6151 Calibration Jobs - Page 28

As a quality control professional, you will be expected to strictly adhere to cGMP norms and safety rules within the factory premises. Your key responsibilities will include verifying logbooks, records, and other analytical documents on a daily basis to ensure their correctness and completeness. It will be your duty to ensure the timely preparation and revision of SOPs, STPs, and other Quality Management System (QMS) documents. You will also be responsible for the prompt completion of investigation activities related to Quality Control (QC) aspects such as Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and out-of-compliance (OOC) activities. Moreover, you will be accountable for the implementation of Corrective and Preventive Actions (CAPAs) as identified, ensuring their completion within the set timelines and evaluating their effectiveness. Additionally, you will prepare and revise calibration and preventive maintenance schedules as per the requirements of the facility. Your role will involve overseeing the calibration of instruments and equipment, both internally and externally, as per the defined schedule and maintaining proper documentation for the same. It will also be your responsibility to review audit trails for all application software used in the QC department to ensure sustained compliance with regulatory standards. Furthermore, you will review documents related to the qualification of working standards and reference standards, ensuring their accuracy. You will also be involved in the preparation and review of protocols for stability studies, instrument/equipment master lists, and quality risk assessments as needed. In the absence of the Deputy General Manager (DGM) or Deputy Chief Manager (DCM) of Quality Control, you may be required to deputize for them and undertake any specific tasks assigned by the Head of Quality. Your role is crucial in maintaining the quality standards and regulatory compliance within the organization.,

As an Instrumentation Technician at our Hubli (Shiggaon) location in Karnataka, you will be responsible for working in the Instrumentation Department. We are looking for individuals with an ITI or Diploma qualification and at least 5 to 6 years of experience in Industrial Instrumentation. Your primary responsibilities will include calibration, Instrument Commissioning to DCS, and Field Instrument Maintenance. If you meet the qualifications and possess the necessary skills, please send your updated resume to hrhubli@ambujagroup.com. We look forward to potentially welcoming you to our team and working together to achieve our goals.,

VMC Setter (Vertical Machining Center Setter) Job Responsibilities:Set up and operate Vertical Machining Center (VMC) machines according to production specifications. Read and interpret engineering drawings, blueprints, and technical documents. Load tools and materials into machines and ensure proper alignment and positioning. Adjust machine settings (feeds, speeds, cutting tools) for optimum performance. Perform first piece inspection and ensure dimensional accuracy using instruments like Vernier calipers, micrometers, and height gauges. Troubleshoot and correct any issues during setup or production. Maintain machine cleanliness, lubrication, and basic maintenance. Collaborate with quality control and production teams to ensure product quality and efficiency. Requirements:ITI / Diploma in Mechanical or related field. 2–5 years of experience in VMC machine setting. Strong understanding of G-code, CNC programming basics, and machining operations. Ability to work independently with minimal supervision. Knowledge of precision measuring instruments and quality standards. VTL Setter (Vertical Turning Lathe Setter) Job Responsibilities:Set up and operate Vertical Turning Lathe (VTL) machines to produce precision metal components. Interpret technical drawings, component tolerances, and machining instructions. Select appropriate cutting tools, fixtures, and materials for each job. Ensure proper machine calibration and tool alignment before running production. Perform test runs and inspect first article pieces for accuracy. Adjust machine parameters as needed for consistent output. Conduct in-process inspection and document results. Maintain tools and machine cleanliness for safe operation. Requirements:ITI / Diploma in Mechanical or Turner Trade. Minimum 2 years of hands-on experience in VTL machine operation and setting. Good understanding of machining practices, tooling, and material properties. Ability to read and interpret machining blueprints and specifications. Familiarity with quality control processes and measurement tool

Quality Control Operations: Supervise and manage all daily QC activities including raw material, in-process, and finished goods inspections. Monitor and ensure adherence to company and regulatory quality standards. Develop, implement, and maintain QC procedures and protoc Team Management: Lead, train, and evaluate QC staff. Assign tasks and responsibilities, ensuring effective team collaboration and performance. Documentation & Reporting: Maintain accurate and detailed QC records, including test results, non-conformance reports, and corrective actions. Prepare and submit periodic quality reports to management. Lab Equipment & Calibration: Oversee maintenance and calibration of testing equipment and laboratory instruments. Ensure compliance with safety and operational standards in the QC lab. Root Cause Analysis & CAPA: Investigate quality issues and customer complaints. Conduct root cause analysis and implement Corrective and Preventive Actions (CAPA). Compliance & Audit Readiness: Ensure compliance with ISO, GMP, HACCP, or other applicable regulatory standards. Prepare for and participate in internal and external audits. Continuous Improvement: Participate in quality improvement initiatives. Analyze QC data and trends to suggest improvements in products or processes.

Job Opening: Marketing & Sales Executive – Material Testing Machines Location: Pimple Saudagar, Pune Company: MTMS Engineers Industry: Material Testing, Calibration & Engineering Solutions ______________ About Us: MTMS Engineers is a trusted name in the field of material testing machines and calibration services, offering innovative and precise solutions across industries. With a strong customer base and commitment to quality, we are looking to expand our dynamic team. ______________ Position: Marketing & Sales Executive Key Responsibilities: • Generate leads and identify new sales opportunities for material testing machines. • Conduct client visits, product demonstrations, and presentations. • Build and maintain strong customer relationships. • Understand client requirements and provide appropriate solutions. • Collaborate with technical and support teams to ensure smooth sales and after-sales service. • Prepare reports and maintain sales records. ______________ Eligibility Criteria: • Gender: Male candidates preferred (due to field travel) • Experience: Minimum 2 years in marketing/sales (preferably in industrial or technical product sales) • Education: Diploma or Degree in Engineering (Mechanical/Electrical) preferred • Technical background will be an added advantage • Must own a 2-wheeler for field visits • Good communication and presentation skills • Ability to work independently and handle client interactions confidently

Maintenance & Calibration: Perform preventive and corrective maintenance on field instruments such as pressure, temperature, level, and flow devices. Calibrate instruments as per industry standards and ensure they operate within required tolerances. Troubleshooting: Diagnose faults and breakdowns in field instruments. Support urgent repair work to minimize downtime during equipment failure. Compliance & Safety: Ensure all instrumentation work complies with refinery safety standards and environmental regulations. Follow hazardous area classification protocols and work permit systems (PTW/LOTO).

