6151 Calibration Jobs - Page 23

Join our team as a Service Engineer in a leading Electrical MNC! As a Service Engineer in the Agriculture Department, your primary responsibility will be to perform on-site installation, servicing, maintenance, and repair of agricultural electrical products in Delhi & Uttar Pradesh (Ghaziabad & Kanpur) locations. You will be working on a third-party parole with a salary range of up to 35K in hand per month. This is a contract position with a duration of 1 year, renewable based on performance. To qualify for this role, you should have a Diploma in Electrical with 1 to 7 years of experience. Your duties will include identifying and resolving technical issues using diagnostic tools, configuring and calibrating electrical systems per specifications and customer requirements, investigating and rectifying faults in electrical equipment to minimize downtime, and effectively communicating with customers to provide technical support. It is crucial to maintain detailed service records, including work performed and customer feedback. Adherence to all safety protocols and regulations while performing fieldwork is mandatory. If you are ready to take on this challenging role, submit your resume to contact@authentic-staffing.com and call us at +91 70418 69674. Join us today and make a difference in the field of agricultural electrical services!,

Job Description: Service Engineer Position: Service Engineer – Rajasthan We are hiring Service Engineers with 2-4 years of experience in maintaining, calibrating, and troubleshooting environmental monitoring instruments such as CEMS, AAQMS, and meteorological stations. Candidates should be proficient in installation, commissioning, and customer training. Field experience in analyzers and knowledge of safety protocols, HVAC, and data transmission to pollution control boards is preferred. Keywords: Service Engineer, CEMS, AAQMS, Instrumentation, Calibration, Environmental Monitoring Mandatory Key Skills (at least 1): Field Service of Environmental Monitoring Systems Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹40,000.00 per month Benefits: Flexible schedule Health insurance Provident Fund Application Question(s): Do you hold a degree in Electrical, Electronics, Instrumentation How many years of experience do you have in service? Willingness to travel: 50% (Required) Work Location: In person

Group Company Vantage Nutrition LLP Primary Responsibilities C.Strategic and planning Functional Core  Ensure proper planning and execution of preventive and periodic maintenance to control the down time,by preparation of list of various machine equipment’s required for preventive maintenance and ensures periodic preventive maintenance of such equipment through proper preventive machine maintenance, ensures tripping free running of all machines. Attend and analyse the breakdown maintenance,Suggests and implements necessary preventive checks, correctives and modifications managing breakdowns within the standard timings with the help of SOPs it will reduce the breakdown timing. Ensure proper troubleshooting, electrical, mechanical maintenance of utilities and machines,Resolve recurring problems Seeks expert guidance from ACPL, PAM, APT to understand the processes effectively to ensures that all the equipment’s are maintained in proper working conditions and control the down time. Plan the external /internal calibration schedule , Ensures proper inspection of the spares / production equipment’s received from suppliers vendors,with the help of external service agencies we validate all the instruments to get accurate results and to meet the statutory compliances. Execute GMP, ISO, FSSC ,KOSHER , Halal ,customer audits /internal audits, safety and statutory compliances with help of periodic schedule and adhering to standards to maintain compliance to policies and procedures of the organisation. Key Result Areas Preventive and periodic maintenances Equipment uptime Statutory compliances Energy consumption Key Interfaces Internal Interfaces External Interfaces Production Quality Control HR and Admin Finance Store External service providers /agencies. Vendor. Purchase Product development Competencies GMP Basic Utility and Maintenance Operation Knowledge of SAP Continuous Improvement Pharmaceutical / Continuous process Spare parts, Accessories and AMC

Job Title: CSSD Technician Location: AIG Hospitals, Gachibowli, Hyderabad, Telangana Appointment Type: Full‑time, Permanent Key Duties: Handle sterilization cycle operations (Steam & E.T.O.) Monitor and document indicators (biological, chemical etc.) Maintain equipment calibration and load records Supply sterile instruments and linen to wards effectively Follow sterilization manuals and safety protocols Essential Qualifications: Diploma in CSSD or relevant field Active Paramedical Registration Minimum 1 year CSSD experience (1–5 years preferred) Working Conditions: Rotational shifts including mornings, days, and nights Benefits: Health insurance, provident fund, sick leave and leave encashment Job Type: Full-time Pay: ₹250,000.00 - ₹450,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Work Location: In person

Position: Mechanical Engineer Location : SHRIRAMPUR Reporting: - Plant Maintenance Manager - Engg & Maintenance Educational Qualificatio n – BE (Mechanical Engineering) Experience - 7-8 Years in Mechanical Maintenance Field – Preferably from Dairy Processing Nature of Experience: Experience of Food / Dairy processing industry maintenance for Milk Dryers, Cheese, Paneer, Milk Pre-processing etc. Exposure to Dairy Processing equipment like Rotary Equipment Centrifugal, Lobes, Gear, Vacuum, High Pressure Pumps, Gearbox, Agitators, Mixers High Speed Machines - Separators, Bactofuge, Decanters Air Compressors, Refrigeration System, Boilers, HVAC, Managing & Upkeep, Calibration, Predictive & Preventive Maintenance Strategy Execution of large Instrumentation and Automation System etc. Analytical Skill to anticipate, understand and resolve issues. Co-ordinate with shift engineers work with production team and make machines availability. Maintaining checklist and comply to requisite Food safety and Human safety standards. Diagnosing problems when machinery breaks down and deciding best way to repair. Identification of Maintenance prone areas, analysing and taking corrective actions to avoid repeated issues. Maintaining history cards, daily log books, ISO Documents Certifying bills for outsourced jobs and estimation for new /modification jobs. Planning and execution of shutdown jobs. Maintaining stock of spares for routine and breakdown maintenance. Preparation of Monthly Presentation for Maintenance. Inspect, Instruct, Training & development of technicians for Best Engg practices. Monthly MIS Presentation and preparation. Maintain Data, records for machines/equipment’s Exposure to TPM, QMS, ISO Systems, SAP

