520 Jobs in Ahmednagar - Page 2

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Manager - Engineering Date: May 17, 2025 Location: Ahmednagar - Plant Company: Sun Pharmaceutical Industries Ltd Responsible for Design and establish the system for maintaining all documents and records of Mechanical as per regulatory requirement. Responsible for Engineering and Project coordinate with site Engineering and Project team to synchronized with site Quality, Production, Health and Safety Dept. To guide and train the department personnel by identifying the training needs. Preparation of annual Engineering Budget (Opex & Capex) to meet the Business Plan. Monitor a list of project activities and key milestones (on the critical path) in line with the project plan. Maximize the resource utilization and flexibility while minimizing the energy, water and utility costs to achieve the target. Responsible to design and establish the systems for maintaining all documents and records of mechanical / electrical maintenance as per regulatory requirements. Responsible to coordinate with vendor and site contractor and sync with site quality, production, Health & Safety department. Propose annually a list of activities and project key milestones (on the critical path) in line with the project plan and consolidates annual objectives. Monitoring the regulatory compliances, Audits and Compliances. To develop system and processes to monitor and optimize engineering resource utilization. Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Sr. Manager - Micro Lead Date: Jun 3, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Title: Manager / Sr.Manager – Micro Lead Job Grade: G10 / G9B Function: Global API Business Sub-function: Manager’s Job Title: Skip Level Manager’s Title: Function Head Title: Location: Ahmednagar No. of Direct Reports (if any) Areas of Responsibility To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipment’s during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Travel Estimate Job Requirements Educational Qualification M.Sc (Microbiology) Specific Certification Skills Experience 15 to 18 Yrs Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Manager Corporate Quality Projects Date: May 19, 2025 Location: Ahmednagar - Plant Company: Sun Pharmaceutical Industries Ltd Position: Manager-1 - Corporate Quality Projects Grade: G10 Education: M.Sc / B.Pharma / M.Pharma Job Location: Vadodara Job Profile: LIMS Lead is responsible for To have good experience & exposure of LIMS System implementations (Project developments support, validation, enhancements & implementations) across various site To ensure the dynamics of computerized systems w.r.t regulatory standards (21 CFR part 11, EU Annexure 11, & GAMP 5). To have good experience & exposure of SAP-HANA system, well aware of SAP system functionality. To have very good experience & expertise of Quality Control Systems & process (Functional expertise on sample management & Stability programme) To have very good experience & expertise of Quality Assurance process. To have knowledge of Quality control instruments handlings like HPLC, GC & UV for Sample Managements (Testing), Test Calculations (as per pharmacopeia general chapters & Monographs) & good understanding of Test different-different scenarios (like Dissolution & CU) for fate value check (Pass/fail) To provide guidance/Support sites for all the major regulatory audits by Remotely & Onsite visit Evaluation, assessments of different business requirements received, it’s impact assessments and decision for its consideration for digitization, simplification & automations. To identify the roadblocks and ensure the smooth execution of assigned projects. Responsible to ensure smooth functioning of the team operations and routine activities. Encouraged and developed the subordinates to explore their capabilities and take challenge to grow further. To identify the actionable and accomplish the project milestone. To prepare and review CSAP, qualifications scripts and ensure execution of qualification. To prepare, ensure and support for the preparation of database and design as per compliance requirements and functional needs. To ensure technical training / support for each site, whenever required. To ensure successful handover of projects to Site/Sites & support site SME’s for Stabilization of projects at sites. To conceptualize and frame a consolidated approach for new identified technique. To ensure vendor support for technical discussion on finalize of projects. To perform the activities as per the project plan / assigned scheduler. To execute, support other Quality project initiated for simplification, harmonization and productivity enhancement. To work in collaboration with IT, API, SGO, vendor, Site Quality and different teams for identification of the right solution /tool/Vendor, to resolve the “Specific problem” and have correct solution for the organization. Basic Expectation Candidate should Have a balance of technical knowledge & managerial skills Be able to prioritize & multi -task Be able to work independently with limited supervision Manage stakeholders & get work done Be able to create project plans/Charters which is efficient from a time, cost & effort perspective, while understanding at the long term impact of decisions Analytical & Report Creation Skills - Proficiency in Excel, Word & PowerPoint. Basic understanding of MySQL & Oracle database Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Micro Lead - API Date: May 16, 2025 Location: Ahmednagar - Quality Control Company: Sun Pharmaceutical Industries Ltd Job Description Title: Micro Lead API Location: Ahmednagar Grade: G9B- Sr. Manager 2 JOB RESPONSIBILITIES To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To check method validation of bacterial endotoxin test and microbial quality of products. To procure, receipt, storage, maintenance, its use and reconciliation of biological indicator, media, reagents standard cultures and bioball etc. To ensure and check calibration and Operation of TOC analyzer Execute breakdown (If any) in consultation with vender. To ensure environmental monitoring activities performed as per schedule and to check the environmental monitoring reports. To review qualification, Calibration of all instruments in microbiology laboratory as per SOP/Schedule. To participate in investigation and to review of deviations/OOS/OOT/OOC/Lab Event / & review of SOPs as per revision date in micro section online in track wise system. To highlight observations, rejection / failure, quality related concern in time and contribute in troubleshooting To ensure and review all logbooks and registers are maintained on line and available at designated place. Preparation and review of GMP documents related to activities. To review and ensure fumigation activity and its verification as per SOP/Guidelines. To prepare / review trends for water and environment monitoring, Summary report of water and environment monitoring. Responsible to follow online good documentation practices for data recording and monitoring. To ensure and review validation of autoclave, Dry heat sterilizer (DHS), Incubators, Laminar Air flow, HVAC. To ensure and review preparation of reagents and volumetric solution and its standardization as per specification / SOP. To ensure and review inventory and stock record of media/reagents/culture/lysate/CSE/LRW. To ensure to follow the GLP as per current practice in the laboratory. To ensure safety and use of personnel protective equipments during day to day activities Responsible for carrying out any other responsibilities assign from time to time orally or in writing by Quality head, however related training imparted to concerns. To support for review and compliance activity in quality function and to support for any time readiness as well as enhancement of system and practices. To Coordinate with corporate functions with respect to microbiology activity. Education : Graduates - Microbiology/ Equivalent ( experience In Micro testing / leading ) Apply Now » Apply Now Start applying with LinkedIn Please wait... Show more Show less

