The LED TV and Audio Systems Technician is responsible for the installation, maintenance, repair, and troubleshooting of LED televisions and audio systems. This role requires expertise in the setup and calibration of home entertainment systems ,commercial audio-visual setups, and multimedia devices. The technician ensures all systems operate effectively and meets the quality expectations of clients or internal users. Additionally other HA products also will be serviced by the technician Note- You will be get reimbursement of petrol claim for 3rs per KM a part from salary and other benefits like you will also et incentive for every sale of Extended Warranty (EW) and Annual maintenance charges (AMC) Job Type: Full-time Pay: ₹19,000.00 - ₹20,000.00 per month Benefits: Life insurance Provident Fund Schedule: Day shift Application Question(s): Do you have two wheeler? Education: Diploma (Preferred) Experience: total work: 1 year (Preferred) Field service: 1 year (Preferred) Willingness to travel: 50% (Preferred) Work Location: In person

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 PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers Responsible for allotting the work to the chemist within the section. Responsible for performing the calibrations of all instruments in section 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 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, OOT, OOC and deviations investigations 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. 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 SFTI. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches Responsible for training the contract persons and helpers on glassware cleaning.

Responsibilities:- Perform preventative maintenance Installation Qualification IOP Perform Calibartion & validation Troubleshooting Identify and resolve issues with various equipment On Site Service Regular visiting different client locations Accidental insurance Annual bonus Performance bonus Mobile bill reimbursements Gratuity Provident fund Travel allowance Food allowance

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 PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers Responsible for allotting the work to the chemist within the section. Responsible for performing the calibrations of all instruments in section 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 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, OOT, OOC and deviations investigations 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. 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 SFTI. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches Responsible for training the contract persons and helpers on glassware cleaning.

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 PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers Responsible for allotting the work to the chemist within the section. Responsible for performing the calibrations of all instruments in section 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 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, OOT, OOC and deviations investigations 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. 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 SFTI. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches Responsible for training the contract persons and helpers on glassware cleaning. 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.

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 PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers Responsible for allotting the work to the chemist within the section. Responsible for performing the calibrations of all instruments in section 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 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, OOT, OOC and deviations investigations 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. 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 SFTI. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches Responsible for training the contract persons and helpers on glassware cleaning. 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 Control Executive / Sr. Executive (Male Candidates Only) Department: Quality Control (QC) Location: [Specify location if needed] Experience: 3 – 8 Years (Formulations – Pharmaceutical Industry) Qualification: B.Sc / M.Sc in Chemistry Salary: As per industry standards, based on current CTC and experience Job Description: We are seeking a male QC professional with a strong academic background in Chemistry and 3–8 years of hands-on experience in Quality Control within a pharmaceutical formulations manufacturing environment . Key Responsibilities: Conduct analysis of raw materials, in-process samples, finished products, and stability samples. Perform analytical tests using HPLC, UV, FTIR, Dissolution, GC, and other instruments as per specifications and SOPs. Prepare and review analytical reports, COAs, and ensure timely documentation. Ensure compliance with cGMP, GLP, and regulatory requirements. Support method validation and transfer activities. Maintain laboratory records, equipment calibration, and sample management. Participate in investigations of OOS/OOT results and deviations. Handle audit queries and support in regulatory inspections (USFDA, MHRA, etc.). Requirements: Only male candidates are eligible for this position. Must have experience in formulations (oral solid dosage or other) in a regulated environment. Sound knowledge of regulatory guidelines and documentation practices . Proficiency in operating analytical instruments. Strong communication, teamwork, and analytical skills. Willing to work in shifts if required. Interested can call/ WhatsApp: 7396423749., Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹60,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Job Title: Assistant Quality Manager / Quality Engineer Experience: 2–5 Years Department: Quality Assurance / Quality Control Industry: Medical Devices / Pharma / Healthcare Standards: ISO 13485, QMS, Regulatory Compliance Job Responsibilities: Assist the Quality Manager in maintaining and improving the Quality Management System (QMS) as per ISO 13485 requirements. Prepare and update Standard Operating Procedures (SOPs), Work Instructions, and Quality Manual. Participate in internal audits , supplier audits, and external regulatory audits (e.g., ISO, FDA). Support CAPA (Corrective and Preventive Action) and non-conformance investigations. Monitor and ensure document control , calibration, validation, and traceability of processes and equipment. Conduct training and awareness programs on QMS and regulatory requirements. Assist in product quality inspections and manage deviations and change controls. Maintain risk management files as per ISO 14971 (if applicable). Coordinate with cross-functional teams (R&D, production, supply chain) to ensure compliance. Prepare and maintain quality reports, metrics, and audit findings. Key Skills Required: Strong understanding of ISO 13485 QMS principles. Knowledge of GMP, CAPA, NCR, RCA, Validation, Risk Management . Proficient in internal audit processes and documentation practices. Attention to detail and analytical thinking. Excellent communication and organizational skills. Job Type: Full-time Pay: ₹30,000.00 - ₹40,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Role & responsibilities · Promote and sell annual maintenance contracts (AMCs) , comprehensive maintenance contracts (CMCs) , and installation & calibration services for biomedical equipment. · Identify and develop new service business opportunities in existing and prospective customer accounts. · Generate leads through market research, cold calling, and site visits to hospitals, diagnostic labs, and clinics. · Prepare technical and commercial proposals in line with customer requirements. · Work closely with the service delivery team to ensure quality and timely execution of services sold. · Maintain and grow relationships with biomedical engineers, hospital administration, and procurement departments . · Negotiate contracts and close agreements to maximize profits while ensuring client satisfaction. · Keep track of service contracts, renewals, and upsell opportunities. · Maintain accurate records of client interactions and sales activities using CRM tools. · Stay updated on product developments, competitors, and industry trends. Preferred candidate profile · Bachelors degree in Biomedical Engineering , Electronics , Life Sciences , or a related field. · 1-5 years of experience in sales or service of medical/diagnostic equipment . · Experience with equipment like ventilators, patient monitors, analyzers, or imaging devices is an added advantage. · Willingness to travel extensively within the assigned region. · Any graduate/ Diploma holder with medical equipment sales can apply Role: After Sales Service & Repair - Other Industry Type: Medical Devices & Equipment Department: Customer Success, Service & Operations Employment Type: Full Time, Permanent Role Category: After Sales Service & Repair Education UG: Any Graduate Key Skills Skills highlighted with ‘‘ are preferred keyskills Strong knowledge of biomedical equipment Target Achievementproven ability in service salesMedical Equipment Sales Job Type: Full-time Pay: ₹20,000.00 - ₹250,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person Application Deadline: 20/06/2025