The role entails the analysis of samples, preparation of reagents, and maintenance of the chemical data book, stock of Acids, chemicals, and glassware, among others. You will be responsible for accurate and impartial reporting as per QMS standards. Proper handling and maintenance of instruments and equipment are also crucial aspects of the role. Additionally, ensuring QHSE procedures are implemented and followed in the laboratory is a key responsibility. Your main accountabilities will include preparing SOPs for testing procedures, verifying goods" descriptions, ensuring compliance with SOP and FIM instructions, and preparing MIS reports for management. Standardization and preparation of solutions of different normalities, as well as creating lab reports, quality reports, worksheets, registers, and laboratory charts will also be part of your responsibilities. Effective communication with office personnel and clients on testing-related matters is essential. Ensuring proper storage of samples, chemicals, and records as per QMS standards and handling testing equipment while maintaining and calibrating them as required by the system are also important tasks. Performance indicators for this role will include monitoring the percentage of testing errors, verifying errors, the number of tests undertaken, the number of different items tested, cost and time savings, and the results of training tests and annual technical assessments. Qualifications required for this position include a B.Sc in Chemistry (inorganic division) or a related field of Science based on business requirements. Freshers with excellent academic records are welcome for entry-level positions, while candidates with 1-2 years of experience as a Chemist are preferred for autonomous roles. Specific training or experience in testing particular products like coal, iron ore, or manganese will be considered advantageous. This is a full-time position that offers benefits such as commuter assistance and a performance bonus. The work schedule is in the morning shift, and a Bachelor's degree is preferred. The work location is in person.,

About Us Nanofilm, listed on the Mainboard of the Singapore Exchange, is a leading provider of nanotechnology solutions in Asia, featuring its own proprietary technologies. Our products and services are integral to the smooth functioning of many technologies and tools essential to modern life. Our solutions serve as key catalysts, enabling our customers to achieve high value-add advancements in their end-products in an environmentally sustainable manner. Founded in 1999 as a high-tech spin-off from Nanyang Technological University, we offer surface solutions based on vacuum deposition, including our proprietary Filtered Cathodic Vacuum Arc (FCVA) technology. Headquartered in Singapore, the company has over 3,000 employees across Singapore, India, Germany, Japan, China, and Vietnam. We aim to achieve technological breakthroughs, redefine the boundaries of material sciences, and develop nanotechnology solutions that enable new end-product possibilities. Our goal is to be a future generation technology-based solutions company, with a vision of our advanced materials and nanoproducts being integrated into the daily lives of consumers worldwide. Job Purpose Responsible for quality management and optimization of PVD coating processes during New Product Introduction (NPI) and Mass Production (MP) phases. Ensures products meet quality standards and customer requirements, drives continuous improvement in product development and production processes. Responsibilities NPI Phase Quality Management NPI Participate in new product development and process design, defining quality objectives and inspection standards for NPI. Monitor trial production processes to ensure compliance with required parameters and equipment performance. Collect and analyze trial production data, lead quality issue resolution and closed-loop management. MP Phase Quality Management Establish and enforce quality standards and inspection protocols for mass production, ensuring product consistency and reliability. Oversee production processes, including parameter monitoring and equipment performance, to prevent and resolve quality issues. Analyze non-conforming products and customer complaints, conduct root cause investigations, and propose improvement measures. Process Optimization & Continuous Improvement. Optimize PVD coating processes to improve yield and production efficiency. Monitor trial production processes to ensure compliance with required parameters and equipment performance. Equipment & Testing Management Manage quality inspection tools and equipment to ensure measurement accuracy. Participate in equipment maintenance and calibration to ensure stable operation. Cross-Functional Collaboration & Reporting Collaborate with R&D, Production, and Supply Chain to support new product development. Prepare quality reports, summarize quality performance, and propose improvement actions. Requirements Bachelor’s degree or higher in Materials Science, Mechanical Engineering, Chemical Engineering, or related fields. 3-5 years of experience in PVD coating or related industry quality management, familiar with NPI and MP quality processes. Proficient in quality management tools and inspection equipment operation. Strong analytical, problem-solving, and communication skills. Detail-oriented, proactive, and team-oriented with a strong sense of responsibility. Working location Nanofilm Advanced Material India Pvt. Ltd. Salcomp Technology India Pvt. Ltd. (STIPL2) Nokia Telecom SEZ, Krishna Nagar, Sriperumbudur

India LOCATION Raigarh, Chhattisgarh WORK LOCATION TYPE On-site DATE POSTED 2025-07-26 CATEGORY Engineer Job Summary: We are seeking a highly motivated and results-driven Senior Biomedical Engineer to join our team. The Biomedical Engineer is responsible for the installation, maintenance, calibration, and repair of all medical equipment and associated technologies. Location- Raigarh (Chhattisgarh) Job Description Key responsibilities: Lead and manage the biomedical engineering team at the facility. Troubleshoot and perform corrective maintenance of critical care diagnostic and general BME. Plan and execute PM schedule for all biomedical equipment. Maintain complete documentation, service records, calibration reports and asset inventories. Coordinate with OEM’s, vendors and service providers for spares, repairs and equipment AMC/CMC. Ensure adherence to NABH/NABL. Requirements : Bachelors/ Diploma in Biomedical engineering/Electronics/ ITI 1-3 years in biomedical equipment maintenance Excellent communication and interpersonal skills. Willingness to travel within state as per demands.

