5113 Calibration Jobs - Page 23

As a Shift Engineer at Adani Power Limited (APL), your primary responsibility is to manage the optimal performance and reliability of Control & Instrumentation (C&I) systems for BTG (Boiler, Turbine, Generator) through vigilant maintenance, calibration, and troubleshooting. This entails ensuring the availability and functionality of all C&I systems related to BTG and BOP during your shift, attending routine maintenance of BTG Motor Operated Valves (MOVs) and auxiliaries, executing calibrations as per schedule, and maintaining the healthiness of C&I parameters in coordination with Operations. You will be required to provide immediate and effective response to emergencies to safeguard personnel and equipment, troubleshoot breakdowns of equipment promptly to minimize downtime, and maintain Flue Gas Discharge (FGD) systems to ensure operational efficiency. Additionally, you will need to coordinate with other departments to minimize delays in maintenance and operational activities, follow safety protocols diligently to ensure zero accidents, and monitor compliance with environmental regulations, particularly in relation to FGD systems. Furthermore, you will be responsible for implementing comprehensive digitization strategies and automation solutions to optimize operational efficiency, adopting newer technologies and innovative ideas, and utilizing advanced technology to streamline maintenance and operational processes. It is essential to ensure compliance with safety audit observations, follow the CHETNA process diligently, and implement MoC (Management of Change) protocols to ensure safe and compliant modifications to equipment and processes. To qualify for this role, you should hold a Bachelor's degree in C&I or Electronics & Communication or equivalent degree and have at least 6+ years of experience in power plant operations or maintenance, with specific exposure to BTG and C&I systems. Experience in the power generation industry, particularly in thermal power plants with knowledge of DCS, FGD systems, and safety protocols, will be advantageous. Join Adani Power Limited to contribute to the operational excellence and business sustainability of one of the largest private thermal power producers in India.,

Description Amazon Finance Operations – Accounts Receivable AR is looking for a Training Specialist. If you are a professional who thrives in a dynamic, ever-changing environment with experience in training delivery and management, we want to speak with you! Key job responsibilities The Training Specialist will be responsible for designing new training content and delivery of approved training content. Responsible for training of all AR employees- new hires as well as existing employees. Deliver our blended learning (instructor led training both in-class and virtual) classes, programs for new hires, new skills (cross-training), continuing education, and refreshers as necessary for global associates. Develop and implement market/site specific training programs that align with global training program, including employee on-boarding and ongoing training programs Plan, coordinate and deliver programs to enhance the knowledge and skills of GAR employees in the site and channel assigned, including email handling, call handling, customer handling, and account handling skills for the respective Channel/Site Work with local management and global leads to identify training needs and implement mechanisms to continuously assesses employee’s needs for training Support and coach operations managers with training techniques for ongoing employee development Conduct weekly one-on-ones with each member of the team, which includes call / email reviews, live monitoring, and role plays Conducting call practice and calibrations for target audience, and providing feedback on mock calls/role plays, case studies and difficult customer scenarios, including call listening and comprehension on use cases identified from time to time Supporting trained new joiners, side-by-side in a Go-Live support environment, to monitor live calls and subsequently providing feedback, conducting refreshers, and discussing difficult scenarios for communication enhancement. Conducting call calibrations sessions with stakeholders and participating in AR wide monthly calibration. Sharing use cases for discussions within teams. Basic Qualifications Expertise in planning, implementing and assessing training Excellent communication skills for the purpose of knowledge transfer and skill development, including superior skill in explaining technical topics to novices and collaborating with subject matter experts and managers. Excellent coordination, classroom management and organization skills. Ability to use multiple learning methods and link appropriate methods with subject matter. Excellent one-to-many and one-to-one communication skills in both classroom and tutorial settings. Knowledge of adult learning and training practices, especially in technical support contexts. Certified trainer with excellent communication skills – oral and written 6 to 8 years of relevant experience in learning and development Bachelor’s degree or equivalent Preferred Qualifications Creative problem solver and strong analytical skills Consistent record of process improvement within the training and development domain Comfortable in a fast-paced, multi-tasked, high-energy environment Content development / Instructional design experience Experience using instructional design tools such as Storyline, Captivate is preferred Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Company - ADCI - Maharashtra Job ID: A3035297

You will be joining the Bio Analytical Department at PTC - MORAIYA as a Probationer-R&D Executive. With 2-3 years of experience and an educational background in M.Sc or B. Pharma, you will be responsible for various tasks including sample preparation, method development, method validation, and subject sample analysis. Your role will involve operating, calibrating, and maintaining equipment while keeping track of the equipment log. You will also be required to review bio analytical data, prepare and review SOPs, protocols, plans, and reports. Additionally, you will play a vital role in executing and maintaining GLP, GCP, Safety, and Quality systems within the department. Maintaining displays such as labels, SOPs, charts, etc., will also be part of your responsibilities. If you are an employee from the QC department looking for a new opportunity, you are encouraged to apply and contribute to the dynamic environment at PTC - MORAIYA.,

