3118 Calibration Jobs - Page 11

Seeking On-site Service Engineers to handle troubleshooting, installation, and servicing of AIR GAUGES AND MECHANICAL INSTRUMENTS. Must have strong technical understanding and hands-on skills in precision instruments. contact: 9840682273 (Vetrisree) Required Candidate profile Diploma/BE Mechanical Engineer with knowledge of air gauges & mechanical instruments. Skilled in troubleshooting, servicing & client handling. Freshers or 1–2 yrs experience preferred.

Minimum 5+ years of relevant experience in SAP PP/ QM and well-versed in S4 HANA/ ECC with good analytical skills along with domain experience in manufacturing industry Experience in Implementation and Support Projects. In-depth knowledge in the below areas: Master Data - Bill of materials, Work centers/ Resources, Routings/ Recipe, Production versions, Inspection Plan, Master inspection, Characteristics, Catalogues and Code groups Material Requirement Planning - Configuration and Integration with, Procurement, Sales and Distribution, New strategy definition Production Order Execution - Order confirmation, Goods issue, Goods receipt and Back flushing Quality Management - Quality in Procurement, Quality in Production, In process inspection, Calibration and Quality in Sales Should have experience in writing Functional Specification, co-ordination with ABAP team, testing of new functionalities. Must have experience in SAP PP-QM integration with third party tool A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to get to the heart of customer issues, diagnose problem areas, design innovative solutions and facilitate deployment resulting in client delight. You will develop a proposal by owning parts of the proposal document and by giving inputs in solution design based on areas of expertise. You will plan the activities of configuration, configure the product as per the design, conduct conference room pilots and will assist in resolving any queries related to requirements and solution design You will conduct solution/product demonstrations, POC/Proof of Technology workshops and prepare effort estimates which suit the customer budgetary requirements and are in line with organization’s financial guidelines Actively lead small projects and contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Ability to develop value-creating strategies and models that enable clients to innovate, drive growth and increase their business profitability Good knowledge on software configuration management systems Awareness of latest technologies and Industry trends Logical thinking and problem solving skills along with an ability to collaborate Understanding of the financial processes for various types of projects and the various pricing models available Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Client Interfacing skills Project and Team management Infosys Ltd. is committed to ensuring you have the best experience throughout your journey with us. We currently have open positions in a number of locations across India - Bangalore, Pune, Hyderabad, Chennai, Chandigarh, Trivandrum, Indore, Nagpur, Mangalore, Noida, Bhubaneswar, Kolkata, Coimbatore, Mumbai, Jaipur, Vizag, Mysore, Hubli. While we work in accordance with business requirements, we shall strive to offer you the location of your choice, where possible.

Job Overview: We are seeking a seasoned and dynamic professional helping organization to establish better Quality systems and compete with quality performance AGM/DGM - Quality to lead our Quality Team in the Aerospace Manufacturing industry. The ideal candidate will have deep knowledge of AS9100 Standards, QA, Calibration, Metrology, Metallurgy, Supplier Quality and Well versed with Quality Tools, Techniques, Standards & OEM requirements Responsibilities Rich experience in AS9100, AS9102 standards and NADCAP requirements, implementation, as a Auditor/Quality professional and Certified for self release system per SAE 13001 Certified DQR. Well versed with Quality Tools/Techniques, Standards & OEM requirements. Expertise to Lead and build the team, Innovative and positive towards challenges. Effective usage and implementation QMS and core tools like, PPAP, SPC, MSA, 8D Methodologies, QC tools, GD&T and QUALITY CLINIC system etc. Expert in FAI-related activities, monitoring all quality activities of respective assigned projects Interaction with Customers, Training on customer-specific requirements to the QA Project Leads Analysis of Customer Complaints and internal rejections Monitoring of corrective action implementation and validating the results Knowledge in GD&T, CMM programming Expert in Quality planning for gauge instruments and inspection methods Good knowledge of the Raw Material Approval process Educational Qualifications Diploma / B.E in Mechanical / Aeronautical Experience Required: 20 to 30 Years Experience working with senior leadership and managing Quality Tools/Techniques, Standards & OEM requirements. Industry Type: Aerospace / Aviation Industry