India LOCATION Kochi, Kerala WORK LOCATION TYPE On-site DATE POSTED 2025-07-18 CATEGORY Engineer Job Summary: We are seeking a highly motivated and results-driven Specialist Engineer (MRI – Wipro GE) to join our team. The MRI Specialist Engineer is responsible for the installation, calibration, maintenance, and repair of MRI systems. Job description Key Responsibilities: Assist in the installation and site preparation of MRI systems. Perform system calibration and functional testing during installation. Ensure proper integration with PACS and hospital networks Perform scheduled preventive maintenance per specifications. Diagnose and repair system faults, RF issues, gradient coil problems, and software errors. Maintain detailed service logs and ensure minimal downtime. Provide real-time technical support to radiographers, radiologists, and clinical staff. Guide users on proper system usage and minor troubleshooting. Ensure MRI safety standards (RF shielding, cryogen levels, magnet quench protocol) are followed. Monitor image quality performance and calibrate systems for optimal diagnostics Skills Required In-depth understanding of MRI physics, software platforms, DICOM, and imaging protocols. Experience with MRI QA tools, RF shielding, and room site planning. Strong analytical and problem-solving abilities. Adaptability Team Work Good communication Skills Proficiency in MS Excel & Computer Data Management Willingness to Travel Requirements 4–5 years of experience in MRI maintenance Familiarity with GE MRI system No of Positions: 1

India LOCATION Kochi, Kerala WORK LOCATION TYPE On-site DATE POSTED 2025-07-18 CATEGORY Sales Job Summary : We are seeking a Self-driven and customer-oriented Area Sales Manager - Service Sales, to promote and sell after-sales services for biomedical equipment and solutions. The ideal candidate will be responsible for achieving Sales targets, building long-term client relationships, and ensuring high levels of customer satisfaction in the biomedical domain. Job Description Key responsibilities : Promote and sell annual maintenance contracts (AMCs), comprehensive maintenance contracts (CMCs), and installation & calibration services for biomedical equipment. Identify and develop new service business opportunities in existing and prospective customer accounts. Generate leads through market research, cold calling, and site visits to hospitals, diagnostic labs, and clinics. Prepare technical and commercial proposals in line with customer requirements. Work closely with the service delivery team to ensure quality and timely execution of services sold. Maintain and grow relationships with biomedical engineers, hospital administration, and procurement departments. Team management Negotiate contracts and close agreements to maximize profits while ensuring client satisfaction. Keep track of service contracts, renewals, and upsell opportunities. Maintain accurate records of client interactions and sales activities using CRM tools. Stay updated on product developments, competitors, and industry trends. Requirements : Any Bachelor’s degree/ Diploma 4+ years of proven experience in Service sales in medical devices / Health care Strong Communication, Negotiation and interpersonal skill Ability to work independently and manage time effectively. Willingness to travel as per business needs. No of positions : 1

India LOCATION Kottayam, Kerala Kasaragod, Kerala WORK LOCATION TYPE On-site DATE POSTED 2025-07-18 CATEGORY Engineer Job Summary : We are seeking a self-driven and customer-oriented Service Sales Executive to promote and sell after-sales services for biomedical equipment and solutions. The ideal candidate will be responsible for achieving service sales targets, building long-term client relationships, and ensuring high levels of customer satisfaction in the biomedical domain. Job Description Key Responsibilities : Promote and sell annual maintenance contracts (AMCs), comprehensive maintenance contracts (CMCs), and installation & calibration services for biomedical equipment. Identify and develop new service business opportunities in existing and prospective customer accounts. Generate leads through market research, cold calling, and site visits to hospitals, diagnostic labs, and clinics. Prepare technical and commercial proposals in line with customer requirements. Work closely with the service delivery team to ensure quality and timely execution of services sold. Maintain and grow relationships with biomedical engineers, hospital administration, and procurement departments. Negotiate contracts and close agreements to maximize profits while ensuring client satisfaction. Keep track of service contracts, renewals, and upsell opportunities. Maintain accurate records of client interactions and sales activities using CRM tools. Stay updated on product developments, competitors, and industry trends. Requirements : Bachelor’s degree/Diploma in Biomedical Engineering, Life Sciences, or a related field No educational barriers for experienced candidates 1-3 years of experience in sales or service of medical/diagnostic equipment. Freshers also welcome. Experience with equipment like ventilators, patient monitors, analyzers, or imaging devices is an added advantage. Willingness to travel extensively within the assigned region. No of Positions : 1 for each location

