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0 years
0 Lacs
Mumbai, Maharashtra, India
On-site
Company Description Athena Instruments Pvt Ltd specializes in high-precision laboratory equipment, providing innovative and high-quality products to scientists, researchers, and industries globally. As an ISO 9001:2015-certified company, we maintain the highest standards in scientific instrumentation, ensuring accuracy and reliability. Our advanced product line includes nitrogen evaporators, probe sonicators, hydrogen and nitrogen gas generators, and custom scientific solutions. We serve laboratories across various industries, partnering with research labs and institutions in numerous regions, including India, the USA, Europe, the Middle East, South East Asia, and Africa. Role Description This is a full-time on-site role located in Mumbai for an Analytical Instruments Specialist at Athena Instruments Pvt Ltd. The role involves day-to-day tasks such as instrumentation, troubleshooting, calibration, preventive maintenance, and supporting research activities to ensure the efficient operation of laboratory equipment. The specialist will work closely with various departments to maintain high precision and performance of all instruments. Qualifications Strong skills in Instrumentation and Calibration Experience in Troubleshooting and Preventive Maintenance Research skills to support scientific and industrial applications Excellent problem-solving and analytical thinking abilities Ability to work independently as well as collaboratively in a team Degree in Engineering, Physics, Chemistry, or a related field is preferred Experience in the laboratory equipment industry is a plus
Posted 1 week ago
9.0 - 12.0 years
0 Lacs
Bengaluru, Karnataka, India
On-site
Date: 31 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Designation: AQA Reviewer Job Location: Bangalore Department: Analytical Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Key Responsibilities Review of analytical raw data (through ELN / manual) generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and specification. Ensuring, verifying, and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. Review of Outsourced analytical report. Review of logbooks with respect to all activity performed in the lab. Responsible for taking any other job allocated by Department Head / Department In charge. Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document. Responsible to ensure review and release of raw material and packing material in LIMS/SAP. Responsible to ensure review and release of cleaning samples, inprocess samples, calibration reports and standard qualification reports. Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. Review the documents for completeness, compliance to good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable Review of all the tests as specified in the specification/Request for analysis /validation protocol/sampling protocol have been carried out Review of all supporting documents like chromatograms, balance print outs, Instrument printouts are enclosed in sequential manner to the parent report with signature as applicable Review of the test results in COA against specification along with other relevant sample information before approval. In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Involving in the Laboratory incident investigation, review, and approval. Educational Quali fi cation: M. Sc (Life science / Chemistry)/ M. Pharm Technical/functional Skills Good exposure in Enterprise Applications like SAP, Learning Management Systems, Trackwise, and Analytical laboratory Applications like Chromatography and Non-chromatography data Management. Well versed in electronic data audit review. Good Knowledge on handling the application software. Establish good Interpersonal skills with cross-functional teams. Experience: 9 to 12 Years experience in life science industry. Behavioural Skills Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
Posted 1 week ago
5.0 years
0 Lacs
Ahmedabad, Gujarat, India
On-site
Position: Hardware Product Manager Location: Ahmedabad Experience: 5+ years of experience in electronics product development or QA/testing in IoT or embedded hardware domains CTC: 8-9 LPA Key Responsibilities ● Production Oversight & QA/QC Management ○ Own the full hardware production lifecycle, from prototype validation to final production QA before shipping. ○ Ensure strict adherence to Standard Operating Procedures (SOPs) and quality benchmarks across every production batch. ○ Lead in-house electronics and production hardware testing – including PCB validation, component-level checks, and functional on-device verifications. ● Hardware & Embedded Systems Testing ○ Debug firmware on embedded systems (C/C++ and Python) and support real-time validation. ○ Perform rigorous on-device testing for hardware-software integration, edge-case simulations, and the product’s environmental resilience. ● Cross-Functional Coordination ○ Act as the bridge between R&D and Production teams—ensuring smooth handover and documentation of SOPs, Test Procedures, firmware versions, and calibration standards. ○ Collaborate with Hardware Support and Project teams to log, investigate, and resolve product issues and close customer feedback loops. ● Leadership & Team Management ○ Lead the Hardware QA and Production Testing Team with ownership, clarity, and accountability. ○ Establish a culture of discipline, traceability, and continuous improvement in production workflows. ○ Develop internal knowledge bases, SOPs, and training modules for the product onboarding. Eligibility & Requirements ● B.Tech/B.E/M.E in Electronics, Electrical, or Instrumentation. ● 5+ years of experience in electronics product development or QA/testing in IoT or embedded hardware domains. ● Proficient in Embedded C/C++, Python, and the use of hardware testing tools. ● Experience with version control systems (e.g., Git) and product release workflows. ● Proven skills in hardware diagnostics, debugging, and test report generation. ● Strong understanding of quality assurance practices, environmental testing procedures, and certification requirements. ● Excellent communication in English—both verbal and written. If your profile is matching with the requirement & if you are interested for this job, please share your updated resume with details of your present salary, expected salary & notice period.