Job Title: Senior Engineer – Engine Development Company Overview: UD Trucks is a leading international commercial vehicle solutions provider headquartered in Japan. We specialize in the development, production, and sales of heavy, medium, and light-duty trucks, supporting smart logistics solutions across more than 60 countries. Our purpose is to “go the extra mile” for our customers through pioneering technologies that enhance fuel efficiency, reliability, and uptime. Our culture is rooted in diversity, empowerment, and innovation, with over 8,000 passionate professionals working together globally to build a better life for society, our customers, and ourselves. Department Overview – Powertrain Engineering, Bangalore: The Powertrain Engineering Bangalore team is responsible for delivering end-to-end powertrain solutions across the value chain—from concept through validation to production. The department includes experts in engine systems, transmissions, axles, calibration, electronics, certification, and quality support. Position Summary: We are seeking a Senior Engineer – Engine Development, with strong domain expertise in base engine and combustion component development. You will take ownership of components such as the after-treatment system, fuel system, turbochargers, pipes, brackets, oil sumps, heat shields, and seals throughout all phases of a project—from concept design to production and post-launch support. You will act as the technical point of contact for all base engine and combustion hardware development activities and coordinate closely with internal stakeholders and suppliers to deliver high-quality, validated solutions. Key Responsibilities: Lead the design and development of base engine and combustion hardware components. Coordinate with in-house teams and suppliers to develop, validate, and release CAD models, drawings, and documentation within Volvo/UD systems. Develop and maintain technical documentation including installation requirements, technical regulations, and design standards. Ensure full QDCF (Quality, Delivery, Cost, Feature) alignment by engaging cross-functional teams (R&D, Purchasing, Manufacturing, Aftermarket, Quality, PRM). Define and execute verification and validation plans using simulation tools, test rigs, and vehicle-level testing. Support resolution of field quality issues and lead root cause analysis and corrective actions. Identify and drive cost optimization and localization initiatives for components. Collaborate with suppliers to define long-term technical strategies and roadmaps. Contribute to the creation of design and verification guidelines for platform development. Prepare and manage project budgets for new development and maintenance activities. Required Qualifications: Bachelor’s/Master’s degree in Mechanical Engineering or equivalent. 6–8 years of experience in engine component development (preferably in the commercial vehicle or automotive industry). Strong knowledge of overall powertrain systems and engine integration. Proficiency in CAD modeling using Pro/Engineer (Creo). Excellent communication skills in English—both written and verbal. Key Competencies & Attributes: Strong team player with a collaborative and proactive mindset. Passionate about automotive technology and innovation. Structured, analytical thinker with problem-solving orientation. Experience in leading cross-functional teams and driving design decisions. Ability to manage conflicts and influence stakeholders effectively. Self-starter with strong technical leadership and project management capabilities. Capable of managing multiple complex projects simultaneously. Skilled in communicating technical details to internal and external stakeholders including global suppliers and customers. Why Join UD Trucks? Work in a diverse, inclusive, and international environment. Opportunity to innovate and lead in a high-performance organization. Flexible, modern work culture with a focus on learning, balance, and growth. Be part of a purpose-driven company building solutions for smart logistics and sustainable transport.

Job Description: The BMS Operator is responsible for operating and maintaining the Building Management System (BMS) in a facility or building. They ensure the efficient operation of the BMS by monitoring, controlling, and troubleshooting various systems, including HVAC (Heating, Ventilation, and Air Conditioning), lighting, security, AAS / FMS, PA System along with other building automation systems. The BMS Operator plays a crucial role in maintaining occupant comfort, energy efficiency, and overall facility performance. Key Responsibilities: Monitor and Control: Operate the Building Management System to monitor and control various building systems, including HVAC, lighting, security, fire alarms, CCTV, access control and other related equipment. Troubleshooting: Identify and resolve issues with the BMS and associated systems by analyzing system logs, alarms, and other data. Perform diagnostics and troubleshoot malfunctions to ensure proper functioning. Maintenance: Perform routine maintenance tasks on the BMS and associated equipment, such as calibration, sensor testing, software updates, and equipment inspections, following manufacturer guidelines and maintenance schedules. Alarm Management: Respond to alarms and alerts generated by the BMS promptly. Investigate the cause of alarms and take appropriate actions to address the issues. Energy Management: Optimize the performance of building systems to achieve energy efficiency and cost savings. Make adjustments to system settings and schedules as needed. Data Analysis: Analyze data collected by the BMS, generate reports, and provide insights on system performance, energy consumption, and potential areas for improvement. Collaboration: Coordinate with facility management, maintenance staff, and external vendors for repair and maintenance activities. Collaborate with other departments to ensure seamless integration and operation of the BMS with other building systems. Documentation: Maintain accurate records of maintenance activities, system configurations, operational procedures, and other relevant documentation. Safety and Compliance: Follow safety protocols and ensure compliance with building codes, regulations, and industry standards.

Key Responsibilities: Respond to customer queries, complaints, and service requests via email within defined TAT & quality SLAs Investigate and resolve issues while adhering to regulatory and company guidelines Draft clear, professional, and empathetic responses aligned with brand tone Escalate unresolved or complex queries to relevant internal stakeholders Maintain detailed case logs, follow-up trackers, and closure documentation Identify recurring issues and flag them to supervisors for resolution Ensure full compliance with RBI, TRAI, or other relevant regulatory frameworks (as applicable) Support internal audit requests by providing email logs and response samples Participate in periodic quality audits, calibration sessions, and feedback reviews Key Requirements: Minimum 2 years of experience in email-based customer support in a regulated industry (FinTech, BFSI, Insurance, Telecom, etc.) Excellent written communication and comprehension skills Strong attention to detail, tone, and accuracy in responses Familiarity with CRM tools like Freshdesk, Zendesk, Salesforce, or in-house systems Understanding of compliance and data confidentiality protocols Ability to work independently and manage high ticket volumes with discipline Comfortable working in rotational shifts (if applicable)