Date: 30 Jun 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Role: Lead Maintenance Engineer Job Location: Bangalore Department: Engineering & Maintenance About Syngene: Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose: Leading EAM team & activities at SU3. Execute maintenance and Upgradation projects. Ensures Safety & GMP compliance at SU3. Common Responsibilities Responsible for EAM activities in the Biologics Operations Unit Ensuring all assigned mandatory trainings related to data integrity, health and safety measures are completed on time. Develop and contribute to development of procedures, practices and setup that ensures safety operations compliant to company and regulatory norms. Specific Responsibilities Leading engineering and maintenance team for GMP areas at Biologics Manufacturing and Biologics Process Development. Able to handle minor project, design review and execute and Facility modification in a GMP facility. Exposure in handling Process, Electrical, HVAC, Utilities and instrumentation teams. Ensuring the related facility, equipment and maintenance systems are in GMP compliance state. Adherence to established procedures and policies of the company on Quality and Safety, ensuring the team adheres the same. Responsible for managing maintenance activities within framework of Quality management systems. Ensuring work management through defined SOPs, Change control, deviations and CAPA, review and approval through Trackwise and EDMS. Represent the function during audits and ensuring agreed actions are acted upon timely. Ensure followings are complying: Equipment master list, Preventive Maintenance and calibration planners are prepared timely. Preventive maintenance and Calibration of equipment and facility are executed as per the planner. Qualification of equipment and facility and area validation for GMP blocks as per schedule. Operations and maintenance of Utilities to enable operations Service contracts for equipment and Instruments are planned and executed. Ensure that team comprising of on-roll engineers and contract manpower are trained on GMP requirements. Evaluation, assessment and selection of vendors for providing services for maintenance, calibration and validation Overall maintenance management that includes handling unscheduled breakdowns and other general upkeep activities are as per requirement to enable operations. Identifying and maintaining Inventory of equipment spares required for maintaining continuous operations. Reviewing and analysing the energy and utility consumption like electricity units, water etc. and take measures for control. Implementing the energy saving initiatives. Facility design, detail engineering and execution of any new requirements for business growth. Preparing and presenting the MIS reports Maintaining and improving departmental operational performance, to meet the requirements of regulatory authorities, company procedures, internal and external customers with respect to quality, service, lead time and cost. Good exposure in Regulatory audit handling. Educational Qualification: BE/BTech in Mechanical or Electirical or Instrumentation. Technical/functional Skills Responsible for EAM activities in the Biologics Operations Unit Ensuring all assigned mandatory trainings related to data integrity, health and safety measures are completed on time. Develop and contribute to development of procedures, practices and setup that ensures safety operations compliant to company and regulatory norms. Leading engineering and maintenance team for GMP areas at Biologics Manufacturing and Biologics Process Development. Able to handle minor project, design review and execute and Facility modification in a GMP facility. Ensuring the related facility, equipment and maintenance systems are in GMP compliance state. Experience: 15 years or above within Biologics manufacturing plant, with at-least 6-7 years of experience in Leading Engineering team, Projects & Maintenance. Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, colour, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Show more Show less

Dear Candidate, We are hiring the Position of E&I Sr Engineer / Asst Manager - QA/QC for Drillmec International Pvt Ltd (MEIL Group) Job Responsibilities: 1. Conduct QAP (Quality Assurance Plan) verifications to ensure compliance with industry standards and customer requirements. 2. Perform inspections of oil rig equipment for drilling operations, ensuring adherence to specifications and quality standards. 3. Ensure compliance with applicable regulations, codes, and standards related to oil and gas industry practices. 4. Coordinate with vendors and clients to address quality-related issues, resolve conflicts, and maintain effective working relationships. 5. Facilitate coordination between various stakeholders at project sites to ensure the smooth execution of Electrical and Instrumentation activities. 6. Collaborate with cross-functional teams to identify and implement process improvements, cost-saving initiatives, and quality enhancements. 7. Conduct and oversee Quality activities, including interpreting and evaluating test results. 8. Provide technical support and guidance to the project team, assisting in problem-solving and decision-making processes. 9. Prepare and maintain accurate documentation, reports, and records related to quality control activities. 10. Stay updated with the latest advancements and best practices in the field of Electrical & Instrumentation engineering and quality control. Interested and suitable candidates can share below details and your updated CVs by Mentioning subject of "E&I Sr Engineer / Asst Manager - QA/QC" to careers@drillmecinternational.com / snaveenkumar@drillmecinternational.com Candidate Name : Qualification : Stream : Current Employer : Designation : Work Exp : Current CTC : Expected CTC : Notice Period : Current Location : Native : For more job related updates, please follow our WhatsApp Channel https://whatsapp.com/channel/0029Vb52rZSD8SDpr06qQl1M

Knowledge of measuring instrument Knowledge of Drawings Knowledge of QMS Knowledge of Excel, Word, Power point etc. Knowledge of Calibration Knowledge of standard room

Sampling and Inspection of received goods in stores, observation to be maintain. Operation, calibration and record maintained of Q.C Instruments Handling of sophisticated instruments (like GC, HPLC, UV.etc)