Posted 1 week ago
3.0 - 6.0 years
0 Lacs
Hyderabad, Telangana, India
On-site
Job Summary We're looking for a highly skilled and detail-oriented Senior Test and Validation Engineer to join our Quality Department in Hyderabad. In this role, you'll be instrumental in ensuring the quality and reliability of our LED lighting products by planning, executing, and documenting comprehensive validation and quality assurance tests. If you have strong expertise in photometric, functional, and accelerated life testing, coupled with a deep understanding of relevant national and international standards, we encourage you to apply! Key Responsibilities Develop and Execute Test Plans: Create and implement thorough test plans for LED lighting products, covering all critical aspects. Perform Diverse Testing: Conduct a wide range of tests including photometric (luminous flux, efficacy, beam angle, CCT, CRI as per LM-79 and IS 16106), functional, electrical safety (as per IS 10322 Part 5/Section 1 to 8), and accelerated life tests. Ensure Compliance: Guarantee strict adherence to BIS, IS, IEC, and LM standards, along with relevant certification requirements. Lab Operations: Perform tests in dark rooms, dedicated test labs, and environmental chambers. Documentation & Reporting: Meticulously document and report test procedures, observations, and results with accuracy and completeness. Collaborate & Resolve: Work closely with R&D, Production, and Supply Chain Management (SCM) teams to effectively resolve any quality and performance issues. Maintain Lab Infrastructure: Oversee the maintenance, calibration, and overall management of lab testing instruments and infrastructure. Support Audits: Provide support for both internal and external audits (BIS, ISO, customer inspections), including NABL documentation and surveillance assessments. Mentor & Train: Train and mentor junior engineers and technicians on QA processes and established standards. Qualifications & Experience Minimum Bachelor’s Degree in Engineering (B.E.) – Electrical, Electronics, or related field. 3 to 6 years of hands-on experience in product testing, preferably in LED lighting, electronics, or electrical manufacturing. Experience with testing procedures under BIS (IS 10322, IS 16101), IEC 60598, IEC 61000, LM79, and LM80 standards. Experience in a NABL or BIS-accredited lab is a plus. Skills Required Strong analytical and documentation skills. High attention to detail in testing and report generation. Familiarity with Microsoft Excel, Word, and standard QA software tools. Good verbal and written communication skills. Problem-solving mindset with a collaborative work ethic. Conduct photometric measurements (luminous flux, efficacy, beam angle, CCT, CRI, etc.) as per LM-79 and IS 16106. Perform electrical safety tests for luminaires as per IS 10322 (Part 5/Section 1 to 8). Operate and calibrate instruments such as: Goniophotometer / Integrating sphere with spectrometer Hi-pot tester, Earth continuity tester, Insulation resistance tester Thermal chamber, Lux meters, Multimeters Ensure test methods and conditions comply with NABL / ISO/IEC 17025 standards. Document and prepare technical test reports with accuracy and completeness. Maintain traceability and calibration status of all test equipment. Assist in method validation, uncertainty calculation, and internal audits. Coordinate with the Quality/Accreditation team to support NABL documentation and surveillance assessments. Ensure safe and efficient operation in the laboratory environment. Degree in Electrical, Electronics, or related field. Sound knowledge of: 10322 series, LM-79, IS 16106, IEC 60598, and related standards. Familiarity with test equipment, measurement procedures, and lab documentation practices. Good written and verbal communication skills. Attention to detail and ability to follow standardized procedures. Instrumentation & Equipment Experience (Preferred) Photometric Testing Goniophotometer Integrating Sphere Lux Meter Luminance Meter Dark Room Setup Electrical & Functional Testing Digital Power Analyzer (e.g., Yokogawa, Fluke) High Voltage / Hipot Tester Surge Generator / EFT Simulator LCR Meter Oscilloscope, Multimeter Functional Testing Rigs Environmental & Reliability Testing Accelerated Life Test (ALT) Chambers Thermal and Humidity Chambers Salt Spray Chamber Burn-in Racks Drop Tester / Vibration Table IP Testing Setup
Posted 1 week ago
9.0 - 12.0 years
0 Lacs
Bengaluru, Karnataka, India
On-site
Date: 31 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Essential Functions Job Title: QMS Coordinator Job Location: Syngene International Limited, Bengaluru About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’ s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose Of The Role This is an exciting opportunity to play a pivotal role in driving quality excellence at Syngene through the QMS function. The role offers exposure to implementing cutting-edge quality practices and refining compliance workflows, ensuring operational efficiency and regulatory readiness. It provides a platform to proactively identify improvement areas, embed quality culture across functions, and stay ahead of evolving standards in Formulations. Role Accountabilities Drive the continuous enhancement of Syngene’s Quality Management System by developing robust, in-house processes that reduce dependency on external audits and consultants. Begin by performing an in-depth review of existing QMS frameworks and regulatory guidelines. Design and implement optimized quality workflows leveraging digital tools and risk-based thinking. Evaluate system effectiveness through CAPA trends, and compliance metrics to identify process improvement hotspots. Based on these insights, the QMS evolved to support readiness for global regulatory expectations. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Demonstrated Capability Education Experience Candidate should have 9 -12 years exposure in Oral Solid Dosage forms and injectable facility quality assurance activities. Candidate should have USFDA audit exposure. Establish good Interpersonal skills with cross-functional teams. Skills And Capabilities Expertise in handling multiple expression platforms Capable of thinking scientifically to address complex problems and develop solutions Work as a team and have collaborative mindset Good communication skills Education B. Pharm/ M. Pharm Job Description Key Responsibilities: Create/ revise procedures and other related documents as applicable. Review of SOPs, IOPs, EOPs, Protocol and Reports for Formulation Facilities. Handling of Change Controls, Deviations, CAPA, Customer complaints, Self-Inspection and Internal Quality Audit. Perform Trending of Change Controls, Deviations, CAPA, LIR and Customer complaints. Ensure compliance with observations of Self Inspection, Internal Quality Audit and client or regulatory audit. Perform activities related to SAP. Vendor qualification of raw material, packing material, consumables, contractors engaged in manufacturing pertaining to GMP manufacturing with respect to vendor questionnaire verification, vendor audit and compliance report verification for approval. Approval of vendors by desktop and site audits. (As required) Review of Risk assessment document from the vendor. Verification of vendor rating documents from the purchase. Inspection of RM, PM and consumables for any damage and discrepancy possible during receipt, storage dispensing and handling of these materials in warehouse. Review of vendor Quality Agreement. Preparation and updation of requalification schedule for Manufacturers. Archival of documents. Issuance of annexures and logbooks. Provide data for QMR and QGF meeting. Provide line clearance to Dispensing, Manufacturing and Packaging area. Provide dispatch clearance for Shipment. Preparation & Review of RSG report. Review and Approval of Calibration Certificate. Review of executed BMR and BPR. Responsible for review and release of Batches. Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
Posted 1 week ago
3.0 - 5.0 years
0 Lacs
Hyderabad, Telangana, India
On-site
Job description: Job Description Role Purpose The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction ͏ Do 1. Conduct process quality audits as per plan Conduct various process audits as per guidelines and SPO’s defined in QMS Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridge any skill gap due to these changes 2. Conduct analysis, report generation and process compliance in different areas like metrics office, CAG, Process Definition Ensure processes to be followed in Wipro in terms of all quality norms in the areas of project management and highlight potential risks Provide insights and process guidance to the projects as per the need Prepare timely dashboards, reports, insights and share with the central quality and delivery teams to ensure minimum client escalation From time to time highlight any critical escalations where the central quality team’s intervention is required in any BU project team Automate the report generations etc to ensure minimization of non-value added tasks, ensuring maximum utilization of existing platforms and their increased adoption ͏ Deliver No. Performance Parameter Measure 1.Quality Standards Timely generation of reports, dashboards, insights to the respective team Accuracy of the data Feedback from the project teams on the insights Quality of insights shared with the team ͏ ͏ Mandatory Skills: Quality Assurance . Experience: 3-5 Years . Reinvent your world. We are building a modern Wipro. We are an end-to-end digital transformation partner with the boldest ambitions. To realize them, we need people inspired by reinvention. Of yourself, your career, and your skills. We want to see the constant evolution of our business and our industry. It has always been in our DNA - as the world around us changes, so do we. Join a business powered by purpose and a place that empowers you to design your own reinvention. Come to Wipro. Realize your ambitions. Applications from people with disabilities are explicitly welcome.