Urgent Requirement for the following position below : Profile Position : LAB TECHNICIAN PATHOLOGY - For the Healthcare Sector in Diagnostics Labs. Company Name : REXPRESS Health Solution Pvt Ltd -Head Office in Naraina New Delhi, Location Required - - DELHI ,ONLY Local candidate of DELHI Experience - 2-4 yrs Qualifications -MLT Pathology, DMLT Pathology Diploma, Degree and Graduate and Post - Graduate. Salary - 15k -25k Skills ,Knowledge And Technical Experience - EM200,H360,ERBA LAURA MACHINE know to Operate, NABL knowledge, Blood Collection , QC and Calibration Running, Bio Chemistry, Operate Machine Clia based Maglumi X3 fully automatic , Basic Knowledge of Laboratory can operate Fully Automatic Machines. Communication skills, Interpersonal Skills, Computer Savvy- Excel, MS office, MS Word, PowerPoint, Employment Type- Full Time Immediate Joiner . If you are interested share your CV OR DM on given email id, contact number below: rexpresshr@rakkshak.in Job Type: Full-time Pay: Up to ₹25,000.00 per month Experience: total work: 4 years (Preferred) Work Location: In person

Job Title: B. Pharma Lab Executive Location: Eternal Life Ayurveda Pvt. Ltd. Job Type: Full-Time Experience: 0–2 years Qualification: B. Pharma (Bachelor of Pharmacy) Job Summary: Eternal Life Ayurveda is seeking a detail-oriented and disciplined B. Pharma graduate to join our R&D and quality control team. The ideal candidate will be responsible for assisting in formulation development, testing of raw materials and finished products, and maintaining lab documentation as per regulatory and Ayurvedic standards. Key Responsibilities: Conduct routine testing and analysis of raw materials, in-process, and finished Ayurvedic products. Assist in formulation and development of herbal and Ayurvedic products like powders, tablets, oils, and syrups. Maintain proper documentation, including batch records, lab notebooks, and test reports. Support the Quality Control and Quality Assurance team in executing quality checks. Handle lab equipment with care and follow calibration and maintenance schedules. Ensure adherence to GMP (Good Manufacturing Practices) and SOPs. Coordinate with the production team to provide lab support during manufacturing. Participate in R&D activities for new product development under senior supervision. Skills Required: Sound knowledge of basic pharmaceutical and Ayurvedic principles Familiarity with laboratory instruments like pH meter, viscometer, balance, etc. Understanding of standard lab practices, safety, and hygiene Good observation and record-keeping skills Ability to work as part of a team and meet deadlines Basic knowledge of MS Office (Excel, Word) for lab documentation Job Type: Full-time Pay: ₹15,153.62 - ₹25,000.00 per month Schedule: Day shift Work Location: In person