Execution of IQ, OQ and PQ for new equipment, facility & utility system, report preparation and maintenance of record. Execution of Periodic performance verification activities for equipments, facility, utilities and its report preparation. Review Initial qualification master document like URS, GxP assessment, DQ, FAT, SAT, IQ, OQ, PQ and PPV of EFU system and all executed report. Handling of departmental QMS activity through track wise software, discrepancy / deficiency activity compliance of observation, summary preparation for regulatory submission. Qualification and Periodic performance verification activity execution, compilation, review of reports [Filter integrity test (PAO), air velocity, non-viable particle count, air flow pattern as per define schedule, review of calibration certificate for measuring devices]. Ensure and updation of periodic performance verification, calibration, Bulk SIP and smoke study schedule as per available data. Review of all AHU PAO test and NVPC report form for periodic verification, Filter Replacement intimation form, Equipment/instrument inward & Deletion intimation slip & all equipments print reports during qualification. Preparation of master document for periodic performance verification of EFU system Preparation & review of SOPs through EDMS Software Execution of FAT and SAT of equipment, facility and utilities as per requirement. Equipment Periodic performance verification schedule preparation, review, updation and provide data required for monthly report preparation. QE related Instrument calibration schedule preparation (Ellab wireless system, Ellab wired system, Rotronic data loggers certificate review and updation as per available data

Experience of PLC & SCADA programming Understanding of P&IDs and Control Systems Site Visit based on project requirement PLC Programming (Ladder, ST,FBD) Experience with Profibus, Modbus, CAN implementation SCADA Development(GUI Designing, Scripting, SCADA Database Configuration) Experience with Codesys, TIA Portal, Studio 5000 PLC softwares Experience with WinCC, Factorytalk SCADA/HMI Softwares Experience in PLCs & SCADA tools from ABB, Siemens, Rockwell, etc Understanding of Controls and automation invovled in plant process Experience in calibration of field sensors, drives, motors, pumps,etc Involvement in budgeting and procurement of project related resources Good analytical, integration and debugging skills are necessary Very Good oral and written communication and multitasking skills are expected

We are looking for a motivated and enthusiastic Trainee Engineer to join our engineering team at our pharmaceutical manufacturing plant. As a Trainee Engineer, you will gain hands-on experience in the operations and maintenance of plant equipment, while adhering to safety and regulatory standards. This role provides a unique opportunity to develop technical skills and knowledge in the pharmaceutical manufacturing environment. Key Responsibilities Equipment Maintenance: Assist in the routine maintenance and troubleshooting of production and utility equipment (e.g., pumps, motors, HVAC systems, etc.). Project Support: Support senior engineers in project planning, execution, and documentation for plant modifications or upgrades. Process Optimization: Assist in the analysis of manufacturing processes and suggest improvements to enhance efficiency, reduce downtime, and optimize production. Documentation: Ensure proper documentation for compliance with GMP (Good Manufacturing Practice) standards, including equipment logs, maintenance records, and calibration reports. Safety Compliance: Ensure adherence to safety protocols and contribute to the identification and rectification of potential safety hazards within the plant. Technical Troubleshooting: Provide troubleshooting support to resolve technical issues in production and utility systems to ensure continuous operations. Collaborative Work: Work closely with the quality assurance, production, and maintenance teams to ensure that all operations comply with industry standards and regulatory requirements. Training & Development: Participate in ongoing training to keep up to date with technological advancements and regulations in the pharmaceutical industry. Skills & Qualifications Educational Qualification: Bachelor’s degree in Mechanical, Electrical, Chemical, or Instrumentation Engineering (or equivalent). Technical Skills: Basic knowledge of mechanical, electrical, and instrumentation systems; familiarity with pharmaceutical production processes (preferred). Regulatory Knowledge: Understanding of GMP, SOPs, and other regulatory requirements in the pharmaceutical industry (preferred).

Your tasks Communication Strategy development Support the Communication Manager in further development and implementation of a global communication strategy for the IT department that aligns with organizational goals and enhances employee engagement Identify key messages and communication channels to effectively reach diverse audiences within the organization Content Creation and Management Develop and implement high-quality communication measures for internal communication across various channels (e.g., intranet, management meetings, MS Teams, etc.) Create engaging materials such as videos, infographics, and presentations to convey complex IT concepts in an accessible manner. Internal events and meetings Organize and facilitate hybrid dialog meetings to foster collaboration among employees and internal events to promote IT initiatives Your Qualifications Enthusiasm, creativity and experience in content creation, media and global collaboration Master degree in Communication, Business Administration, or a related field 3 years proven experience in internal communications, preferably within a technology or IT environment. Strong writing and editing skills, with the ability to convey complex information clearly and concisely Proficient in Microsoft Office, particularly PowerPoint Experience with social collaboration platforms (e.g., Microsoft Teams, SAP Work Zone, Microsoft SharePoint) as well as video and image editing software Independent, reliable, and structured working style Very good English language skills Interested? We are looking forward to receiving your application! Ideally, you should apply online with the reference number. If you have any questions, please feel free to contact your recruiting contact via LinkedIn or XING. We promote equal opportunities and welcome applications from people with and without disabilities. We offer an inclusive work environment where all individuals can develop their skills and talents regardless of gender, nationality, ethnic and social background, religion, worldview, age, sexual orientation, identity, and other characteristics. Rohde & Schwarz is a global technology company with approximately 14,000 employees and three divisions Test & Measurement, Technology Systems and Networks & Cybersecurity. For 90 years, the company has been developing cutting-edge technology, pushing the boundaries of what is technically possible and enabling customers from various sectors such as business, government and public authorities to maintain their technological sovereignty. Rohde & Schwarz is a leading supplier of solutions in the fields of Test and Measurement, Broadcasting, Radio monitoring and Radiolocation as well as Mission-critical Radio communications. For more than 80 years, company has been developing, producing and marketing a wide range of electronic products. Headquarters in Munich with subsidiaries and representatives active in over 70 countries around the world, Rohde & Schwarz has achieved its global presence greatly. In India the company is present as Rohde & Schwarz India Pvt. Ltd (RSINDIA) which is 100% owned subsidiary of Rohde & Schwarz GmbH KG & Co, Germany, whose head office is located in New Delhi and branch offices in Bangalore, Hyderabad, Mumbai and Field presence at Ahmedabad, Chennai and Pune. With more than 10 channel partners situated at key industrial locations we serve across the country. Our emphasis is to provide outstanding sales, service and support to our customers. The company has invested sustainably to increase the local support capability as well as to provide a fully automated Calibration facility for most of the products sold. Rohde & Schwarz India has ISO 9001 2015 certified Quality Management Systems and ISO 17025 NABL Accreditation. The company continuously invests in training its service and sales personnel regularly to maintain a high level of technical competence in pre- and post-sales support and outstanding quality in services viz. Repairs, Calibration, Product support & Project management. Rohde & Schwarz India is a financially stable company rated by CRSIL as SME 1 for more than 5 years now. This rating is the highest in its category. Rohde & Schwarz India is committed to 100% customer satisfaction through innovative product offerings and outstanding support and services. Our comprehensive and continuously growing range of services are designed to provide customers with the highest level of quality and value throughout the life cycle of our products.