Posted 1 week ago
0.0 - 1.0 years
0 - 0 Lacs
Haldwani, Uttarakhand
On-site
HR CUM DEPUTY QUALITY MANAGER * Required Qualification A. MBA IN HR B Min. Exp. 1-5 * Roles & Responsiblities 1. DAILY RESPONSIBILITIES Area Tasks HR - Record biometric attendance - Monitor staff presence, punctuality, and behaviour. - Resolve minor grievances and support daily HR queries. - Check staff hygiene and dress code - Track /leave/overtime etc. - Manage hiring through job portals, agencies, and local networks ( if required) - Conduct initial screening, interview, and coordinate final selection with top management ( if requirements) - handle grievances, resolve conflicts, and ensure a healthy workplace culture. - Maintain compliance with health & safety norms. - Staff shift roster planning Quality - Supervise article receiving & lot making. - Coordinates with the team in hallmarking Process, ensures documentation - Monitor equipment condition. - Review customer complaints, after not resolving, coordinate with management if any -Monitor the daily work of the Quality Manager in his/ her absence. Reporting - Daily working report review of all employees. - Prepare a Daily working report. - Article in/out status, stock verification. - Equipment status log (e.g., XRF machine working) 2. WEEKLY RESPONSIBILITIES Area Tasks HR - Prepare and submit a weekly HR report to management - Staff shift roster planning - Leave and overtime summary - Cleanliness and workplace inspection Quality - Internal checklist audit of process (lot tracking, SOP adherence) - Equipment maintenance check - file review Coordination - Team meeting with staff and Quality Manager. - Feedback review from customers. - Ensure stock of labels, tags, consumables, etc. 3. MONTHLY RESPONSIBILITIES Area Tasks HR - Salary sheet preparation with Accounts - Review attendance register and leave register - Update employee records and ID cards -Submit a monthly HR report (new hires, etc) Quality - Review and update SOPs if needed - Monthly internal quality audit - Maintain calibration schedule - Review turnaround time and rejections of hallmarking. Reporting - Monthly HR & Quality report - Consumables stock statement - MIS report for hallmarking volumes 4. QUARTERLY RESPONSIBILITIES Area Tasks HR - Conduct employee performance review meetings - Plan skill development/refresher training - Update manpower requirement (if any) - HR Policy Review and Amendments. - Set KPIs for performance and appraisal. - Conduct a workshop on workplace ethics, soft skills, and compliance.. - Arrange a Skill development session. Quality - Conduct NABL/BIS readiness mock audit - Submit internal audit report to Quality Manager - Review non-conformance & CAPA implementation - Coordinate calibration with external agency (if due) 5. ANNUAL RESPONSIBILITIES Area Tasks HR - Support HR policy updates & revisions - Plan annual health check-up or wellness programs - Prepare appraisal data for increments - Employee data verification for renewal - Conduct regular employee performance reviews annual basis. Quality - Assist in annual NABL/BIS audits - Update QMS documentation - Annual maintenance contract (AMC) check of XRF/equipment & software - Audit review & final reporting - Coordinate quality training for all technical staff Reporting - Submit annual HR & Quality summary report - Review of SOPs & statutory compliance documents. Job Types: Full-time, Permanent Pay: ₹12,500.00 - ₹20,000.00 per month Schedule: Day shift Rotational shift Experience: HR sourcing: 1 year (Preferred) Location: Nainital, Uttarakhand (Required) Work Location: In person Expected Start Date: 31/07/2025
Posted 1 week ago
0 years
0 Lacs
Pune, Maharashtra, India
On-site
Job Title: Manager-T&Q Job Description Key Responsibilities: Design quality monitoring frameworks, standards, and procedures. Regularly review calls, emails, chats, and other interactions to assess adherence to quality standards and identify areas for improvement. Analyse quality data to pinpoint recurring issues, process gaps, and training needs. Participate in calibration sessions with other stakeholders to ensure consistent and fair scoring of interactions. Create regular reports on quality metrics, trends, and improvement initiatives for management review. Supervise, mentor, and develop a team of quality analysts and trainers. Oversee the effective use of call recording, evaluation software, and other quality management systems. Evaluate effectiveness of TQ interventions Accurately capture SLA/SLO metrics, the reporting needs of each of the client and set up / customize processes to seamlessly meet client's expectation Provide crisp and specific feedback to Front Line Recruitment Teams on quality of new hires Design comprehensive training curriculum for new hires, ongoing skill development, and product/process updates. Facilitate engaging and effective training sessions using various methodologies (classroom, virtual, e-learning, on-the-job). Develop engaging and informative training materials, including presentations, manuals, job aids, and e-learning modules. Identify skill gaps and training requirements through needs analysis, performance data, and feedback from stakeholders. Desired Skills: Ability to provide clear, concise, and constructive feedback. Ability to interpret data, identify root causes, and recommend solutions. Ability to effectively deliver training and present quality findings. Ability to work effectively with agents, supervisors, and other departments. Understanding the importance of the customer experience and advocating for customer needs. Ability to motivate, guide, and develop a team of quality analysts. Process Oriented, Planning, Decision making, Data Handling, Ability to prioritize, Ability to meet deadlines and work under pressure Researching and implementing new training methodologies and tools to enhance learning effectiveness. 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: Design quality monitoring frameworks, standards, and procedures. Regularly review calls, emails, chats, and other interactions to assess adherence to quality standards and identify areas for improvement. Analyse quality data to pinpoint recurring issues, process gaps, and training needs. Participate in calibration sessions with other stakeholders to ensure consistent and fair scoring of interactions. Create regular reports on quality metrics, trends, and improvement initiatives for management review. Supervise, mentor, and develop a team of quality analysts and trainers. Oversee the effective use of call recording, evaluation software, and other quality management systems. Evaluate effectiveness of TQ interventions Accurately capture SLA/SLO metrics, the reporting needs of all clients and set up / customize processes to seamlessly meet client's expectations Provide crisp and specific feedback to Front Line Recruitment Teams on quality of new hires Design comprehensive training curriculum for new hires, ongoing skill development, and product/process updates. Facilitate engaging and effective training sessions using various methodologies (classroom, virtual, e-learning, on-the-job). Develop engaging and informative training materials, including presentations, manuals, job aids, and e-learning modules. Identify skill gaps and training requirements through needs analysis, performance data, and feedback from stakeholders. Key