About The Position We are looking for someone who has an Engineering Degree with Materials, Metallurgy with a minimum experience of 4 years in the Quality function. Quality Control- ✓ Process and Product Deviation Control (“All 5 plants - Melting & Atomization, Annealing, Mixing, INSIP & SSP” & “Raw Materials”) ✓ MSA Plan and execution ✓ SPC monitoring and process control ✓ Round Robin Test (Global lab conformity test) ✓ Product Specific Investigation Inclusion Analysis & Cross Contamination of Iron and Iron Alloys – Metallography analysis to report submission DC Correlation for critical grades (Base Powder + Mixes) Sintering Furnace Calibration and Mapping XRF – Method development, Calibration, Troubleshooting ✓ Review of Product analysis and its approval in IB ✓ Maintaining Automix System ✓ Product Specification creation in M3 & CRAM ✓ Procurement & Inventory Management for lab stocks through M3 ✓ Product related documentation Export documents to logistic Legal documents for Govt. requirements Declaration / Statements for customers Monitor & share 4M changes to customer Sample documents to logistic Samples to customers Working at Höganäs We aim to offer a great and meaningful place to work where you can fulfill your potential and ambitions. We welcome all applicants and strive for diversity. We have a clear management philosophy, and just like us you believe that through collaboration and openness we develop as individuals and as a company. We see all employees, regardless of position, as leaders when we approach the challenges that the world - and we - face. Höganäs ambition is to lead the transformation to better meet the needs of tomorrow and become the preferred supplier of sustainable metal powder on a global scale – join us in our journey of sustainable change and towards net-zero climate emissions. More About Höganäs Höganäs is the world leader in the market for metal powders, with a yearly capacity of 500,000 tons. Höganäs vision is to inspire the industry to make more with less, and its ambition is to be the preferred supplier of sustainable metal powders. In close cooperation with customers, Höganäs develops tomorrow's solutions for automotive components, electrical motors, brazing, surface coating, and additive manufacturing. Höganäs operates 17 production centres across the globe and has a workforce of 2,400 employees. The turnover for 2024 was €1.034 biljons. Höganäs, which was founded in 1797, is owned by Lindéngruppen and Wallenberg owned FAM. Interested? Apply today! Show more Show less