Job Summary: We are looking for motivated and technically skilled ITI students/graduates with specialization in Electrical or Electronics to assist in installation, maintenance, troubleshooting, and repair of electrical systems and electronic devices in industrial or commercial settings. Key Responsibilities: For Electrical Students: ● Installation of electrical wiring, panels, switches, and distribution systems. ● Preventive and corrective maintenance of electrical systems and equipment. ● Reading and interpreting electrical circuit diagrams and technical drawings. ● Conducting routine checks on power supply, earthing, and circuit safety. ● Assisting in electrical testing using tools like multimeters, megger, etc. ● SupporƟng senior technicians in HT/LT line maintenance (if applicable). ● Ensuring compliance with electrical safety regulaƟons. For Electronics Students: ● Assembly, installation, and repair of electronic circuits and systems. ● Testing and calibration of sensors, controllers, and PCBs. ● Troubleshooting faults in industrial electronic devices like PLCs, SMPS, or control panels. ● Soldering, DE soldering, and basic electronic circuit modifications. Required Skills: ● Basic understanding of electrical/electronic components. ● Ability to read circuit diagrams and follow safety protocols. ●. Familiarity with tools like muleteers, testers, soldering kits, etc. ● Willingness to work in field/site condones or production environments. And Good teamwork and communication skills. MOB : 6366263951 / 7760122268 / 9243878059

Job Title: Medical Equipment Executive / Manager Location: Bangalore / Hyderabad Company: Portea Medical Experience: 3-4 Years Employment Type: Full-Time About the Company: Portea is India’s largest in-home-healthcare service provider company, is headquartered in Bengaluru and was founded in the year 2013. Portea leads the in-home-healthcare service with operations in 42 cities of India. It is involved in giving hospital - quality healthcare in the comfort of one’s home. Job Summary We are looking for a knowledgeable and proactive Medical Equipment Executive/Manager to manage the end-to-end operations of medical equipment, including inventory, procurement, maintenance, and logistics. The ideal candidate should have prior experience in medical equipment management and warehouse operations, and must be well-versed with the healthcare industry standards. Key Responsibilities: � � Manage inventory of medical equipment including beds, oxygen concentrators, monitors, etc. � � Coordinate procurement, delivery, installation, and maintenance of medical devices. � � Monitor equipment movement between warehouses and patients’ homes. � � Ensure timely servicing and calibration of equipment as per standards. � � Liaise with vendors for procurement and repair of equipment. � � Maintain documentation for audit, warranty, and compliance purposes. � � Collaborate with clinical and operations teams for smooth delivery of care services. � � Conduct periodic audits and maintain asset tracking systems. Requirements: ✅ Bachelor's Degree (Science/Engineering/Healthcare background preferred) ✅ Minimum 2 years of experience in medical equipment management ✅ Experience in warehouse/inventory operations ✅ Familiarity with DME (Durable Medical Equipment) and HME (Home Medical Equipment) ✅ Proficient in MS Excel, basic ERP tools, and equipment tracking systems ✅ Strong communication and coordination skills ✅ Ability to handle field operations and vendor negotiations ✅ Must be fluent in English (regional language a plus) Nice to Have ➕ Certification or knowledge of biomedical equipment ➕ Exposure to NABH/JCI standards ➕ Experience in home healthcare or hospital equipment logistics. Apply Now � � Send your CV to Arjith.jithu@porteamedical.com Join Portea Medical in delivering world-class home healthcare services across India!

Job Summary: The QC Lab Chemist is responsible for conducting routine testing and analysis of water and packaging materials to ensure all products meet BIS, FSSAI, and internal quality standards. The chemist ensures compliance with regulatory norms and supports continuous improvement in product quality. Key Responsibilities: Sampling & Analysis Collect samples of raw water, RO water, treated water, rinsed water, and packaged product from various plant locations as per sampling plan. Perform physical, chemical, and microbiological analysis as per BIS 14543, FSSAI, and company standards. Test parameters include pH, TDS, Turbidity, Conductivity, Hardness, Alkalinity, Chlorides, Sulphates, Nitrates, Fluorides, Metals, Pesticides, and Microbial load (TPC, Yeast & Mold, Coliform, etc). Documentation Maintain daily laboratory records, test reports, calibration logs, and sample registers. Ensure traceability of all records for audits and compliance. Process Control Monitor online and offline water parameters, provide feedback to production for corrective actions. Conduct periodic line audits (rinsing, filling, capping, packaging). Calibration & Maintenance Calibrate and maintain all laboratory instruments (pH meter, TDS meter, Turbidity meter, Spectrophotometer, Incubator, Autoclave, etc). Ensure timely AMC and troubleshooting of laboratory equipment. Raw & Packaging Material Testing Test preforms, caps, bottles, labels, and packing materials for compliance to standards. Perform sensory and migration tests if required. Regulatory & Compliance Prepare and maintain all documentation required for BIS, FSSAI, and other regulatory inspections. Participate in internal and external audits. Reporting & Communication Report non-conformities and deviations immediately to the QC Manager. Prepare daily/weekly QC reports for management review. Hygiene & Safety Follow Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and plant safety norms. Ensure proper disposal of laboratory waste. Continuous Improvement Suggest and implement improvements in lab processes and product quality. Participate in trainings and skill-upgradation programs. Key Skills & Competencies: Knowledge of BIS 14543, FSSAI, and ISO standards for packaged drinking water Sound understanding of water chemistry and microbiology Hands-on with laboratory instruments & analytical methods Meticulous documentation and record-keeping Analytical thinking, troubleshooting skills, and attention to detail Good communication and teamwork Educational Qualification: B.Sc./M.Sc. in Chemistry, Microbiology, or equivalent (preferably with food/water testing experience) Experience: 0–3 years in QC lab, preferably in bottled water/beverage/food industry Work Environment: Laboratory & plant floor, regular interaction with production and QA teams, 3-shift rotation may be required.

