspection. 4. Responsible to face regulatory and customer audits. 5. Ensure to follow quality culture in organization.
Delivery: 1. To achieve the weekly plan schedule NLT 90%. 2. Responsible to perform the Operation, machine setting, cleaning, in process checks, challenge test and Trouble shooting. 3. To ensure no machine functioning parameters/facility by passed. 4. Proper operation and setting of machines to minimize the spillage and rejection. 5. To maintain the machine, accessories, documents, area, materials, and all other things are in place. Ensure things are in their designed place and vice versa. 6. To maintain machine, area and accessories with minimum breakdown. PMP and spares management. 7. Involved in the dispensing of raw materials. Storage and material movement of dispensed materials. 8. Verification of dispensed materials and in process storage materials against the batch record. 9. Ensure and discuss with supervisor and above if any special precaution (Like staggering during breaks, sensitive product, new product, new PM, new market, offline activity, special/critical product, new manpower, machine issues etc.). 10. Preparation and storage of disinfectant solution and cleaning agents. 11. Issuance and integrity checking of sieves, screen, filter bags, hose pipes, silicon tubes etc. 12. Cleaning and checking of tools before and after completion of batch. 13. Cleaning and storage of Utensils and Production accessories. 14. Indenting, storage, issuance, usage, and destruction of silica gel. 15. Responsible to prevent the cross contamination during manufacturing. 16. Execution of necessary document during cleaning, line clearance and BMR. 17. Performance of in process check and challenge test as per BMR and if any abnormalities observed inform to the superior and QA. 18. Responsible to Monitoring of Environmental condition and reporting maintenance team if any abnormalities noticed. 19. Involved in the Equipment PMP activities along with engineering person. 20. Ensure the calibration of weighing balance & instruments as per the calibration schedule. 21. To give Training to junior level operators and newly joined persons. 22. Identification and initiation of improvement projects in manufacturing. 23. Based on requirements to carry out the activity whenever assigned by management
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

We are looking for Engineer Manufacturing – Engine APP with 3-6 Yrs of Experience for our esteemed client for Chennai Location. Note : Freshers Please Excuse – Please do not apply if you don’t meet minimum experience criteria Key Skills:  MBOM, SWES, Time study, Virtual Build of EngineThis is an immediate requirement. Please apply if you can join within 20 days or close to 20 days.Candidate must be willing to work from client location in Chennai.Requirements

Virtual build, Assembly process planning and Manufacturing services in Caterpillar are preferred.

MBOM, SWES, Time study, Virtual Build of Engine , and systems.Previous experience in Engine product design, quality, manufacturing process, application and installation, Assembly Process Planning, product performance/support.BenefitsYou will be working with a trusted global product engineering and lifecycle services partner to the world’s most recognized companies in the Aero Engines, Aerospace & Defense, Hi-Tech, Transportation (Auto and Rail), Power and Industrial, Oil & Gas, and Medical Devices industries. With 12K+ experts, and a global presence in 73 locations across 15 countries, it believes that it is at the forefront of the convergence of mechanical, electronics, software, and digital engineering innovations to enable solutions for a safer, cleaner world. A Strong Process based organization Certified for CMMI L5 and multiple other certifications of the process and one of the few organizations which are ranked as best place to work.

We are looking for Engineer Manufacturing – Engine Virtual Build with 3-6 Yrs of Experience for our esteemed client for Chennai Location. Note : Freshers Please Excuse – Please do not apply if you don’t meet minimum experience criteria Key Skills:  Virtual build, VDRA Projects Engine OEM/ Shop floor experiencesThis is an immediate requirement. Please apply if you can join within 20 days or close to 20 days.Candidate must be willing to work from client location in Chennai.RequirementsManufacturing Engineer- VDRA/VB Prior working experience in Virtual build, VDRA Projects in Caterpillar are preferred.Strong fundamental understanding of Engine, Power train and its systemsEngine OEM/ Shop floor experiences preferred.BenefitsYou will be working with a trusted global product engineering and lifecycle services partner to the world’s most recognized companies in the Aero Engines, Aerospace & Defense, Hi-Tech, Transportation (Auto and Rail), Power and Industrial, Oil & Gas, and Medical Devices industries. With 12K+ experts, and a global presence in 73 locations across 15 countries, it believes that it is at the forefront of the convergence of mechanical, electronics, software, and digital engineering innovations to enable solutions for a safer, cleaner world. A Strong Process based organization Certified for CMMI L5 and multiple other certifications of the process and one of the few organizations which are ranked as best place to work.

Quality Control Analyst
Date: Oct 27, 2025
Location:
Chennai, India,
Company: Teva Pharmaceuticals
Job Id: 64341
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**How you'll spend your day**
+ To perform Stability analysis.
+ Maintenance of operating instruments / equipment.
+ To maintain the assigned Laboratory workplace, instruments and equipment etc.
+ To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.
+ Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance.
+ Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.
+ Performing stability testing (Assay, RS & Dissolution) of all formulations by HPLC and UV techniques.
+ Preparing samples and executing the same as per the Method of Analysis and Verification of sample set sequence in applicable software's.
+ Interpreting chromatographic data and ensuring proper documentation of all analytical activities in compliance with GLP / GDP requirements
+ Reporting of interpreted data in line with specification, compliance and regulatory standards and maintaining data integrity throughout the analytical lifecycle.
+ Evaluation of reported results and reporting of any abnormal results to the supervisor ontime.
+ Handling of laboratory software's.
+ Ensure to use safety apparels and PPEs while working in the laboratory.
+ Ensure timely completion of assigned training.
**Your experience and qualifications**
+ M.Sc., Chemistry
+ 7+ years of experience
**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 ( 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.
EOE including disability/veteran

**Job Description Summary**
To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.