488 Jobs in Halol - Page 6

Job Title: Project Manager – Green Field Company Name : Indore Composite Private Limited Location : Gujarat, Halol About Indore Group Indore Group is a leading Indian multinational specializing in advanced materials for cable reinforcement and protection. With over 25 years of industry leadership , we serve the world’s top cable manufacturers, delivering high-performance products including FRP rods, ARP, coated glass fibers, tapes, yarns, and gels . Operating four world-class manufacturing facilities —three in India (Pithampur, Ambernath, Umbergaon) and one in Tangier, Morocco —we support customers in over 60 countries across North America, Europe, Russia, Africa, and Asia . Over 60% of our production is exported, reflecting our strong global presence. At the forefront of composite innovation , we continue to expand our portfolio with next-generation materials such as carbon composite cores for HTLS conductors and pultruded components for wind energy . We are also India's first manufacturer of LFT compounds for the automotive and engineering sectors under the brand RePlet , developed in collaboration with Plasticomp, USA. Driven by continuous R&D investment , cutting-edge technology, and a dedicated workforce of over 700 professionals , Indore Group remains committed to sustainability, quality, and innovation . Our mission is to deliver reliable, future-ready solutions for the telecommunication, energy, and transportation industries worldwide. Job Summary: We are looking for a highly experienced Project Manager to lead and execute complex greenfield projects in the mechanical and/or electrical domains. This role requires a strong technical background, leadership skills, and proven experience in delivering projects within budget and schedule. The ideal candidate will manage all phases of project lifecycles, from planning through construction and commissioning. Experience in electrical and/or mechanical systems is a must, while civil engineering experience is not preferred. Key Responsibilities: Project Planning & Execution : Develop detailed project plans, including scope, schedule, budget, and resource allocation. Ensure project execution adheres to plans, specifications, and timelines. Monitor project progress, identify risks, and implement corrective actions. Lead and manage project teams, including engineers, technicians, and contractors. Technical Expertise : Provide technical oversight for electrical and/or mechanical systems design, installation, and commissioning. Ensure compliance with industry standards, codes, and regulations. Review and approve technical drawings, specifications, and calculations. Lead system design reviews for electrical or mechanical systems. Stakeholder Management : Act as the primary point of contact for clients, contractors, and stakeholders. Build and maintain strong relationships to ensure effective communication and collaboration. Manage stakeholder expectations, addressing concerns promptly and professionally. Project Control & Reporting : Develop and maintain project budgets and schedules. Track project costs and identify cost-saving opportunities. Prepare and present regular project reports to management and clients. Lead project risk assessments and develop mitigation plans. Safety & Quality : Ensure compliance with safety protocols and regulations. Implement and oversee quality control and assurance programs. Conduct regular site inspections and audits to ensure safety and quality standards are met. Greenfield and Brownfield Expertise : Demonstrated experience managing both greenfield and brownfield projects. Ability to adapt project strategies to meet the unique challenges of each environment. Strong understanding of integration challenges when working within brownfield sites. Qualifications & Experience: Education : Bachelor’s or Master’s degree in Electrical Engineering or Mechanical Engineering . Experience : Minimum 10 to 15 years of experience in project management, particularly with greenfield projects . Proven track record of managing complex electrical and/or mechanical projects. Experience managing project budgets upwards of 100 Cr . Proficiency in project management tools like MS Project or Primavera . Strong problem-solving and decision-making abilities. Preferred Qualifications: Certifications : PMP (Project Management Professional) or other relevant certifications. Industry Experience : Experience in the continuous production manufacturing , cable , or FRP industries (preferred but not mandatory). Compensation: Competitive salary based on experience and industry standards. Share cv to - mahesh.naik@indore.co.in Company Website: www.indore.co.in

Welding Process Engineering Basics of Jigs and Fixtures, Geometric Dimensioning and tolerancing, PPAP, ISO 9001 Quality systems, Machine design 3-4 years of experience for injection moulding process (4-wheeler) AutoCAD, CATIA, NX, SolidWorks Software