You will be joining the Bio Analytical Department at PTC - MORAIYA as a Probationer-R&D Executive. With 2-3 years of experience and an educational background in M.Sc or B. Pharma, you will be responsible for various tasks including sample preparation, method development, method validation, and subject sample analysis. Your role will involve operating, calibrating, and maintaining equipment while keeping track of the equipment log. You will also be required to review bio analytical data, prepare and review SOPs, protocols, plans, and reports. Additionally, you will play a vital role in executing and maintaining GLP, GCP, Safety, and Quality systems within the department. Maintaining displays such as labels, SOPs, charts, etc., will also be part of your responsibilities. If you are an employee from the QC department looking for a new opportunity, you are encouraged to apply and contribute to the dynamic environment at PTC - MORAIYA.,

The job involves being a team member of the Engineering Maintenance & Reliability Team within the Active Pharmaceutical Ingredient department of the Manufacturing division. Your primary responsibility is to execute maintenance activities in the plant, ensuring minimal breakdowns and maximum efficiency while adhering to safety and GMP standards. You will support the Senior Engineer in planning, scheduling, and executing maintenance activities to ensure plant and equipment availability, capacity, integrity, and reliability as per company policies and procedures. Additionally, you will be responsible for maintenance tasks in the Manufacturing, Packing, and utility areas as assigned by the Senior Engineer. In this role, you will be accountable for executing shift maintenance activities, including managing available resources to achieve maintenance targets, analyzing breakdowns, diagnosing faults, and supervising equipment repairs. You will also be involved in executing a comprehensive maintenance plan, preventive maintenance, calibration, and condition monitoring activities, ensuring adherence to standards and documenting all related activities. Handling breakdown maintenance to prevent recurrence, operating equipment efficiently as per SOP, implementing new technologies to improve machine performance, managing spares, adhering to EHS compliance, and ensuring cGMP compliance are also key aspects of the role. Moreover, you will be required to provide suggestions for process optimization, continuous improvements, and self-development in mechanical engineering and leadership aspects. Major challenges include adherence to budget constraints, cost vs. performance trade-offs, aging assets leading to escalating costs, and ensuring personnel and service providers" capability and competence. You will interact internally with Central Engineering, EHS, Site and Unit heads, and externally with OEMs, maintenance contractors, industry bodies, and statutory bodies. The role requires a BE/BTech in Mechanical Engineering with 2-5 years of experience in manufacturing, maintenance, and projects. You should have a deep understanding of manufacturing processes, organizational skills, technical knowledge of Pharma/API machinery, experience in project execution, knowledge of GMP and regulatory requirements, and leadership skills in mechanical engineering activities.,

You will be responsible for issuing and receipting raw materials required for manufacturing Peptide Products. This includes charging batches and executing all activities related to the process in accordance with Batch Manufacturing Records (BMR) and documented procedures. Your role will involve the manufacturing of peptide products as per BMR and written procedures in the Peptide plant. Additionally, you will be in charge of operations, calibration, cleaning, and maintenance of process equipment. It will be essential to accurately record the usage logs of the equipment. Monitoring the process and cleaning turn around time (TR) during the synthesis and purification of Peptide products will also be part of your duties. You will play a crucial role in monitoring process parameters and yield to ensure efficiency. Your focus will be on reducing solvent usage, minimizing instrument downtime, and decreasing batch failures, hold-ups, and waste generation.,

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Senior Officer - Quality Assurance Date: Jul 16, 2025 Location: Paonta Sahib - Quality Assurance Company: Sun Pharmaceutical Industries Ltd Job Responsibilities: Monitoring: In-process monitoring of Manufacturing & Packing activities of Tablets and Capsules. Ensure compliance to cGMP Regulations, established SOPs, FO/MI and PO/PI and for all operational activities, area and equipment’s. Perform QA review of executed batch production records and ensure the submission of Batch production record in the document cell. Calibration & maintaining documentation of In-process Quality Assurance (IPQA) instruments. Data back-up activities for IPQA instruments as per defined SOP frequency. Monitor the environmental conditions mentioned in the batch production record and SOP. Certification of batch production records for compliance and stage-wise compliance. Reporting any GMP related discrepancies, non-conformances and deviations to superiors immediately. Collection and entry of data for APR preparation. Imparting training to subordinates. Line Clearance: Ensure physically that the area and equipment to be used for manufacturing and packaging of next product/batch are free from any material/remnants of previous product. Ensure to prevent mix up and cross contamination. Check for proper environmental conditions with respect to temperature, Relative humidity, differential pressure etc. Ensure that the Batch Production record is completed up to the previous stage. Verify the material with respect to the container labels and quantity from the batch production record. In-Process Checks: Ensure the calibration of instruments for in-process checks. In-process checks as per the approved manufacturing and packaging instructions. Enclose all the printouts generated during in-process checks along with the batch production record. All printouts shall be duly signed after checking. Inform the production manager, supervisor and quality assurance manager about the in-process failure observed during in-process checks. To record all the observations in the Batch Production Record. Inspection: Inspection of the Bulk Tablets/Capsules as per respective SOP. Inspection of the Finished Goods inspection as per SOP and clearance of Transfer Ticket by ensuring the quantity and batch details. Sampling: Ensure for usage of appropriate sampling tool for sampling. Ensure sampling device cleaning prior to the sampling. Sampling procedure to be followed as per SOP. Ensure sampling of in-process finished product, process validation, cleaning validation, control samples, EU Lab testing samples & stability samples as per SOP. Approval: Approval of coding pattern on immediate pack and secondary pack to be verified as per the approved packaging instructions / written procedures. Apply Now » Apply Now Start applying with LinkedIn Please wait...