Job Title: communications trainer II Job Description Concentrix is a technology-enabled global business services company specializing in customer engagement and improving business performance. We partner with ambitious, progressive executives around the world to future-proof their business and stay ahead of the competition and customer expectations. Role and Key Responsibilities: Support Front Line Recruitment Teams to assess the quality of new hires Consistent alignment with operations by auditing calls , e-mails and chats. Understanding needs, conducting refresher training in English - as per requirement Demonstrating innovation in training by incorporating the floor requirement into the curriculum. Maintaining Data and MIS as per the training BPMS / requirement Supports intra & inter function collaboration Proactively implement best practices and add value across locations Attend the mandatory TTT program Interfaces with customers as per requirement Conducts Need Analysis and shares feedback with the stakeholders Meeting the monthly Conversion & Effectiveness targets Providing Feedback to the New Hires on Soft Skills and basic grammar Mentoring the New Trainers Participate in calibration of Trainers, QAs and Voice Coaches within the team and with the TTBU training team Analyze and report findings for Process Training batches Conduct refreshers basis TNA, publish and execute for 100% closure every month Meet the training requirements of the BU basis TNA Design & develop training processes (need identification to feedback and follow through) in consultation with the training teams Track and report improvements Key Skills and knowledge: : CAT Score of 6.5 or above Excellent communication skills (English & Hindi). Excellent facilitation and presentation skills Data handling / data interpretation and Data Management. Good people management and Interpersonal Skills. Good knowledge of computers and MS Office (Excel, Power point). Strong organizational and presentation skills Educational Qualification – Graduation / Diploma (15 years of formal education) in any discipline. Disclaimer:- 'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities. Location: IND Gurgaon Building 14 - 11F, Tower D Language Requirements: Time Type: Full time If you are a California resident, by submitting your information, you acknowledge that you have read and have access to the Job Applicant Privacy Notice for California Residents

This role is for one of our clients Industry: Administrative and Support Services Seniority level: Associate level Min Experience: 1 years Location: Gurgaon JobType: full-time As a Quality Assurance Specialist within the Student Admissions team, you will play a mission-critical role in safeguarding the integrity of our student experience. Your core responsibility will be to monitor, evaluate, and enhance the performance of Admissions Mentors through structured audits and actionable insights. By driving operational excellence and continuous improvement, you will ensure that our communication, documentation, and service standards consistently exceed expectations. What You’ll Do Interaction Quality Audits Evaluate mentor-student conversations across channels (WhatsApp, email, CRM, and call recordings) for clarity, empathy, accuracy, and alignment with brand voice. Use a structured scoring rubric to assess interaction quality and flag deviations from communication guidelines. Provide mentors and their managers with constructive, data-driven feedback for improvement. ️ Documentation & CRM Review Audit CRM entries and student records to ensure completeness, accuracy, and consistency with key milestones (e.g. application, visa, fee payments). Identify missing data, improper tagging, or outdated notes that could impact student outcomes. Drive adherence to real-time data capture policies and SOPs. Process Adherence Monitoring Cross-check mentor workflows against standardized operating procedures to ensure protocol compliance. Highlight process breakdowns, missed timelines, or critical errors requiring intervention. Collaborate with Team Leads and Trainers to reinforce best practices. Reporting & Insight Generation Develop and maintain quality dashboards, audit reports, and performance summaries. Identify recurring issues, trending behaviors, and team-level gaps in service delivery. Share audit insights with Training and Leadership teams to guide improvements. Feedback & Skill Development Support mentors with performance coaching by pinpointing strengths and areas for growth. Recommend targeted learning interventions to enhance communication, compliance, or documentation skills. Assist Training teams in updating playbooks, SOPs, and communication templates based on quality findings. Risk & Issue Escalation Act as a frontline defense against high-risk or subpar student experiences. Proactively flag critical issues such as misinformation, documentation delays, or potential escalation risks. Work with leadership to ensure timely resolution and safeguard student trust. Standardization & Calibration Participate in regular calibration sessions to align QA evaluations across the team. Help refine audit scorecards and quality benchmarks to match evolving expectations and business goals. Continuous Improvement Identify systemic issues and recommend enhancements to tools, processes, or training methodologies. Stay informed about trends in student communication and digital onboarding to ensure audits remain relevant and effective. Who You Are Detail-oriented with a structured approach to reviewing large volumes of communication and documentation. Strong communicator with the ability to deliver honest, constructive feedback in a supportive manner. Analytical thinker who can spot trends, identify root causes, and suggest practical solutions. Comfortable working independently with cross-functional stakeholders including Training, Operations, and Leadership. Required Skills Quality Auditing (voice/chat/email) CRM & Documentation Analysis Compliance Monitoring Process Evaluation & SOP Enforcement Communication Coaching Reporting & Data Interpretation Preferred Qualifications Bachelor’s degree in Business, Education, Communications, or related field. Experience in a quality assurance, auditing, or compliance role—preferably in education, edtech, BPO, or student services. Familiarity with CRM systems (e.g., Salesforce, HubSpot), LMS platforms, or quality scorecard frameworks.