Job Title: Production Manager – Spray Drying Operations Company: Venkatesh Naturals Extract Pvt. Ltd. Location: Chhindwara, Madhya Pradesh Experience Required: Minimum 5 years in Spray Drying Machinery and Production Management Industry: Herbal Extracts / Natural Ingredients / Food & Nutraceuticals About Us: Venkatesh Naturals Extract Pvt. Ltd. is a leading manufacturer and exporter of high-quality herbal extracts and natural ingredients. With a strong commitment to innovation, quality, and sustainability, we specialize in delivering premium-grade natural products for the dairy creamer , NDC , nutraceutical, pharmaceutical, and food industries. Position Overview: We are seeking an experienced and results-driven Production Manager to lead and manage our spray drying plant operations in Chhindwara. The ideal candidate will possess in-depth knowledge of spray drying machinery and proven expertise in managing end-to-end production processes, ensuring optimal productivity, quality, and safety. Key Responsibilities: Oversee daily operations of the spray drying unit and other associated production processes. Plan and manage production schedules to meet output targets and delivery timelines. Ensure proper functioning, maintenance, and calibration of spray drying equipment and related machinery. Supervise production staff, provide training, and enforce operational protocols and safety standards. Coordinate with R&D, quality control, and logistics teams to streamline production activities. Monitor process parameters, raw material usage, and yield optimization to reduce production costs. Maintain accurate production records, reports, and documentation for compliance and audit purposes. Implement continuous improvement strategies to enhance efficiency, reduce downtime, and uphold product quality. Qualifications & Skills: Bachelor’s degree/Diploma in Chemical Engineering, Food Technology, or related field. Minimum 5 years of hands-on experience in spray drying machinery and production management. Strong knowledge of plant operations, GMP, HACCP, and safety regulations. Leadership skills with the ability to manage and motivate a team. Problem-solving mindset with a focus on productivity and quality. Excellent organizational, communication, and analytical skills. Preferred Attributes: Experience in the herbal/natural extract or nutraceutical industry. Familiarity with ISO, FSSAI, and other regulatory compliances. Job Type: Full-time Location: Chhindwara, Madhya Pradesh Salary: Commensurate with experience and industry standards

Company Description Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. In 2024, Sika’s around 33,000 employees generated annual sales of CHF 11.76 billion. Job Description Title : R&D Technician - cementitious mortar - 3rd Party Payroll Department: Technology Location : Nerul, Navi Mumbai R&D Reports To : Executive/Manager- cementitious R&D Company Profile Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 102 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. In 2024, Sika’s more than 34,000 employees generated annual sales of CHF 11.76 billion. Overview The Lab Technician has the technical responsibility to support his supervisor on Trial Modification of Mortar, Grouts, Tile adhesive etc Duties And Responsibilities Support the trial mix for research and development purposes, which is not limited to weighing, flow/ slump testing, cleaning of mixing tools, water permeability test, rheology, RCPT, wash out, etc. Supporting the application technician for physical parameter testing of competitor sample, raw material, etc. Conducting field test at the site as per the instruction from the supervisor. Testing of sands, cement, chemical materials and finished goods i.e. sieving, flow, strength, Carry out and compile laboratory test results such as sieve analysis, water absorption, moisture content, specific gravity, etc, marsh cone & other test. Maintenance of samples, testing apparatus, tools preparation for corrosion testing, testing as ASTM G 109. Supporting the supervisor for collecting the data with regards to shrinkage & tam study of the admixture. Stability sample preparation & support the supervisor for observation of the sample. Cube de-molding, cube cleaning & cube testing in CTM. Updating of the strength in the trail sheet. Monitors the overall raw material stock availability for conducting lab trails and ensure appropriate use of them. Pick up of the raw material from production site. Housekeeping of Acid, Alkali cabinet, RM storage, application and lab areas. Sample preparation & raw material arrangement for trials. Storage of cements, sand and materials. Monitors availability and implementation of PPEs and relevant essential tools. Continuous support to training calendar. Supporting the supervisor for calibration of the equipment. Unloading of raw material received from the site. 5 s of the raw material storage area. Supporting the supervisor which is not limited to removing of the sludge from ETP sludge bed, drying the material, filling of the same in bin & labelling. Segregation of hazardous & non-hazardous material. Operating of ETP & updating the same in the record book. Housekeeping of the outdoor premises & main lab area which is not limited to arranging the aggregates, cementitious as per the customer identification, removal of unwanted material, cleaning of the area, etc. Housekeeping of the sample preparation area which is not limited to identification, cleaning, segregating of raw material, etc. Housekeeping of the other lab area. Provides overall assistance to development team in various technical activities. Performs other duties as assigned by the supervisor for smooth functioning of the R&D premises. Performs other duties as assigned by the supervisor such as MSEB, MTNL, TTC, etc. work for smooth functioning of the R&D premises. Maintenance of safety shower, eye wash & water level check of the fire hydrant tank. Maintenance of concrete mixer & as a back-up for the siren testing & DG operation. Back-up for night shift & testing of cube as & when required. Maintenance of electrical, mechanical & other equipment, which is not limited to DG operation, UPS, Siren, AC’s, lights, etc. present in the R&D premises. Supporting the third-party vendor for maintenance of the major equipment such as DG, UPS, Electrical Equipment’s, Fire Hydrant, Fire Panel, Fire Fighting Equipment’s, Panel area, etc. for smooth functioning of R&D premises. Supporting the third-party environmental testing. Pick up of the raw material from the gate. Qualifications/Experience Graduate Minimum 2 years of experience in product development in Chemical Manufacturing Company Knowledge on construction chemicals, application, R&D, QC is preferred. Helpful if having Knowledge on Cement, concrete Admixture and Related Raw material functions. Analytical equipment handling Basic computer knowledge. Competencies Passion for innovation Behavioura l Self-starter Work management