Key Responsibilities: • Quality Management System: o Develop, implement, and maintain QMS in accordance with ISO 9001, ASME, API, and client-specific standards. o Ensure compliance with project specifications and applicable codes and standards. • Inspection and Testing: o Oversee all stages of fabrication inspection, including material inspection, welding, NDT (RT, UT, PT, MT), dimensional checks, and final product testing. o Approve and review inspection test plans (ITPs), method statements, and quality control procedures. • Documentation and Reporting: o Ensure proper documentation of quality records, inspection reports, weld maps, material traceability, and calibration records. o Prepare and submit quality dossiers as per project/client requirements. • Team Management: o Lead and train a team of QC inspectors and NDT personnel. o Conduct performance evaluations and technical mentoring of the QA/QC team. • Client Coordination: o Liaise with client representatives and third-party inspectors (TPI) for quality audits and inspections. o Address NCRs (Non-Conformance Reports), CARs (Corrective Action Reports), and ensure timely closure. • Audit and Compliance: o Plan and execute internal quality audits. o Ensure compliance with HSE and quality standards throughout the fabrication processes. • Continuous Improvement: o Implement root cause analysis (RCA) and corrective/preventive actions (CAPA). o Drive quality improvement initiatives and defect reduction in fabrication processes. Key Skills & Competencies: • Strong knowledge of welding processes, fabrication techniques, NDT, and relevant oil & gas codes/standards. • Proficiency in ISO 9001, ASME Sec VIII / B31.3, API 650/1104. • Leadership and team management skills. • Analytical thinking and problem-solving. • Communication and client handling skills. Qualifications & Experience: • Education: Bachelor’s degree in Mechanical / Metallurgical / Production Engineering or related field. • Experience: 8–12 years in quality management in an oil & gas fabrication/pressure vessel/piping environment.

Job Description Summary Responsible for driving improvements in product quality related to rejections from Customers & Internal yields. Responsible for quality of output from the manufacturing line - Track and close quality issues in the manufacturing line & returns from customer. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job Description Roles & Responsibilities. Responsible for driving improvements in product quality related to rejections from Customers & Internal yields. Responsible for quality of output from the manufacturing line - Track and close quality issues in the manufacturing line / returns from customer. Interface with Supplier Quality on supplier related defects. work with suppliers on RMA/RTV, drive Root cause analysis against part quality Issues. Ensure compliance through Validation and Verification (V&V). Compliance to quality management systems & EHS in all activities. Identify and report any quality or compliance concerns and take immediate corrective action as required. Equipment Calibration Activities, Coordination with calibration agencies and the periodic calibration complete. Creation of Standard Operating Procedures, release & training to Production line operators. Root Cause Analysis against Quality Issue – CAPA Process. Define Incoming Acceptance Plan for Parts. Engagement with Customers to drive product quality improvement actions. Work on Lean Initiatives, Kaizen Implementation etc.… Attend Line Breakdown, drive fixes to minimize the production down time. Work with equipment manufacturers in establishing preventive controls or maintenance. Qualifications Bachelor’s degree in mechanical engineering/industrial engineering. Demonstrated ability to lead and develop teams. Demonstrated ability to identify and implement Best Practices and deal with high levels of ambiguity. Desired Characteristics Strong oral and written communication skills. Inclusion and Diversity GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support. Additional Information Relocation Assistance Provided: No

Job Description Summary Responsible for driving improvements in product quality related to rejections from Customers & Internal yields. Responsible for quality of output from the manufacturing line - Track and close quality issues in the manufacturing line & returns from customer. GE HealthCare is a leading global medical technology and digital solutions innovator. Our purpose is to create a world where healthcare has no limits. Unlock your ambition, turn ideas into world-changing realities, and join an organization where every voice makes a difference, and every difference builds a healthier world. Job Description Roles & Responsibilities. Responsible for driving improvements in product quality related to rejections from Customers & Internal yields. Responsible for quality of output from the manufacturing line - Track and close quality issues in the manufacturing line / returns from customer. Interface with Supplier Quality on supplier related defects. work with suppliers on RMA/RTV, drive Root cause analysis against part quality Issues. Ensure compliance through Validation and Verification (V&V). Compliance to quality management systems & EHS in all activities. Identify and report any quality or compliance concerns and take immediate corrective action as required. Equipment Calibration Activities, Coordination with calibration agencies and the periodic calibration complete. Creation of Standard Operating Procedures, release & training to Production line operators. Root Cause Analysis against Quality Issue – CAPA Process. Define Incoming Acceptance Plan for Parts. Engagement with Customers to drive product quality improvement actions. Work on Lean Initiatives, Kaizen Implementation etc.… Attend Line Breakdown, drive fixes to minimize the production down time. Work with equipment manufacturers in establishing preventive controls or maintenance. Qualifications Bachelor’s degree in mechanical engineering/industrial engineering. Demonstrated ability to lead and develop teams. Demonstrated ability to identify and implement Best Practices and deal with high levels of ambiguity. Desired Characteristics Excellent oral and written communication skills. Inclusion and Diversity GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support. Additional Information Relocation Assistance Provided: No

Job Title: Electrical and Instrumentation Engineer/Mechanical Maintenance Engineer Department: Engineering / Maintenance Reports To: Maintenance Manager / Plant Head Qualification and Experience: • Diploma / B.E. / B.Tech in Instrumentation or Electrical Engineering. • 3–7 years of experience in a chemical/process industry with multi-disciplinary maintenance exposure. • Working knowledge of chemical plant safety standards and statutory compliance is preferred. Key Responsibilities: Instrumentation Responsibilities: • Install, calibrate, troubleshoot, and maintain field instruments (pressure, flow, temperature, level, analytical). • Ensure proper functioning and upkeep of control systems. • Schedule and conduct preventive maintenance for all instrumentation and control systems. • Maintain calibration records and ensure statutory compliance (e.g., ISO, IEC standards). • Work with process teams to improve instrumentation-based process control and automation. Electrical Responsibilities: • Troubleshoot and maintain LT/HT panels, transformers, motors, MCCs, VFDs, and power distribution systems. • Conduct regular inspection and preventive maintenance of electrical infrastructure. • Ensure compliance with safety standards related to electrical systems in hazardous areas (ATEX/Flameproof equipment). • Liaise with utility services (DG sets, UPS, lighting systems, etc.) for operational reliability. Mechanical Maintenance Responsibilities: • Support/manage mechanical maintenance of pumps, compressors, agitators, valves, pipelines, heat exchangers, and utility systems. • Management of mechanical overhauls, shutdowns, and emergency repairs. • Monitor equipment performance and conduct root cause analysis for failures. Key Skills and Competencies: • Good technical knowledge of instrumentation, electrical, and mechanical systems. • Experience in process industry automation and control. • Hands-on experience with calibration tools, test equipment, and safety instruments. • Familiarity with electrical safety codes, hazardous area classification, and mechanical troubleshooting. • Knowledge of ERP software for maintenance tracking. • Analytical, proactive, and problem-solving mindset. • Strong communication and team coordination skills. Work Environment: • Plant-based role with exposure to chemical processing units. • May involve shift work, call-outs during breakdowns, and participation in shutdown activities.