Role & responsibilities : Minimum 1 Years experience is mandatory in CASA sales . Acquire new customers for liabilities from open market. (CASA) Assist the customers for conversion of existing borrowing customers for liabilities • Enhance the relationship with the existing customers by cross-selling products and services as per the profile & need of the customers Interested Can Share you updated resume - mahesh.dolare@ujjivan.com / 8855042842

4 yrs of exp in Home loan and LAP - Prime team handling Required Candidate profile Location- Ahmednagar Graduate Share CV's on Sweetiec@onboardhrservices.com

Position- Manager- Customer Experience Experience: Preferably healthcare. Role & responsibilities: Operational To be responsible for supervising all customer touch points like IPD, OPD and Support Services, including Housekeeping, Security and Food & Beverage and ensure an exceptional level of customer experience To conduct detailed daily rounds of patient rooms and to meet patients and their relatives and address grievances, thereby, ensuring optimum patient satisfaction in all areas To supervise the activities of customer experience team and ensure their interaction with customers reflect positively on the company To assist in designing and implementing a mechanism to assign complaints and concerns to respective HODs for corrective action with closure timelines and due follow up. To submit operational tracker to the COO on a daily basis Strategy & Planning To develop and implement Customer engagement plans, programs, and initiatives. To define and implement standards/procedures for ensuring optimal customer experience. To identify opportunities for enhanced service delivery through online and e-services delivery and the application of social media, mobile apps and technologies to optimize customer experience. To design and develop methodology and tools to capture and generate recurring complaint analysis reports for daily consumption and actionable. To prepare and implement the SOP to handle VIP/celebrity patients. To prepare and implement the room readiness SOP To create and implement an escalation matrix for complaint handling with adherence to level wise TAT. To prepare an SOP for Fam Trip(Patients/clients for understanding the facilities available) Feedback Mechanism: To adapt a robust feedback mechanism that has all the listening and learning ports available to capture Patient feedback from all touch points and to resolve concerns and grievances and focus on reducing repeats. To ensure cross department collaboration and routine feedback and interaction mechanisms. To review feedback and interaction mechanisms routinely and analyse gaps for further improve and enhance. To capture service gaps/customer grievances in the form of a dashboard and actively work towards gap closure through appropriate action plan OPD: To set up systems and processes to handle heavy OPD flows in order to minimize /eliminate delays. To ensure a system to reduce turnaround time for reports. To develop standard operating procedures for Corporate and VIP customers and ensure the best service. To continuously review the process flow to ensure smooth transactions. To ensure that the Front Desk of the hospital is always ready in all aspects to process new admissions and service existing customers To monitor OPD waiting time, and track mandatory reports(OPD Cancellation, Appointment Cancellation, Change in OPD timings/days) To track daily OPD conversions to various departments OPD schedule to be updated on monthly basis and mailed to all concerned IPD: To streamline the Admission and Discharge process and implement a smooth billing process. To ensure a robust room allocation procedure and room reservation system is in place. To ensure standards for handling patient visitors/patient companions are being implemented. To prepare an SOP for in-room admission/discharge for VIP/celebrity patients Call Centre: To ensure the customer appointment booking process functions smoothly. To develop a robust database of Customers for the Sales and Marketing department. To assist the Sales & Marketing team is advertising the organization as well as make cold calls. To review the process flow routinely. The list of duties and responsibilities mentioned above is indicative, not exhaustive.

