4845 Calibration Jobs - Page 21

Job Title: Quality Engineer (SQM & IQC) Company: Jagan Lamps Ltd. Location: Kundli, India Website: www.jaganlamps.com Qualifications Gender: Male Education: Diploma in Engineering / ITI Experience: 1-2 Year Specialization: Electrical, Electronics, Mechanical, or Instrumentation Technician Industries: Automotive / Engineering / Assembly / Lighting / Electrical / Electronic / Home Appliance Job Description As a Supplier Quality Management (SQM) and Incoming Quality Control (IQC) Quality Engineer , you will be responsible for ensuring the quality of incoming materials and products from suppliers. Your role will involve developing and implementing quality control procedures, collaborating with suppliers to drive continuous improvement, and ensuring compliance with industry standards and company requirements. Key Responsibilities Manage and maintain QA/QC documentation, including certificates, calibration records, test results, inspection requests, non-compliance reports (NCRs), and site instructions. Ensure proper handling and verification of permanent materials delivered to the facility. Oversee the closure of non-conformances (NCRs) and site instructions, ensuring corrective and preventive actions are implemented effectively. Conduct daily defect analysis, identifying root causes and implementing corrective and preventive measures. Ensure that all quality control processes align with regulatory standards and company policies. Monitor daily product quality to ensure targets are met and maintained at the highest standards. Collaborate with internal teams and suppliers to drive continuous improvement in product quality. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Experience: total work: 1 year (Required) Location: Kundli, Haryana (Required) Work Location: In person Application Deadline: 30/04/2025 Expected Start Date: 20/07/2025

Do you want to be a part of the fascinating story of over 500 iconic brands spanning across more than 100 countries Being the best beer company starts with finding the best people. While we have big brands, we have bigger opportunities as well. AB InBev India is looking to hire a Senior Manager - Quality Analyst for its supply team based out of Aurangabad, Maharashtra. As a Senior Manager - Quality Analyst, you will be responsible for handling instruments like GC, Alcolyser, DMA, Sodium Meter, pH Meter, and Gas Generators. Your role will involve the calibration and maintenance of all BQA instruments while strictly following BQA SOPs. You will be analyzing in-process samples, highlighting deviations, and examining incoming brewing raw materials. Adhering to SOP's for all analysis, you will ensure reliable and accurate data is supplied through the use of BWC and control charting. Maintenance of all records and updating the AB datasheet regularly will be part of your duties. Additionally, you will conduct PRP audits and 5S Audits at regular intervals, maintaining 5S in the lab, and serving as a subject matter expert on instruments like GC's, Alcolyser, DMA, Sodium Meter, pH meter, Generators, centrifuge, sonicator, hot water bath, and Mash Bath. As a Senior Manager - Quality Analyst, you will play a crucial role as an enthusiastic team player in the Environmental Pillar, a qualified taster, and a trainer of new Brewing Quality Analysts. Your responsibilities will include brewing quality improvement analysis, developing and implementing process checklists and audits, as well as conducting and tracking CAR of brewery PRP audits. You will ensure all BQA lab consumables and inventory are maintained, adhere to safety requirements, and review daily data, control charts, calibration, and maintenance logs. Key dimensions of this role include being accountable for the Director (Supply & Logistics) KPI, Brewery Sensory Score, Regional BOP KPI, and VPO Implementation Department-specific KPI such as BPI & Plant Micro Index. Above all, a passion for beer is essential to excel in this role. Quench your thirst for success by joining AB InBev India as a Senior Manager - Quality Analyst. Come, sit at the tab and be a part of our dynamic team in Aurangabad, Maharashtra.,

Job Title: QA/QC Manager Location: Bhiwandi, Maharashtra Department: Quality Assurance / Quality Control Reporting To: Plant Head / Operations Manager / Director Job Purpose We are seeking an experienced QA/QC Manager to lead and manage the Quality Assurance and Quality Control functions at our manufacturing unit. The role focuses on ensuring all products and processes comply with internal quality standards, customer specifications, and ISO requirements. This includes implementing robust inspection systems, conducting in-line checks, and driving continuous improvement across CNC machining, hose assembly, and related manufacturing processes. Key Responsibilities 1. Quality Management & Compliance Implement, maintain, and enhance compliance with ISO 9001, ISO 14001, and ISO 45001 standards. Prepare and maintain quality documentation including Quality Manual, SOPs, Work Instructions, NCR reports, CAPA, etc. Lead internal audits and coordinate external audits (e.g., TUV, customer audits). Oversee calibration of measuring instruments and ensure proper traceability. 2. In-line Quality Checks Design and enforce inspection protocols at various production stages (cutting, CNC, drilling, crimping, testing). Ensure execution of First Piece Inspection (FPI), In-Process Inspection (IPI), and Final Inspection (FI) with accurate record-keeping. 3. CNC Machining Quality Review machining tolerances, surface finishes, and geometric dimensions. Interpret engineering drawings and verify components using instruments such as calipers, micrometers, height gauges, and CMM (if available). Maintain control plans and inspection criteria for CNC parts. 4. Hose Assembly Quality Control Validate crimp dimensions, pressure test results, and visual inspection standards. Document hydrostatic test reports, burst test data, and ensure batch traceability. Maintain jigs, gauges, and Go/No-Go standards. 5. Team Leadership & Training Supervise and guide quality inspectors and technicians. Conduct training programs to enhance quality awareness on the shop floor. Foster a culture of continuous improvement. 6. Root Cause Analysis & CAPA Investigate internal and external quality complaints. Use tools such as 5-Why, Fishbone Diagram, Pareto Analysis for root cause identification. Implement corrective and preventive actions (CAPA) and monitor effectiveness. Key Deliverables (KPIs) Reduction in rejection/rework rates Customer complaint index improvement Timely closure of internal audit findings ISO compliance score maintenance Minimization of inspection backlog and cycle time Coverage of employee training initiatives Qualifications Diploma or Degree in Mechanical / Production Engineering Minimum 2–5 years of experience in QA/QC within a manufacturing environment Knowledge of ISO 9001, ISO 14001, ISO 45001 standards (certifications preferred) Experience in CNC machining, hose assembly, and hydro testing is an advantage Familiarity with tools like 8D, 5S, SPC, MSA, and FMEA Skills Required Strong attention to detail and commitment to process discipline Proficiency in MS Excel, Word, and QA software tools Effective communication and documentation skills Leadership and training capability Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹50,000.00 per month Work Location: In person