India LOCATION Kochi, Kerala WORK LOCATION TYPE On-site DATE POSTED 2025-07-18 CATEGORY Engineer Job Summary: We are seeking a highly motivated and results-driven Specialist Engineer (Cath lab) to join our team. The Cath Lab Specialist Engineer is responsible for the installation, maintenance, calibration, and repair of all cardiac catheterization laboratory equipment and associated technologies. Job description Key Responsibilities: Install and configure Cath lab. Assist with system integrations (e.g., PACS, EMR). Conduct routine preventive maintenance and calibration of Cath lab equipment Diagnose and troubleshoot malfunctions or failures in real-time to minimize procedure downtime. Provide technical support during cardiac catheterization procedures. Train Cath lab personnel on proper equipment usage and troubleshooting techniques. Skills Required: Troubleshooting of biomedical instruments Multimodality Adaptability Team Work Good communication Skills Proficiency in MS Excel & Computer Data Management Willingness to Travel Requirements 4–5 years of experience in Cath lab maintenance Proficiency in troubleshooting imaging systems and networked medical devices. Familiarity with systems from vendors such as GE, Siemens, Philips, or Canon No of Position: 1

India LOCATION Bangalore, Karnataka WORK LOCATION TYPE On-site DATE POSTED 2025-07-18 CATEGORY Engineer Job summary: Seeking a skilled Biomedical Equipment Field Service Engineer with 3–8 years of experience in troubleshooting, calibrating, and maintaining critical medical devices (X‑Ray, Dialysis, ICU/OT, Lab), who thrives in a collaborative, innovative environment and is ready to support healthcare delivery across diverse locations. Key Responsibilities: Maintain & Troubleshoot: Handle breakdown and preventive maintenance for critical equipment like X-Ray, Dialysis, ICU/OT systems, and lab instruments. User Support: Provide technical assistance and training to healthcare professionals. Vendor Coordination: Liaise with OEMs and vendors for spares and technical support. Multi-Modal Expertise: Manage equipment across ICU, OT, Imaging, and Lab settings. Travel Ready: Willingness to travel extensively within assigned territories. Qualifications and Skills: 3-8 years in biomedical equipment service and maintenance. Proficiency in troubleshooting, calibration, and performance testing. Excellent interpersonal and communication skills. Degree/Diploma in Biomedical, Medical Electronics, or Electronics & Instrumentation. No of positions: 1

As a trusted global leader and industry partner who is reimagining plasma and exploring its untapped potential, Takeda’s Plasma-Derived Therapies (PDT) Business Unit is dedicated to transforming the lives of patients worldwide who rely on these lifesaving and life-sustaining therapies. With an 80-year legacy of developing treatments for rare and complex chronic diseases, we thrive on innovation, offering a broad, differentiated portfolio of more than 20 plasma medicines with integrated care solutions to patients in more than 80 countries. Powered by ~ 17,000 Takeda employees, our ~230 high-quality BioLife donation centers, a dedicated R&D team, and eight world-class plasma manufacturing facilities, we are unleashing data, digital and technology to transform our end-to-end operations and set new industry standards. This enables us to innovatively and sustainably meet the growing and changing needs of patients, our people, and our planet, today and in the future. Job ID R0159348 Date posted 07/30/2025 Location Bengaluru, Karnataka I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’sPrivacy Noticeand Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description The Future Begins Here At Takeda, we are leading digital evolution and global transformation. By building innovative solutions and future-ready capabilities, we are meeting the need of patients, our people, and the planet. Bengaluru, the city, which is India’s epicenter of Innovation, has been selected to be home to Takeda’s recently launched Innovation Capability Center. We invite you to join our digital transformation journey. In this role, you will have the opportunity to boost your skills and become the heart of an innovative engine that is contributing to global impact and improvement. At Takeda’s ICC we Unite in Diversity Takeda is committed to creating an inclusive and collaborative workplace, where individuals are recognized for their backgrounds and abilities they bring to our company. We are continuously improving our collaborators journey in Takeda, and we welcome applications from all qualified candidates. Here, you will feel welcomed, respected, and valued as an important contributor to our diverse team About the role: As a Senior Software Developer in the Calibration Management System (CMS) space within the Plasma-Derived Therapies (PDT) business unit, you will focus on developing IT Service Management solutions using ServiceNow by customizing the product. Your role involves translating functional specifications into logical, component-based technical designs and developing new ServiceNow workflows and processes. Collaborating closely with multiple stakeholders, you will translate business needs into effective technical solutions, maintaining continuous dialogue with both business and IT teams to ensure robustness, accuracy and consistency. By designing and implementing sophisticated IT Service Management solutions, this role directly contributes to PDT’s ability to harness data effectively, enhancing decision-making capabilities, and ultimately, competitive advantage in the market. You will be adopting cutting-edge technologies and methodologies which will help Takeda drive innovation, adapt to new opportunities, and continuously evolve in an ever-changing business/technological landscape. This position will align to Cloud & Custom Development chapter of the ICC and initially report to the PDT Delivery Lead for strategic direction as well as day-to-day management until the role of Technical Program Manager for CMS is filled within Takeda ICC. This is expected to be completed by Dec 2024, post which the reporting and managerial responsibilities will be transitioned accordingly. How you will contribute: Design, develop, and implement customized solutions on the ServiceNow platform, specifically focusing on Nuvolo applications to meet requirements and enhance operational efficiency Integrate Nuvolo with other enterprise systems and automate workflows to streamline processes and improve data accuracy and accessibility Provide technical expertise and support for Nuvolo applications, including troubleshooting, performance tuning, and ensuring system stability and reliability Work closely with business analysts, project managers, and other stakeholders to gather requirements, provide technical insights, and ensure successful project delivery Stay updated with the latest ServiceNow and Nuvolo features and best practices, and proactively suggest improvements to existing solutions to drive innovation and efficiency Minimum Requirements/Qualifications: Bachelor’s degree in Computer Science, Information Technology, Software Engineering, or a similar field required. Master's degree in a similar field would be a plus 5-8 years experience in developing and customizing applications on the ServiceNow platform, including scripting, workflows, and integrations - Nuvolo/ServiceNow across Nuvolo GXP Lab asset management, ServiceNow scripting experience using JavaScript, HTML, CSS, XML and web services integration (SOAP, WSDL, REST) Experience of working with Data Migration and ERP/IWMS/EAM Implementation engagements Hand on experience in all client side and server-side objects of ServiceNow like Client Scripts, Catalog Client Scripts, UI Policy, Catalog UI Policy, BR, Script Include, ACL, Form Design, Form Layout changes, writing Email scripts, Email notification, Email Templates etc. Software integration experience utilizing Web Based API - SOAP, REST API Understand technical and functional design requirements related to ServiceNow Excellent troubleshooting skills with ability to demonstrate influence in a consultative fashion to stakeholders and other team members Preferred requirements: Good understanding in service portals and hands-on experience in Widget, Instance, and Pages Integration experience with Web Services, Middleware Solutions such as TIBCO, J2EE, J2ME, JSP, Servlets, JDBC, AJAX, XML, SQL Server 2008R/2012, Oracle 9i/10g/11g, MS-Access, My SQL, EDI, XSLT, .Net or other integration technologies Ability to develop custom UI changes with usage of Web Technologies such as DOM, HTML changes BENEFITS: It is our priority to provide competitive compensation and a benefit package that bridges your personal life with your professional career. Amongst our benefits are: Competitive Salary + Performance Annual Bonus Flexible work environment, including hybrid working Comprehensive Healthcare Insurance Plans for self, spouse, and children Group Term Life Insurance and Group Accident Insurance programs Employee Assistance Program Broad Variety of learning platforms Diversity, Equity, and Inclusion Programs Reimbursements – Home Internet & Mobile Phone Employee Referral Program Leaves – Paternity Leave (4 Weeks) , Maternity Leave (up to 26 weeks), Bereavement Leave (5 calendar days) ABOUT ICC IN TAKEDA: Takeda is leading a digital revolution. We’re not just transforming our company; we’re improving the lives of millions of patients who rely on our medicines every day. As an organization, we are committed to our cloud-driven business transformation and believe the ICCs are the catalysts of change for our global organization. #Li-Hybrid Locations IND - Bengaluru Worker Type Employee Worker Sub-Type Regular Time Type Full time