Summary: Avantive Solutions is looking for a Voice and Text Analytics, who can contribute enormously to implementing solutions leveraging AI tools to improve sales, customer satisfaction, and compliance adherence. Trained in scoping improvement projects and carrying out action plans utilizing speech analytics software within strict timelines under the guidance of Speech analytics Manager. Display a keen interest in detail-oriented analytics, be a self-starter, and attentive to observing process failures/opportunities through communication at all levels and validate them through data. Proactively delve into data to discover scope of improvement and have great aptitude to devise solutions. Key Responsibilities: · Recognize agent or process opportunities from operation’s meetings, calibration, call scores, dashboards, KPI targets, quality reports, and AI-based tool reporting · Build queries on an AI tool for capturing opportunities, failures, gaps, improving scorecards, for specific business requirements, improving sales, and on requests from Operations or Quality teams. Schedule reporting from the AI tool to all the stakeholders · Perform a daily system test of the speech analytics tool, report the identified issues to the vendor, and if necessary, to the internal stake holders · Update the news article on the tool requested by Marketing, Operations, and Quality teams. Identify the need for coaching on specific topics/campaigns/procedures to build news articles and publish on the tool · Add and update activities on the AI tool for any survey, poll, rewards, or KPI and review the result in reports and dashboards · Coordinate with Operations, Quality and Leadership to discuss the modification, addition, or deletion in scorecards · Review the accuracy of scorecards timely. Take input from Operations and Quality to improve scores · Monitor manual scoring by QAs and QA reports on the AI tool. Point out inaccuracies, give feedback, refreshers, and prepare Job aids to keep everyone in agreement with the process ·Prepare detailed AI-driven reports highlighting agent performance, sentiment trends, and compliance adherence, process KPIs, and custom KPIs ·Monitor AI-generated predictive analytics to anticipate potential performance risks and proactively implement solutions Skills and Qualifications: · Strong experience with speech analytics and AI-based quality monitoring tools (e.g., NICE Nexidia, Verint, CallMiner, Observe.AI, or similar) · Analytical mindset with the ability to interpret AI-generated insights and translate them into actionable strategies · Advanced knowledge of call center KPIs, compliance frameworks, and quality assurance methodologies · Proficiency in reporting tools, dashboards, and data visualization platforms (Excel, Power BI, Tableau, PPT etc.) · Excellent communication skills, both written and verbal. Spanish is a plus, not required Ability to collaborate with different teams to effectively leverage AI tools for process improvement Education Qualifications & Experience: Bachelor’s degree in any field, Data or Business Analytics or a related field (preferred) 5+ years of experience in internation call centre quality assurance, Good to have experience with at least 2 years working with speech analytics or AI-driven monitoring tools