Position: Head of Manufacturing (Plant Head) API Job Location : Ahmednagar Job summary: Overall responsibility and accountability for the Manufacturing including Production, Engineering, Ware house and all support functions across location. Which will include conducting operations review, drive compliance to all regulatory & statutory requirements and demonstrate Sun Pharma values and improvement /Corporate initiatives, policies at the site with a focus on compliance to environmental standards with the objective of achieving the business target and building potential for sustained revenue growth. Area of responsibility: Overall responsibility for manufacturing activities across location. Create and implement best practice manufacturing vision, strategy, policies, processes and procedures to aid and improve business performance. Ensure that manufacturing strategies and processes are in place to meet business objectives and operational needs in terms of price, quality and delivery targets and which enables the company to function and compete effectively in the market. Evaluate the challenges faced by the business and take action to mitigate risks and develop opportunities. Contribute to overall business strategy and annual budget process. Take ownership of the manufacturing policy, guidelines and any associated documents. Initiate and develop creative and innovative manufacturing processes. Conduct timely Review meetings like Back Order, Demand vs Commit vs Supply and ensure meeting set out targets and to improve the plant volume Achieve Annual Work Plan of the plant with adherence to cost. Control and review Quality related systems, processes to adhere to the regulatory requirement. Monitor timely delivery of products as per Organizational mandates. Provide Site switch and support R&D for commercial scale up batches and new product launches. Ensure continuous higher levels of productivity, manufacturing yields & by optimizing the available resources. Plan and coordinate all activities leading to timely delivery of new product launches and site transfers. Ensure maintenance and up-keep of production, support systems and facility. Develop and maintain high level of morale and motivation amongst employees, capacity building and maintain disciplined workforce at plant. Conceive plan and implement capital expenditure proposals as sanctioned for capacity up-gradation and other routine activities within stipulated time and cost. Ensure regulatory compliances and to oversee the execution of self-inspection and other inspections. Maintain all time preparedness for Regulatory Audit/Inspections. Establish & ensure the cGMP requirements for Investigational Medicinal Products (IMP) manufacturing. Monitor environment, health and safety and ensure all EHS compliances. Coordinate team activities to optimize cost performance of the plant through capital investment programs, optimizing operating working capital usage and minimizing waste through the development of a continuous improvement culture encompassing lean principles and clear strategic development Provide leadership to departments under control and coach, mentor and develop direct reports and manage a high performing team that delivers continuous improvement, added value and cost reductions. Establish strategy and best practices for staff to ensure achievement of overall business objectives. Work with the Manufacturing team to translate site strategy into specific annual performance goals and departmental objectives including KPIs, and to track them. Ensure strong communication between teams under leadership to facilitate exchange of information and in order to implement change and improvements. Responsible for developing the appropriate organizational structure, resource plans and culture to support the business objectives and deliverables. Skills and Attributes: Proven leadership and management skills with the ability to optimize team performance and development. Excellent relationship management skills with the ability to engage, negotiate and manage key stakeholders and suppliers. Strong and confident negotiator with the ability to negotiate at all levels Excellent communication, interpersonal and influencing skills. Excellent analytical and problem solving abilities. Results orientated with ability to plan and deliver against project deadlines. Commercially and financially astute with experience of managing budgets. Resilient, self-motivated and able to work well under pressure. Technical mindset. Qualifications and Experience Levels: M.Sc / B.E / B.Tech Chemical with 22 to 25 Yrs experience . Demonstrable experience of leading a manufacturing function with a proven track record in strategic manufacturing leadership delivering effective manufacturing strategies, policies, processes and systems. Ability to add value, reduce costs and make business improvements. Proven project management and build quality experience. Experience of operating and influencing at a strategic level. Knowledge and technical understanding of manufacturing. Show more Show less

Role : Site Quality Head Business Unit: Global Quality & Compliance Location: Ahmednagar POSITION SUMMARY Ensure the supply of high quality, GMP compliant products, define operational strategy for quality system management at site, finalize site quality assurance and quality control goals, objectives and strategies in line with Sun Pharma compliance, product quality management objectives and regulatory requirements. Provide leadership and direction to ensure achievement of all site accountabilities for QA, QC and Stability at site. Proactively assess quality issues at site and ensure compliance to QA/QC regulatory requirements in manufacturing operations at the site and track quality assurance/control metrics with site manufacturing and drive them down. Assure all time readiness of site for regulatory agency inspections\internal audits at any given point The incumbent will assure individual compliance with the all concerned regulatory requirements, GxP’s and applicable department programs, including training, documentation, Standard Operating Procedures, and Sun Pharma Global Quality Policies, Standards and Procedures. Key responsibilities: 1. Assess quality issues at site and ensure compliance to QA/QC regulatory requirements in manufacturing operations at site and track quality metrics with site manufacturing management and drive them down. 2. Accountable for designing/implementing and ensuring compliance to all quality related SOPs, Policies, Standards and Quality systems at the site 3. Design and execute continuous improvement initiatives at the site to enhance compliance, drive efficiencies and cost effectiveness. 4. Responsible for ensuring availability of adequate resources, including manpower to maintain compliance with GXP requirements. 5. Facilitate harmonization and consistent implementation of Quality Systems and procedures at site, in alignment with Global Quality policies\standards. 6. Ensure market complaints, failures, deviations are investigated and corrective and preventive actions are implemented with adherence to timelines 1. Assure all time readiness of site for regulatory agency inspections\internal audits and appropriate implementation of corrective actions regarding observations made by the agencies\internal audit teams 2. Monitor industry trends/issues faced internally and identify scope for improving Site quality management and processes. 3. Ensure compliance to regulatory requirements on product, process and release procedures. 4. Prepare site quality revenue and capital budgets and headcount projections, track and manage expenditures and headcount to budget over the fiscal year. 5. Ensure release of safe and effective drug products from site as per cGMP requirement and regulatory commitment. 6. Responsible for ensuring smooth collaboration with all Sun Pharma sites and functions to leverage synergies. 7. Follow the EHS policy, laboratory standard operating procedures and maintain the compliance to GMP requirements Educational Qualification M.Sc / B.Pharm / M.Pharm Work Experience: 18 to 22 Yrs Show more Show less