skills and knowledge: Ability to provide clear, concise, and constructive feedback. Ability to interpret data, identify root causes, and recommend solutions. Ability to effectively deliver training and present quality findings. Ability to work effectively with agents, supervisors, and other departments. Understanding the importance of the customer experience and advocating for customer needs. Ability to motivate, guide, and develop a team of quality analysts. Process Oriented, Planning, Decision making, Data Handling, Ability to prioritize, Ability to meet deadlines and work under pressure Researching and implementing new training methodologies and tools to enhance the learning effectiveness. Education: Graduation Disclaimer: 'Neither Concentrix nor any authorized 3rd party who assist with our recruitment process, ever ask candidates for ‘recruitment’, ‘processing’ or any other kind of fees in exchange for offer letters from Concentrix. Offer letters and other recruiting correspondence from Concentrix are printed on Concentrix letter head with authentic signatures of appropriate Concentrix authorities.' Location: IND Pune - Amar Tech Centre S No.30/4A 1 Language Requirements: Time Type: Full time If you are a California resident, by submitting your information, you acknowledge that you have read and have access to the Job Applicant Privacy Notice for California Residents R1632907
Posted 1 week ago
0 years
0 Lacs
Gurugram, Haryana, India
On-site
Seeking a detail-oriented and technically competent Technical Executive to support our PV Module Testing and Lab Operations . The ideal candidate should have strong knowledge of photovoltaic (PV) technology, testing protocols, and lab equipment. This role will involve day-to-day execution of module testing, maintaining testing equipment, supporting data analysis, and ensuring compliance with relevant standards and safety protocols. Key Responsibilities: Perform PV module testing using electroluminescence (EL), I-V curve tracing, insulation resistance, Hi-Pot, and other diagnostic techniques. Support lab-based testing operations such as Flash test , EL Imaging ,Thermal Imaging, Visual Inspection, etc. Assist in the handling, preparation, and testing of modules as per IEC standards (e.g., IEC 61215, IEC 61730). Ensure proper calibration and upkeep of lab equipment. Maintain accurate records of test data, observations, and results in prescribed formats. Coordinate with internal and external stakeholders for module movement, test scheduling, and reporting. Contribute to root cause analysis for defective or underperforming modules. Ensure implementation of safety and quality protocols in lab operations. Support technical evaluations and validations related to warranty claims and supplier discussions. Participate in regular audits and maintain documentation for internal and third-party evaluations. Technical Skills: Working knowledge of PV modules, test standards, and testing equipment. Familiarity with EL Imaging, IR Thermography, IV Curve measurement. Basic understanding of solar PV system behavior and failure mechanisms. Ability to interpret technical data and test reports. Software Skills: MS Excel, basic data analysis; exposure to PVsyst, LabVIEW or testing software is a plus
Posted 1 week ago
5.0 - 8.0 years
0 Lacs
Dahej, Gujarat, India
On-site
Essential Functions: JOB DESCRIPTION Operate and monitor equipment used in various stages of API production such as reactors, centrifuges, dryers, millers, sifters, etc. Ensure cleanliness and readiness of equipment before batch charging through visual verification procedures. Maintain accurate records, including Batch Manufacturing Record (BMR), Batch Cleaning Record (BCR), Batch Packing Record (BPR), equipment usage logs, and deviation reports. Execute batch operations strictly as per SOPs and GMP guidelines. Monitor and record process parameters in real-time to ensure adherence to specifications and quality. Report and coordinate with Engineering for any equipment breakdowns during the shift. Coordinate with QA for issuance and submission of documents and with the warehouse for material movement. Handle raw materials, intermediates, and APIs, ensuring proper storage, reconciliation, and documentation. Follow standard procedures for sampling and in-process testing of materials and intermediates. Maintain cleanliness and good housekeeping in the designated manufacturing area. Monitor utilities in the plant (e.g., steam, vacuum, chilled water) and report abnormalities. Monitor and record environmental conditions like temperature, humidity, and differential pressure in clean areas (Level-I, II, III). Perform daily verification and calibration checks of weighing balances. Participate in periodic equipment cleaning and preventive maintenance. Ensure proper handling and disposal of hazardous materials as per environmental guidelines. Identify process deviations, malfunctions, or quality concerns and report them immediately. Support continual improvement by suggesting ideas for optimization, efficiency, and waste reduction. Take mandatory safety and operational training via AIMS software and participate in hands-on skill-building sessions. Adhere strictly to safety practices and use PPE as per company safety protocols. Participate in emergency response activities such as managing spills or operational incidents. Ensure timely inventory of plant/process-related consumables. Review completed manufacturing records for accuracy, completeness, and compliance with SOPs. Additional Responsibilities: Support implementation of process improvement initiatives and lean manufacturing practices. Assist in the qualification and validation of equipment and processes as per regulatory and internal guidelines. Ensure readiness of the area for internal, external, and regulatory audits. Support investigation and documentation of deviations, change controls, and CAPAs in coordination with QA. Participate in cross-functional meetings to discuss production schedules, quality concerns, and improvement plans. Maintain discipline and GMP compliance on the shop floor and promote a culture of accountability. Train and mentor junior staff/operators on standard procedures and safe working practices. Assist in preparation and review of SOPs related to manufacturing activities. Support periodic review of equipment performance and suggest improvements for efficiency. Ensure adherence to environmental and safety norms in chemical handling and waste disposal. Actively participate in safety drills, risk assessments (HIRA), and incident investigations. Coordinate with stores for timely availability of raw materials, consumables, and packing materials. Report daily production updates to the shift in-charge or supervisor as required. Qualifications :- Education: Master Degree, M. Sc – Organic Chemistry - Preferred Bachelor Degree, B. Pharma – Preferred B.E. Chemical – Required B. Tech Chemical – Required Experience: 5 to 8 years in API/Intermediate manufacturing operations Skills: API Manufacturing Operations – Intermediate to Advanced Batch Documentation (BMR/BCR/BPR) – Intermediate GMP Compliance and Data Integrity – Intermediate Process Monitoring and Troubleshooting – Intermediate SOP Adherence and Equipment Operation – Intermediate Safety and Emergency Response – Intermediate Material Handling & Inventory Control – Basic to Intermediate Utilities & Cleanroom Parameter Monitoring – Basic Team Coordination and Communication – Intermediate. QUALIFICATIONS Qualifications :- Education: Master Degree, M. Sc – Organic Chemistry - Preferred Bachelor Degree, B. Pharma – Preferred B.E. Chemical – Required B. Tech Chemical – Required