Quality Control Officer – Ayurvedic, Nutraceutical & Healthcare Manufacturing Location: Faridabad, Haryana, 121001 Company: Vedic Herbal Concept Experience: 2–5 Years Qualification: B.Sc / M.Sc in Chemistry, Biotechnology, or B.Pharm / M.Pharm Industry: Ayurvedic | Nutraceutical | Healthcare About Us Welcome to Vedic Herbal Concept , your trusted partner in manufacturing premium healthcare and wellness products. We specialize in Ayurvedic formulations, nutraceuticals, and high-quality personal care solutions. Rooted in tradition and powered by science, our state-of-the-art manufacturing facilities uphold the highest standards of purity, sustainability, and efficacy. We are looking for a detail-oriented Quality Control Officer to join our team and ensure our products consistently meet the regulatory and quality expectations of both national and international markets. Key Responsibilities Conduct quality checks on raw materials, packaging materials, in-process, and finished goods as per FSSAI, GMP, and internal specifications. Perform chemical and physical tests to evaluate product safety, consistency, and compliance. Maintain and review test records, COAs, calibration logs, and SOPs in accordance with regulatory guidelines. Monitor and ensure adherence to GMP, FDA, HACCP, and ISO 22000 quality systems. Conduct root cause analysis and implement corrective and preventive actions (CAPA) for non-conformance or deviations. Coordinate with R&D, production, and QA teams for new product validations, process improvements , and batch release decisions. Ensure proper calibration and functioning of laboratory instruments and cleanliness of QC lab. Stay updated with FSSAI guidelines and Ayurvedic pharmacopoeia . Key Skills Required Sound knowledge of FSSAI regulations, Ayurvedic quality norms, and ISO/GMP documentation . Experience with lab testing instruments (pH Meter, Gravity, Moisture Analyzer, Ash etc.). Excellent analytical, documentation, and report-writing skills. Ability to work independently and manage multiple product lines (Ayurvedic, nutraceuticals). Strong interpersonal skills and attention to detail. What We Offer A collaborative work environment that values tradition, innovation, and integrity. Opportunity to work with a diverse product range across Ayurvedic, nutraceutical, and beauty categories. Competitive salary and growth-oriented career path. Join Us If you are passionate about quality and want to make a real difference in the wellness industry, we invite you to apply and grow with Vedic Herbal Concept . Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Performance bonus Education: Bachelor's (Required) Experience: QC: 2 years (Required) Location: Faridabad, Haryana (Preferred) Work Location: In person Application Deadline: 16/06/2025

Exposure to industrial DCS and PLC systems, Experience performing calibrations on transmitters, flowmeters, valves, etc. Maintenance of various types of Pressure, Temperature, Flow and Level transmitter. Maintenance of various types of controls valve. Loop checking of various types of Working on RTD and Working on various types of Pressure, Temperature and Level switch. Handle the Installation Erection & commissioning of instruments. Desired Skills Maintaining calibration reports of the team. (Daily, Monthly, Quarterly, Half yearly and yearly). - Maintaining AMC records (Annual maintenance calibration) IQ, OQ and PQ documents of instruments. - To coordinate with engineering department for the support and service in case of breakdown of any instruments/Equipment’s. - Follow up of instrument maintenance in case of failure, perform troubleshooting, coordinate with service engineer, and get the instrument repaired. Also, responsibility is to provide / ensure uninterrupted utilities services to all plant operations, Monitor Plant-operating functions in accordance with Operating Procedures. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Work Location: In person