Supervise and schedule all Final Inspection and Lab and testing activities inorder to achieve maximum effectiveness and efficiency. Design and prepare procedures to support Quality operations. Maintain effective operations selection, development, training andmotivation of personnel. Coordinate and conduct customer and accreditation audits of the Qualityoperations. Ensure that Gage/Tools/Dies calibration system is effective and complieswith company operating procedures. Ensure that testing operations are performed within guidelines of customerand accreditation requirements. Maintain a record and documentation system for testing and calibration thatcomplies with both internal and customer accreditation requirements. Maintenance of all necessary requirements of the ISO9000/API approvedsystem Acts as a key contact with customers, suppliers, auditors, manufacturing, andsupport resources to ensure the execution of corrective actions and that theQuality Assurance systems are meeting objectives and continuouslyimproving. Management of external quality and special process audits assuring a highlevel of performance as exhibited by audit results. This includes preparationof necessary documentation to support an international customer base Enhance and implement effective measurement on quality performance withspecific focus on customer complaints and product consistency Job Type: Full-time Pay: ₹700,000.00 - ₹800,000.00 per year Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Job Title : Machine Operator Location : Ernakulam, Kerala Experience : 1–2 Years Industry : Manufacturing / Engineering / Industrial Employment Type : Full-time Job Summary : We are seeking a skilled and motivated Machine Operator with 1–2 years of hands-on experience in operating, maintaining, and troubleshooting production machinery. The ideal candidate will be responsible for ensuring machine functionality, quality output, and safety in our Ernakulam-based manufacturing facility. Key Responsibilities : Operate and monitor machines (e.g., CNC, lathe, milling, printing, or packaging) efficiently Perform basic setup, calibration, and routine maintenance of machines Inspect finished products for quality assurance and report deviations Adhere to standard operating procedures (SOPs) and safety guidelines Maintain cleanliness and safety of the work area Record production logs and report daily outputs Required Qualifications : ITI / Diploma in Mechanical, Production, Tool & Die, or related field 1–2 years of machine operation experience in a factory or plant environment Ability to read technical drawings and basic measurements Basic knowledge of machine safety protocols Preferred Skills : Familiarity with CNC or lathe machine operation Problem-solving ability and attention to detail Willingness to work in shifts (rotational, if required) Job Types: Full-time, Permanent Pay: ₹8,086.00 - ₹18,000.00 per month Benefits: Food provided Schedule: Day shift Supplemental Pay: Performance bonus Experience: Machine operator: 1 year (Required) Work Location: In person Application Deadline: 28/06/2025

Dialysis Procedure Management : Set up and operate hemodialysis machines and related equipment. Prepare dialysis solutions and ensure proper functioning of the machine before each session. Initiate, monitor, and terminate dialysis sessions for patients according to prescribed protocols. Patient Care & Monitoring : Monitor patients’ vital signs before, during, and after treatment. Recognize and report any adverse reactions or complications during dialysis. Assist in managing vascular access (AV fistula, graft, catheter). Infection Control and Hygiene : Maintain a sterile environment to prevent infections. Disinfect machines and clean dialysis stations thoroughly after each session. Record Keeping : Maintain accurate patient records including treatment parameters, duration, and any issues noted during dialysis. Document machine calibration and maintenance logs. Equipment Maintenance : Conduct regular checks and basic maintenance of dialysis machines. Report any technical issues or need for repairs to the biomedical/maintenance team. Patient Communication & Support : Provide emotional support and guidance to patients undergoing long-term treatment. Educate patients on pre- and post-dialysis care, fluid restrictions, and dietary guidelines (in coordination with dietitian/nurse). Emergency Handling : Respond promptly to any complications or emergencies during dialysis. Assist in basic life support procedures if needed.