🔧 Job Title: GDC Head (Gravity Die Casting) 🏢 Company: Klassic Wheels Ltd. 📍 Location: MIDC, Ahmednagar 🔹 Responsibilities: Lead & manage Gravity Die Casting (GDC) operations Ensure production targets, quality, and safety compliance Oversee die/mould maintenance and manpower planning Drive process improvements and reduce rejections ✅ Requirements: Diploma/BE in Mechanical Engineering 10+ years’ experience in GDC operations Strong leadership & technical knowledge 📌 How to Apply: Interested candidates can send their updated CV to kwl2.hr@gmail.com 📱 Or WhatsApp us at 8766980771 Show more Show less

Dalmia Cement Bharat Ltd is looking for Technical Services Engineer to join our dynamic team and embark on a rewarding career journey. Provide technical support and guidance to clients via phone, email, and in- person interactions Troubleshoot technical issues and identify and implement solutions Maintain and troubleshoot technical systems and infrastructure, including servers, networks, and hardware Keep up to date on industry trends and best practices in technical support and infrastructure management Maintain accurate and up- to- date documentation of technical systems and processes Collaborate with other teams and departments to ensure smooth and efficient operations

Company Description We suggest you enter details here. Role Description This is a part-time hybrid role as a Sales Executive at Arvind Agro And Oil Industries. The Sales Executive will be responsible for generating leads, pitching products, closing sales, and maintaining customer relationships. The role is located in Ahmednagar with the flexibility for some work from home. Qualifications Sales Skills, Communication Skills, and Negotiation Skills Experience in lead generation and sales pitching Customer Relationship Management skills Proven track record of meeting sales targets Ability to work independently and in a team Knowledge of the agricultural or oil industries is a plus Bachelor's degree in Business Administration or related field Show more Show less

FREE JOB FREE JOB WE ARE HIRING!!! COMPANY NAME - SFO Technology Pvt Ltd LOCATION : Wasuli Phata, Chakan Pune QUALIFICATIONS: 10th, 12th, ITI, Graduation SALARY: 17,321 + 500 3-Year Diploma Certificate 2,000 Retention Bonus FACILITIES: Attendance Bonus Bus & Canteen Available Open for Both Male & Female candidates Company Address : B-21, Chakan MIDC Phase-II Wasuli, Taluka, Khed taluka, Maharashtra - 410501 Office Address : Talentcorp Solutions Pvt Ltd, Shree Gajanan Commercial Complex, Chakan-Talegaon Road, Chakan, Pune, Maharashtra - 410501 CONTACT NUMBER : 9226514199 | 7219570521 | 7875724537 Talentcorp Solutions Pvt Ltd,

FREE JOB | FREE JOB HAIER APPLIANCES INDIA PVT LTD Location - Ranjangaon (Pune) REQUIRED DIPLOMA, GRADUATE BA, B.COM, B.SC, BBA, BCA, M.COM, MA,M.SC, MCA (NATS APPRENTICESHIP) Last 5 Years Graduation Passout (2025, 2024, 2023, 2022, 2021, 2020) DIPLOMA STIPEND : 20000/- GRADUATE STIPEND : 18500/- 8 Hours Duty Bus Canteen Facility Total Requirements - 500 Contact Number : Rudra Mam : 9226569240 Bhumika Mam : 9226569233 Namdev Sir : 8208872829 Sarang Sir : 7397971322 Shivanand Sir : 9226541390 Nana Sir : 9975722151 Resume + Qualification Documents + Aadhar Card + Pan Card + 4 passport size photo + Wear shoes Address: Talentcorp Solutions Pvt. Ltd., First Floor, Sadguru Krupa Complex, Yesh Inn Chowk, Near Ganga Grand Restaurant, Karegaon, Maharashtra 412220 Address Link : https://g.co/kgs/E8hzP3M