The Planning and Billing Engineer with NABL Certification is responsible for managing project schedules, ensuring the timely completion of all tasks, and overseeing the billing process in accordance with contract specifications and legal requirements. This role requires a deep understanding of project planning, resource management, and cost estimation, along with the application of NABL standards for testing and calibration. The engineer will also ensure that the required laboratory testing and calibrations adhere to international quality standards and will be involved in coordinating between various departments, clients, and contractors. Key Responsibilities: Planning and Scheduling: - Develop and maintain detailed project plans, including defining project scopes, setting deadlines, and allocating resources effectively. - Monitor and track project progress, adjusting plans as necessary to ensure timely completion. - Collaborate with project teams to assess risks and establish mitigation strategies. - Ensure that all work activities are planned according to NABL certification requirements and other quality standards. - Prepare and update detailed project reports on schedule performance, risks, and other critical factors. Billing and Cost Control: - Prepare, review, and process project invoices in accordance with contractual terms and conditions. - Ensure that all billing milestones are met based on the project schedule and deliverables. - Track project expenses and ensure that all financial transactions align with the budget. - Coordinate with procurement, accounting, and finance departments for the accurate and timely submission of billing documents. - Resolve any billing discrepancies and disputes promptly. Quality Assurance and NABL Compliance: - Ensure that all laboratory activities (testing, calibration) conform to NABL standards and relevant certifications. - Collaborate with quality assurance teams to maintain compliance with all NABL procedures and requirements. - Review test reports and certifications to verify that all processes are conducted in accordance with NABL accreditation guidelines. - Keep abreast of changes in NABL standards and help implement these changes within the project workflows. Documentation and Reporting: - Maintain proper documentation for all project planning, testing, and billing activities. - Create regular status reports and dashboards that provide insights into project progress, billing status, and NABL compliance. - Ensure that all documentation for NABL certification and accreditation processes is current and readily available for inspection. Collaboration and Stakeholder Communication: - Act as a liaison between project stakeholders, including clients, contractors, engineers, and vendors. - Provide technical support to teams working on testing, calibration, and other engineering aspects of the project. - Address any queries or concerns raised by clients or internal teams, ensuring effective communication and problem resolution. Risk Management: - Proactively identify and assess risks related to project planning, billing, and quality standards. - Develop strategies to minimize potential risks and prevent issues related to project delays or cost overruns. Continuous Improvement: - Contribute to the continuous improvement of processes, systems, and procedures for project planning, billing, and NABL compliance. - Implement lessons learned from previous projects to enhance future project execution. Required Qualifications: Education: - Bachelors degree in Engineering (Civil, Mechanical, Electrical, or related field). - NABL certification or accreditation in quality management is required. Experience: - Minimum of 3-5 years of experience in project planning, billing, or related roles within industries that require NABL certification, such as construction or manufacturing. - Familiarity with scheduling software (e.g., MS Project, Primavera) and ERP or billing software. - Experience in managing projects requiring NABL accreditation is highly desirable. Skills: - Strong understanding of project planning, scheduling, and billing. - Knowledge of NABL standards, testing, calibration, and quality assurance processes. - Proficiency in MS Office Suite (Excel, Word, PowerPoint) and project management tools. - Analytical and problem-solving abilities, especially in relation to project scheduling and billing processes. - Excellent communication and interpersonal skills. - Ability to work under pressure and manage multiple tasks simultaneously. - Attention to detail, especially when it comes to billing accuracy and compliance. Preferred Qualifications: Certifications: - NABL Accreditation Certification in relevant engineering disciplines. Experience: - Previous experience working in a project environment that is NABL-accredited or deals with high-standard testing and calibration. Knowledge of Standards: - Knowledge of international standards (ISO/IEC) related to testing and calibration.,