Essential Functions: JOB DESCRIPTION Operate and monitor equipment used in various stages of API production such as reactors, centrifuges, dryers, millers, sifters, etc. Ensure cleanliness and readiness of equipment before batch charging through visual verification procedures. Maintain accurate records, including Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch Packing Record (BPR), equipment usage logs, and deviation reports. Execute batch operations strictly as per SOPs and GMP guidelines. Monitor and record process parameters in real-time to ensure adherence to specifications and quality. Report and coordinate with Engineering for any equipment breakdowns during the shift. Coordinate with QA for issuance and submission of documents and with the warehouse for material movement. Handle raw materials, intermediates, and APIs, ensuring proper storage, reconciliation, and documentation. Follow standard procedures for sampling and in-process testing of materials and intermediates. Maintain cleanliness and good housekeeping in the designated manufacturing area. Monitor utilities in the plant (e.g., steam, vacuum, chilled water) and report abnormalities. Monitor and record environmental conditions like temperature, humidity, and differential pressure in clean areas (Level-I, II, III). Perform daily verification and calibration checks of weighing balances. Participate in periodic equipment cleaning and preventive maintenance. Ensure proper handling and disposal of hazardous materials as per environmental guidelines. Identify process deviations, malfunctions, or quality concerns and report them immediately. Support continual improvement by suggesting ideas for optimization, efficiency, and waste reduction. Take mandatory safety and operational training via AIMS software and participate in hands-on skill-building sessions. Adhere strictly to safety practices and use PPE as per company safety protocols. Participate in emergency response activities such as managing spills or operational incidents. Ensure timely inventory of plant/process-related consumables. Review completed manufacturing records for accuracy, completeness, and compliance with SOPs. Additional Responsibilities: Support implementation of process improvement initiatives and lean manufacturing practices. Assist in the qualification and validation of equipment and processes as per regulatory and internal guidelines. Ensure readiness of the area for internal, external, and regulatory audits. Support investigation and documentation of deviations, change controls, and CAPAs in coordination with QA. Participate in cross-functional meetings to discuss production schedules, quality concerns, and improvement plans. Maintain discipline and GMP compliance on the shop floor and promote a culture of accountability. Train and mentor junior staff/operators on standard procedures and safe working practices. Assist in preparation and review of SOPs related to manufacturing activities. Support periodic review of equipment performance and suggest improvements for efficiency. Ensure adherence to environmental and safety norms in chemical handling and waste disposal. Actively participate in safety drills, risk assessments (HIRA), and incident investigations. Coordinate with stores for timely availability of raw materials, consumables, and packing materials. Report daily production updates to the shift in-charge or supervisor as required. Qualifications :- Education: Master Degree, M. Sc – Organic Chemistry - Preferred Bachelor Degree, B. Pharma – Preferred B.E. Chemical – Required B. Tech Chemical – Required Experience: 4 to 6 years in API/Intermediate manufacturing operations Skills: API Manufacturing Operations – Intermediate to Advanced Batch Documentation (BMR/BCR/BPR) – Intermediate GMP Compliance and Data Integrity – Intermediate Process Monitoring and Troubleshooting – Intermediate SOP Adherence and Equipment Operation – Intermediate Safety and Emergency Response – Intermediate Material Handling & Inventory Control – Basic to Intermediate Utilities & Cleanroom Parameter Monitoring – Basic Team Coordination and Communication – Intermediate. QUALIFICATIONS Qualifications :- Experience: 2 to 5 years in API/Intermediate manufacturing operations

JOB DESCRIPTION Description: Plan, procure, evaluate, and control inventories of raw materials and packaging materials in line with production requirements. Coordinate with the Purchase department to ensure timely availability of materials. Coordinate with Quality Control for timely release of materials as per production schedule. Prepare, review, and implement departmental SOPs. Train subordinates on departmental SOPs and updates. Ensure strict adherence to SOPs and cGMP during warehouse operations. Prepare and submit MIS reports as required. Verify and maintain the integrity of all cGMP and statutory records. Ensure receipt, storage, and dispensing of materials are carried out per defined procedures, with reference to relevant MSDS and safety requirements. Oversee proper return or destruction of rejected materials in compliance with procedures and MSDS guidelines. Ensure weighing balances are verified and calibrated per SOPs. Maintain environmental conditions of designated storage and dispensing areas as per SOP. Coordinate with the Engineering department to execute preventive maintenance of departmental equipment. Ensure calibration of standard weights, balances, and instruments is done before the due date. Enforce safety protocols and ensure all team members follow defined safety measures during operations. Monitor receipt, storage, and issuance of engineering and miscellaneous materials as per SOPs. Prepare and review equipment qualification protocols and reports in collaboration with the Engineering department. Assist in conducting qualification studies and temperature mapping protocols. Ensure timely dispatch of finished goods to customers with proper documentation. Maintain overall housekeeping and upkeep of warehouse areas. Lead and coordinate change controls, deviations, and ensure timely closure. Represent the department during audits and ensure prompt compliance with audit observations. Essential Functions: Warehouse QMS-related activities Dispensing of materials as per production plan Dispatch of materials as per plan Additional Responsibilities: Raise material/service indents and prepare Capex proposals as needed. Manage departmental inventory effectively. Attend technical workshops/seminars and explore new techniques and technologies relevant to the warehouse function. Education: Qualifications : B.Sc. / B. Pharma – Preferred B.Com or equivalent – Acceptable Experience: 10–12 years of relevant experience in warehouse and distribution, preferably in a pharmaceutical or regulated industry. Skills: Documentation & Data Review Interpretation & Statistical Analysis Strong knowledge of cGMP, SOPs, and warehouse compliance systems Good communication and coordination abilities across departments Experience: QUALIFICATIONS 10–12 years of relevant experience in warehouse and distribution, preferably in a pharmaceutical or regulated industry.