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: MES Co-ordinator Date: Jul 10, 2025 Location: Halol 1 - Information Technology Company: Sun Pharmaceutical Industries Ltd Job Title: Manager, MES & L2 project coordinator Job Grade (refer to JE) G10 Function: Global IT Sub-function: Manufacturing IT Location: Halol/Baska Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summary: We are seeking a seasoned professional with 7-9 years of experience in the pharmaceutical industry, including hands-on expertise in Manufacturing Execution Systems (MES) and L2 integration. The Site Project coordinator for MES Implementation will be the primary coordinator for all MES-related activities at the Halol / Baska sites. This role demands dedicated full-time support to the project to ensures smooth execution, alignment with the global MES strategy, and timely delivery of milestones to enhance manufacturing efficiency, compliance, and digital transformation. The role will work closely with internal teams—including QA, IT, SAP, business users, and L2 integration—as well as external vendors and infrastructure leads. Responsibilities include stakeholder management, managing project timelines, risks, and dependencies, ensuring infrastructure readiness, facilitating change management, and maintaining compliance with site validation and quality standards. As the single point of contact for MES implementation at the site, the site coordinator plays a critical role in driving collaboration and successful deployment. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) Previous experience with Werum (Korber Pharma) for pharma industry is a big plus Project Coordination: Lead and coordinate all MES implementation activities at the site, ensuring alignment with the global MES strategy. Stakeholder Management: Serve as the single point of contact for site-level stakeholders, including QA, QA IT, IT, SAP, and business users (Production & Engineering) Vendor & Partner Collaboration: Work closely with MES vendors, infrastructure teams, and integration partners to ensure smooth execution. Timeline & Risk Management: Manage project schedules, track milestones, identify risks, and implement mitigation plans. Infrastructure & Readiness: Ensure site infrastructure (network, servers, systems) is ready and validated for MES deployment. Compliance & Validation: Oversee adherence to site quality standards, IT validation (CSV), and regulatory requirements. Communication & Reporting: Maintain clear and timely communication with the Global Project Manager and other stakeholders; provide regular updates and escalate issues as needed. Change Management: Facilitate change control processes and support user readiness and adoption. Travel Estimate Less Job Scope Internal Interactions (within the organization) Global Project Manager – MES Program Site QA and QA IT teams Site IT and Infrastructure teams Production, Operations teams SAP Coordinators Site SME and Global SME External Interactions (outside the organization) MES vendors and implementation partners System integrators (L2/PLC/SCADA) Infrastructure service providers (network/server) Validation consultants (if outsourced) Auditors (during validation or compliance reviews) Geographical Scope Halol/Baska site Financial Accountability (cost/revenue with exclusive authority) No direct financial authority Job Requirements Educational Qualification Bachelor’s degree in Engineering, Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field. Preferred: Master’s degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Project Management, Operations Management, Industrial Automation, or Pharmaceutical Technology. Specific Certification PMP – For Structured Project Execution (Preferred) GAMP5 or CSV Training – for compliance in regulated environments Experience 7–9 years of experience managing IT or digital transformation projects, preferably in pharmaceutical manufacturing. Hands-on experience with MES platforms, L2/PLC systems, and SAP integration and Edge Cloud IoT. Proven track record in project planning, stakeholder coordination, and cross-functional team leadership. Strong background in GxP compliance, CSV, and validation protocols (IQ/OQ/PQ). Experience working on the shop floor and with QA, IT, and business teams in a regulated environment. Skill (Functional & Behavioural): Functional: Strong project management expertise in IT/digital systems, Knowledge of MES platforms, L2/PLC systems, and SAP integration, Familiarity with GxP, CSV, and validation protocols (IQ/OQ/PQ), Understanding of pharmaceutical manufacturing processes and shop floor operations, Proficiency in stakeholder coordination and cross-functional collaboration Behavioral: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, Ability to work under pressure and manage multiple priorities, Team-oriented with a focus on collaboration and accountability Additional Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s). Apply Now » Apply Now Start applying with LinkedIn Please wait...

We required Graduate person Department : Store Location : Surat Post : As Store Supervisor Salary : 25000 TO 35000 Time : 9 to 7 Mo No : +91 90816 99500 / 90816 99400 /+91 90816 88600 / 90816 99800

Job Title: Manager / Sr. Manager Engineering (Projects) Location : Central India (Greenfield Project) Responsibilities- Overall experience in USFDA Injectable Plants, handling Qualification of HVAC, Designing, Installation, Commissioning Clean Utilities Black Utilities Overall, In charge of Piping, Utilities & HVAC Systems for installations at Site. Based on the received drawings & documents, assign work and timelines and ensures the implementation of the same. Ensure collection of data; do analysis to achieve relevant construction quality and safety. Help overcome constraints, work out alternatives to the design in case of difficulties Retention of records in respective area. Preparation & completeness of documentation for Qualifications. Give final acceptance of construction quality for piping and utilities. Review measurements sheets. Ensure schedule updates in primavera and send progress reports in terms of schedule work quantity, progress, constraints, snaps and etc. Coordination with Boiler Inspector and other statutory agencies Execute construction quality audits for piping and utilities. Responsible for construction quality; finishes, Operations, Performance and safety at site. He will report quantity variation and scope change Educational Qualification Bachelor's degree in Mechanical Engineering Experience : Tenure : 14 to 17 Years ( Pharmaceutical Industry with Injectable experience mandatory)