As a global leader in precision measurement sensing technologies, VPG addresses an expanding array of applications in which accuracy, reliability, and repeatability make the difference. Whether in the design and safety of new generations of cars, trucks, and planes or optimizing advanced medical equipment and consumer products, VPG’s deep engineering expertise makes the world safer, smarter, and more productive. We are seeking a highly motivated Process Engineer to join our Engineering team on a full-time basis. Major Responsibilities & Accountabilities: New Product Implementation, transferring of new product to Mass production by guiding production team & coordinating with all Support teams - main contact point to R&D/Electrical. Prepare Work Instruction, SOP, PN creation and updating, ECR, PCO, Drawing verification PCBA faulty analysis (Analog & Digital PCB), Product/Process Failure RCCA, Product qualification Knowledge base: SMT process and PCBA manufacturing / assembly process. Process automation & Jigs & Fixtures design and implementation ESD-Knowledge base and digital-setups training for Production operators Supporting local Sales team with troubleshooting Digital products. CFT follow ups and support of continuous improvement Critical skills & Attributes: Soft Skills: Teamwork & Collaboration Result Orientation Communication Problem Solving and critical thinking Adaptability & flexibility Essential Competencies: People Handling Failure analysis capability NPI EMS Product knowledge Good to have Competencies: APQP PPAP PFMEA Technical Competencies: Basic knowledge on PCBA design, CAN BUS, Graphical user interface (GUI), circuit debugging, Gerber knowledge, SMT, Altium, Hand Soldering experience, Advantech modules, Thermal and electrical interferences and problem solving for EMI, RFI & ESD, Microcontrollers, In-circuit testing jigs, Programming – Microcontrollers and interfacing communication networks, Electrical testing - electrical noises – EMI / RFI etc.,, Connectors fastness and calibration, EEPROM programs for communication interfaces, Exposure to IPC 610 & 620 standards, Breadboard circuitry, Communication protocols and the buses – RS232, I2C, RS 485, Embedded System Benefits: Best In Industry

The team you will be a part of will be responsible for commissioning and maintaining I&C systems. Your duties will include conducting pre-job briefings, isolating systems, removing instruments, cleaning, decontamination, physical inspections, testing, troubleshooting, repairing, calibrating, filling data sheets, normalization, and providing feedback to ENC. This is a full-time position with a rotational shift schedule. The required education for this role is a Diploma. You should have at least 3 years of work experience and 3 years of experience in Electrical Engineering. Proficiency in Hindi is preferred for this role. The work location will be in person. If you are looking for a challenging role where you will be involved in a wide range of activities related to I&C systems, this position could be a great fit for you.,

Warehouse - SafetyMalur Posted On 15 Jul 2025 End Date 31 Aug 2025 Required Experience 0 - 1 Years Basic Section No. Of Openings 1 Designation Grade Safety Engineer - M21 Freshers/Experience Experience Employee Bonus Regular Organisational GPCOMP Pon Pure Chemicals Group Company Name Pon Pure Chemical India Private Limited Department Warehouse - Safety Country India State Karnataka Region Malur Branch Malur Skills Skill SAFETY Minimum Qualification BE CERTIFICATION No data available Working Language No data available Job Description 1. Daily Report / TBM Report / Deviation Report, Weekly Report / Bimonthly Report, Weighing Scale Calibration Report/ Boundary Rounds report, Fire Drill Training Report, Mock Drill Report 2. Training to Warehouse Employees, Near Miss, Incident CAPA & Near Miss, Incident CAPA Training, New Joiners Induction Training, Drivers Training 3. Preventive Maintenance Record, Fire Extinguisher / Fire Hydrant Maintenance, Earth Pit Maintenance, Tools & Equipment's Checklist. 4. Factory License Requirements, PCB Requirements / Hazardous waste Disposal, Fire Department Requirements.

Job title : Manager - Instrumentation and Electricals Entity : Evonik Specialty Silica India Pvt. Ltd. work location : Jhagadia, Gujarat Purpose of the Position: Safe and efficient management of preventive maintenance & breakdown of instruments and electrical equipments through effective engineering norms of ESSIPL to meet or exceed maintenance requirements. Communicating with authorities and complying with all associated legal requirements. Co-ordinating with regional PT Team for implementation of best maintenance practices like Risk Based Maintenance (RBM), EPS in Instrumentation and Electrical streams. Digitalization initiatives like OT security, and act as LOSC. Key Responsibilities: Management of Departmental Activities for Instrumentation and Electrical side. Handling and ensuring compliance related to Nucleonic Gauge (Should have completed Training through A.E.R.B./BARC) Work as Radiological Safety Officer for Organization. Ensure timely compliance of Instrumentation ( Weights and Measure Metrology related, GPCB related, etc.) Ensure timely compliance of Electrical (Annual Inspection, DG set registration & Duty filing, Communication with DGVCL/GETCO, Etc.) Experience on Rockwell Automation PLC System (Control Logix, PLANT PAX, FT BATCH, SCADA AND LOGIC programming development) . Experience of SAP and SAP Plant Maintenance module. ( Notification, Work Order management). Experience on filter press Hydraulic system, Spray Dryer Burner System, Boiler Burner and safety interlocking system. Ensure timely calibration of field instruments, MCI and various measuring instruments. Ensure timely attendance to break-down and emergency repair jobs. Guide subordinates to repair the equipment and keep it ready to use as per requirement. Ensure proper and safe operation of equipments used during maintenance and calibration. Install, commission and validate new equipment. Instrument and Electrical related Mechanical support designing, fabrication through vendor. Sizing and Selection of proper instrument (knowledge of Mass Flow meter, Pressure transmitter, Thermocouple, Magnetic Flowmeter, pH Meter, Turbidity meter, Conductivity meter, Ozone Generator, Weighing system, Etc) Telephone EPBX programming, Configuration, CCTV Configuration Etc. Contract man power planning, assigning them jobs daily and ensuring safe maintenance. Plan, schedule and carry out shut down maintenance jobs. Support in controlling maintenance cost, analyzing breakdown, Prepare CAPA, diagnosing, identifying the root cause and implementing the actions. Coordination with external vendors and other departments and sustain team work. Carry out cost estimate for equipment maintenance, repair and replacement. Attend assigned EHSQ and GMP related actions. Meet the applicable EHS legal and Evonik requirements. To ensure safe maintenance through adherence to the EHS policy, Life Saving Rules, Work Permit, use of Personal Protective Equipments, Management of Change, Pre-Job Plan, Incident Reporting, EHS procedures etc. Prepare and maintain documents like Equipment History Card, Maintenance Checklist, Reports to Management, Standard Practice Instruction, ISO related etc. Communication with authority and compliance of legal requirements. Active participation in conceptualization to execution to commissioning of projects. Ensure availability of spares by working with Purchase department and Engineering Stores by implementing Min/Max system for spares. Preparation of Appropriation Request for major expenditures. Responsible for imparting training on SAP Maintenance Module to all new joiners of the department. Digitalization initiatives like OT security including global policy/standard implementation, act Education & Experience Required : B.E. / B.Tech. – Instrumentation or Electronics & Communication with 10-12 years of experience in maintenance of plant. Additional requirements - Training cum Certification- course on Radiation Safety Aspects of Nucleonic Gauges. Active registration on ELORA AERB Website for Radiation Professional. Additional skills and abilities required for this position Man-power management. Fluency in English, Gujarati and Hindi language. Experience in SAP is preferred. PLC programming Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal . Further information about Evonik as Employer can be found at https://careers.evonik.com . Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Sagar Khedekar Company is Ev Spec Silica India