Company Description Sika is a specialty chemicals company with a globally leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protection in the building sector and industry. Sika has subsidiaries in 103 countries around the world, produces in over 400 factories, and develops innovative technologies for customers worldwide. In doing so, it plays a crucial role in enabling the transformation of the construction and transportation industries toward greater environmental compatibility. In 2024, Sika’s around 33,000 employees generated annual sales of CHF 11.76 billion. Job Description Title : Executive / Sr Executive - QA/QC Department: Quality Location : Turbhe Reports To : Manager Quality Company Profile Sika is a specialty chemicals company with a leading position in the development and production of systems and products for bonding, sealing, damping, reinforcing, and protecting in the building sector and motor vehicle industry. Sika has subsidiaries in 100 countries around the world and manufactures in over 400 factories. Its 33,000 employees generated annual sales of CHF 11.7 billion in 2024.. Duties And Responsibilities Responsible for performing and supervising the testing of Mortar/ Flooring/RM and PM as per the specification provided by R&D. Responsible for performing and supervising the testing of Intermediates and Finished products as per the specification provided by R & D. Ensuring the recording of test results in Hard copy as well in soft copy. Statistical Data analysis and improvement in process with the help of Analyzed data. Responsible for authorizing and executing the RM/PM/ FG release in ERP. Responsible for the generation of non-conforming material note in case of any rejection of RM, PM, Intermediates and F.G. Responsible for the modification of First Time Failure batches as per R & D guidelines. Ensuring that the status of nonconforming raw, packing materials, intermediate and finished products are identified with proper label. Ensuring that the raw materials which are being used are supplied by an approved vendor. Ensuring that the ‘Monitoring and Measurement of product procedure’ mentioned in our Quality Manual is followed in his location. Responsible for the calibration of the testing equipments available in his location both external & internal. Ensure all the lab equipments are maintained in good condition. Handle Customer Complaint and RCA for the failure. Implement corrective actions against the Root Causes analysis. To ensure compliance to ISO and EHS Standards at tolling Assist technical team in establishing new products at Plant level. To ensure compliance to all kinds of audits done in the laboratory. Ensure continual improvements in the testing procedures of raw material, packing material and finished goods. Assist Procurement/ R&D for New Raw material/Packing material / Vendor development. Conduct regular process audits and ensure Corrective action against observation/ Non conformance. Ensure good housekeeping and 5S in Lab. Coordinate with Tolling units for QC operation, new product setup, daily and monthly reporting. Training to the plant lab staff on various quality and safety related topic Ensure compliance to Sika quality management system at Tolling location. Monitor overall operation at tolling location. Coordinate with cross functional team for day-to-day operation at tolling site. Qualifications/Experience M.Sc. in Chemistry with 2 to 3 years of experience or B.Sc. in Chemistry / Diploma in Civil with 3 – 5 years of experience in relevant field / working in Quality control Lab Construction Chemical/Chemical Manufacturing Company Knowledge of ERP/ SAP Competencies Functional Knowledge of good laboratory practice with Safety first. Good understanding of routine QC methods, procedure and equipment handling. Knowledge of IMS (Integrated Management System) Good in MS Office, Basic Computer Behavioral Self-starter Analytical mind Team player Qualifications Qualifications/Experience: M.Sc. in Chemistry with 2 to 3 years of experience or B.Sc. in Chemistry / Diploma in Civil with 3 – 5 years of experience in relevant field / working in Quality control Lab Construction Chemical/Chemical Manufacturing Company Knowledge of ERP/ SAP

Job Description Key Responsibilities: Conduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental conditions Communicate findings and recommendations to stakeholders and management Participate in environmental remediation and restoration projects Ensure compliance with environmental regulations and standards Growth promotion test, Media preparation, Autoclave operation, Cleaning and disinfectant preparation. Calibration of instruments. Qualifications Qualification: M.Sc (Microbiology) Experience: 2-7 years Person having work experience in GLP section in Microbiology section.

Role & responsibilities We are looking for highly skilled and process-driven professionals to join our Quality Assurance (QA) team at a cutting-edge surgical gloves manufacturing facility. The ideal candidate will play a key role in ensuring that every aspect of production especially raw material evaluation , packing material testing , process validation , and regulatory compliance meets stringent national and international standards for Class B, C and D medical devices. Quality Management System (QMS): Design, implement, and monitor QMS as per ISO 13485 and MDR 2017 . Maintain SOPs, work instructions, and controlled documents. Regulatory Compliance: Ensure adherence to CDSCO regulations , BIS 13422 (Surgical Gloves), BIS 15354 (Examination Gloves), and GMP guidelines. Support during audits (internal, external, and regulatory). Validation & Process Control: Oversee validation protocols including cleaning, packaging, and sterilisation (ETO/Gamma). Conduct risk assessments , change control , and CAPA implementation. Batch Records Review: Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) . Ensure traceability from raw materials to finished goods using batch/lot numbers. Packaging Material Testing & Traceability: Verify and test all packaging materials against relevant standards. Maintain Certificates of Analysis (COA) for inward materials, including packing components. Ensure complete traceability for raw materials , packaging , and finished gloves . Training & Documentation: Conduct training on QA procedures, GMP, and regulatory updates. Manage deviation reports and QA documentation flow across production and QC. Mandatory Requirements: Prior experience in a CDSCO-approved manufacturing facility handling Class B, C & D medical devices. Strong understanding of: ISO 13485 MDR 2017 BIS 13422 / BIS 15354 GMP/QMS documentation Hands-on with internal audits, regulatory inspections, and validation processes. Inward Raw Material Testing: Evaluate incoming latex and other input materials using lab instruments such as viscometers, tensile testers, hardness testers, etc. Test and verify packaging materials as per standard requirements. Attach and maintain Certificates of Analysis (COA) for all inward materials, including packaging materials. Sample Preparation: Prepare glove samples for technical evaluation, customer trials, and tender submissions. In-Process Quality Checks: Monitor ongoing production to ensure compliance with defined AQL levels and physical parameters. Identify and classify critical defects during manufacturing. Packaging & Sterilization Checks: Conduct QC checks at all packing stages: Valeting, Pouching, and Sterilization (ETO/Gamma). Verify packaging integrity and labeling accuracy. Final Product Inspection: Perform thorough inspections of finished goods, including Pre-Dispatch Inspections (PDI) . Traceability & Documentation: Maintain batch and lot numbers for raw materials, packing materials, and finished goods to ensure full traceability. Generate daily QC reports, maintain batch records, and ensure proper documentation flow. Preferred candidate profile Education: B.Sc / M.Sc in Chemistry, Microbiology, or Polymer Science OR B.Tech in Chemical Engineering, Rubber Technology, or Biomedical Engineering Experience: 37 years in QA roles within the medical devices industry (gloves manufacturing preferred) Skills: Proficiency in QA documentation , process audits , and compliance systems Experience with ERP tools (SAP or equivalent), Excel , and root cause analysis Familiarity with AQL standards , though not primary in QA, is a plus Proficiency in using QC lab instruments and interpreting test results Familiarity with Excel , ERP systems (SAP or equivalent) Knowledge of internal audits , root cause analysis , and process validation