Job Title Manager, MES & L2 project coordinator Job Grade (refer to JE) G10 Function Global IT Sub-function Manufacturing IT Location: Halol/Baska Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Position Summary We are seeking a seasoned professional with 7-9 years of experience in the pharmaceutical industry, including hands-on expertise in Manufacturing Execution Systems (MES) and L2 integration. The Site Project coordinator for MES Implementation will be the primary coordinator for all MES-related activities at the Halol / Baska sites. This role demands dedicated full-time support to the project to ensures smooth execution, alignment with the global MES strategy, and timely delivery of milestones to enhance manufacturing efficiency, compliance, and digital transformation. The role will work closely with internal teams—including QA, IT, SAP, business users, and L2 integration—as well as external vendors and infrastructure leads. Responsibilities include stakeholder management, managing project timelines, risks, and dependencies, ensuring infrastructure readiness, facilitating change management, and maintaining compliance with site validation and quality standards. As the single point of contact for MES implementation at the site, the site coordinator plays a critical role in driving collaboration and successful deployment. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) Previous experience with Werum (Korber Pharma) for pharma industry is a big plus Project Coordination Lead and coordinate all MES implementation activities at the site, ensuring alignment with the global MES strategy. Stakeholder Management Serve as the single point of contact for site-level stakeholders, including QA, QA IT, IT, SAP, and business users (Production & Engineering) Vendor & Partner Collaboration Work closely with MES vendors, infrastructure teams, and integration partners to ensure smooth execution. Timeline & Risk Management Manage project schedules, track milestones, identify risks, and implement mitigation plans. Infrastructure & Readiness Ensure site infrastructure (network, servers, systems) is ready and validated for MES deployment. Compliance & Validation Oversee adherence to site quality standards, IT validation (CSV), and regulatory requirements. Communication & Reporting Maintain clear and timely communication with the Global Project Manager and other stakeholders; provide regular updates and escalate issues as needed. Change Management Facilitate change control processes and support user readiness and adoption. Travel Estimate Less Job Scope Internal Interactions (within the organization) Global Project Manager – MES Program Site QA and QA IT teams Site IT and Infrastructure teams Production, Operations teams SAP Coordinators Site SME and Global SME External Interactions (outside the organization) MES vendors and implementation partners System integrators (L2/PLC/SCADA) Infrastructure service providers (network/server) Validation consultants (if outsourced) Auditors (during validation or compliance reviews) Geographical Scope Halol/Baska site Financial Accountability (cost/revenue with exclusive authority) No direct financial authority Job Requirements Educational Qualification Bachelor’s degree in Engineering, Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field. Preferred: Master’s degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Project Management, Operations Management, Industrial Automation, or Pharmaceutical Technology. Specific Certification PMP – For Structured Project Execution (Preferred) GAMP5 or CSV Training – for compliance in regulated environments Experience 7–9 years of experience managing IT or digital transformation projects, preferably in pharmaceutical manufacturing. Hands-on experience with MES platforms, L2/PLC systems, and SAP integration and Edge Cloud IoT. Proven track record in project planning, stakeholder coordination, and cross-functional team leadership. Strong background in GxP compliance, CSV, and validation protocols (IQ/OQ/PQ). Experience working on the shop floor and with QA, IT, and business teams in a regulated environment. Skill (Functional & Behavioural) Functional: Strong project management expertise in IT/digital systems, Knowledge of MES platforms, L2/PLC systems, and SAP integration, Familiarity with GxP, CSV, and validation protocols (IQ/OQ/PQ), Understanding of pharmaceutical manufacturing processes and shop floor operations, Proficiency in stakeholder coordination and cross-functional collaboration Behavioral: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, Ability to work under pressure and manage multiple priorities, Team-oriented with a focus on collaboration and accountability Additional Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let’s create a brighter future together! Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).

Company Description Team Computers is a leading IT Infrastructure and Information Solution Provider, serving businesses' needs with high-quality, affordable IT solutions. The company, founded in 1987 by IIT-Kanpur alumnus Ranjan Chopra, has a turnover of 3500+ Cr, 25+ offices across India, and a workforce of over 5000 members. Known for its proactive approach and customer-centric service, Team Computers prides itself on creating outstanding customer experiences. With 38 years of experience, the company continues to be a platform where individuals with innovative ideas can thrive and succeed. Role Description This is a full-time on-site role for an Asset Executive, located in Halol. The Asset Executive will be responsible for managing and overseeing the company’s IT assets. Duties include tracking asset locations, maintaining asset records, ensuring timely updates, coordinating with various departments for asset allocation, managing asset lifecycle, and implementing asset management policies. The role also involves performing regular audits and ensuring compliance with asset management guidelines. Qualifications Proficiency in IT Asset Management and understanding of IT Infrastructure Strong organizational and record-keeping skills Experience in conducting audits and ensuring compliance Excellent coordination and communication skills Ability to work independently and manage multiple tasks Bachelor’s degree in IT, Computer Science, or related field is preferred