Job Summary: Responsible for maintaining quality standards and ensuring that sheet metal components and assemblies meet design specifications, customer requirements, and industry standards. Key Responsibilities: In-Process and Final Inspection Perform dimensional and visual inspection of sheet metal components. Monitor quality at various stages of fabrication (laser cutting, bending, welding, powder coating, etc.). Quality Documentation Prepare and maintain inspection reports, NCRs (Non-Conformance Reports), and CAPA (Corrective and Preventive Action) records. Update control plans, SOPs, and checklists. Supplier Quality Conduct incoming inspection of raw materials and bought-out items. Coordinate with the purchase team and vendors for quality issues. Standards Compliance Ensure compliance with ISO 9001:2015 and customer-specific standards. Assist during internal and external audits. Problem Solving Participate in root cause analysis and implement corrective actions using 5 Why, Fishbone (Ishikawa), or Pareto analysis. Continuous Improvement Identify quality improvement opportunities and implement Kaizen initiatives. Collaborate with production to reduce rework and rejection. Tool Handling & Measurement Use measurement tools like Vernier Caliper, Micrometer, Height Gauge, Welding Gauge, etc. Maintain calibration records of measuring instruments. Drawing Reading & Interpretation Accurately interpret engineering drawings, GD&T symbols, and material specifications for inspection and verification. Production Coordination & Follow-Up Closely follow up with the production team to ensure timely corrective actions and resolution of quality issues. Assist in aligning production output with quality standards Key Skills: Good understanding of sheet metal fabrication processes 2 Years (preferably in mechanical / sheet metal industry) Diploma / B.E. / B.Tech – Mechanical Engineering or relevant field Drawing reading and interpretation skills Knowledge of GD&T, Engineering drawings Basic knowlege in Autocad Basic knowledge of welding quality Experience with tools like 7QC, 5S, and Lean principles Familiar with Odoo or similar platforms Proficient in MS Office, especially Excel Behavioural Skills: Attention to detail Proactive problem-solving Team collaboration Good communication skills Time management Job Type: Full-time Pay: ₹12,483.50 - ₹43,322.31 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person

Job requisition ID :: 84124 Date: Jun 9, 2025 Location: Chennai Designation: Senior Executive Entity: Overview of role and associated job description Economic Sanctions and Screening team responsible for developing, enhancing, and validating sanctions screening frameworks and models. This role plays a pivotal part in fortifying the firm's financial crime risk posture by ensuring our screening capabilities align with global regulatory expectations and industry best practices. Responsibilities Design and Development: Develop, test, and optimize sanctions screening frameworks including name and payment screening methodologies. Model Enhancement: Evaluate existing sanctions models (fuzzy matching algorithms, rules logic, thresholds) and propose enhancements based on regulatory guidance and operational feedback. Framework Review: Conduct periodic and event-driven reviews of sanctions screening models to ensure continued relevance and compliance with OFAC, EU, UN, and other regulatory standards. Scenario Calibration and Tuning: Support tuning and threshold analysis for match scoring, leveraging historical alert data and false positive metrics. Data Analytics and Insights: Analyze screening outcomes to identify gaps, trends, and patterns that inform risk mitigation strategies and enhance effectiveness. Documentation and Governance: Prepare and maintain comprehensive model documentation, validation reports, and technical specifications in line with model risk governance frameworks. Stakeholder Engagement: Collaborate with compliance officers, technology teams, and business stakeholders to gather requirements, explain model logic, and support audits and regulatory reviews. Required Experience and Skills: Domain Expertise: 1-3 years of hands-on experience in sanctions screening framework development, tuning, and validation. Familiarity with leading screening platforms (e.g., FircoSoft, Bridger, Actimize, Oracle Watchlist Screening, etc.) and list management practices. In-depth understanding of global sanctions regimes (OFAC, EU, UN, HMT) and related regulatory expectations. Experience in integrating sanctions screening models with broader AML/CFT frameworks. Exposure to AI/ML techniques for entity resolution or fuzzy matching optimization. Prior involvement in regulatory examinations or independent validations of screening tools. Technical Proficiency: Strong programming and scripting skills (Python, R, SQL, SAS). Experience in data modeling, scoring logic calibration, and large-scale dataset analysis. Analytical Thinking: Ability to conduct root cause analysis on alert quality issues. Strong quantitative and qualitative problem-solving capabilities. Communication: Strong written and verbal communication skills, including the ability to explain technical models to non-technical stakeholders. Ability to craft data-backed narratives and present recommendations with clarity. Education Bachelor's Degree / Master's Degree Location Chennai /Bengaluru / Mumbai