About Newtronic Newtronic Lifecare has established itself as one of the leading brands in the space of Laboratory Equipment. https://newtronic.in/news-and-media/# Designation - AC Technician /Service Engineer / Refrigeration Engineer Education - 10th and above / ITI/ Diploma/ BE Job Location - Ahmedabad/Vadodara/ Vapi/Daman/ Ankaleshwar No of positions - 2 each location Field work – Yes Training will be provided - Yes ,On the job training will be provided Remuneration - Salary + Travelling allowance + incentive +PF+ESIC+Bonus (as applicable) Job summary You will visit various organization indian and international MNCs for Installation, maintenance, repair , and calibration for instruments (Stability chambers, Walk in chambers , Oven, Incubators etc ) candidate who are working in AC repairs/ Cold storage equipment / calibration engineers /maintenance engineers are more aligned with this profile JOB ROLES & RESPONSIBILITY : 1) Installation, Repair, Testing and Maintenance of various equipment at clients end. 2) Training and demonstrating the equipment to new users, if required. 3) Servicing, calibration, validation of instruments. 4) Providing after-sales service of machines at customer end. 5) Troubleshooting of various equipment. 6) Co-ordinate with team & provide the inputs regarding the call. Please share your cv at hr@newtronic.in with the following details · Name · Contact number · Education · Preferred work location · Current organization and designation · Current location · Current in hand salary · Expected in hand salary · Notice period Job Type: Full-time Pay: ₹15,000.00 - ₹27,000.00 per month Benefits: Commuter assistance Provident Fund Work Location: In person

Job Title: QC Chemist Department: Quality Control / Laboratory Experience: 0-2 Years Location: Gujarat Reports To: QC Manager / Senior Chemist Qualifications: • Bachelor’s degree in chemistry, Pharmaceutical Sciences, or a related field. • 0–2 years of experience in a pharmaceutical, chemical, or food testing laboratory (freshers may be considered). • Basic knowledge of chemical analytical techniques and laboratory safety. • Proficiency in Microsoft Office (Excel, Word). • Good communication, organizational, and documentation skills. Job Summary: The QC Chemist is responsible for performing routine laboratory testing and analysis of raw materials, in-process samples, and finished products to ensure compliance with established specifications and regulatory requirements. The role supports quality assurance through accurate documentation, data analysis, and adherence to Good Laboratory Practices (GLP) and standard operating procedures (SOPs). Key Responsibilities: • Conduct chemical and physical analysis on raw materials, intermediates, and finished goods. • Perform routine and non-routine tests as per SOPs and analytical methods. • Operate and calibrate laboratory instruments such as GC, pH meters, and balances. • Record and interpret test results accurately and report any deviations or non-conformities to supervisors. • Maintain lab notebooks and documentation in compliance to standards. • Support stability studies and sample management. • Assist in method validation and verification activities. • Ensure the cleanliness, calibration, and maintenance of laboratory equipment. • Adhere to safety protocols and maintain a clean and organized laboratory environment. • Participate in internal and external audits as required. • Collaborate with production and QA teams to resolve quality issues. Preferred Skills: • Hands-on experience with analytical instruments (e.g., GC,). • Exposure of SAP or ERP. • Ability to work independently as well as part of a team. • Strong attention to detail and accuracy.

Job Responsibilities Monitoring : In-process monitoring of Manufacturing & Packing activities of Tablets and Capsules. Ensure compliance to cGMP Regulations, established SOPs, FO/MI and PO/PI and for all operational activities, area and equipment’s. Perform QA review of executed batch production records and ensure the submission of Batch production record in the document cell. Calibration & maintaining documentation of In-process Quality Assurance (IPQA) instruments. Data back-up activities for IPQA instruments as per defined SOP frequency. Monitor the environmental conditions mentioned in the batch production record and SOP. Certification of batch production records for compliance and stage-wise compliance. Reporting any GMP related discrepancies, non-conformances and deviations to superiors immediately. Collection and entry of data for APR preparation. Imparting training to subordinates. Line Clearance : Ensure physically that the area and equipment to be used for manufacturing and packaging of next product/batch are free from any material/remnants of previous product. Ensure to prevent mix up and cross contamination. Check for proper environmental conditions with respect to temperature, Relative humidity, differential pressure etc. Ensure that the Batch Production record is completed up to the previous stage. Verify the material with respect to the container labels and quantity from the batch production record. In-Process Checks : Ensure the calibration of instruments for in-process checks. In-process checks as per the approved manufacturing and packaging instructions. Enclose all the printouts generated during in-process checks along with the batch production record. All printouts shall be duly signed after checking. Inform the production manager, supervisor and quality assurance manager about the in-process failure observed during in-process checks. To record all the observations in the Batch Production Record. Inspection: Inspection of the Bulk Tablets/Capsules as per respective SOP. Inspection of the Finished Goods inspection as per SOP and clearance of Transfer Ticket by ensuring the quantity and batch details. Sampling: Ensure for usage of appropriate sampling tool for sampling. Ensure sampling device cleaning prior to the sampling. Sampling procedure to be followed as per SOP. Ensure sampling of in-process finished product, process validation, cleaning validation, control samples, EU Lab testing samples & stability samples as per SOP. Approval: Approval of coding pattern on immediate pack and secondary pack to be verified as per the approved packaging instructions / written procedures.