ProductionAhmedabad Posted On 15 Jul 2025 End Date 31 Aug 2025 Required Experience 2 - 3 Years Basic Section No. Of Openings 1 Designation Grade Senior Executive -M24 Freshers/Experience Experience Employee Bonus Regular Organisational GPCOMP Pon Pure Chemicals Group Company Name Pon Pure Chemical India Private Limited Department Production Country India State Gujarat Region Ahmedabad Branch Ahmedabad Skills Skill MANUAL TESTING & AUTOMATION TESTING Minimum Qualification MSC CERTIFICATION No data available Working Language ENGLISH HINDI GUJARATI Job Description S. No. Responsibilities 1. Ensure the safety in laboratory. 2. Management of samples (RM/PM/IP/FP). 3. Analysis of sample as per standard testing procedure(RM/PM/IP/FP). 4. Handling of Instrumentation : GC, UV, FT-IR, KF Titrator. 5. Documentation: SOP/STP Preparation,Maintain Record of Analysis, COA and Instruments logbook. 6. Ensure AMC and Calibration of Apparatus/instruments. 7. To maintain stability samples along with their analysis records 8. Maintain stock registers for lab.consumables and non-consumables 9. Knowledge in Change control, CAPA, OOS. 10. Handling of customer compliant. 11. Review of BMR/BPR. 12. Batch Release and Rejection. 13. Quality Management system. 14. Analytical method validation and method verification.

Warehouse - MaintenanceMadhavaram Posted On 15 Jul 2025 End Date 31 Aug 2025 Required Experience 5 - 13 Years Basic Section No. Of Openings 1 Designation Grade Assistant Manager - M3 Freshers/Experience Experience Employee Bonus Two Month Organisational GPCOMP Pon Pure Chemicals Group Company Name Pon Pure Chemical India Private Limited Department Warehouse - Maintenance Country India State Tamil Nadu Region Madhavaram Branch Madhavaram Skills Skill SURVIVABILITY REGULATORY AUDITS CONTINUITY OF OPERATIONS SENIOR EXECUTIVE LEADERSHIP Minimum Qualification B.TECH/BE CERTIFICATION No data available Working Language TAMIL ENGLISH HINDI Job Description 1. Availability and Inspection of Tools & Equipment (All Locations) Conduct periodic inspection and condition assessments of tools and material handling equipment. Maintain a central inventory of all tools and ensure calibration and servicing as required. Ensure availability of necessary tools and spares at each site based on criticality and usage. Rectify and maintain defective tools and equipment in coordination with the local team. Provide training on Material Handling Equipment (MHE) to operators and technicians. 2. Equipment Maintenance and AMC Management Ensure AMC (Annual Maintenance Contract) renewals are done before expiry. Include newly procured equipment in the SOP, AMC, and maintenance checklist. Regularly review service provider reports and ensure action on critical observations. Arrange spares and consumables based on AMC reports and predictive needs. Prepare and update preventive maintenance checklists for both electrical and mechanical assets. Schedule and track periodic preventive maintenance (PPM) and report status monthly. 3. Regulatory Compliance and Legal Requirements Ensure calibration and stamping of weighing scales, Weighing bridge , and stones (manual & electronic). Obtain and maintain competency certifications for Forklift operators and ensure Safe waste oil Storage & Disposal to authorise Vendor . Coordinate with regulatory authorities for pressure vessel inspections and records. Maintain compliance related to DG set emissions and ensure timely disposal of hazardous waste . Co-ordinate and implement the action plan effectively for the Audit findings related to Tools and equipment. 4. Revamping, Modification, Erection & Commissioning (Key Managerial Role) Estimate and prepare Bill of Materials (BOM) and coordinate with procurement for materials and tools. Develop and update technical drawings and layouts before and after modifications. Conduct Pre-Startup Safety Reviews (PSSR) and support HIRA documentation for new or modified installations. Oversee erection, commissioning, and testing of new or refurbished equipment. Ensure documentation and execution of DQ (Design Qualification), IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) protocols. As per the Department Business plan requirement studying the feasibility and installing the necessary Tools and Equipment. 5. Preventive Maintenance & Repairs Implement and monitor site-wise Preventive Maintenance schedules for all Equipment. Conduct routine inspections to identify wear, damage, or abnormal operating conditions. Troubleshoot mechanical and electrical faults and coordinate corrective actions . Maintain minimal downtime by timely diagnosis and resolution of issues. Propose upgrades and process improvements based on failure history and trends. 6. Operational Efficiency & Downtime Management Reduce equipment downtime and maintain operational continuity. Maintain detailed logs of breakdowns, repairs, and modifications . Analyze trends to improve Equipment performance and reliability . 7. Coordination & Documentation Maintain detailed records of all maintenance tasks, AMC schedules, spares used, and service history . Collaborate with vendors and service contractors for sourcing, repair, and overhauls. Coordinate with warehouse and operations teams to minimize disruption during maintenance work. Use CMMS or Excel-based tracking tools for equipment health monitoring . 8. Training & Team Development Provide Technical training to ITI and Diploma technicians at site on preventive maintenance and equipment handling. Conduct weekly reviews (WIG-Meetings) with Maintenance and Safety Engineers for performance tracking and issue resolution. Promote a S afety Culture, Accountability, and Continuous improvement across all sites.