Job Requirements Role/Job Title : Associate Relationship Manager-Personal Loan Function/Department: Rural Banking Job Purpose To Start Personal Loan in Rural Market and service and source the product. Roles & Responsibilities Identifying Business owners / entrepreneurs in the defined catchment and identifying / assessing their business loan needs. Map out prospects in the town to scope business potential. Disburse Personal loans based on needs assessment. Conduct end-use checks as specified post disbursal of loans. Achieve monthly and annual loan booking targets. Cross-sell products and services to both new and as well as existing customers as per their lifestyle, risk profiling and requirements. Contribute to penetration of liabilities business in Rural markets through lead generations and account opening as per needs of customer. Secondary Responsibilities Maintain high collections efficiency through discipline and drive. Preparation of accurate documentation of loans. Coordinate with operations officer to ensure timely data entry. Nudge behavioural changes in customers to move towards online banking. Ensure compliance as per the bank requirements. Education Qualification Graduation: Any Graduate Experience: 2 to 5 years of relevant branch banking experience.

Working with high and low voltage equipment Designing systems and products using computer software Managing and maintaining building services, such as lighting, heating, ventilation and lift systems Budgeting and estimating

Hi, We are having an opening for Manager IT - MES SME at our Halol or Baska(Gujarat) location. Job Summary : We are seeking a seasoned professional with 6-8 years of experience in the pharmaceutical industry, including technical and functional experience in MES & L2 systems. The Site SME MES Project is a key functional and technical expert responsible for supporting the successful implementation of the Manufacturing Execution System (MES) & L2 at the Halol & Baska pharmaceutical manufacturing sites. This role ensures that site-specific manufacturing processes are accurately captured and reflected in the global MES solution. The SME is also accountable for leading site-level validation activities and technical owner responsibility , and managing all GxP documentation related to the MES & L2 system. The Site SME is the go-to authority for end-to-end MES product knowledge. This includes a deep understanding of system functionality, configuration, and compliance requirements.The SME also serves as the first point of contact for any MES front-end application issues, supporting users in troubleshooting, training, and ongoing system usage post-go-live. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) Previous experience with Werum (Korber Pharma) for pharma industry is a big plus Areas Of Responsibility : MES Implementation: Representing site-specific needs during MES design, configuration, and deployment. Validation Leadership: Leading IQ, OQ, PQ, UAT, and traceability matrix execution. Documentation Ownership: Managing GxP documentation (URS, FS, DS, test cases, validation plans/reports). MES Product Expertise: Maintaining deep knowledge of MES functionality and architecture. Front-End Support: Acting as the first point of contact for MES application issues and user support. Training & Adoption: Delivering training and ensuring user readiness for MES usage. Data Management: Supporting data collection, migration, and master recipe creation. Audit Readiness: Ensuring all documentation and systems are compliant and audit-ready. Educational Qualification : Bachelors degree in Engineering - Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field. Preferred: Masters degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Industrial Automation, Pharmaceutical Technology or related technical fields Specific Certification : GAMP 5 for system validation in regulated environments. CSV (Computer System Validation) for compliance with GxP. MES Platform Certifications e.g., Werum PAS-X, Siemens Opcenter, or Rockwell 21 CFR Part 11 Compliance Training for electronic records and signatures Experience : 6 to 8 years of experience Pharmaceutical Manufacturing: Strong understanding of pharma shop floor operations and regulatory requirements. MES or Digital Systems: Prior hands-on experience with MES platforms or similar systems in GxP-regulated environments. Validation Expertise: Proven experience in validation documentation and execution, especially for GxP Category 4 & 5 systems. Application Support: Experience in resolving front-end MES issues and supporting end-users post-deployment. Audit Experience: Familiarity with audit processes and documentation expectations Skill (Functional & Behavioural): Functional: MES system configuration, deployment, and validation, Front-end application troubleshooting and user support, GxP and 21 CFR Part 11 compliance, Validation protocol development and execution (IQ, OQ, PQ, UAT), Documentation management (URS, FS, DS, traceability matrices), Data migration and master recipe creation Behavioral: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, Ability to work under pressure and manage multiple priorities, Detail- oriented with a focus on compliance and quality, Proactive problem-solving and decision-making, Comfortable working on the shop floor and in technical environments Additional Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases

Role & responsibilities Training of all the members to identify risk hazards and unsafe conditions. Identification of near misses and other incidents and ensuring countermeasures. Create and maintain safety awareness in Junior Engineers & Associates. Identify training needs, prepare skill matrix, prepare yearly training plan as per the skill level. Should have experience in Spot welding, MIG welding and metal finishing operations. Encourage Engineers & Associates to identify and execute Kaizens and improvements. Ensure effective implementation of all the quality standard requirements. Line side productivity improvement and achieving production targets Develop, coordinate, review & update JES, SOS, PFMEA, PPSR Ensuring effective TPM done in fixtures, tools & equipments in the line. Ensure jobs are running necessary to meet proper cycle time and/or product quality. Execute the scheduled plan. Support Lead Associates to resolve ANDON calls. Ensure all Body vehicle is passed to the customer with Best Quality Standards. Monitor and control of effective implementation of improvements & Kaizens. Monitor and control factory supplies and rejection costs in the Group with JEs. Ensure Business KPIs of SPQRC is met and within target. Preferred candidate profile Problem Solving, Project Management, Technical Skills. Motivate the team with friendly manner Co-ordinate & facilitate shop problem resolution activities Able to achieve results given by Shift Managers in the individual line. To ensure the cleanliness of the area is maintained by his leader and Associates.

Required Candidate Only From Cable manufacturing Accessories Business & management principles involved in strategic planning,resource allocation human resources modeling,leadership technique,sales techniques sales control systems supervise. Required Candidate profile Knowledge of principles & methods for showing, promoting and selling product services. This includes marketing strategies and tactics, product demonstration, sales techniques & sales control systems

Hi, We are having an opening for Manager IT-MES & L2 project coordinator at our Halol/Baska(Gujarat) location. Job Summary : We are seeking a seasoned professional with 7-9 years of experience in the pharmaceutical industry, including hands-on expertise in Manufacturing Execution Systems (MES) and L2 integration. The Site Project coordinator for MES Implementation will be the primary coordinator for all MES-related activities at the Halol / Baska sites. This role demands dedicated full-time support to the project to ensures smooth execution, alignment with the global MES strategy, and timely delivery of milestones to enhance manufacturing efficiency, compliance, and digital transformation. The role will work closely with internal teams including QA, IT, SAP, business users, and L2 integrations as well as external vendors and infrastructure leads. Responsibilities include stakeholder management, managing project timelines, risks, and dependencies, ensuring infrastructure readiness, facilitating change management, and maintaining compliance with site validation and quality standards. As the single point of contact for MES implementation at the site, the site coordinator plays a critical role in driving collaboration and successful deployment. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) Previous experience with Werum (Korber Pharma) for pharma industry is a big plus Areas Of Responsibility : Project Coordination: Lead and coordinate all MES implementation activities at the site, ensuring alignment with the global MES strategy. Stakeholder Management: Serve as the single point of contact for site-level stakeholders, including QA, QA IT, IT, SAP, and business users (Production & Engineering) Vendor & Partner Collaboration: Work closely with MES vendors, infrastructure teams, and integration partners to ensure smooth execution. Timeline & Risk Management: Manage project schedules, track milestones, identify risks, and implement mitigation plans. Infrastructure & Readiness: Ensure site infrastructure (network, servers, systems) is ready and validated for MES deployment. Compliance & Validation: Oversee adherence to site quality standards, IT validation (CSV), and regulatory requirements. Communication & Reporting: Maintain clear and timely communication with the Global Project Manager and other stakeholders; provide regular updates and escalate issues as needed. Change Management: Facilitate change control processes and support user readiness and adoption. Educational Qualification : Bachelors degree in Engineering, Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field. Preferred: Masters degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Project Management, Operations Management, Industrial Automation, or Pharmaceutical Technology. Specific Certification : PMP for structured project execution (Preferred) GAMP5 or CSV Training for compliance in regulated environments Experience : 9 to 10 years of experience managing IT or digital transformation projects, preferably in pharmaceutical manufacturing. Hands-on experience with MES platforms, L2/PLC systems, and SAP integration and Edge Cloud IoT. Proven track record in project planning, stakeholder coordination, and cross-functional team leadership. Strong background in GxP compliance, CSV, and validation protocols (IQ/OQ/PQ). Experience working on the shop floor and with QA, IT, and business teams in a regulated environment. Skill (Functional & Behavioural): Functional: Strong project management expertise in IT/digital systems, Knowledge of MES platforms, L2/PLC systems, and SAP integration, Familiarity with GxP, CSV, and validation protocols (IQ/OQ/PQ), Understanding of pharmaceutical manufacturing processes and shop floor operations, Proficiency in stakeholder coordination and cross-functional collaboration Behavioral: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, Ability to work under pressure and manage multiple priorities, Team-oriented with a focus on collaboration and accountability Additional Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases

Hi, We are having an opening for Manager IT - MES SME at our Halol or Baska(Gujarat) location. Job Summary : We are seeking a seasoned professional with 6-8 years of experience in the pharmaceutical industry, including technical and functional experience in MES & L2 systems. The Site SME MES Project is a key functional and technical expert responsible for supporting the successful implementation of the Manufacturing Execution System (MES) & L2 at the Halol & Baska pharmaceutical manufacturing sites. This role ensures that site-specific manufacturing processes are accurately captured and reflected in the global MES solution. The SME is also accountable for leading site-level validation activities and technical owner responsibility , and managing all GxP documentation related to the MES & L2 system. The Site SME is the go-to authority for end-to-end MES product knowledge. This includes a deep understanding of system functionality, configuration, and compliance requirements.The SME also serves as the first point of contact for any MES front-end application issues, supporting users in troubleshooting, training, and ongoing system usage post-go-live. The ideal candidate will ensure adherence to global regulations (FDA 21 CFR Part 11, EU GMP, GAMP5) Previous experience with Werum (Korber Pharma) for pharma industry is a big plus Areas Of Responsibility : MES Implementation: Representing site-specific needs during MES design, configuration, and deployment. Validation Leadership: Leading IQ, OQ, PQ, UAT, and traceability matrix execution. Documentation Ownership: Managing GxP documentation (URS, FS, DS, test cases, validation plans/reports). MES Product Expertise: Maintaining deep knowledge of MES functionality and architecture. Front-End Support: Acting as the first point of contact for MES application issues and user support. Training & Adoption: Delivering training and ensuring user readiness for MES usage. Data Management: Supporting data collection, migration, and master recipe creation. Audit Readiness: Ensuring all documentation and systems are compliant and audit-ready. Educational Qualification : Bachelors degree in Engineering - Information Technology, Computer Science, Production, Pharmaceutical Sciences, or a related technical field. Preferred: Masters degree (e.g., MBA, M.Tech, M.Pharm) with specialization in Industrial Automation, Pharmaceutical Technology or related technical fields Specific Certification : GAMP 5 for system validation in regulated environments. CSV (Computer System Validation) for compliance with GxP. MES Platform Certifications e.g., Werum PAS-X, Siemens Opcenter, or Rockwell 21 CFR Part 11 Compliance Training for electronic records and signatures Experience : 6 to 8 years of experience Pharmaceutical Manufacturing: Strong understanding of pharma shop floor operations and regulatory requirements. MES or Digital Systems: Prior hands-on experience with MES platforms or similar systems in GxP-regulated environments. Validation Expertise: Proven experience in validation documentation and execution, especially for GxP Category 4 & 5 systems. Application Support: Experience in resolving front-end MES issues and supporting end-users post-deployment. Audit Experience: Familiarity with audit processes and documentation expectations Skill (Functional & Behavioural): Functional: MES system configuration, deployment, and validation, Front-end application troubleshooting and user support, GxP and 21 CFR Part 11 compliance, Validation protocol development and execution (IQ, OQ, PQ, UAT), Documentation management (URS, FS, DS, traceability matrices), Data migration and master recipe creation Behavioral: Strong communication and interpersonal skills, Proactive problem-solving and risk management, High attention to detail and compliance mindset, Ability to work under pressure and manage multiple priorities, Detail- oriented with a focus on compliance and quality, Proactive problem-solving and decision-making, Comfortable working on the shop floor and in technical environments Additional Skills: (Good to have) Knowledge of data analytics tools Edge Cloud deployment experience with (IoT and and IIoT) L2 integration with MES MES integration with SAP Understanding of network and databases

Manager - Civil Projects (Greenfield project) Role & responsibilities To coordinate with CIVIL- site contractors for planning and scheduling for different civil work. Update, day to day work with effective watch over Work Quality; Quantity variations and joint measurements. Also coordinate with other team members to achieve project milestones. Preferred candidate profile Team player of Civil Construction team at Site Based on the received drawings, assign work and timelines and ensures the implementation of the same. Ensure collection of data; analyze to achieve relevant construction quality and safety. Help overcome constraints , work out alternatives to the design in case of difficulties Retention of records in respective area. Preparation & completeness of documentation for qualification in terms of facility. Prepare snag list. Give final acceptance of construction quality for civil components / systems after fixing it. Review measurements sheets. Ensure Schedule updates in primavera and send progress reports in terms of schedule work quantity, progress, constraints, snaps and etc. Coordinate with factory inspector, External approving agency, water, IDC and etc. Execute construction quality audits, Internal / External audits for Civil Responsible for Construction quality; finishes, Operations, Performance and safety at site Report quantity variation and scope change Educational Qualification B.E. in Civil Engineering. Technical Skills/Competencies (Software packages, experience with specific machines etc.) MS Office ,Auto cad, Statutory / govt licensing procedures & requirements Excellent communication skills, strong collaborator, problem solving, interdepartmental coordination, and team leadership. Experience (8 to 10 Years of experience in relevant field in Pharmaceutical Industry.)