We are Hiring Asst Quality Controller Key Responsibilities: Assist in inspecting incoming raw materials such as kraft paper, adhesives, and liners for quality compliance. Monitor in-process quality during the manufacturing of corrugated boxes (printing, cutting, slotting, pasting). Conduct regular checks on dimensions, GSM, bursting strength, edge crush tests (ECT), and moisture levels. Identify and report defects or deviations from specifications and assist in corrective action implementation. Maintain proper documentation of inspection records and quality reports. Support the Quality Controller in root cause analysis and continuous improvement activities. Ensure products meet customer specifications before dispatch. Assist in calibration of testing instruments and equipment. Coordinate with the production and packing teams to ensure compliance with quality standards. Job Type: Full-time Pay: ₹17,000.00 - ₹20,000.00 per month Work Location: In person

Responsible to assist installation & commissioning of plant machinery. Responsible for qualification & documents related to qualification of plant machinery. Responsible for executing and installation of plant equipment’s and monitor the site execution work in project. Responsible for maintenance and breakdown activity related to plant equipment / machineries. Responsible to procure & maintain the critical spares inventory. Responsible to update and maintain all cGMP documents related to breakdown & preventive maintenance of plant machinery as per SOP. Responsible to supervise the calibration activity and maintain the related documents. Responsible to generate tools and parts requirement for daily breakdown and preventive maintenance. Responsible to carry out all work as per cGMP and GEP. Responsible to update and maintain all cGMP documents related to breakdown and preventive maintenance as per SOP. Responsible for handling quality management documents i.e., Change control, Deviation, CAPA, Quality Risk Management etc.. Responsible for co-ordination with vendors and purchase department Responsible for qualification & documents related to qualification of plant machinery. To ensure that Preventive and Predictive Maintenance is carried out in co-ordination with the concerned departments as per planner. Preparation and review of QMS documentation. Education: Diploma/ B.E. Total Experience - 3 - 7 Years of experience in engineering plant maintenance role for sterile manufacturing plant

Operate and monitor manufacturing equipment and Instrument used in various stages of API production, such as reactors, Centrifuge, Dryer, Miller, sifter etc. Maintaining accurate records and documentation of production activities, including batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch Packing Record (BPR) records, Equipment’s usage logs and Deviation reports if, any. To co-ordinate with engineering department for the shift break down jobs. To monitor the utility operation in the plant and report any abnormality to engineering department. Collaborate with other shop floor personnel, shift in-charges, and cross-functional teams to ensure efficient and coordinated production. Before charging of batch, cleanliness of Equipment’s to be verified by visual verification procedure. To maintain good housekeeping in respective manufacturing area during process. Receive, store, and handle raw materials, intermediates, and finished products. Maintain accurate reconciliation records and follow proper material handling procedures. Follow established procedures to maintain product quality and consistency. This may involve sampling and testing intermediates, raw materials, and finished products. To monitor the process online and record/fill the entire document legible. Continuously monitor & maintain process parameters as per the desired product specifications and quality. To record and maintain all the documents online as per CGMP. Execute batch processing tasks according to standard operating procedures (SOPs), Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch packing Record (BPR), and maintain the details of records in equipment usage logs Ensure that all steps are carried out accurately and in a timely manner. To monitor and record temperature, Humidity and differential pressure in clean area (Level-I, Level-II & III). To check and record daily weighing balance calibration and verification. To take training online in AIMS software. Participate in training programs to enhance knowledge and skills related to API/Intermediate’s manufacturing and safety point of view. Adhere to and promote safety practices, including the use of personal protective equipment (PPE) and following safety procedures to prevent accidents or incidents. Be prepared to respond to emergencies, such as spills, leaks, or safety incidents, by following established emergency procedures. Participate in equipment cleaning and maintenance activities to ensure equipment is in good working condition. Identify and address issues or deviations in the manufacturing process, such as equipment malfunctions or variations in product quality. Comply with environmental regulations, including proper waste disposal and following procedures for managing hazardous materials. Identify opportunities for process optimization, efficiency improvements, and waste reduction and communicate suggestions to higher-level personnel. To co-ordinate with QA department for documents issuance/submission and warehouse for RM, Intermediate, API issuance/submission as per requirement. To be maintained plant/process related consumable items Inventory as per requirement. To review the manufacturing department executed documents like, Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch packing Record (BPR) etc.. Qualification - B.E Chemical / B. Tech Chemical