As an Automation Engineer at DigitalSync Automation Solutions, you will play a crucial role in the design, development, testing, and deployment of industrial automation systems. Your responsibilities will involve collaborating with senior engineers and technicians to implement automation solutions for a wide range of industrial processes in sectors such as steel, packaging, printing, food & beverages, and more. Your key responsibilities will include assisting in the design and programming of automation systems, which encompasses PLCs, HMIs, SCADA, and drives. You will also provide support for field assignments like system installation, troubleshooting, and commissioning. It will be essential for you to accurately read and interpret electrical schematics and panel layouts, as well as collaborate with the engineering team to define system specifications and testing procedures. Moreover, you will aid in the integration and calibration of various control systems and visit client factories and sites to implement and support automation solutions. Additionally, you will participate in internal training sessions to enhance your skills in automation tools and logic development. Joining DigitalSync Automation Solutions will provide you with an opportunity to work on diverse automation projects in a learning-focused environment with real-time field exposure. You can expect flexible growth and learning opportunities in cutting-edge automation systems, contributing to your professional development. DigitalSync Automation Solutions is a growing industrial automation company that specializes in providing end-to-end automation services. Their expertise spans PLC programming, HMI & SCADA development, control panel wiring and designing, and VFD/Servo drive commissioning. The company operates across various industries, delivering efficient, reliable, and smart automation systems. If you are a passionate and skilled professional eager to work on cutting-edge automation projects and grow with a dynamic company, we invite you to apply and become a part of our team at DigitalSync Automation Solutions.,

Be the First to Apply Job Description Responsible to maintain the laboratory as per good laboratory practices, good documentation practices, 21 CFR guidance and meets cGMP Requirement. Responsible to adhere with data integrity policy, ALCOA++ principle during performing any activity inside the company premises. To follow the administrative policies including personal hygiene, HR procedures, environmental and safety regulations within the site premises. To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness. Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor / HOD-QC / Head-Quality as and when required. To receive the analysis sample includes packing materials, raw materials, In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Responsible for analysis of test parameters includes description, solubility, Water content, Purity/ related substances by GC, Assay by GC etc.by using approved testing procedure. To execute the analysis activity by completing all necessary documentation related to instrument logbooks, analytical test report, analysis worksheets, analytical hard books and document archival after approval of samples. To perform the wet lab instrument calibration as per the schedule and respective SOP as and when required. To perform the GC instrument calibration as per the schedule and respective SOP and qualification of GC instruments as and when required. To execute the chemical analysis of additional studies like stability study, method validation/ verification study/ any investigation purpose analysis. Destruction of samples after approval and subsequent record to be updated. To ensure the availability of valid working standards, impurity standards, reference standards and its management during usage. To Support to maintain GC columns within the laboratory and ensure the stock availability. Report any non-conformance i.e. Laboratory Incidence, OOS/OOT/OOC to Immediate supervisor for further action. Department: Quality Control Location: Digwal Job Overview: To perform Quality Control actives as per GMP & Safety Travel Requirements: NA Reporting Structure Reports to Manager - QC Key Stakeholders Internal: Production, QA, SCM, IT, Engineering & Maintenance, TSD & Safety External: Customers Experience 4-8 Year Experience in Quality Control Chemical and Instrumentation Analysis for In-process, Stability, Raw Materials, Working standard/Reference standard, Packing Materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC (API) as per Pharma Manufacturing GMP requirements. Responsibilities Key Roles & Responsibilities Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC. Responsible for allotting the work to the chemist within the QC department. Responsible for performing the calibrations of all instruments in QC as per the schedule. Responsible for maintaining all the documentation online. Responsible for maintaining the minimum stock for working standards, reference standards and impurity standards and ordering as and when required. Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares and solvents required for analysis. Responsible for keeping instruments neat and clean and overall housekeeping in the FP section. Responsible for review of analytical data, calibration data, qualification data. Responsible for keeping all instruments within the calibrated status. Responsible to do the analysis, review and release on time to support the production. Responsible for reducing the lab incidences, repeat analysis and no Data Integrity issues. Responsible for real time data monitoring. Responsible for reviewing the analytical data received from external laboratory. Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates and working/reference standard certificates. Responsible for maintaining the consumption records and traceability of working/reference standards. Responsible for OOS investigations, deviations and CAPA implementations Responsible for review of SOP’s , test procedures and specifications Responsible for providing the training on GLP/GMP to the employees working the section. Responsible for releasing the batches timely manner to achieve the site requirement. Responsible for preparing the COA’s as per the customer requirement Responsible for approving/rejecting the batches in SAP Responsible for Controlling the cost and operate within the approved budget. Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments. Responsible for carrying out the analytical method transfers, Method validations, Method equivalency study and Method verification activities. Responsible for keeping the critical spare parts of the instruments. Responsible for Safe working conditions and clean environmental practices. Responsible for usages of required safety appliances in the section. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches. Responsible to train the contract persons and helpers on glassware cleaning. Qualifications B.Sc (Chemistry) / M.Sc (Chemistry) / B. Pharmacy / M. Pharmacy Required Skills GC & Wet analysis handling About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders. PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators. Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space. Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment. Job Info Job Identification 8977 Job Category Quality Control Posting Date 07/14/2025, 06:25 PM Apply Before 08/14/2025, 06:25 PM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN

Be the First to Apply Job Description Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor / HOD-QC / Head-Quality as and when required. To receive the analysis sample includes packing materials, raw materials, In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Responsible for analysis of test parameters includes description, solubility, Water content, Purity/ related substances by GC, Assay by GC etc.by using approved testing procedure. To execute the analysis activity by completing all necessary documentation related to instrument logbooks, analytical test report, analysis worksheets, analytical hard books and document archival after approval of samples. To perform the wet lab instrument calibration as per the schedule and respective SOP as and when required. To perform the GC instrument calibration as per the schedule and respective SOP and qualification of GC instruments as and when required. To execute the chemical analysis of additional studies like stability study, method validation/ verification study/ any investigation purpose analysis. Destruction of samples after approval and subsequent record to be updated. To ensure the availability of valid working standards, impurity standards, reference standards and its management during usage. To Support to maintain GC columns within the laboratory and ensure the stock availability. Report any non-conformance i.e. Laboratory Incidence, OOS/OOT/OOC to Immediate supervisor for further action. Qualifications BSC/ MSC/ B Pharmacy / M Pharamcy Required Skills Handling of GC with Empower software & handling of Balance,KF,IR About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders. PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators. Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space. Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment. Job Info Job Identification 8978 Job Category Quality Control Posting Date 07/14/2025, 06:26 PM Apply Before 08/14/2025, 06:26 PM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN

Selected Intern's Day-to-day Responsibilities Include Inspection and report preparation of incoming parts, subassemblies, and assemblies at supplier place. Help document and segregate conforming and non-conforming materials. Distribute controlled DMR documents to manufacturing and suppliers. Assist in coordinating calibration schedules for tools, instruments, and fixtures. Support in reporting and documenting process deviations. Participate in internal audits Support in preparation of CAPA records related to NCPRs and customer complaints and assist in tracking CAPA implementation and effectiveness review. Help in data collection for supplier evaluation. Participate in KAIZEN activities and support implementation. About Company: Perfint Healthcare is a world leader in planning and targeting solutions for image-guided interventional procedures, with an emphasis on oncology and pain care. Perfint's products are installed at some of the world's top hospitals and are CE marked. Radiologists around the world use Perfint's Robotic solutions for image-guided interventional procedures like biopsy, drug delivery, ablation, drainage, fine needle aspiration, and varied pain care procedures for both cancerous and non-cancerous pain. Perfint's newest product, MAXIO, is set to change the world of interventional oncology. MAXIO will allow clinicians to visually plan, execute, and validate ablation procedures on a single system, and all in 3D. MAXIO has been designed to make complex, multi-probe ablations simpler, which will help to make these life-saving procedures available to more cancer sufferers than ever before.

You will be joining Autoprint as a skilled and detail-oriented Quality Executive within the Quality Control team. Your primary responsibility will be to ensure the quality and compliance of machinery by conducting thorough inspections and maintaining documentation throughout all production stages. Your key responsibilities will include performing quality inspections, conducting Pre-Delivery Inspections (PDI) and Finished Goods (FG) checks, executing assembly and spot inspections, documenting and reporting findings, conducting supplier quality audits, identifying and resolving problems, managing calibration and tools, driving process improvement initiatives, collaborating with team members, and ensuring compliance with standards. To qualify for this role, you should possess a Diploma or Bachelor's Degree in Mechanical Engineering (DME / BE Mechanical) and have a minimum of 3-5 years of experience in a quality control or inspection position. Additionally, you must have a strong grasp of mechanical drawings and inspection tools, proficiency in documentation and report writing, experience with cylindrical grinding, CNC reports, and calibration, excellent communication and problem-solving abilities, the capacity to work independently as well as in multidisciplinary teams, and a willingness to travel for supplier audits as required.,

Selected Intern's Day-to-day Responsibilities Include Inspection and report preparation of incoming parts, subassemblies, and assemblies at supplier place. Help document and segregate conforming and non-conforming materials. Distribute controlled DMR documents to manufacturing and suppliers. Assist in coordinating calibration schedules for tools, instruments, and fixtures. Support in reporting and documenting process deviations. Participate in internal audits Support in preparation of CAPA records related to NCPRs and customer complaints and assist in tracking CAPA implementation and effectiveness review. Help in data collection for supplier evaluation. Participate in KAIZEN activities and support implementation. About Company: Perfint Healthcare is a world leader in planning and targeting solutions for image-guided interventional procedures, with an emphasis on oncology and pain care. Perfint's products are installed at some of the world's top hospitals and are CE marked. Radiologists around the world use Perfint's Robotic solutions for image-guided interventional procedures like biopsy, drug delivery, ablation, drainage, fine needle aspiration, and varied pain care procedures for both cancerous and non-cancerous pain. Perfint's newest product, MAXIO, is set to change the world of interventional oncology. MAXIO will allow clinicians to visually plan, execute, and validate ablation procedures on a single system, and all in 3D. MAXIO has been designed to make complex, multi-probe ablations simpler, which will help to make these life-saving procedures available to more cancer sufferers than ever before.

The role of a SLAM Engineer at Peppermint Robotics involves developing autonomous navigation and mobility functions for robots designed for floor cleaning and material handling across various environments. You will be responsible for enhancing the capabilities of the navigation stack, refining mapping algorithms, and working on localization algorithms using different sensors to navigate dynamic environments such as airports, parking lots, warehouses, and malls. Integration and synchronization of data from sensors like Depth Camera, LiDARs, and IMUs with embedded development boards will be crucial to build a robust robot navigation system. The products you work on will be of world-class quality, manufactured in Pune (India), and distributed globally. Your key responsibilities will include developing and deploying localization, mapping, and calibration algorithms, staying updated with the latest advancements in robotics, collaborating with diverse teams for system integration, and optimizing algorithms for real-time performance. Hands-on experience with SLAM, robot navigation, sensor fusion, and various perception sensors will be essential for this role. Strong communication skills, a Bachelor's degree in Robotics, Computer Science, Electrical Engineering, or a related field, and at least 2 years of relevant experience are required. Proficiency in C++ programming, familiarity with Python, experience with ROS1 and/or ROS2, and a passion for developing software for cutting-edge robots are highly valued. You will report to the Lead - Robotics Engineer and collaborate with teams based in India, MEA, and the USA. Expect cross-team collaboration, hands-on learning, and professional attire in the office with necessary protective gear in the assembly area. As part of a fast-growing startup, you will be involved in planning and executing short and long-term robotic software plans and will be expected to align with Peppermint's work ethos, code of conduct, and culture of clear communication and continuous learning. If you are enthusiastic about working on a world-class product, possess a strong sense of curiosity, and are eager to learn and grow in the field of robotics, this role at Peppermint Robotics may be the perfect fit for you. To apply, please send your resume to allen.louis@peppermintrobotics.com.,