Job Description Summary Candidate will be responsible to plan, conduct and monitor quality of a product line including incoming, in-process and final inspection of parts and shall be accountable for on-time inspection of parts to meet the customer demand with almost focus on quality objectives. Job Description Company Overview: Working at GE Aerospace means you are bringing your unique perspective, innovative spirit, drive, and curiosity to a collaborative and diverse team working to advance aerospace for future generations. If you have ideas, we will listen. Join us and see your ideas take flight! Site Overview Our Multi-modal Manufacturing Facility (MMF) in Pune plays a crucial role in manufacturing key aerospace components, supporting not only India’s defense and commercial sectors but also global aviation supply chains. Our relationships with Indian suppliers, combined with our world-class local facilities and global reach, continue to shape India’s aerospace ecosystem. Role Overview Plan, conduct and monitor quality of a product line including incoming, in-process and final inspection of parts and shall be accountable for on-time inspection of parts to meet the customer demand with almost focus on quality objectives Approve in-process production by confirming required specifications, conducting visual and measurement tests, and communicating the required adjustments to the production supervisor Approve all finished products by confirming specifications and conducting required tests Candidate with good knowledge in welding and having experience to work in heavy fabrication will be preferred. Document and update inspection results by completing reports and logs Investigate customer complaints and non-conformance issues Develop, recommend and monitor corrective and preventive actions Document internal audits and other quality assurance activities Evaluate audit findings and implement appropriate corrective actions Proactively identifying areas of obstruction / breakdowns and take steps to rectify the problem at early stage Assist Manufacturing in investigations of process related quality issues Tracking and controlling the rejection by raising alarm/ NC with immediate effect and maintaining CoQ as per organizational requirements Involved in Kaizen and other process improvements like suggestion activities. Manage MRB & RTV and ensure on-time disposition / drive supplier recovery as applicable; also maintain critical supplier score card Participate in HPT Team discussions (HPT = High Performance Teams) and provide insights on quality, quality escapes and issue resolution, RCA, CAPA etc. Shall be responsible for total compliance to Quality Management System and Lead key initiatives; align the function with business goals to support 2x growth of the business Year-Over-Year Use experience and expertise to perform the assigned tasks himself and provide leadership to quality inspectors, mentor & train them and ensure their skill enhancement continuously. Own Quality Metrics including COQ, FPY, DPU, Escaping Defects, Customer Issue Resolution, On-Time Qualification etc. for the product line Calibration Management of all gauges / instruments / fixtures; deploy smart gauges (blue tooth enabled) to help accelerate digitization of manufacturing operations The Ideal Candidate In this role, you will be responsible for tasks that require a basic understanding of quality principles and problem-solving tools. Hands-on experience with measuring instruments and familiarity with locomotive products are preferred. Required Qualification Education: Diploma in in Mechanical, Electrical or Production Engineering from a reputed college /university 2 - 3 years hands on experience in Quality for locomotive products. Shall be willing to work in shifts to meet the organizational goals. Strong oral and written communication skills, with the ability to communicate across levels. Experience to work in Heavy Fabrication with good knowledge on welding. The candidate shall be highly energetic and passionate with positive attitude. He shall be able to explain clearly business drivers and organizational objectives to team Whether we are manufacturing components for our engines, driving innovation in fuel and noise reduction, or unlocking new opportunities to grow and deliver more productivity, our GE Aerospace teams are dedicated and making a global impact. Join us and help move the aerospace industry forward Additional Information Relocation Assistance Provided: No

Job Summary Our organization is looking for highly skilled individuals who have what it takes to be an electronic technician. Your ideas and expertise can help our company fine tune our production and manufacturing processes and influence changes to the way we do business. As an electronic technician, your input could push our organization closer to our monthly and quarterly sales goals. You can join our multidisciplinary team of experts and develop new knowledge and skills in the industry. Responsibilities and Duties Purchase and Evaluate electronic components related to the production process or the quality of final product parts and determine when there is a need for changes to the process. Decipher complex plans, drawings, diagrams, blueprints and instructions in order to complete installation or practice troubleshooting of electronics systems, parts or wiring networks. Record information and results about product or electronic performance by detailing testing methods, documenting possible issues and listing part specifications. Partner with mechanical or electrical engineers to fine tune the repair and diagnostic process in the work environment. Diagnose and repair problems with malfunctioning circuitry networks, ineffective electronic pieces, and missing or inoperative parts. Maintain all equipment and components by performing scheduled maintenance tasks, ensuring calibration of equipment and scheduling replacement when needed. Communicate with customers, team members, engineers or management to determine possible problems or update individuals with work progress. Required Experience, Skills and Qualifications Assembling Troubleshooting SMT Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Work Location: In person

This is a QC/QA executive role including responsibilities like Raw material Analysis, FG Analysis, maintaining daily calibration & quality documents, quality assurance activities on the floor, Sampling, Training, Implementing GMPs & creating, implementing and maintaining SOPs/documents as required. Experience with maintaining documentation for Various certification standards like FSSC, ISO and BRC is preferred Other Qc related activities may be assigned as needed. A B. tech. Food technology or equivalent degree is mandatory for this role along with at least 2 years of experience in any Food manufacturing company. Job Type: Full-time Pay: ₹22,000.00 - ₹30,000.00 per month Schedule: Day shift Weekend availability Education: Bachelor's (Required) Experience: Food industry: 2 years (Required) License/Certification: Fostac (Preferred) Work Location: In person