Key Responsibilities: Develop and implement quality assurance standards, processes, and procedures for HVAC products and installations. Conduct inspections and audits on raw materials, in-process components, and finished HVAC units to ensure conformity to specifications. Collaborate with engineering and production teams to resolve quality issues. Analyze test data and root causes of defects or failures, and recommend corrective and preventive actions (CAPA). Maintain calibration records for all testing equipment and ensure timely recalibration. Assist in the preparation and execution of ISO, ASHRAE, or customer-specific audits. Ensure compliance with industry standards and customer requirements. Develop quality documentation including inspection reports, SOPs, and quality manuals. Conduct training for shop floor staff on quality practices and product standards. Monitor supplier quality performance and initiate corrective actions for non-conformities. Support continuous improvement initiatives Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Company Description SAA Vishnu Bakers Pvt. Ltd. is a leading manufacturer and supplier of high-quality bakery products, committed to delivering taste, hygiene, and innovation. Established with a vision to create wholesome snacking experiences, we specialize in producing a wide range of biscuits, cookies, and baked treats that cater to diverse consumer preferences across India. Role Description This is a full-time on-site role for a Lab Chemist at Saa Vishnu Group located in Ranchi. The Lab Chemist will be responsible for conducting analytical tests, operating laboratory equipment, carrying out laboratory procedures, ensuring quality control measures, and performing calibrations. Qualifications • Analytical and Laboratory Skills • Experience with Laboratory Equipment • Knowledge of Quality Control and Calibration Processes • Attention to detail and precision • Strong problem-solving abilities • Ability to collaborate effectively in a team • Bachelor's degree in Chemistry or related field in Food Tech

As an Instrumentation Engineer is responsible for designing, installing, maintaining instruments that measure & control industrial processes. Design, Installation, Commissioning, Calibration, Maintenance Troubleshooting, Spares & Material Management Required Candidate profile Nature of exp: Chemical, Pharma, Argo industries, Instrumentation Engg. must have specific exp. & skills to ensure the effective operation, calibration & maintenance safety & regulatory compliance. Perks and benefits Canteen, Transportation/GTLI/GPA/GMC

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. 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. 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.

Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. 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. 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 Title: Quality Analyst Location Hyderabad/Chennai Functional: Digital Sales Sub Department Digital Channel Reference / Version No: Last Updated Date: PURPOSE OF THE POSITION: Looking for a result-driven Quality Analyst to be responsible for monitoring and supervising a team of non - sales to achieve the organization’s objectives and increase sales through Digital Process DUTIES & RESPONSIBILITIES: Analyze /Audit Calls to identify the areas of Improvement which did not meet the predefined performance standards of Medvarsity. Provides Structured and timely feedback of the audits Verbal/Written to all the stakeholders within the organization and helps ISM's in improving their performance. Performs Mock -Calls with new hires post-training to determine readiness for moving into teams. Quality Analyst is responsible for facilitating calibration/group sessions regarding quality programs Need the ability to work in a constructive, unbiased, and collaborative manner by establishing positive work relationships & partnering with the Leadership team & Training Team. This Position requires the ability to gain the confidence and trust of others by demonstrating professionalism and expertise in an ever-changing environment. The Quality Analyst is responsible for the overall quality of the customer interactions, making improvement recommendations to the sales team leader and monitoring the result of the stated recommendation Desired Candidate Profile: 7 QC tool experience Excellent communication skills Outbound calls quality check Contact/whatsapp:7801027439 Job Type: Permanent Pay: ₹4.00 - ₹5.00 per year Benefits: Provident Fund Schedule: Day shift Application Question(s): Do you have experince as Quality Analyst Experience: BPO /Telecalling: 3 years (Required) Language: Do you speak Kannada or Marathi (Required) Work Location: In person Speak with the employer +91 7801027439

Job Description: Skills: High Analytical skills Investment operations exposure is mandate (Stock, Bond, Mutual Funds). Strong project management orientation. Ability to extract information with apt precision and shorter timelines and communicate to others. Ability to navigate, research, and utilize processing guidelines...And add value as needed. Strong problem-solving and decision-making skills through effective calibration of inputs. Strong Numerical ability…needs to be a role model for peers. Ability to innovate with new ideas for continuous process improvement. Ability to work in a team-oriented, collaborative environment…proactive help offering as needed. Strong customer service orientation, with close watch on set procedures. Quick learner with attention to detail. Comfortable with Night shifts. Knowledge: Advance knowledge in MS Excel / any other tools used in the process required Enhanced knowledge on SOPs & procedures for aligned process. Possess significant investment domain expertise to align with our processes. Ability to develop dashboard & measures to proactively manage multi- client level impacts and shares with the appropriate audience as per expected schedules Location: This position can be based in any of the following locations: Chennai, Gurgaon Current Guardian Colleagues: Please apply through the internal Jobs Hub in Workday