Posted 1 week ago
8.0 - 15.0 years
0 Lacs
Khed, Maharashtra, India
On-site
Job Description Summary We are seeking experienced professional in the nickel electroplating field to join our manufacturing team. In this leadership role , you will establish ,control and optimize the electroforming process ensuring the highest standards of safety and quality while driving operational efficiency . Job Description Company Overview: Working at GE Aerospace means you are bringing your unique perspective, innovative spirit, drive, and curiosity to a collaborative and diverse team working to advance aerospace for future generations. If you have ideas, we will listen. Join us and see your ideas take flight! Site Overview Our Multi-modal Manufacturing Facility (MMF) in Pune plays a crucial role in manufacturing key aerospace components, supporting not only India’s defense and commercial sectors but also global aviation supply chains. Our relationships with Indian suppliers, combined with our world-class local facilities and global reach, continue to shape India’s aerospace ecosystem. Role Overview Daily monitoring of electroforming process operations and documentation, equipment, instruments , maintenance and checks of the electroforming process. Operation and control of daily output, safety and quality parameters of the electroforming process to Ensure that the documented work instructions and the router requirements are implemented as per operation sequence. Root cause analysis for the process defects and implementation of the corrective actions. Qualification and Training of operators on the special processes and related equipment. Coordination with Quality team for the calibration of instrumentation of process equipment and ensuring process and quality compliance. Preparation of Standard work, EHSRA, Heat Map and SOD and periodic review. Preparation of PFMEA and periodic review. Control of consumables and Implementing ideas for cost reduction. Generate and implement Productivity improvement ideas. Ensure compliance to customer specifications - requirements and NADCAP special process requirements. Technical Skills Strong, in depth understanding of chemical processes and material properties related to plating. Hands on experience in the electroplating process including nickel plating, nickel hard plating, thorough understanding of electroplating processes. ability to set up and operate the electroplating tanks, rectifiers and associated equipment. knowledge of plating chemistry, ability of safe handling chemicals, proper surface preparation, cleaning techniques like polishing, buffing, cleaning. familiarity with different plating solutions, quality control methods, solution control and analysis, monitoring of plating thickness and ensuring consistency, thorough understanding of principles of electrolysis, current density, anode, cathode functions. chemical compositions of the nickel plating baths, pH levels, additives and their impact of nickel plating quality, ability to use the instruments techniques, methods for the plating / coating thickness measurement, Proven ability for problem solving – diagnosing the issues with plating quality trouble shooting of common issues like pitting, burning, poor adhesion and complex plating problems and corrective action implementation. Understanding of the hazards associated with the plating process, chemicals , handling of the chemicals and handling procedures , awareness of environmental regulations , waste water treatment , disposal of associated hazardous wastes. Experience in preparation for NADCAP audits. training and mentoring of the processing engineers for the safety and quality best practices. Ideal Candidate An ideal candidate is a skilled professional with expertise in electroplating processes, coating of aerospace components and assemblies. Required Qualification B.E./ B Tech in Chemical / Mechanical engineering/ MSc Chemistry with 8 to 15 years of experience in Electroplating, coating of aerospace components and assemblies Preferred Qualifications Experience in leadership role within the plating environment in aerospace supplier industry Familarity with automated plating systems and advanced plating technologies Certification in plating technology or related field strong attention to detail and commitment to maintain high quality of safety and quality standards Strong written and verbal communication and leadership skills Ability to work collaboratively in a team oriented environment Proactive problem solving approach and continuous improvement mindset Ability to guide and lead team of engineers working for the process Whether we are manufacturing components for our engines, driving innovation in fuel and noise reduction, or unlocking new opportunities to grow and deliver more productivity, our GE Aerospace teams are dedicated and making a global impact. Join us and help move the aerospace industry forward. Additional Information Relocation Assistance Provided: Yes
Posted 1 week ago
5.0 years
0 Lacs
Rohtak, Haryana, India
On-site
Job Title: QMS Engineer/Manager Location: Rohtak, Haryana Experience: 5 to 6 Years Industry: Automotive / Engineering / Manufacturing Company: Hiltasu India Pvt Ltd ⸻ About Hiltasu India: Hiltasu India Pvt Ltd is a fast-growing sourcing and manufacturing company, delivering smart solutions in automotive components, precision fasteners, and electronic assemblies. We are driven by innovation, quality, and strong customer relationships, building reliable partnerships across industries. ⸻ Job Overview: We are looking for a dedicated QMS Engineer/Manager with 5–6 years of hands-on experience in quality management within a manufacturing setup. The ideal candidate will lead QMS implementation and audits, ensure adherence to ISO/IATF standards, and play a key role in continuous improvement initiatives. ⸻ Key Responsibilities: • Implement and maintain ISO 9001/IATF 16949-compliant Quality Management System. • Plan and execute internal audits; support external and customer audits. • Manage quality documentation: SOPs, manuals, WI, control plans, etc. • Handle customer complaints, conduct root cause analysis, and drive CAPA. • Collaborate with cross-functional teams to improve product and process quality. • Monitor and report quality KPIs: rejection trends, in-process defects, and customer returns. • Ensure calibration and upkeep of quality tools and measuring instruments. • Support APQP, PPAP, and FMEA activities for new product launches. • Conduct quality training and awareness programs for employees. ⸻ Desired Candidate Profile: • Degree/Diploma in Mechanical/Industrial/Production Engineering. • 5–6 years of relevant experience in QMS in a manufacturing/automotive firm. • Sound knowledge of ISO 9001:2015 / IATF 16949 implementation and auditing. • Familiarity with PPAP, APQP, MSA, SPC, and FMEA. • Experience in customer complaint handling and documentation practices. • Excellent communication, team coordination, and problem-solving skills. • Proficiency in MS Office and quality management tools/software. ⸻ Preferred Qualifications: • Lead Auditor Certification (ISO 9001/IATF 16949). • Prior experience in fasteners, hinges, or PCB assembly domains. • Understanding of BIS certification process and regulatory standards. ⸻ Apply Now 📧 Email: dinesh@hiltasu.com 📞 Contact: +91 81999 90846 🌐 Website: www.hiltasu.com 📍 Job Location: Rohtak, Haryana