As an Instrumentation Manager at Genuine Biosystem Pvt Ltd in Chennai, you will play a crucial role in overseeing the design, installation, calibration, and maintenance of all instrumentation systems. Your responsibilities will include developing and implementing preventive maintenance programs, ensuring compliance with regulations, and effectively managing the instrumentation team. To excel in this role, you should have experience in the design, installation, calibration, and maintenance of instrumentation systems. Your knowledge of preventive maintenance programs and regulatory compliance will be essential. Strong leadership and team management skills are required to lead the instrumentation team successfully. Excellent problem-solving and troubleshooting abilities will enable you to address any issues effectively. Technical proficiency in instrumentation technology and systems is a must for this position. A Bachelor's degree in Instrumentation Engineering, Electrical Engineering, or a related field is required. Certifications in instrumentation maintenance and management would be considered a plus. Join Genuine Biosystem Pvt Ltd and contribute to the continuous maintenance of high production standards in the field of (IVD) Invitro Diagnostic reagents, kits, and Laboratory Medical equipment. Your expertise will ensure quality and workmanship satisfaction for our customers.,

As a Quality Control Technician III at TAPI, you will be an integral part of the leading international supplier of active pharmaceutical ingredients (APIs). TAPI boasts the industry's broadest portfolio, which includes over 350 API products. With a rich history spanning over 80 years, we are recognized as one of the most trusted API suppliers globally, catering to 80 PERCENT of the top 50 pharmaceutical companies. At TAPI, our commitment to excellence is driven by our experience, expertise, cutting-edge technologies, and unwavering dedication to exceptional customer service. Your primary responsibilities will include maintaining 24/7 audit readiness, possessing expertise in Wet Chemistry, and being flexible to work in different shifts. You will actively participate in internal, external, and regulatory audits, ensuring full compliance with CAPA trainings. Additionally, you will be responsible for initiating and investigating LIR, OOS, OOT, and borderline results, promptly reporting them to the designated authority. Collaborating with various departments, you will facilitate the sharing of necessary documents from Quality Control to Regulatory Affairs and other relevant areas. In your role, you will play a crucial part in determining team priorities aligned with the plant's requirements, while coordinating effectively with team leaders and managers. Upholding stringent quality standards, you will adhere to housekeeping practices, cGMP, GLP, and Safety Guidelines within the laboratory. Your duties will encompass sampling and analyzing raw materials, finished goods, intermediates, and cleaning samples as per specific requirements, meticulously documenting results in analytical sheets, QA forms, LIMS, and online systems to ensure data integrity. Furthermore, you will conduct analytical tests following established monographs and SOPs, oversee the calibration and verification of instruments, and manage the reserved samples room along with chambers, autoclaves, and incubators. Your support will also be essential in preparing department-related documents such as STPs, SOPs, and more. Ensuring the timely sampling, approval, and rejection of labels for various products and maintaining accurate stock records of chemicals will be among your key responsibilities. To excel in this role, you should hold a Bachelor's or Master's degree in Chemistry and possess a minimum of 3 years of relevant experience in a similar capacity. Your dedication to upholding Teva's Equal Employment Opportunity commitment, which includes supporting diversity and providing equal opportunities to individuals with disabilities and veterans, is paramount in our inclusive work environment.,