As a Shift Engineer at Adani Power Limited, your primary responsibility is to ensure the optimal performance and reliability of Control & Instrumentation (C&I) systems for Boiler, Turbine, Generator (BTG) through vigilant maintenance, calibration, and troubleshooting. You will be tasked with managing the healthiness of C&I parameters, providing rapid response to emergencies, and maintaining equipment such as Motor Operated Valves (MOVs) and Flue Gas Discharge (FGD) systems. Your key responsibilities include: - Ensuring the availability and functionality of all C&I systems related to BTG and Balance of Plant (BOP) during your shift. - Performing routine maintenance of BTG Motor Operated Valves (MOVs) and auxiliaries. - Executing calibrations as per schedule and preparing detailed reports. - Maintaining C&I parameters" healthiness in coordination with Operations, including bypassing interlocks and protections when required. - Providing DCS historian data for analysis and other purposes. - Managing timely startup of the unit to meet operational demands and maintain power generation schedules. - Responding immediately and effectively to emergencies to ensure personnel and equipment safety while minimizing operational disruptions. Additionally, you will be responsible for: - Troubleshooting breakdowns promptly to minimize downtime. - Following equipment maintenance checklists and ensuring timely execution. - Providing resources and guidance to contractor technicians for routine maintenance tasks. - Maintaining Flue Gas Discharge (FGD) systems for operational efficiency. - Coordinating with other departments to minimize delays in maintenance and operational activities. - Reporting unsafe conditions, acts, and near misses to promote a culture of safety. - Implementing digitization and automation strategies to optimize operational efficiency. - Monitoring compliance with environmental regulations and ensuring adherence to statutory compliances and regulations. To qualify for this role, you should have a Bachelor's degree in C&I or Electronics & Communication, or an equivalent degree, along with at least 6 years of experience in power plant operations or maintenance, specifically with 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, is preferred. If you are passionate about ensuring the smooth operation of power generation systems and are committed to safety and compliance, then this role at Adani Power Limited is the perfect opportunity for you to make a significant impact. Apply now and be a part of a dynamic team dedicated to excellence in the energy sector.,

You will be responsible for performing line clearance activities before commencing operations, ensuring a clean and sanitized visual inspection and Packing area, and following the preventive maintenance schedule of machines. Operating the machines efficiently and filling the log of general areas as per SOP and work execution will also be part of your responsibilities. It is essential to adhere to cGMP, GDP, and maintain discipline in the department while ensuring that all employees comply with the same standards. Your role will involve ensuring that all equipment and production lines are in validated and calibrated status, preparing daily production reports based on achieved targets, and creating production plans on a monthly and daily basis according to material availability. Handling tasks such as change control, deviations, CAPA, investigations, and document management including BMRs, BPRs, and master SOPs will be part of your duties. You will also be involved in the preparation, review, revision, control, and implementation of standard operating procedures within the sterile manufacturing department. Conducting line clearance activities before commencing various operations such as manufacturing, sterilization, and filling, as well as checking and maintaining records and logbooks related to manufacturing processes, garment washing, drying, and equipment sterilization are key aspects of your role. Additionally, you will be required to perform any activities as instructed by the HOD, provide training to subordinates, technicians, and operators, and stay updated on self-hygiene practices. Attending training sessions as per the schedule and ensuring compliance with the Training Need Identification (TNI) will also be part of your responsibilities. Qualifications required for this role include M.Sc., B.Pharm, or M.Pharm degree.,

Kaseya® is the leading provider of complete IT infrastructure and security management solutions for Managed Service Providers (MSPs) and internal IT organizations worldwide powered by AI. Kaseya’s best-in-breed technologies allow organizations to efficiently manage and secure IT to drive sustained business success. Kaseya has achieved sustained, strong double-digit growth over the past several years and is backed by Insight Venture Partners www.insightpartners.com), a leading global private equity firm investing in high-growth technology and software companies that drive transformative change in the industries they serve. Founded in 2000, Kaseya currently serves customers in over 20 countries across a wide variety of industries and manages over 15 million endpoints worldwide. To learn more about our company and our award-winning solutions, go to www.Kaseya.com and for more information on Kaseya’s culture. Kaseya is not your typical company. We are not afraid to tell you exactly who we are and our expectations. The thousands of people that succeed at Kaseya are prepared to go above and beyond for the betterment of our customers. Role: Quality Assurance Officer Location: Bangalore - Onsite Duration: Full-Time Timings: 9-6 AM (fixed – 2-4 months) / open to Rotational shift.) Experience: 2-4 yrs Skills to crack: data analysis tools/ contact center/ DA of Raw Data/ COPC/ ISO 9001:2015/ Call-Chat process Job Summary We are seeking a detail-oriented and analytical Quality Analyst to join our Contact Center team. This role is pivotal in enhancing the quality of customer interactions, improving agent performance, and optimizing support processes. The ideal candidate will have a strong background in quality assurance within a contact center environment and a passion for driving continuous improvement. Qualifications 2–4 years of experience in a contact center quality assurance or process improvement role. Previous work experience in an IT industry working with Tickets is a Plus. Strong understanding of QA methodologies, call monitoring tools, and customer service metrics. Proficiency in data analysis tools (Excel, Power BI, or similar). Excellent communication, coaching, and interpersonal skills. Ability to work independently and collaboratively in a fast-paced environment. Preferred Skills Experience with CRM and contact center platforms (e.g., Zendesk, Five9). Familiarity with Six Sigma, Lean, or other process improvement methodologies. Certification in Quality Assurance or Customer Experience (e.g., COPC, ISO 9001, CCXP) is a plus. Key Responsibilities Monitor and evaluate inbound and outbound customer interactions across multiple channels (calls, chats, emails). Analyze agent behavior and adherence to scripts, compliance standards, and customer service protocols. Identify trends, gaps, and opportunities for improvement in agent performance and customer experience. Develop and maintain quality scorecards, evaluation forms, and performance dashboards. Provide actionable feedback and coaching recommendations to supervisors & managers. Collaborate with training and operations teams to design and implement improvement initiatives. Track the effectiveness of quality improvement programs and report on KPIs. Conduct root cause analysis on recurring issues and recommend process enhancements. Support calibration sessions to ensure consistency in quality evaluations. Join the Kaseya growth rocket ship and see how we are #ChangingLives ! Additional Information Kaseya provides equal employment opportunity to all employees and applicants without regard to race, religion, age, ancestry, gender, sex, sexual orientation, national origin, citizenship status, physical or mental disability, veteran status, marital status, or any other characteristic protected by applicable law.