Your challenges Attending Pipettes Maintenance, Repair Calibration of pipettes as per ISO 8655 Knowledge about ISO 17025 standards Installation of Eppendorf general instruments. Attending Breakdown Service of standard & specialty instruments Attending Instruments Maintenance of standard & specialty equipment’s Sending quotations to customers for required spares Achieving the Service business target Achieving AD Goals Service revenue Generation including payment collection Revenue management for the assigned territory Complaint Management for the assigned territory Customer Communication Sending Service/AMC Proposals Customer Presentations Working with the sales & service manager of the Branch Updating the market feedback to the management Daily CRM update (E365). Your expertise Minimum 2 to 3 year’s industry related Calibration experience. Key understanding to handle customer complaints and workflows. Excellent verbal and written communication skills. Professional experience in MS office tools is desired. Bachelor's degree in B.Tech / Diploma (ECE/ EEE or equivalent). Your benefits at Eppendorf We truly appreciate our employees and their performance We offer a wide range of learning and development opportunities to allow you to deepen your technical knowledge and for continuous growth By working with us, you will make a meaningful contribution to improving human living conditions Attractive salary, employee benefits and performance bonus. Eppendorf is an equal opportunity employer. We offer all qualified employees and applicants identical chances.

Location: Hyderabad, TG, IN Areas of Work: Supply Chain Job Id: 13338 External Job Description Role Description Job Purpose To ensure that inspection and all related activities are carried out as per the defined quality system and only conforming product batches are released, in quick time, for packing. Primary Responsibilities Business Responsibility Areas (Please detail out at least 8-10 responsibility areas) Key Performance Indicators Daily Activities Getting the details about status of different batches in various Pug mills, Mixers, reactors, TSDs etc from the preceding shift Officer-Level I. Making a list of approved, pending batches, and obtaining any special instructions or communication regarding batches, processes, practices etc in the previous shift. Ensuring implementation of 5S activities on the shopfloor and QA lab. Ensuring the regular updation of various ledgers and log books regarding the parameters checked for batches and other tests done. Undertaking calibration of various instruments like color computer etc for future usage. Inspecting various finished products and intermediates as per the specifications and test methods laid out in the master files. Analyzing batch cards of finished products intermediates for observed deviations in process controls availability of data for future analysis etc. Coordinating with production in case of deviations w.r.t completion of batches, recording details of the same and ensuring that these do not recur in subsequent batches. Ensuring periodic updation of various ledgers, files as per the laid down procedures in accordance with ISO requirements. Looking after the smooth operating and maintenance of various instruments like colour computer, penetrometer, viscometer, gyroshaker etc. Making daily rounds to the shopfloor and processing floor to ensure that the activities are carried down as per the laid down procedures/systems. Communicating with production department regarding status of various batches, approvals, problems related to batches etc. Weekly/Monthly/Ad hoc Activities Getting the weekly/ monthly plan from the Planning department and checking for the availability of specifications, test methods, Master samples, and Standard shade panels. In case of non-availability of the above, informing Planning cell immediately and taking steps to procure the same. Analysing customer complaints thoroughly as per the system guidelines and handling customer queries. Ensuring that feedback for customer complaints goes within 48 hours for product complaints and within 24hrs for packing complaints. Conducting of various products cum process audits, packing audits, batching audits etc. Conducting Other Tests as per the required frequency. Ensuring that master samples are generated before one month of the expiry period. Ensuring that standard shade panels are procured from technical function one month before the expiry period. For new designs, ensuring that first three batches are subjected to other tests and sending the samples to Technical Function. Communicating the results to respective persons. Providing all the necessary data required for monthly report preparation. Ensuring that stability studies and exposure studies are conducted as per the guidelines and informing the technical function about the deviations. Providing the necessary support for analysis of deviant batches. Referring the matter to Technical function in the following cases:

Your challenges Attending Pipettes Maintenance, Repair Calibration of pipettes as per ISO 8655 Knowledge about ISO 17025 standards Installation of Eppendorf general instruments. Attending Breakdown Service of standard & specialty instruments Attending Instruments Maintenance of standard & specialty equipment’s Sending quotations to customers for required spares Achieving the Service business target Achieving AD Goals Service revenue Generation including payment collection Revenue management for the assigned territory Complaint Management for the assigned territory Customer Communication Sending Service/AMC Proposals Customer Presentations Working with the sales & service manager of the Branch Updating the market feedback to the management Daily CRM update (E365). Your expertise Minimum 2 to 3 year’s industry related Calibration experience. Key understanding to handle customer complaints and workflows. Excellent verbal and written communication skills. Professional experience in MS office tools is desired. Bachelor's degree in B.Tech / Diploma (ECE/ EEE or equivalent). Your benefits at Eppendorf We truly appreciate our employees and their performance We offer a wide range of learning and development opportunities to allow you to deepen your technical knowledge and for continuous growth By working with us, you will make a meaningful contribution to improving human living conditions Attractive salary, employee benefits and performance bonus. Eppendorf is an equal opportunity employer. We offer all qualified employees and applicants identical chances.