Trending Job Description Key Roles & Responsibilities: Oversee and support the overall activities during the product development life cycle from quality perspective in R&D (API and intermediates). To understand the site needs with respect to system establishment and sustainability. Author/ Review and approve the SOPs/work directions required for implementing the Quality systems in R&D activities as per GLP and regulatory requirements. Ensure effective implementation of SOPs/ work directions. Review and approve Lab Familiarization Reports (LFR), Product development reports (PDR), Technology transfer, product specifications & STPs, analytical method validation, method transfer, qualification, calibration, process validation protocol and reports. Ensure effective execution of these activities. Periodic audits of R&D laboratory. Ensure online documentation and review lab notebooks, PDR/LFR documents, analytical documents and stability data. Effective maintenance of R&D records, distribution and archival systems. Perform cGMP audit of R&D facilities and operations. Assist the team in auditing contract manufacturers/ vendors/ contract testing laboratory. Ensure R&D team is trained for their relevant job function and GMP/ GLP training. Provide quality related inputs to new projects, existing project, up gradations etc. Participate in identification of key starting material (KSM)/ registered starting material (RSM) and ensure that it is correctly identified. Participate in handling of OOS, OOT, Deviations, Batch failures, investigations and CAPA implementation at site. Establish raw material standards by studying manufacturing/ R&D requirements-conferring with suppliers. Responsible to follow the safety and environmental procedures deployed in the site. Qualifications Graduation and above in Science / Pharmacy Required Skills Analytical development (API /CDMO) with DQA experience About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 8598 Job Category Quality Assurance Posting Date 07/29/2025, 04:50 PM Apply Before 08/04/2025, 04:50 PM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN

Job Description: As a valued member of our company's lab Operations team, you will be responsible for a variety of key roles and responsibilities. Your primary tasks will include working with instrumentation such as Pressure and Temperature sensors, as well as possessing knowledge of soldering techniques. Additionally, you will need to have a good understanding of Electrical Panels, particularly 230V and 420V systems, and be skilled in instrumentation wiring and panel wiring for pressure sensors. It will be essential for you to be able to interpret panel drawings and schematic layouts accurately. Your commitment to safety will be crucial, including knowledge of safety protocols like LOTO and HIRA. Understanding I/O modules and basic calibration principles will also be part of your daily duties. You will collaborate closely with engineers, technicians, lab and test operations personnel, and product validation teams. Proficiency in basic computer operations, Windows operating systems, and Microsoft Office will be advantageous. Additionally, you will conduct lab testing activities and set up equipment while ensuring adherence to 5S practices in the work area. Requirements: To excel in this role, you should possess a minimum of 2 to 4 years of experience in a relevant field. A degree in Mechanical Engineering or a related discipline, such as a B.E. or Diploma, will be required to demonstrate your qualifications for this position.,

As a member of Jubilant Pharma Limited, you will be responsible for various sampling analysis of raw materials, water samples, swab samples, compressed air monitoring, and microbial load in production areas. You will conduct MLT validation and investigate deviations, incidents, and OOS. Your role will involve recording analytical data and preparing worksheets for raw materials, finished products, water samples, and swab samples. Furthermore, you will ensure proper storage and destruction of samples after testing, as well as validate and calibrate instruments and equipment. You will also investigate deviations, incidents, and OOS. In this position, you will interact with auditors, quality control lab, production, warehouse, and quality assurance teams. Jubilant Pharma's revenue has been consistently growing, reaching INR 53,240 million during the Financial Year 2018-19 compared to INR 39,950 million in the Financial Year 2017-18. For more information about the organization, please refer to www.jubilantpharma.com.,

The role is accountable for ensuring adherence to quality norms. The key responsibility of this position is to ensure that products meet specified quality standards. This position involves conducting product testing in accordance with quality norms, managing shift operations, and reporting shift outcomes to the reporting manager. Customer Quality - Verify that product-specific quality requirements are fulfilled. - Maintain the hygiene of the department. - Report any abnormalities identified during testing. RM Testing & Approval - Ensure timely approval of raw materials. - Maintain the testing equipment used for analysis. - Manage the inventory of consumables needed for testing. - Maintain and calibrate equipment. Audits & Compliance - Comprehend the requirements of quality and safety audits. - Understand roles and responsibilities and execute tasks accordingly. Quality - Ensure that tasks are executed following defined procedures to meet quality standards. - Report any quality-related anomalies to superiors. Safety - Ensure tasks are performed as per defined procedures to meet safety requirements. - Report any safety-related irregularities to superiors. People Management - Effectively communicate work instructions to shift employees. - Ensure that work is carried out as per procedures. - Provide necessary support as needed.,

Job Description Key Roles & Responsibilities: Oversee and support the overall activities during the product development life cycle from quality perspective in R&D (API and intermediates). To understand the site needs with respect to system establishment and sustainability. Author/ Review and approve the SOPs/work directions required for implementing the Quality systems in R&D activities as per GLP and regulatory requirements. Ensure effective implementation of SOPs/ work directions. Review and approve Lab Familiarization Reports (LFR), Product development reports (PDR), Technology transfer, product specifications & STPs, analytical method validation, method transfer, qualification, calibration, process validation protocol and reports. Ensure effective execution of these activities. Periodic audits of R&D laboratory. Ensure online documentation and review lab notebooks, PDR/LFR documents, analytical documents and stability data. Effective maintenance of R&D records, distribution and archival systems. Perform cGMP audit of R&D facilities and operations. Assist the team in auditing contract manufacturers/ vendors/ contract testing laboratory. Ensure R&D team is trained for their relevant job function and GMP/ GLP training. Provide quality related inputs to new projects, existing project, up gradations etc. Participate in identification of key starting material (KSM)/ registered starting material (RSM) and ensure that it is correctly identified. Participate in handling of OOS, OOT, Deviations, Batch failures, investigations and CAPA implementation at site. Establish raw material standards by studying manufacturing/ R&D requirements-conferring with suppliers. Responsible to follow the safety and environmental procedures deployed in the site. Qualifications Graduation and above in Science / Pharmacy About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide.