Kaseya® is the leading provider of complete IT infrastructure and security management solutions for Managed Service Providers (MSPs) and internal IT organizations worldwide powered by AI. Kaseya’s best-in-breed technologies allow organizations to efficiently manage and secure IT to drive sustained business success. Kaseya has achieved sustained, strong double-digit growth over the past several years and is backed by Insight Venture Partners www.insightpartners.com), a leading global private equity firm investing in high-growth technology and software companies that drive transformative change in the industries they serve. Founded in 2000, Kaseya currently serves customers in over 20 countries across a wide variety of industries and manages over 15 million endpoints worldwide. To learn more about our company and our award-winning solutions, go to www.Kaseya.com and for more information on Kaseya’s culture. Kaseya is not your typical company. We are not afraid to tell you exactly who we are and our expectations. The thousands of people that succeed at Kaseya are prepared to go above and beyond for the betterment of our customers. Role: Quality Assurance Officer Location: Bangalore - Onsite Duration: Full-Time Timings: 9-6 AM (fixed – 2-4 months) / open to Rotational shift.) Experience: 2-4 yrs Skills to crack: data analysis tools/ contact center/ DA of Raw Data/ COPC/ ISO 9001:2015/ Call-Chat process Job Summary We are seeking a detail-oriented and analytical Quality Analyst to join our Contact Center team. This role is pivotal in enhancing the quality of customer interactions, improving agent performance, and optimizing support processes. The ideal candidate will have a strong background in quality assurance within a contact center environment and a passion for driving continuous improvement. Qualifications 2–4 years of experience in a contact center quality assurance or process improvement role. Previous work experience in an IT industry working with Tickets is a Plus. Strong understanding of QA methodologies, call monitoring tools, and customer service metrics. Proficiency in data analysis tools (Excel, Power BI, or similar). Excellent communication, coaching, and interpersonal skills. Ability to work independently and collaboratively in a fast-paced environment. Preferred Skills Experience with CRM and contact center platforms (e.g., Zendesk, Five9). Familiarity with Six Sigma, Lean, or other process improvement methodologies. Certification in Quality Assurance or Customer Experience (e.g., COPC, ISO 9001, CCXP) is a plus. Key Responsibilities Monitor and evaluate inbound and outbound customer interactions across multiple channels (calls, chats, emails). Analyze agent behavior and adherence to scripts, compliance standards, and customer service protocols. Identify trends, gaps, and opportunities for improvement in agent performance and customer experience. Develop and maintain quality scorecards, evaluation forms, and performance dashboards. Provide actionable feedback and coaching recommendations to supervisors & managers. Collaborate with training and operations teams to design and implement improvement initiatives. Track the effectiveness of quality improvement programs and report on KPIs. Conduct root cause analysis on recurring issues and recommend process enhancements. Support calibration sessions to ensure consistency in quality evaluations. Join the Kaseya growth rocket ship and see how we are #ChangingLives ! Additional Information Kaseya provides equal employment opportunity to all employees and applicants without regard to race, religion, age, ancestry, gender, sex, sexual orientation, national origin, citizenship status, physical or mental disability, veteran status, marital status, or any other characteristic protected by applicable law.

As a Production Manager, you will need to hold a degree in B.Sc/M.Sc/B.Pharm/M.Pharm with FDA approval in topical preparations. With a CTC of 7 to 8 lac per year, you will be required to work in 8-hour shifts and possess at least 10 to 15 years of experience in topicals. Your responsibilities will include production planning based on clients" purchase orders and ensuring its successful implementation. You will be responsible for verifying dispensed raw materials, maintaining and updating the Production Module on the PERP system, and overseeing the manufacturing of cream, ointment, and lotion. It will be crucial for you to execute instructions related to production operations and in-process control. Furthermore, your duties will involve online documentation such as Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), and updating logbooks. You will also be accountable for maintaining calibration, validation, and associated documents, handling change controls and deviations, and ensuring the preventive maintenance of equipment is carried out regularly. In case of incidents, you will be required to conduct investigations and provide necessary training to new recruits. Collaboration with the Quality Assurance (QA), Quality Control (QC), and Store departments will be essential. You will be responsible for the upgrade of the PERP system and its related documents and supervising all manufacturing activities. Your role as a Production Manager will encompass a wide range of tasks, from overseeing production processes to ensuring compliance with regulations and maintaining a high standard of quality throughout the manufacturing operations.,

You will be joining our team as a Cleanroom Operator where your primary responsibility will involve performing manufacturing, assembly, and support tasks in a controlled cleanroom environment. It is essential to strictly adhere to cleanliness and safety protocols to ensure the quality of the operations. Your key responsibilities will include operating equipment and executing processes within the cleanroom environment, handling sensitive components like wafers, sensors, and optical parts using cleanroom gloves and tools. You will be required to follow standard operating procedures (SOPs), work instructions, and cleanroom protocols such as GMP, ESD, and gowning procedures. Monitoring cleanliness, particulate levels, and preventing material contamination will also be part of your duties. Additionally, you will support routine maintenance, cleaning, and calibration of cleanroom tools and instruments, accurately log data in batch sheets, maintenance records, or electronic systems, and collaborate with engineering and QA teams during process trials or inspections. Ensuring adherence to safety protocols and reporting any equipment malfunctions or unsafe conditions promptly is crucial. To be successful in this role, you should hold a Diploma or B.E. in Electrical and Mechanical or a related field. Although 2 years of experience in a cleanroom, lab, or production environment is preferred, freshers are also welcome to apply. A basic understanding of cleanroom protocols, contamination control, and ESD safety is required. Good hand-eye coordination, attention to detail, willingness to work in shifts, wear cleanroom gowns, and adhere to hygiene practices are essential. You should also possess the ability to maintain accurate documentation and follow process discipline effectively.,