http://nauk.in/bpfLwvP Key Responsibilities: Perform analysis of raw materials, intermediates, and finished products of Active Pharmaceutical Ingredients (APIs) as per approved specifications and SOPs. Operate and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, Karl Fischer, Melting Point Apparatus, etc. Review and verify analytical data and ensure proper documentation in line with cGMP and GLP guidelines. Prepare and standardize volumetric solutions and reagents. Carry out stability studies and maintain stability data as per ICH guidelines. Ensure timely calibration of laboratory instruments. Perform method validation/transfer activities as per regulatory and internal requirements. Involve in investigations related to OOS/OOT/Deviations and CAPA implementation. Coordinate with cross-functional departments like QA, Production, and R&D for smooth workflow. Comply with all safety protocols and maintain a clean and organized lab environment. Desired Candidate Profile: Hands-on experience in analytical techniques (HPLC/GC) is a must. Good knowledge of regulatory guidelines (ICH, WHO, USFDA, etc.) Strong documentation and communication skills. Experience in a regulated API manufacturing unit is preferred. Industry Type: Pharmaceutical & Life Sciences Department: Corporate Quality Control Employment Type: Full Time, Permanent

This role is for one of our clients Industry: Hospitals and Health Care Seniority level: Associate level Min Experience: 1 years Location: Ranchi JobType: full-time Role Overview We are looking for a qualified and proactive Nuclear Medicine Technologist cum Radiation Safety Officer to join our state-of-the-art multispeciality hospital in Ranchi. This hybrid role blends technical expertise in nuclear imaging with critical responsibilities in radiation safety management, making it ideal for professionals who excel at combining clinical precision with regulatory compliance. You will be instrumental in delivering high-quality diagnostic imaging services using radiopharmaceuticals, while ensuring that radiation protection practices across the department meet the highest safety standards as per AERB guidelines. Key Responsibilities Nuclear Medicine Technologist Prepare, handle, and administer radiopharmaceuticals safely and accurately for diagnostic procedures. Operate nuclear medicine imaging systems including PET/CT, SPECT/CT, and gamma cameras . Assist physicians in performing and interpreting nuclear imaging studies to support clinical diagnoses. Monitor patients throughout imaging procedures for safety, comfort, and response to radiopharmaceuticals. Maintain detailed patient records, dosage logs, imaging documentation, and reports. Follow strict protocols for waste disposal, decontamination, and infection control within the imaging unit. Radiation Safety Officer (RSO) Oversee implementation and enforcement of radiation protection policies across the nuclear medicine department. Ensure ongoing compliance with AERB regulations , license conditions, and institutional safety protocols. Conduct routine radiation surveys , leak tests, exposure monitoring, and safety audits of equipment and premises. Maintain radiation monitoring instruments and ensure proper calibration and usage. Manage and submit regulatory documentation , maintain records for inspections, and act as liaison with regulatory authorities. Educate and train staff on radiation safety protocols , emergency response procedures, and best practices. Candidate Requirements Educational & Regulatory Qualifications Bachelor’s or Master’s degree in Nuclear Medicine Technology from a recognized institution. Certified Radiation Safety Officer – Level 2 , recognized by the Atomic Energy Regulatory Board (AERB) . Experience Minimum 1 year of hands-on experience in a hospital-based nuclear medicine department. Familiarity with PET/CT and SPECT/CT procedures, equipment handling, and post-procedure care. Technical Proficiency Skilled in radiopharmaceutical preparation, imaging protocols, and patient monitoring. Strong understanding of radiation physics, occupational exposure limits, and regulatory reporting. Experience in maintaining dosimetry records and conducting radiation safety training sessions is desirable. Preferred Attributes Attention to detail and ability to maintain high standards of safety and accuracy. Strong organizational and documentation skills, especially for regulatory compliance. Effective communicator with the ability to work well in cross-functional teams. Ability to respond to emergencies involving radioactive exposure or contamination confidently and calmly.