As a key member of the Quality Control team, your main responsibility will involve performing laboratory analysis and instrumentation tasks efficiently. This will include conducting analytical tests on raw materials, finished products, and various samples within specified timelines. You will also play a crucial role in maintaining control of the data generated from these analyses. To excel in this role, you should possess the following skills: - Proficiency in wet analysis techniques such as titrimetry and other relevant methods - Familiarity with a range of analytical procedures - Hands-on experience in operating instruments for analyzing color, moisture, etc. - Ability to carry out maintenance, calibration, and validation of laboratory equipment - Prior exposure to handling GC/HPLC instruments would be highly advantageous In terms of experience, we are looking for candidates with a minimum of 2-3 years of relevant experience in the food or food-related industry. This experience should cover a broad spectrum of activities related to quality control and laboratory analysis. For more information on our commitment to workplace diversity and inclusion, please visit IFF.com/careers/workplace-diversity-and-inclusion. We look forward to welcoming a dedicated professional like you to our team!,

Apply Now Job Title: Supervisor - Training & Quality Job Description Key Responsibilities: Training: Design, develop, and deliver onboarding and ongoing training programs for call center agents. Conduct training needs analysis and identify skill gaps. Collaborate with team leaders and managers to ensure training aligns with business goals. Maintain training materials and update them regularly based on process or product changes. Monitor and evaluate training effectiveness through assessments and feedback. Quality Assurance: Develop and implement quality monitoring frameworks and scorecards. Monitor and evaluate agent interactions (calls, chats, emails) for quality, compliance, and customer satisfaction. Provide constructive feedback and coaching to agents based on quality evaluations. Analyze quality trends and recommend process improvements. Ensure compliance with internal policies and external regulations. Reporting & Analysis: Generate regular reports on training outcomes and quality metrics. Track performance improvements and identify areas for further development. Present insights and recommendations to senior management. Qualifications: Bachelor’s degree in Business, Communications, or related field (preferred). 3+ years of experience in a call center environment, with at least 1 year in a training or quality role. Strong knowledge of call center operations and customer service best practices. Excellent communication, presentation, and interpersonal skills. Proficiency in MS Office and call center software (e.g., CRM, QA tools). Ability to analyze data and generate actionable insights. Key Competencies: Leadership and team management Analytical thinking and problem-solving Attention to detail Coaching and mentoring Adaptability and continuous improvement mindset Concentrix is a technology-enabled global business services company specializing in customer engagement and improving business performance. We partner with ambitious, progressive executives around the world to future-proof their business and stay ahead of the competition and customer expectations. Training Supervision: Role and key responsibilities: Identify training needs through performance data, feedback, and business goals. Design, implement, and evaluate training programs and workshops. Supervise trainers and ensure consistency in content delivery and facilitation. Maintain training records and ensure compliance with mandatory learning requirements. Monitor training effectiveness through assessments, feedback, and performance metrics. Collaborate with department heads to align training with operational goals. Quality Assurance: Oversee quality monitoring processes and ensure adherence to SOPs and KPIs. Supervise quality analysts and ensure timely audits and feedback loops. Analyze quality data to identify trends, gaps, and areas for improvement. Develop and implement quality improvement plans in collaboration with operations. Conduct calibration sessions to ensure consistency in evaluations. Support root cause analysis and corrective action planning. Key Skills And Knowledge: Proven experience in training methodologies, and soft skills (communication skills, critical thinking, time management, team building, etc.) Strong oral and written communication skills Proficient in Microsoft Office Demonstrated ability to multi-task, prioritize, and meet timelines of deliverables Strong understanding of adult learning principles and instructional design. Excellent communication, presentation, and leadership skills. Proficiency in using Learning Management Systems (LMS) and MS Office tools. Ability to analyze data and generate actionable insights Education - Graduate Disclaimer :- 'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities.' Location: IND Pune - Amar Tech Centre S No.30/4A 1 Language Requirements: Time Type: Full time If you are a California resident, by submitting your information, you acknowledge that you have read and have access to the Job Applicant Privacy Notice for California Residents Apply Now

Job Summary: The Production Chemist is responsible for executing and monitoring all production activities related to the formulation and manufacturing of cosmetic products such as creams, lotions, shampoos, serums, and personal care items. They ensure the batch is manufactured as per cGMP and regulatory standards while maintaining quality, safety, and efficiency. Key Responsibilities: Batch Manufacturing: Execute batch manufacturing of cosmetics as per Batch Manufacturing Records (BMR). Weigh, mix, and blend raw materials following standard operating procedures (SOPs). Maintain batch records, equipment logs, and production data accurately. Process Monitoring: Monitor and control production processes, ensuring consistency and quality. Adjust formulations or parameters when needed, based on in-process testing results. Coordinate with QA/QC for sample testing and approval. Compliance & Documentation: Ensure adherence to GMP, ISO, and other regulatory guidelines. Maintain detailed documentation for traceability and audits. Participate in internal and external audits. Equipment Handling: Operate, clean, and maintain manufacturing equipment (mixers, homogenizers, filling machines, etc.). Perform equipment calibration and report any maintenance issues. Material Management: Coordinate with the stores department for raw material availability. Minimize wastage and monitor usage efficiency. Safety & Hygiene: Maintain a clean and safe working environment. Follow safety protocols for chemical handling and personal hygiene.