Your challenges Attending Pipettes Maintenance, Repair Calibration of pipettes as per ISO 8655 Knowledge about ISO 17025 standards Installation of Eppendorf general instruments. Attending Breakdown Service of standard & specialty instruments Attending Instruments Maintenance of standard & specialty equipment’s. Sending quotations to customers for required spares Achieving the Service business target Achieving AD Goals Service revenue Generation including payment collection Revenue management for the assigned territory Complaint Management for the assigned territory Customer Communication Sending Service/AMC Proposals Customer Presentations Working with the sales & service manager of the Branch Updating the market feedback to the management Daily CRM update (E365). Your expertise Minimum 2 to 3 year’s industry related Calibration experience. Key understanding to handle customer complaints and workflows. Excellent verbal and written communication skills. Professional experience in MS office tools is desired. Bachelor's degree in B.Tech / Diploma (ECE/ EEE or equivalent). Your benefits at Eppendorf We truly appreciate our employees and their performance We offer a wide range of learning and development opportunities to allow you to deepen your technical knowledge and for continuous growth By working with us, you will make a meaningful contribution to improving human living conditions Attractive salary, employee benefits and performance bonus. Eppendorf is an equal opportunity employer. We offer all qualified employees and applicants identical chances.

Description At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment. Brief Job Overview This is a hands-on, non-supervisory professional position that supports the important work of USP’s Quality Assurance Activities. The Quality systems Associate is the expert in management of the tool of Quality Management System (MasterControl) including all quality documentation and training with respect to business objectives, provides guidance regarding Document workflow, proof-reading, and accuracy of documents. All Document Control functions must be compliant with applicable ISO Requirements and industry best practices. This position is responsible for managing user accounts, organizing, maintaining, and updating all controlled documents and ensuring training is assigned and executed in a timely manner. The Quality System Associate trains all levels of users in QMS tool and collaborates with all departments to maintain a compliant document management/training system and meet business needs. This position works independently, with minimal supervision, to accomplish daily tasks by efficiently and effectively utilizing the Company’s QMS tool. The Quality System Associate will drive continuous improvement within the system and create/report metrics regarding document status, priority, change management, training completion, and issue management. This position is also leading/supporting workflow development by utilizing the QMS tool to enhance the quality system and improve the process efficiency. This position is also responsible for performing documentation review/release of lab projects, batch records, and equipment qualification. This position will also support the Global Supplier Quality Management Program. How will YOU create impact here at USP? As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments. The Quality System Associate Has The Following Responsibilities Document Control activities (at least 50%) : The Quality System Associate is the QMS tool SME, responsible for managing all aspects of the document management processes, as well as training. Review, edit and format documents, approves document change requests, release approved documents and manages document workflows, including new document, document revision and document obsoletion. Review of Standard Operating Procedures (SOPs) and other documentation, including work instructions, to ensure accuracy and compliance. Manages QMS tool users including activating and deactivating users, assigning appropriate roles per business needs, maintaining/assigning job codes, creation of new hire training infocard and assigning new hire mandatory trainings. Creation of training courses, sessions, and support trainers on updating of class roll. Serves as the MasterControl System Administrator/SME and provides training/guidance to all levels of system end-users regarding processes of document management and training, and QMS tool(s). Resolve issues during trouble-shooting requests. Designs/develops/maintains training courses, instructional materials, and training records for the various levels of system users. Improves and streamlines processes of document management, training, issue management and user management. Develop, improve workflows in the QMS tool to enhance the efficiency of processes. Develops/maintains/reports metrics periodically regarding document management, training, issue management, user management. Identifies negative data trends and escalates immediately as necessary. Tracks/follows up key activities, e.g., miss assigned document review, overdue triennial review, pending/ overdue training tasks, etc. Prioritizes activities by compliance and business requirements Communicates effectively with cross-functional and external stakeholders Coordinate with USP Global Site SME’s and MasterControl Customer Support Team to resolve any application issues/glitches for a quick resolution. Assumes other responsibilities as assigned by Adhere and promote USP core values & DEIB (Diversity, Equity, Inclusion and Belonging) within the department and throughout the organization. Other QA activities (not more than 50%): Review/approve the following QA activities Equipment IQ/OQ/PQ documents Equipment calibration documents Quality-related issues, complaints, deviations, and investigations with appropriate corrective/preventive actions. Review/approval of technical and analytical documents of moderate to high complexity for Reference Standards and/or Analytical Reference Materials (ARM) Batch Records Lab data projects Support the Supplier Quality Management program by conducting supplier evaluations, audits, and supplier performance/metrics. Other assignments as required Who is USP Looking For? The Successful Candidate Will Have a Demonstrated Understanding Of Our Mission, Commitment To Excellence Through Inclusive And Equitable Behaviors And Practices, Ability To Quickly Build Credibility With Stakeholders, Along With The Following Competencies And Experience Master's degree in Science(M.Sc Chemistry/M.Pharm) with 5-7 years relevant experience in a pharmaceutical industry preferably working in QA Document Control function/Analytical Reviewer role/Quality Control in API or formulations industry. 1-2 years of document control experience in a pharmaceutical, biotech, or other regulated industry Hands-on experience in laboratory, handling of analytical equipment, qualification of analytical equipment, calibration, metrology and other laboratory activities is preferable. Strong computer working knowledge of MS Word, PowerPoint, Excel etc., Demonstrated initiative and ability to work independently while handling multiple tasks, as well as part of a team in a dynamic environment. Must have strong technical writing and proofreading skills, as well as exemplary attention to detail due to demand for accuracy in controlled documents. Ability to clearly communicate, both verbal and written and interface with customers and third parties, and diverse audiences at all levels of the organization. Strong focus on internal and external customer service Additional Desired Preferences Experience in managing QMS tool(s) as an Administrator Understanding of GMP, GLP, and ISO regulations and the integration of the regulations into working systems in the laboratory. Excellent written and verbal communication skills including well-developed interpersonal skills used to influence the behavior of others. Any diploma in computers or relevant QA/QC/QMS certifications on document management systems and good documentation practices is an added advantage. Outstanding organizational skills and ability to work systematically and cross-functionally, driving assigned tasks to completion. Strong knowledge of MS office tools such as Word, Excel, and power point presentation. Supervisory Responsibilities None Benefits USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected. Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP Job Category Quality Assurance Job Type Full-Time