Posted 1 week ago
2.0 years
1 Lacs
Calicut
On-site
Location: Chennai, Tamil Nadu(Candidates only) Experience: 2+ years in hospital/clinical biomedical equipment Job Type: Full-time Job Description: We are seeking an experienced and driven Senior Biomedical Engineer to lead biomedical equipment maintenance, calibration, and support operations in healthcare facilities across Chennai. The ideal candidate will have a deep understanding of diagnostic, critical care, and imaging equipment, with strong problem-solving skills and a commitment to safety and quality. Key Responsibilities: Supervise installation, preventive maintenance, and repair of biomedical equipment (ICU, OT, NICU, imaging, lab devices). Ensure compliance with healthcare standards and safety regulations. Liaise with OEMs for service coordination and warranty management. Provide technical guidance to junior engineers and hospital staff. Maintain documentation, service logs, and equipment inventory. Qualifications: B.E./B.Tech in Biomedical Engineering (or equivalent) Minimum 5 years of hands-on experience in a hospital or service company In-depth knowledge of ventilators, monitors, syringe pumps, anesthesia machines, lab analyzers, etc. Strong troubleshooting, communication, and team management skills Preferred Skills: Experience with brands like GE, Dräger, Philips, Mindray, Siemens, Olympus, etc. Familiarity with NABH or JCI standards Willingness to travel within Chennai and surrounding regions apply directly through Indeed Job Type: Full-time Pay: From ₹10,252.77 per month Schedule: Day shift Work Location: In person
Posted 1 week ago
0 years
2 - 4 Lacs
India
On-site
Job Title: CSSD Technician Location: AIG Hospitals, Gachibowli, Hyderabad, Telangana Appointment Type: Full‑time, Permanent Key Duties: Handle sterilization cycle operations (Steam & E.T.O.) Monitor and document indicators (biological, chemical etc.) Maintain equipment calibration and load records Supply sterile instruments and linen to wards effectively Follow sterilization manuals and safety protocols Essential Qualifications: Diploma in CSSD or relevant field Active Paramedical Registration Minimum 1 year CSSD experience (1–5 years preferred) Working Conditions: Rotational shifts including mornings, days, and nights Benefits: Health insurance, provident fund, sick leave and leave encashment Job Type: Full-time Pay: ₹250,000.00 - ₹450,000.00 per year Benefits: Health insurance Leave encashment Provident Fund Work Location: In person
Posted 1 week ago
3.0 - 5.0 years
0 Lacs
Hyderābād
On-site
Location: Hyderabad, IN Employment type: Employee Place of work: Office Offshore/Onshore: Offshore TechnipFMC is committed to driving real change in the energy industry. Our ambition is to build a sustainable future through relentless innovation and global collaboration – and we want you to be part of it. You’ll be joining a culture that values curiosity, expertise, and ideas as well as diversity, inclusion, and authenticity. Bring your unique energy to our team of more than 20,000 people worldwide, and discover a rewarding, fulfilling, and varied career that you can take in anywhere you want to go. Job Purpose Performs administrative and technical duties in the Quality domain, such as complex report running, providing necessary support to Quality employees Job Description • Follows internal procedures and Quality System (QS) and other governmental and customer requirements and specifications • Collects and analyses data related to Quality, and identifies possible inconsistencies • Participates in the calibration of equipment in laboratories • Manages all documentation related to Quality • Receives, classifies, reconciles, interprets, consolidates, and/or summarizes documents and information related to quality • Maintains records and balance information for control purposes • Compiles reports, drawing data from a variety of sources within the quality department • Regularly contacts Quality employees outside the immediate work area to exchange information • Assists with internal quality audits You are meant for this job if: • Certificate or equivalent / technical background • 3 to 5 years of experience • Knowledge of Information Systems Skills Additional Skills Being a global leader in the energy industry requires an inclusive and diverse environment. TechnipFMC promotes diversity, equity, and inclusion by ensuring equal opportunities to all ages, races, ethnicities, religions, sexual orientations, gender expressions, disabilities, or all other pluralities. We celebrate who you are and what you bring. Every voice matters and we encourage you to add to our culture. TechnipFMC respects the rights and dignity of those it works with and promotes adherence to internationally recognized human rights principles for those in its value chain. Date posted: Jul 29, 2025 Requisition number: 14386
Posted 1 week ago
5.0 - 7.0 years
8 - 12 Lacs
India
On-site
Education - B. Tech Electronics / Electro-optics Additional Qualification- IPC-WHMA-A620 Specialist Total Experience (Years) - 5 to 7 Years’ relevant Experience Relevant Experience - Good Experience in Assembly, Integration & Testing of Thermal Imaging (Cooled & Un-cooled) Sights in Defence & Aerospace Sector Technical Must have skills Required Level (Basic /Advance / Expert) Electro-Optical Systems Testing & Integration & trouble shooting - E Testing, calibration, Bore-sighting of Cooled & Uncooled multi sensor Systems - E Understanding of sensor calibration and opto-mechanical alignments E Measuring parameters: MRTD, NETD, FOV, bore sighting using collimators. - E Communication & Interpersonal skills - E Documentation as per AS9100D - E Technical Qualifications - B. Tech Electronics / Optics Engineering JOB Description Good Experience in manufacturing and testing of Electro optics systems for the Defense / Aerospace industry. Good understanding of thermal imaging systems technologies, IR Optics, IR detectors, cryogenic systems, Signal and Image processing, gimbal platforms, video electronics. Hands on experience with optical lens, lasers, optical coatings, diffractive optical elements, illumination and imaging optics. Should have good knowledge about different types of glass and glass materials. Experience of manufacturing and testing of cooled / uncooled thermal sights, hand held thermal sights. Possess experience with IR, MTF and Transmission set up, thermal Imaging test stations used in testing of NFOV FLIR, WFOV FLIR. Testing of multi sensor FLIR , CCD, Laser systems, Boresight, MRTD, SNR etc. Capability to own an Electro optics systems task from early design through product delivery. Demonstrated problem solving and risk assessment skills. Experience in Testing as per JSS55555 / MIL 810 G/F, MIL 461 E Understanding and using instruments like multimeters, oscilloscopes, and spectrum analyzers to characterize electrical signals and component . Job Type: Full-time Pay: ₹800,000.00 - ₹1,200,000.00 per year Work Location: In person
Posted 1 week ago
2.0 years
3 - 3 Lacs
Gurgaon
On-site