Job Description Responsible to maintain the laboratory as per good laboratory practices, good documentation practices, 21 CFR guidance and meets cGMP Requirement. Responsible to adhere with data integrity policy, ALCOA++ principle during performing any activity inside the company premises. To follow the administrative policies including personal hygiene, HR procedures, environmental and safety regulations within the site premises. To identify unsafe conditions/ acts inside the laboratory, report to supervisor/ HOD- QC and ensure its completeness. Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required . Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor / HOD-QC / Head-Quality as and when required. To receive the analysis sample includes packing materials, raw materials, In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Responsible for analysis of test parameters includes description, solubility, Water content, Purity/ related substances by GC, Assay by GC etc.by using approved testing procedure. To execute the analysis activity by completing all necessary documentation related to instrument logbooks, analytical test report, analysis worksheets, analytical hard books and document archival after approval of samples. To perform the wet lab instrument calibration as per the schedule and respective SOP as and when required . To perform the GC instrument calibration as per the schedule and respective SOP and qualification of GC instruments as and when required . To execute the chemical analysis of additional studies like stability study, method validation/ verification study/ any investigation purpose analysis. Destruction of samples after approval and subsequent record to be updated. To ensure the availability of valid working standards, impurity standards, reference standards and its management during usage. To Support to maintain GC columns within the laboratory and ensure the stock availability. Report any non-conformance i.e. Laboratory Incidence, OOS/OOT/OOC to Immediate supervisor for further action. Department: Quality Control Location: Digwal Job Overview: To perform Quality Control actives as per GMP & Safety Travel Requirements: NA Reporting Structure Reports to Manager - QC Key Stakeholders Internal: Production, QA, SCM, IT, Engineering & Maintenance, TSD & Safety External: Customers Experience 4-8 Year Experience in Quality Control Chemical and Instrumentation Analysis for In-process, Stability, Raw Materials, Working standard/Reference standard, Packing Materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC (API) as per Pharma Manufacturing GMP requirements. Responsibilities Key Roles & Responsibilities Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC. Responsible for allotting the work to the chemist within the QC department. Responsible for performing the calibrations of all instruments in QC as per the schedule. Responsible for maintaining all the documentation online. Responsible for maintaining the minimum stock for working standards, reference standards and impurity standards and ordering as and when required. Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares and solvents required for analysis. Responsible for keeping instruments neat and clean and overall housekeeping in the FP section. Responsible for review of analytical data, calibration data, qualification data. Responsible for keeping all instruments within the calibrated status. Responsible to do the analysis, review and release on time to support the production. Responsible for reducing the lab incidences, repeat analysis and no Data Integrity issues. Responsible for real time data monitoring. Responsible for reviewing the analytical data received from external laboratory. Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates and working/reference standard certificates. Responsible for maintaining the consumption records and traceability of working/reference standards. Responsible for OOS investigations, deviations and CAPA implementations Responsible for review of SOP’s , test procedures and specifications Responsible for providing the training on GLP/GMP to the employees working the section. Responsible for releasing the batches timely manner to achieve the site requirement. Responsible for preparing the COA’s as per the customer requirement Responsible for approving/rejecting the batches in SAP Responsible for Controlling the cost and operate within the approved budget. Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments. Responsible for carrying out the analytical method transfers, Method validations, Method equivalency study and Method verification activities. Responsible for keeping the critical spare parts of the instruments. Responsible for Safe working conditions and clean environmental practices. Responsible for usages of required safety appliances in the section. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches. Responsible to train the contract persons and helpers on glassware cleaning. Qualifications B.Sc (Chemistry) / M.Sc (Chemistry) / B. Pharmacy / M. Pharmacy About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders. PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators. Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space. Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment.

Job Description Responsible to keep Lab and Instruments neat, clean and in working condition all the time. Timely communicate any abnormalities observed during analysis and escalate it to supervisor for appropriate action. To ensure the analysis activity perform in the laboratory by following approved procedures. To ensure the training on the activity which are assigned by supervisor/ HOD-QC prior to execution. Actively involve and Participate in assessment, investigations, and implementing CAPA effectively. Responsible for Internal & External vendor follow-up and timely completion. Responsible for maintain the minimum stock and Use valid working standards, reference standards, impurity standards, chemicals, reagents, glassware and solvents required for analysis and Ensure availability as and when required. Perform Sampling & analysis of packing materials, raw materials, stability samples, in process and finished products. Responsible to perform and complete the work assigned by supervisor / HOD-QC / Head-Quality as and when required. To receive the analysis sample includes packing materials, raw materials, In-process, Intermediate, API, Finished product samples and make entry in to the respective AR number logs. Responsible for analysis of test parameters includes description, solubility, Water content, Purity/ related substances by GC, Assay by GC etc.by using approved testing procedure. To execute the analysis activity by completing all necessary documentation related to instrument logbooks, analytical test report, analysis worksheets, analytical hard books and document archival after approval of samples. To perform the wet lab instrument calibration as per the schedule and respective SOP as and when required. To perform the GC instrument calibration as per the schedule and respective SOP and qualification of GC instruments as and when required. To execute the chemical analysis of additional studies like stability study, method validation/ verification study/ any investigation purpose analysis. Destruction of samples after approval and subsequent record to be updated. To ensure the availability of valid working standards, impurity standards, reference standards and its management during usage. To Support to maintain GC columns within the laboratory and ensure the stock availability. Report any non-conformance i.e. Laboratory Incidence, OOS/OOT/OOC to Immediate supervisor for further action. Qualifications BSC/ MSC/ B Pharmacy / M Pharamcy About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Critical Care (PCC), under Piramal Pharma Limited (PPL), a subsidiary of Piramal Enterprises Limited, is the third largest producer of Inhaled Anaesthetics and a global player in hospital generics. Motivated by its vision to deliver critical care solutions for patients and healthcare providers across the globe, PCC is committed to enabling sustainable and profitable growth for all its stakeholders. PCC maintains a wide presence across the USA, Europe and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anaesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has wholly-owned, state-of-the-art manufacturing facilities in the US and India that have successfully cleared periodical inspections by the US FDA, UK MHRA and other regulators. Its core strength lies in a highly qualified global workforce of more than 400 employees across 16 countries. PCC is focused on further expanding its global footprint through new product additions in the critical care space. Committed to corporate social responsibility alongside Piramal Group, PCC collaborates with various partner organizations and proudly takes an active role in providing hope and resources to those in need, as well as caring for the environment.

Calibration of customer instruments and maintaining laboratory master equipments