We at Sun Pharma are hiring for the Manager - Operation Excellence role at our Guwahati / Halol/ Mohali plants. Here are the roles and responsibilities of the position: Years of experience: 14-15 years; Pharma industry background mandatory Areas of Responsibility 1. To drive Operational Efficiency Improvements, to build culture of Continuous Improvement (Lean Six Sigma / TPM etc.) 2. To work closely with Site Leadership and help them to identify opportunities for improvement in the areas of Quality, Cost, Productivity & Delivery, and conducting gap analysis and driving OE projects 3. To work on skill improvement roadmap and partnering with HR, to enhance capability proficiency in TPM advanced tools 4. To publish monthly OE MIS reports, including OEE and overall plant performance 5. To coordinate RCA / brainstorming sessions with project teams, help project teams in process mapping, VSM, and statistical analysis. 6. To Conduct training on LSS/TPM tools for production team members 7. To capture the Best Practices and share it with site team and other site teams 8. To evaluate the standard manpower and execution of optimization plan by coordinating with HODs, review of overtime, and reduction of overtime 9. To ensure periodic review of the Quality Management System and continual improvement plans with block heads 10. Deploy IFQM on-site in collaboration with regional stakeholders 11. Tracking of launching plan and Evaluating, Timely executions of launch plan by coordinating with block heads. 12. Any other additional work allocated by reporting authority and site spoke for any improvement initiatives

Distribution of work to operators in order to achieve daily production target.Planning day 2 day production.Product/process quality mgmnt system through internal & External Audits, SQC,BOP inspection.Productivity & quality improvement through Kaizen. Required Candidate profile Line balancing & reducing assembly time using 3M-Methodology.Layout improvement & workstation design. Employ FIFO. Examine needs for training & provide on job training 2 personnel.Capacity improvement

Plant HR Head- Halol Vadodara: Plant HR Head About CMR Group is India'slargest producer of Aluminium and zinc die-casting alloys. With 13state-of-the-art manufacturing plants across the country, CMR has become thepreferred supplier for many of Indias largest automotive industry leaders.Since its inception in 2006, CMR has consistently outpaced competition byfocusing on delivering superior value to its stakeholders. This value is drivenby a strong commitment to technical advancements, quality enhancement, sustainability, and people-centric practices. We believe in an " Employee First " philosophy, ensuring that ourpeople are at the core of our success. Our dedication to fostering an enrichingwork environment is reflected in our recognition as the 'Most Preferred Place for Women to Work' and as one of the Top 25 Mid-Sized Indias BestWorkplaces in Manufacturing for 2025 by Great Place to Work. As CMR continues to chart its growthtrajectory, we remain committed to innovation and excellence. We are alwayslooking for enthusiastic and dynamic individuals to join our team andcontribute to our continued success. Position : Plant HR Head Location: Halol, Near Vadodara Job Band: A/B Designation: AssistantManager /Dy. Manager Reporting to: Administratively to Unit Head & Functionally to Hub Head HR West Qualifications Essential MBA/MSW/ Post graduate degree or diploma in Human Resource management (2 yearsFull Time) from Institute Recognized by UGC/ AICTE. Desired Degree /Dip in T & D, Labour Laws Experience: Around 3 + years of experience in Plant IR/ERfunction preferably in the Manufacturingsector withminimum200andaboveworkforce . Candidate should have at least 2+ years of experience of HR Generalist role as Head ER/ IR or 1+ Years experience as second in command in Employee Relation function in large organization. Job Profile: ThisPosition is Plant Head HR Role. Thispositionisresponsibleforove rseeingtheentiregamutof HR activitiesfor plants andprovidingstrategic H R supporttotheManagement. The objective of the role is to formulate human resources strategies, systems, and processes that help the organization meet its goals and objectivesand facilitate growth and development. The role is also responsible formaintaining security and EHS standards for the organization. Major Jobincludes: Overall HR andIR Management -IR, Legal, Compliances & Audit, Local Govt. Liaison, CSR, Employee Grievances, Apprenticeship, Shop Floor Management, Quality Circle, EHS, Contract Labour Management (including Labor works software), ManpowerPlanning & budget, Org Structure & JD, Talant Acquisition, Onboarding, Performance Management, Training & Development, Emp. Engagement, Group HRInitiatives (Policy drive, GPTW, Talent Mgmt. etc.), HR Presentation, HRMS (CMRConnect), Personal File Mgmt., Payroll, Admin- Canteen, Transportation, Guest House, Visitor Management, etc. Core Competencies: Goodunderstanding about HRMS Operation of HR Automation like SAP HR/ successfactor / Darwin box etc Strongcommunication skills Highattention to detail, clarity Excellentinterpersonal and organizational skills with proven abilities in peoplemanagement, Should beProficient in MS office suite & Analytical skills General Age Around30 years. CTC : 8 to10 LPA. Candidate should not be frequentjob changer. Notice Period - Joiningperiod Max 30 Days. We can buy notice period, if required Location: - Halol : 455/P1/P1, Village Kambola, Taluka- Savli, Vadodara, Gujarat, India-391510