Job Title- Quality Analyst Function - Call Centre Working time 6 Days working (Monday to Saturday) 10 am to 7 pm office hours Sunday Fixed off Minimum Education Graduate Work Experience 2 Years - 8 Years Minimum 2 yrs. of experience as Quality Analyst on papers BPO ONLY. Gender Female/ Male Job Role - Can communicate in Hindi and English both. Call Audit (1) Live Call (2) Recorded Calls Team Strength Call Duration What is AHT? How to share Feedback Call Calibration No of calls audit What is your feedback mechanism? Basic Excel Knowledge DIP Check Knowledge Job Type: Full-time Pay: ₹30,000.00 - ₹33,000.00 per month Work Location: In person Speak with the employer +91 8867151186
Posted 1 week ago
2.0 years
1 - 5 Lacs
Delhi
On-site
Company Overview: Clear Point Instrumentation Pvt. Ltd. (CPIPL) is a trusted provider of industrial automation and instrumentation solutions, serving the oil & gas, power, and process industries. With a commitment to technical excellence and customer satisfaction, CPIPL offers services ranging from installation and commissioning to diagnostics and repairs. Job Summary: We are looking for a detail-oriented and skilled Repair Technician to join our technical service team. The candidate will be responsible for troubleshooting, repairing, and maintaining a wide range of industrial instrumentation and electronic equipments. Key Responsibilities: Diagnose and repair faults in instrumentation and electronic equipment. Perform component-level repair on PCBs on various electronic modules. Perform testing and calibration of equipment as per standard procedures. Maintain a clean, organized, and safe work environment. Required Skills & Qualifications: ITI / Diploma in Electronics or related field. 2+ years of experience in instrumentation or electronics repair (preferred). Ability to read electrical schematics, datasheets, and technical manuals. Experience with soldering, de-soldering, and testing tools (e.g., multimeters, oscilloscopes). Good troubleshooting skills and attention to detail. Basic computer knowledge (MS Office, service documentation). Preferred Qualities: Strong analytical and problem-solving abilities. Ability to work independently and as part of a team. Commitment to quality and safety. Willingness to travel occasionally for onsite service support. Compensation: Competitive salary based on experience and qualifications. Additional benefits as per company policy. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹45,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Performance bonus Willingness to travel: 75% (Preferred) Work Location: In person
Posted 1 week ago
0 years
2 - 3 Lacs
Delhi
On-site
We are seeking a detail-oriented and technically skilled Lab Assistant to support testing, validation, and documentation tasks in our USB product development and compliance lab. The ideal candidate will assist engineers with USB device testing (USB 2.0, 3.x, USB4), maintain lab equipment, and help ensure devices meet industry standards. Key Responsibilities: Assist with testing of USB devices (flash drives, hubs, cables, controllers, etc.) under different conditions. Operate USB protocol analyzers, oscilloscopes, power analyzers, and other lab equipment. Support test setups for electrical compliance, interoperability, and performance testing. Perform functional, stress, and regression tests on USB hardware and firmware. Document test procedures, results, anomalies, and assist in root-cause analysis. Maintain lab inventory and calibration of equipment. Work closely with engineers to follow USB-IF (USB Implementers Forum) testing protocols. Prepare samples for USB-IF compliance testing and maintain logs of certification status. Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Paid sick time Work Location: In person
Posted 1 week ago
5.0 years
2 - 8 Lacs
Brahmapur
On-site
Key Responsibilities BE Civil, 5 years to 8 years of experience as Quality Control Engineer / Supervisor in construction or construction supervision of new construction or construction or pavement rehabilitation of Runways / Roads & Highways 1. Review of plant and machinery, calibration certificate at HMP 2. Quality control of material at production 3. Check of quality as approved QC document 4. Verification of test reports of aggregates 5. Verification of test conducted at HMP, keeping records of temperature control of asphalt machinery 6. Keeping record of machinery failure 7. Ensure appropriate safety during production of material at HMP 8. Co-ordinate resource deployment at site with Contractor 9. Prepare daily work plan in consultation with Client's team and ensure daily progress 10. Supervision of asphalt laying as per approved Method Statement and Quality Control document 11. Prepare and review site construction method statement as required for the works 12. Supervision of laying and compaction of asphalt on the pavement and soil on raded strip 13. Ensure appropriate safety while carrying pavement works Qualifications: Bachelor's degree in Civil Engineering, Construction Management, or related field. PMP (Project Management Professional) certification or equivalent preferred. Minimum of 10 years of experience in project management within the civil engineering and/or laboratory environment. Strong understanding of civil engineering principles, laboratory processes, and relevant industry standards. Excellent communication, leadership, and organizational skills. Ability to manage multiple projects simultaneously while maintaining high-quality standards. Experience with project management software (e.g., MS Project, Primavera, etc.). Knowledge of safety protocols and environmental regulations Job Types: Full-time, Permanent Pay: ₹23,018.15 - ₹70,000.00 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person
Posted 1 week ago
1.0 - 2.0 years
1 - 3 Lacs
Indore
On-site
Job Title: PFT / TMT / EEG / EMG Technician Location: Apple Hospital, Indore Job Type: Full-Time Experience Required: 1–2 years (preferred) About Us: Apple Hospital, Indore is a NABH-accredited multi-specialty healthcare facility committed to providing quality patient care with advanced diagnostic and treatment technologies. We are currently looking for experienced and dedicated technicians to join our Diagnostic Services team. Key Responsibilities: Perform Pulmonary Function Tests (PFT), Treadmill Tests (TMT), Electroencephalograms (EEG), and Electromyography (EMG) procedures accurately and efficiently. Prepare and position patients for diagnostic testing. Operate diagnostic equipment with proper care and adherence to safety protocols. Maintain detailed records and assist in report preparation. Coordinate with consultants and nursing staff for test scheduling and interpretation needs. Ensure proper calibration, cleaning, and maintenance of machines. Requirements: Diploma/Degree in Respiratory Therapy, Neurodiagnostic Technology, or related allied health course. Minimum 1 year of hands-on experience in performing PFT/TMT/EEG/EMG tests. Sound technical knowledge and understanding of safety protocols. Good communication skills and a patient-friendly attitude. Job Type: Full-time Pay: ₹10,000.00 - ₹25,000.00 per month Benefits: Commuter assistance Flexible schedule Leave encashment Paid time off Ability to commute/relocate: Indore, Madhya Pradesh: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: total work: 1 year (Preferred) PFT /TMT: 1 year (Preferred) Shift availability: Day Shift (Preferred) Work Location: In person