Job Summary: We are seeking a qualified and proactive Biomedical Engineer to join our team. The ideal candidate will be responsible for the maintenance, calibration, and repair of medical equipment, ensuring optimal performance, safety, and compliance with health regulations. Key Responsibilities: Install, maintain, and repair biomedical equipment such as ventilators, monitors, defibrillators, and imaging devices. Conduct preventive maintenance and calibration of medical equipment as per schedules. Perform troubleshooting and root cause analysis of faulty devices and ensure timely resolution. Maintain accurate records of equipment performance, repairs, and maintenance logs. Ensure compliance with relevant safety and quality standards (ISO, NABH, etc.). Liaise with vendors for procurement, AMC/CMC, and spare parts management. Provide technical support and training to clinical staff on equipment usage. Assist in evaluation and selection of new medical equipment and technologies. Participate in audits and prepare documentation as per regulatory requirements. Stay updated with advancements in medical technology and industry best practices. Qualifications and Skills: Bachelor’s degree in Biomedical Engineering or related field (Diploma with experience may be considered). 1–3 years of experience in hospital or healthcare equipment management preferred . Strong technical knowledge of diagnostic and therapeutic biomedical equipment. Problem-solving and analytical skills. Excellent communication and coordination skills. Knowledge of hospital safety protocols and regulatory standards. Employment Type: Full-Time Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Provident Fund Schedule: Fixed shift Work Location: In person Expected Start Date: 01/07/2025

Key Responsibilities: Quality Control & Inspection: Supervise and coordinate in-process and final product inspections. Ensure adherence to quality standards, specifications, and procedures. Review and approve inspection reports, test results, and certifications. Team Supervision: Lead a team of quality inspectors and technicians. Assign duties, monitor performance, and provide on-the-job training. Conduct regular team meetings and toolbox talks related to quality. Process & Compliance Audits: Conduct routine audits (internal and external) to ensure compliance with ISO/TS/IATF standards. Support customer and third-party audits. Implement corrective and preventive actions (CAPA) for non-conformities. Documentation & Reporting: Maintain quality records, inspection logs, and test reports. Prepare monthly quality performance reports and trend analyses. Ensure proper calibration of measuring instruments and maintain records. Customer Interaction: Handle customer complaints and quality concerns. Coordinate with production and design teams to address product issues. Support root cause analysis and implement corrective actions. Continuous Improvement: Identify process improvements using tools like 5 Why, Fishbone Diagram, or FMEA. Promote and support quality improvement initiatives (Kaizen, 5S, Lean, etc.) Conduct training sessions on quality tools and awareness. Job Types: Full-time, Permanent Pay: Up to ₹30,000.00 per month Schedule: Day shift Ability to commute/relocate: Ghaziabad, Uttar Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: Quality control: 1 year (Preferred) Work Location: In person

Male candidates may apply. Install, maintain, and repair a wide range of medical equipment (Equipment for OT, CCU, Pathology, Emergency, Dialysis, Radiology Department). Calibration and Testing Troubleshoot technical issues with medical devices and perform necessary repairs to minimize downtime. Preventative Maintenance Biomedical engineers train medical staff on the proper use and maintenance of medical equipment Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Experience: HOSPITAL EQUIPMENT: 5 years (Required) Work Location: In person Application Deadline: 01/07/2025 Expected Start Date: 07/07/2025

Job Description Job Purpose: Deliver all clinical audiology services in Amplifon clinics - audiology diagnostics to hearing aid fitting and verification. Job Specification: Strong and effective communicator. Ability to build trust, value others and demonstrate high integrity. Demonstrable ability to operate all audiometric equipment Demonstrable ability to administer all diagnostic audiological tests for adults and children and also to interpret the results. • Demonstrable ability to subjectively calibrate audiometer and necessary calibration for impedance meter. • Working knowledge of the pathology of all hearing and related speech disorders. Demonstrable ability to counsel adults with hearing loss using various methods in clientcentered approach Good working knowledge on current and past hearing aid and assistive devices technology Demonstrable ability to fit and verify hearing aids and assistive devices to adults with hearing loss Demonstrable ability to maintain records, prepare reports and conduct correspondence related to work. Ability to maintain favorable relations with doctors, customers and all internal stake holders. Willingness and ability to work in different teams in field and head office and show high level of accountability with each and every customer Ability to learn and improvise clinical work as per the inputs provided/ shared Ability to align with organization's objectives and accept the goals designed time to time as per the need of the organization Job Qualifications: Minimum Educational Qualification: Bachelors in Audiology and Speech-Language Pathology (BASLP) or Masters in Audiology and Speech-Language Pathology (MASLP)