Responsible for preparation, review, revision, control, and implementation of standard operating procedures of packing department. Responsible for preparation & review of the master documents of packing. Responsible for preparation and review of Protocols and reports based on the requirements. To assist the officers and Executives for document management and preparation like BPRs master SOPs etc.. Responsible to identify training needs and impart training of SOPs and developmental training within the department and for another department. Responsible for the handling of Change Control, Deviations, CAPA, Investigation etc.. To assist the packing officer for line clearance activity before commencing the operations like labelling and packing operation. To have good communication skill to avoid misunderstanding. Arrange to send requisition in advance to the store get the material required for the next day production plan. Responsible to monitoring of all the activities related to packing. Responsible to give proper planning to subordinates and ensure its implementation. Responsible for preparation of production planning on monthly and daily as per the requirement and availability of materials. Responsible to prepare daily production report as per the production achieved. Responsible to helpful all the types of validation, calibration, and verification. Responsible to check all the record and logbooks related to packing area. Responsible to give training to all the subordinates, technicians, and operators of the department. Responsible to keep area updated with all the document and cleaning. Responsible to provide guidance to subordinates. Responsible to be fully familiar with machine and activities in his work. Education: B.Sc., B.Pharma, M.Sc., M.Pharma Total Experience - 3 - 7 Year in sterile manufacturing- packing

Job Description : We are seeking an Extremely Talented Fresher or Experience candidate to join our team. If you're passionate about Installation Commissioning/Trouble Shooting etc of Process & Analytical Instruments e.g. Gas / Liquid Analyzers, Particulate Monitoring equipment’s, , Flow / Level / Pressure measuring instruments. Roles & Responsibilities: Installation, commissioning, operation, maintenance and troubleshooting of Analytical Air Quality Gas Analyzers, Particulate Monitoring Analyzers, Water Quality Analyzers & other Bhoomi make products. Identifying root cause of failures and implementing quick breakdown solutions to put the equipment back in operation within minimum turnaround time. Involved in the operations, maintenance and troubleshooting of CEMS and Air Quality Monitoring Stations equipped with various Automatic On-line Gas Analysers Monitor and ensure installed Carrying out routine scheduled maintenance work and responding to equipment faults. Ensured spare management for all instruments and analysers also generated, processed & Interpreted air quality data. Involved in the calibration and quality checking of Air Monitoring System. Project Commissioning and Troubleshooting at Client’s end Ensure safety norms are followed during installation and maintenance process. Organized and provided training to the staff of clients. Ensure overall customer satisfaction. Handle customers in professional manner during difficult high-pressure situations Ensure overall customer satisfaction. Qualification - Diploma / Bachelor's degree in Electrical, Electronics and Telecommunication Engineering / Instrumentation or related field Understanding of the latest technologies, trends, and industry standards related to Instrumentation Strong analytical and problem-solving skills are essential for identifying and resolving technical challenges encountered during Product Promotion. Ability to work effectively in a team environment, collaborate with colleagues from different department and contribute to achieving sales goals. Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Provident Fund Schedule: Day shift Education: Bachelor's (Required) Experience: Field service: 2 years (Required) Location: Baroda, Gujarat (Required) Willingness to travel: 100% (Required) Work Location: In person

Job description Key Responsibilities & Duties:Utility Systems Operations & Maintenance Monitor and operate essential utility systems such as HVAC, boilers, air compressors, purified water (PW/WFI) systems, chillers, cooling towers, and effluent treatment plants (ETP/STP). Perform routine preventive maintenance to ensure the efficient and reliable operation of all utilities. Handle breakdown maintenance promptly to minimize downtime and production interruptions. Inspect and calibrate utility equipment as per SOPs and regulatory requirements. Maintain an updated log of all equipment performance data, maintenance activities, and breakdown reports. Regulatory Compliance & Documentation Ensure compliance with GMP, WHO, USFDA, MHRA, and other regulatory standards related to utility systems. Prepare and maintain Standard Operating Procedures (SOPs), maintenance logs, and validation reports for all utilities. Support regulatory audits and inspections by providing documentation and demonstrating compliance. Ensure timely renewal of Annual Maintenance Contracts (AMC), calibration certifications, and validation records . Conduct periodic risk assessments and update risk mitigation plans for utility operations. Energy & Cost Optimization Monitor energy consumption of utility equipment and implement energy-saving initiatives. Analyze breakdown trends and suggest improvement plans to enhance equipment efficiency. Identify and implement cost-saving opportunities by optimizing utility operations. Evaluate and implement modern maintenance techniques such as Total Productive Maintenance (TPM), Root Cause Analysis (RCA), and Predictive Maintenance (PdM). Safety & Team Coordination Ensure adherence to safety guidelines while operating and maintaining utility systems. Conduct training sessions for maintenance staff on best practices, emergency response, and equipment handling. Coordinate with production, quality, and other departments to ensure uninterrupted plant operations. Liaise with vendors and contractors for maintenance support, spare parts, and technical assistance. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Cell phone reimbursement Flexible schedule Health insurance Internet reimbursement Paid sick time Paid time off Provident Fund Schedule: Day shift Night shift Rotational shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