Posted 1 week ago
0 years
3 Lacs
Unjha
On-site
Job Summary: We're seeking a skilled Sortex Machine Operator to oversee the operation and maintenance of Sortex machines, ensuring efficient and accurate sorting of products, such as grains, nuts, or other materials. Key Responsibilities: 1. Machine Operation: Operate and monitor Sortex machines, ensuring optimal performance and minimal downtime. 2. Product Sorting: Ensure accurate sorting of products according to quality and specifications. 3. Machine Maintenance: Perform routine maintenance tasks, such as cleaning and calibration, to ensure machine efficiency. 4. Quality Control: Monitor product quality and report any issues or defects to supervisors. 5. Troubleshooting: Identify and resolve machine issues, collaborating with maintenance teams as needed. 6. Production Targets: Meet production targets and deadlines while maintaining quality standards. 7. Safety Protocols: Follow safety guidelines and protocols to ensure a safe working environment. Requirements: 1. Experience: Previous experience operating Sortex machines or similar equipment. 2. Technical Skills: Understanding of machine operations, maintenance, and troubleshooting. 3. Attention to Detail: Strong attention to detail to ensure accurate sorting and quality control. Job Types: Full-time, Permanent Pay: Up to ₹30,000.00 per month Benefits: Food provided Health insurance Leave encashment Paid time off Provident Fund Work Location: In person
Posted 1 week ago
5.0 years
0 Lacs
India
On-site
Greetings from Farmson!........... We are looking for candidates with the following criteria: Work experience of preventive & breakdown Maintenance of field instruments & instrumentation system Testing & Calibration of instruments with Traceability certification Interested candidates, please provide your CV to the following email ID generalhr5@farmson.com Job Type: Full-time Schedule: Rotational shift Education: Diploma (Preferred) Experience: Instrument Technician: 5 years (Preferred) Work Location: In person
Posted 1 week ago
5.0 years
6 - 8 Lacs
India
On-site
Designation : Associate Manager / Manager QC Location : Ahmedabad Employement Type : Full-Time Company Overview : Panacea Phytoextracts Pvt. Ltd. is a the world class leading manufacturer and sole supplier of optimum quality standardized herbal extracts for the formulation of Herbal Biomedicines, Phytodrugs, Nutraceuticals, Food supplements, Pharmaceutical intermediates, Cosmetics products and most recently, new chemical entities for synthetic drugs in the global market of Herbalism. According to World Health Organization (WHO), 80% of the world population relies on herbal medicines for their primary health care and 45% world natural medicines are from plant origin. Job summary: Online testing of inward material, intermediate products, and finished Product. To ensure that sampling and analysis are as per standard operating procedures. To ensure that all necessary tests are carried put as per written method of analysis. Control of the quality of input and output by developing systems. To ensure that calibration and validation of lab instrument are as per written schedule. Training of QC personnel according to related work cGMP, limit test and analysis. To check and maintain the cleaning of the department and equipment as per written schedule. Evaluation of analyst time to time. Responsible for QC costing. As per testing data prepare & review the analytical report. Ensuring instrument & reagent labelling. Operating of Equipment’s. New product method development. Method verification & method validation activity. As per QMS requirement prepare & review QC related SOP & method of analysis. Properly maintain the retention sample with proper labelling. Properly maintain & store the working standard & reference standard. Testing data result recorded in SAP. To ensure compliance to Good Laboratory Practices (GLP). Handling of QMS Documentation like CAPA, Documentation and data control, Change management system, Handling of Out of specification, Out of Trend analysis, Handling of deviation, Quality Risk assessment. Handling the lab incident procedure Cleaning validation activity. Experience : 5 - 8 Years Education : B.SC M.SC Chemistry Salary : 6 - 8 LPA Why Join Panacea Phytoextracts? Opportunity to lead the technological vision of company. Collaborative and innovative work environment. Competitive salary and benefits package. Commitment to professional development and career growth. For more information about our company, please visit our website: www.panaceaphytoextracts.com In case you seem to be interested in the career opportunity, drop your resume - shreya.hr@meteoricbiopharma.com or contact on +91 9227990526 Job Type: Full-time Pay: ₹600,000.00 - ₹800,000.00 per year Benefits: Health insurance Provident Fund Work Location: In person
Posted 1 week ago
2.0 years
4 - 5 Lacs
India
On-site
Designation : Officer - Production Location : Aslali, Ahmedabad Employement Type : Full-Time Company Overview : Driven by #innovationthrougdiscovery for close to 2 decades, we serve clients across diverse industries worldwide from our headquarters in India, with strategic offices in the USA and Vietnam. Serving over 1000+ customers across 90+ countries. With state-of-the-art analytical and microbiology in-house R & D centers, Meteoric ensures exceptional quality for its clients. Today, we are a one-stop solution for all biological requirements across Enzymes, Probiotics, Bioactives, Formulations, and Animal Health Care. We also offer unique services including Product Customization, Concept Formulation, and Contract Manufacturing under one roof. Job summary: Maintaining the area Monitoring records and differential pressure record. Handling of Batch manufacturing record and batch repacking records. To verify the daily verification activity of weighing balance. To Maintaining the production records i.e., Cleaning Records, equipment usage logs finished goods transfer record etc. To verify the machine cleaning at manufacturing stage. To perform and verify the weighing balance calibration activity. To perform line clearance activity at manufacturing and packing stage. To monitoring of manufacturing and packing activity on daily basis. To monitoring of packing activity for export market. Issuance and retrieval of production documents i.e., Annexure, BMR, logbook, labels etc. Skills: BMR, Production documentation, Batch Manufacturing, CGMP, Production Packing, Production Operation, Production Process, BPR, Biopharma, QMS, Line clearence Experience :2-4 Year Education : Graduation B.sc / B.Pharm required / Knowledge about cGMP Practice / QMS tools knowledge/ Awareness about the documentation process Salary : 35000-40000 Per month Meteoric Biopharmaceuticals is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. For more information about our company, please visit our website: https://www.meteoricbiopharma.com Job Type: Full-time In case you seem to be interested in the career opportunity, drop your resume - shreya.hr@meteoricbiopharma.com or contact on +91 9227990526 Job Type: Full-time Pay: ₹35,000.00 - ₹45,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person
Posted 1 week ago
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