At Jacobs, we're challenging today to reinvent tomorrow by solving the world's most critical problems for thriving cities, resilient environments, mission-critical outcomes, operational advancement, scientific discovery and cutting-edge manufacturing, turning abstract ideas into realities that transform the world for good. Your impact The candidate must be able to integrate well with a large multi-cultural and high performing team and have the flexibility to meet the challenging demands of the project which include quality standards, bridging data gaps, timelines, amongst others. Reporting to the Senior Engineer, the candidate shall be responsible for Work collaboration with other project team members; Have respect for deadlines and achieve targeted results; Analyze data and bridge gaps; Hydraulic modelling in software such as Tuflow, Flood Modeller Pro, Infoworks ICM, HEC-RAS; Hands on experience on Qgis, MapInfo and ArcGIS; Catchment analysis and Hydrology calculations; Options evaluation; Prepare presentations and present the outcomes to the lead office; Undertaking project tasks at various stages in the project life cycle, while ensuring technical excellence and best practice to specification; Provide input to Designers / Draftsmen or other disciplines as per their need; Interact / coordinate with other disciplines for input, other information as required for completion of work for the Project requirements; We value collaboration and believe that in-person interactions are crucial for both our culture and client delivery. We empower employees with our hybrid working policy, allowing them to split their work week between Jacobs offices/projects and remote locations enabling them to deliver their best work. Here's what you'll need The mentioned position shall have the flood hydraulic modelling and hydrology experience on River modelling projects. He shall be a water sector practitioner with thorough experience in the core subject, having a level of expertise and experience commensurate with the position. The candidate must have a minimum of Bachelor of Engineering degree from recognized university, Master’s in environmental/Water Resource Engineering would be an added advantage and must have a minimum of 1 to 3 years’ experience in Hydrology and River Hydraulic Modelling projects. The candidate should have the experience in hydraulic modelling softwares such as Tuflow and Flood Modeller Pro. Experience in Infoworks ICM will be an added advantage. The candidate shall be performing hydraulic analysis, mitigation modelling, calibration, flood mapping, report drafting and co-ordination with the lead offices on various projects.

Company Description Founded in 2019, Sri Lakshmi Industries (CNC & Tooling works) specializes in precise machining for a wide range of parts across various industries. We are committed to delivering exceptional quality and tailor-made solutions to meet each client's needs. Serving notable clients such as Karnataka Turned Components Pvt. Ltd., Omsham Mechatronics System, Omsham Machines & Sensors, and Sri Chakara Engineering, we uphold strict quality control with tooling precision maintained to within +/- 0.01mm. Our principles of reliability, efficiency, and customer satisfaction underpin our growing reputation in the CNC machining sector. Role Description This is a full-time on-site role for a CNC Operator located in Hosur. The CNC Operator will be responsible for setting up and operating CNC machines, interpreting blueprints and technical drawings, and ensuring the precision and quality of machined components. Daily tasks include machine calibration, tool changes, performing quality checks, maintaining equipment, and troubleshooting issues to ensure smooth operations. Qualifications Experience in operating CNC machines and understanding of CNC machining processes Ability to read and interpret blueprints and technical drawings Skills in machine calibration, tool changes, and performing quality checks Proficiency in basic maintenance and troubleshooting of CNC equipment Attention to detail and commitment to precision Good communication skills and ability to work as part of a team Relevant certification or diploma in machining or a related field Fresher will be trained for CNC operation, setting & programming Along with measuring instrument handling.