Role & responsibilities Direct Purchase Buyer: Roles and responsibilities knowledge area: Identifying suppliers having expertise into seating commodity including Weatherstrips, Rubber Molding, Door Handles, Mirrors, Spoilers and Claddings, Exterior Plastics including Molding, Chrome plating and Painting parts Lead and execute sourcing process; floating RFQs, Technical review meetings, supplier negotiation and contract release Should have excellent knowledge about negotiation tools Drive annual contract cost down and generate saving ideas to improve material cost Work closely with VAVE function to drive saving ideas Sourcing expertise to drive localization of imported parts Support cross functional team to drive required inputs from suppliers to achieve desired results Support SQE and SC for on time readiness / delivery of product and services

Responsibilities: * Ensure compliance with safety standards * Collaborate with operations team on preventative maintenance plans * Maintain electrical systems and equipment * Troubleshoot and repair electrical issues promptly Flexi working Annual bonus

• 3-5 years in transformer project engineering, design coordination, or documentation • Familiarity with SAP, drawing workflows, BOM structures, and engineering records • Working knowledge of Monday.com, Excel/Sheets, and dashboard/reporting tools Required Candidate profile Strong interpersonal skills for cross-functional coordination & follow-up Clear understanding of transformer deliverables and design release sequence Required only Transformer Manufacturing Industry

Designation: Purchase Department | Executive/ Sr. Executive Qualifications : Desired - B.E / B. tech in Mechanical Work Experience : 3 yrs ~ 5 Yrs Industry: Candidates should be must from the Automobile , Automotive , auto components industry. Brief Job Description / key responsibilities : 1- Independently working for Regular Monitoring & arranging of clamps from different supplier 2- Closely working with RM team for Clamp RM arrangement. 3- Closely working with Molfex & Vikrant Buyers for clamp MRP requirement 4- Release clamp requirement PO & follow up with suppliers & arrangement of Transportation for clamp inward 5- Knowledge of Working in any ERP MUST 6- Close working with PPC Team for clamp inward as per assy plan 7- Good Computer working knowledge (Excel, PPT) 8- Responsibility to make daily & monthly MIS for KRA review. 9- Knowledge of IATF 16949/OHSAS/ISO 14001 Procedures. Profile Shortlisting Criteria 1. Candidate Must have qualification in SSC,HSC, Graduation or Masters minimum 60% 2. Distance learning will not be considered as Qualification for Graduation and Above. 3. Candidate profile should be stable (No frequent Jump)

Position: Instrumentation Engineer Job Location: Katol Plant (Halol-Gujarat) Education: Bachelor of Engineering - (Instrumentation & Control) Experience: 08 to 10 Years experience in function of DCS & PLC Role & responsibilities 1. Key Result Areas: Preventive Maintenance and Calibration . Major Activities: Execution of Preventive maintenance of equipment. Calibration of all type of transmitter and switches. Monthly monitoring of DCS controller, module and power supply. Outcome: Reduce breakdown of instruments, DCS and PLC hardware. Accuracy in process parameter like temperature, flow, pressure, level. 2. Key Result Areas: Spare part and vendor development. Major Activities: Maintain inventory of Spare part in store. Vendor development for emergency service and imported spare. Outcome: Attained emergency breakdown in minimum time to reduce production loss. 3. Key Result Areas: Emergency Breakdown Major Activities: Troubleshooting of control wiring. Spare replacement, Spare repairing. Outcome: Sustain productivity. Line-up system in minimum breakdown time. 4. Key Result Areas: Small project / CAPEX (Instrumentation) Major Activities: External party selection and quotation review (technical), project execution & completion Outcome: Improvement in process and plant facility 5. Key Result Areas: ISO and Audit compliances. Major Activities: Execute PM and calibration as per plan Record keeping/updating and audit compliance. Calibration of Gas detector as per plan. Outcome: To maintain ISO standard and Quality of product. 6. Key Result Areas: Department work progress Major Activities: Leadership, co-operation and support to technician Outcome: Work efficiency, safety and proper utilization of man hours.

Shreeji Infrastructure is a leading name in the infrastructure and construction industry, known for quality work, timely delivery and strong client relationships. We are currently looking for a dedicated and detail-oriented Store Keeper to join our team at Our Manufacturing Plant. Responsibilities: Maintain accurate records of incoming and outgoing materials. Organize and manage inventory in the store efficiently. Coordinate with the procurement team and site engineers for material requirements. Ensure proper storage, labeling and safety of materials. Conduct regular stock checks and report discrepancies. Maintain documentation for audit and compliance purposes. Requirements: Minimum 2 years of experience as a Store Keeper in a construction or manufacturing setup. Basic computer knowledge with English Proficiency. (Excel, stock management systems). Strong organizational and record-keeping skills. Ability to work independently and handle responsibilities. Qualification: 12th pass or graduate (preferred).