FREE JOB! FREE JOB! Company Name :- Otter Controls India Pvt Ltd Location - Waghjai Nagar, Chakan Qualifications & Salary : ITI - 19,000/- Diploma 21,000/- BE/BTech 22,000/- Facilities : Canteen Available 8 Hours Shift Double OT Only for Male Candidates Contact Number :- 9226514199 | 7219570521 | 7875724537 Interview Address - Otter Controls India Pvt Ltd , Shed No 6, U-Turn Industrial Hub, Kharabwadi, Maharashtra 410501 Address Link - https://g.co/kgs/y7aPCAv Office Address : Talentcorp Solutions Pvt Ltd, Shree Gajanan Commercial Complex, Chakan-Talegaon Road, Chakan, Pune, Maharashtra- 410501 Come with - Resume + Qualification Documents + Adhar card + Pan card + Passport size 4 photos + Bank Pass Book TALENTCORP SOLUTIONS PVT LTD

Develop and implement academic programs, policies, and procedures to ensure high-quality education. Oversee curriculum development, implementation, and evaluation to meet school goals. Manage faculty performance, recruitment, training, and professional development to maintain a skilled team. Foster effective communication among teachers, students, parents, and stakeholders through regular meetings and reports. Ensure compliance with regulatory requirements from relevant authorities (CBSE).

manufacturing unit HR & administration operations IR, TA, PAYROLL, LABOUR, COMPLAINCE, AUDITS, FACTORY ACT, overall factory HR operations management Electronics/EMS working only, male,

Lean Management of manufacturing unit Japanese automobile working candidate only 3-5yrs exp in lean management /operations improvement, processes, waste reduction, smooth functioning

Sr Executive/AM, SUPA, Ahmednagar, Maharashtra, EMS MNC, Role manufacturing unit HR & administration operations - TA, PAYROLL, LABOUR, COMPLIANCE, AUDITS, FACTORY ACT, factory HR operations. manufacturing - Electronics/EMS working only.

chinese interpreter male, for mnc electronics manufacturing in supa, ahmednagar, maharashtra good knowledge of chinese languauge - written and verbal role to translate / interpret chinese to english

MNC working, Role to manage Plant HR & Admin, key skills ; OD, TA, PMS, T&D, Employee engagement, Compliances, IR. 12-15yrs exp. of mfg. MNC- EMS/HA/CD excellent english communication

MNC WORKING, Key skills ; Talent Development & Training, HR & admin operations 5-8yrs exp of mfg. MNC / EMS/Home appliance, Excellent English Communication is must,

Equipment Maintenance, Machine maintenance Industry background: Home appliance / consumer durable Qualification: B.Tech / Diploma in Mechanical Engineering plant maintenance, mechanical maintenance, mnc working, ems / home appliances good exposure

Cadila Pharmaceuticals Limited is looking for Field Officer to join our dynamic team and embark on a rewarding career journey. As a Field Officer, you will be responsible for carrying out various field-related tasks and activities to support the organization's operations and objectives Your role may involve data collection, customer interactions, inspections, assessments, or other field-based tasks, depending on the organization's industry and needs Key Responsibilities:Field Operations:Data Collection: Conduct field surveys, interviews, or assessments to gather relevant data and information Customer Visits: Visit customers, clients, or stakeholders to provide services, collect feedback, or address concerns Inspections: Perform inspections of facilities, equipment, or properties to ensure compliance with regulations and standards Reporting:Data Recording: Accurately record and document field data, observations, or findings Reporting: Prepare and submit reports based on field activities, including data analysis and recommendations Customer Interaction:Customer Support: Provide information, assistance, or support to customers or clients during field visits Issue Resolution: Address customer inquiries, complaints, or issues in a timely and effective manner Compliance:Regulatory Compliance: Ensure compliance with applicable laws, regulations, and company policies during field operations Quality Control: Conduct quality control checks or assessments as required Safety and Security:Safety Protocols: Adhere to safety protocols and guidelines while working in the field Security Measures: Implement security measures to safeguard assets, data, or equipment in the field Logistics and Inventory:Inventory Management: Manage and maintain inventory or supplies required for field operations Training and Development:Training: Participate in training programs and workshops to enhance field-related skills and knowledge