Main job responsibilities of Quality Manager are as follows for both central lab & satellite labs (but not limited to): 1. Quality Assurance System Implementation Ensure the implementation, monitoring, and control of QMS across all diagnostic centres as per ISO/NABL/CAP standards. Responsible for drafting, reviewing, issuing, and updating quality documents including Quality Manuals, SOPs, QMS Procedures, forms, and flowcharts. Monitor compliance and initiate corrective/preventive actions for non-conformities. 2. Accreditation & Audit Management Manage the accreditation lifecycle for NABL & CAP, including applications, reassessments, and documentation of correspondences. Coordinate and face internal and external audits; document and track audit findings, NCs, and ensure closure within timelines. Maintain updated accreditation certificates and display them at all centres. 3. Internal Audits & Management Reviews Plan and conduct periodic internal audits across departments and centres (including reception, phlebotomy, sample receiving, housekeeping, etc.). Organize Management Review Meetings (MRM), prepare MOMs, follow-up on decisions and ensure documentation. Organize safety audits, mock drills, and other quality meetings with documented outcomes. 4. Document Control Maintain a central document control system for all quality documents. Ensure timely revision, issuance, withdrawal, and obsolescence marking of documents and SOPs. 5. Complaint Handling & Incident Management Manage all customer complaints for the central lab and ensure timely investigation, closure, and documentation in complaint logs. Maintain incident/accident records (e.g., needle-stick injuries, spillages) for all centres. 6. Equipment & Calibration Management Prepare calibration and preventive maintenance schedules for all analyzers and equipment. Ensure IQ/OQ/PQ documentation for new instruments and proper documentation of PM and calibration activities. Maintain equipment breakdown logs and ensure regular internal calibration of centrifuges (bi-annually). 7. External Quality Assurance (EQAS)/Proficiency Testing (PT) Oversee all EQAS/PT activities: registration, timely testing, result documentation, and corrective actions for unsatisfactory results. Coordinate root cause analysis and maintain EQAS/PT records as per CAP/NABL requirements. 8. Training & Competency Identify training needs, prepare training plans and materials, and conduct induction and periodic staff training. Collaborate with HR for onboarding lab tours and maintaining training records. Evaluate training effectiveness, especially for new phlebotomists and technical staff. 9. Quality Indicators & Statistical Analysis Define quality indicators and statistically analyze performance every 6 months month. Present quality trends and improvement initiatives in monthly/quarterly lab presentations. 10. Other Responsibilities Ensure proper functioning of the lab's water treatment system. Maintain patient unclear prescription files. Ensure immunization status is updated for all employees. Participate in DSIR approval processes and ethical committee meetings. Maintain various logs and registers including reagent storage, report delay logs, PT records, and doctor rosters. Prepare SOPs for new tests and contribute as CAP Section Director for Lab General Checklist audits. Prepare monthly LAB PPTs and CAP PT survey forms.

ARAI, Pune is a premier Automotive Research Institute, with the Ministry of Heavy Industries, involved in R&D, Homologation, Testing & Certification, Calibration & Skill Development services to Automotive and Allied industries globally. We are looking for the following position for our Quality Management Department (QMD) : Designation: Research Engineer – Quality Management Systems (QMS) (ARAI Contract) – 1 No. Location: Kothrud, Pune + HTC / FID – Chakan, MRC-Takwe and outstation if needed. Work Experience: 2 – 5 Years The candidate should be Diploma in Mechanical, Electrical or Electronics Engineering from reputed College with good record of academic career with relevant experience of 2-5+ years in the Automotive or Automotive ancillary units, MS Word, Excel, Power point operational skill good oral communication skills in English, Hindi and Marathi. Candidates should possess necessary skill sets mentioned in below job description. Job Description: Hands on Experience in: Implementation and maintenance of Management System Standards like ISO 9001, ISO 17025, BIS LRS2020. Planning and execution of Internal Audits of above-mentioned Standards Documents and Records Management System Compilation of Quality related Data for Management Review meeting Various report preparation as per Management System Standards Coordination with Quality Champions for system implementation across all site of ARAI. Various Problem-Solving Techniques like- 8D, 7QC tools, Kaizens, Six Sigma, RCA etc. Preparation for Customer Audits Training of internal / external professionals on various QMS activities Experience/Skills: 2-5+ years of experience in above fields with good communication skills, Presentation Skills, Having Good Knowledge of MS-Office with Advance Excel (Macros), SAP Preferred Industry – Automotive or Automotive ancillary units, Work Experience in ISO 9001, ISO 17025, BIS LRS2020 Accredited Lab is Preferred Note for Contract Position: ARAI Contract for 01-year, Contract will be extended but it depends upon candidate performance. Last Date of Application: 01-JUL-25 Directly Apply on ARAI Career Site : https://www.araiindia.com/pages/career-with-arai