It's about Being What's next. What's in it for you? A Manager in the instrumentation department will be responsible for Erection & commissioning of Instrumentation & Process Control system of medium & small size projects, ensuring safety, quality & timely completion of instrumentation jobs. At Linde, the sky is not the limit. If you’re looking to build a career where your work reaches beyond your job description and betters the people with whom you work, the communities we serve, and the world in which we all live, at Linde, your opportunities are limitless. Be Linde. Be Limitless. Team Making an impact. What will you do? In this role you shall be responsible for erection & commissioning of Instrumentation & Process Control system of medium & small size projects, ensuring safety, quality & timely completion of instrumentation jobs Further you will be customer Focus (Customer relationships) - Uses information on customer issues, satisfaction and needs to increase levels of customer satisfaction Furthermore, you should have a Visible Leadership (Exemplary Leadership) - Drives for high performance and takes personal accountability for results Moreover, you should have a Decision making & execution (Decision making) - Makes decisions based on facts, knowledge and experience after considering viable alternatives Additionally, you should do Personal Development (Resilience) - Handles resistance, set-backs and adversity in a resilient, emotionally mature and self reliant manner Winning in your role. Do you have what it takes? You are a B-Tech instrumentation with 5-7 years of experience Further you have knowledge of analyzers like CO2 trace, O2 purity & trace, Moisture, N2O etc and knowledge in calibration of all type of instruments used in process plant Hands on experience in Control system is required for this role Hands on knowledge in DCS/PLC logic & troubleshooting of DCS/PLC etc You should have knowledge of MS office tools, Word, excel, power point etc. Why you will love working for us! Linde is a leading global industrial gases and engineering company, operating in more than 100 countries worldwide. We live our mission of making our world more productive every day by providing high-quality solutions, technologies and services which are making our customers more successful and helping to sustain and protect our planet. On the 1st of April 2020, Linde India Limited and Praxair India Private Limited successfully formed a joint venture, LSAS Services Private Limited. This company will provide Operations and Management (O&M) services to both existing organizations, which will continue to operate separately. LSAS carries forward the commitment towards sustainable development, championed by both legacy organizations. It also takes ahead the tradition of the development of processes and technologies that have revolutionized the industrial gases industry, serving a variety of end markets including chemicals & refining, food & beverage, electronics, healthcare, manufacturing, and primary metals. Whatever you seek to accomplish, and wherever you want those accomplishments to take you, a career at Linde provides limitless ways to achieve your potential, while making a positive impact in the world. Be Linde. Be Limitless. Have we inspired you? Let's talk about it! We are looking forward to receiving your complete application (motivation letter, CV, certificates) via our online job market. Any designations used of course apply to persons of all genders. The form of speech used here is for simplicity only. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, pregnancy, sexual orientation, gender identity or expression, or any other reason prohibited by applicable law. Linde India Limited acts responsibly towards its shareholders, business partners, employees, society and the environment in every one of its business areas, regions and locations across the globe. The company is committed to technologies and products that unite the goals of customer value and sustainable development. Show more Show less

Operate and monitor machinery involved in the final stages of production, which may include finishing, assembly, testing, or packaging equipment. Perform basic setup, calibration, and adjustments of machinery as required. Conduct visual inspections of finished products to ensure they meet company quality standards and specifications. Identify and segregate defective or non-conforming products. Perform quality checks using basic measurement tools and gauges. Accurately pack finished goods into designated cartons, cases, or containers. Apply correct labels, barcodes, and other identification marks to products and packaging. Ensure all packaging is secure and ready for shipment. Move raw materials, in-process goods, and finished products to and from the back-end production area. Maintain an organized and clean workspace, ensuring materials are stored correctly. Adhere strictly to all company safety policies and procedures to ensure a safe working environment. Wear appropriate Personal Protective Equipment (PPE) at all times. Minimum of a 10th or 12th standard pass. Experience in a similar "back-end" or finishing role will be an advantage. Freshers with a strong willingness to learn may also be considered. Job Type: Full-time Pay: ₹8,000.00 - ₹12,000.00 per month Benefits: Paid sick time Paid time off Schedule: Day shift Supplemental Pay: Overtime pay Work Location: In person Expected Start Date: 16/06/2025