6178 Calibration Jobs - Page 32

We’re building India’s most intensive Full‑Stack Development Bootcamp—240 hours of live, hands‑on training across Architecture, Frontend, Backend, and DevOps. As a Bootcamp Instructor & Coaching Fellow , you’ll be the day‑to‑day backbone of our student experience and learning community. Your Impact Deliver Live Classes Lead live, interactive sessions across two simultaneous cohorts (up to 40 students total), rotating through our four core modules. Facilitate coding workshops, live demos, and guided labs using pre‑built curriculum assets. Mentor & Support Students Host weekly Q&A clinics and mini‑project review sessions to troubleshoot code, clarify concepts, and coach on best practices. Monitor attendance and performance; proactively reach out to students at risk of falling behind. Community Engagement Moderate cohort Slack/Discord channels, answer asynchronous queries, and foster peer‑to‑peer collaboration. Organize and drive peer‑pod meetings (groups of 5–6 students) to build accountability and camaraderie. Quality Assurance Participate in weekly calibration huddles with founders and senior mentors to align on pedagogy, share feedback, and continuously improve delivery. Undergo periodic session audits against our Delivery Scorecard (clarity, engagement, pace, accuracy). Outcome Ownership Drive your cohorts toward ≥85% live‑attendance, ≥4.5/5 teaching ratings, and ≥90% graduation & placement‑interview milestones. Collaborate with our Placement Cell to ensure students complete mock interviews and capstones on time. What We’re Looking For Technical Expertise 1–3 years of professional experience in Full‑Stack Development (MERN, MEAN, Laravel, Django, etc.) and familiarity with DevOps fundamentals (CI/CD, Docker, AWS/Azure). Strong command of architecture patterns, frontend frameworks (React, Vue, Angular), backend languages (Node.js, Python, PHP), and cloud/deployment workflows. Teaching & Communication Skills Exceptional verbal and written English proficiency; comfortable explaining complex concepts in simple terms. Prior experience leading workshops, webinars, or study groups is a plus. Mentorship Mindset Passion for coaching, empathy for learners, and a growth‑oriented attitude. Ability to give constructive feedback and motivate students to overcome roadblocks. Organizational Rigor Strong time‑management skills to juggle multiple cohorts, Q&A sessions, and community channels. Detail‑oriented approach to tracking student progress and administrative tasks. Compensation & Rewards Salary: 2.4 LPA (Base + Bonus) Perks: Direct mentorship from the founding team and senior industry experts Access to our proprietary curriculum, slide decks, and code repositories Opportunity to build your teaching portfolio and grow into a senior instructional role or curricular designer

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Essential Duties And Responsibilities Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management. Assist in decision making for process improvement efforts. Provide quality role in assisting with generating Design Plans, reviewing design inputs, outputs, verification, validation and design transfer strategies. Ensures that activities within the Product Development elements are performed in a manner consistent with the Design and Development Plan, Change Plan and Quality Planning. Support Risk Management activities for sustaining engineering projects. Support post market activities such as complaint investigation, complaint trending, CAPA, and FA Support global manufacturing facilities and associated manufacturing and supplier changes. Preside as key quality participant in compliance audits and FDA/ministry of health (MOH) inquiries. Lead and Support global procedure implementations at site for laboratory process and Analytical Studies. Perform CAPA reviews and provide input to management reviews. Support Supplier quality activities and assist to maintain Approved Entity List for the Site. Support CRO OOL, OOS and insight to the ongoing studies and SCAR. Responsible for Quality Assurance of the Product Development and Lifecycle Management process. Responsible for the compliance and approval of PDLM records to Vantive procedures throughout the product lifecycle. Collaborate with regulatory affairs as needed to guide teams in meeting quality/regulatory requirements based on the regulatory plan/strategy or assessment. Collaborate with teams to provide strategy and guidance for meeting Vantive Requirements and External Quality Standards as appropriate. Qualifications Good interpersonal/communication/influencing/negotiation skills. Good analytical and problem solving skills. Working knowledge of FDA Regulations. Demonstrated ability to lead others within small project or investigational environments. Good technical overview of medical device verification, validation and test automation. Good understanding of 21 CFR Part 820, ISO 13485, EU MDD / EU MDR. Broad working knowledge of Medical Device Software Development Lifecycle and IEC 62304. Good understanding of medical device manufacturing process. Good Understanding of requirements for Calibration and Qualification of Test & Measurement equipment in labs used for Verification and Validation. Education And/or Experience BS engineering and 12 + years in related Quality or Engineering field in the medical products industry. ASQ (e.g., CQE, CMQ/OE, etc.) and/or Six Sigma certification highly preferred. Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

We are looking for a Calibration Engineer to perform in-lab and on-site calibration of measuring instruments across electrical, mechanical, and thermal parameters. The role involves maintaining calibration records, ensuring compliance with ISO/IEC 17025:2017, and supporting customer requirements. Key Responsibilities: Calibration of instruments and equipment. Prepare and review calibration certificates and reports. Ensure traceability and documentation as per ISO 17025 standards. Coordinate with clients and internal teams. Willingness to travel for field work. Qualifications: Diploma / B.Tech / B.Sc. in Mechanical, Electronics, Instrumentation, or Physics. Basic knowledge of measuring instruments. Good communication and documentation skills. Job Types: Full-time, Permanent, Fresher Pay: ₹12,500.00 - ₹15,000.00 per month Benefits: Cell phone reimbursement Health insurance Provident Fund Ability to commute/relocate: Surajkund, Faridabad, Haryana: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Language: Hindi, English (Preferred) License/Certification: Driving Licence and Passport (Preferred) Location: Surajkund, Faridabad, Haryana (Preferred) Shift availability: Day Shift (Preferred) Willingness to travel: 75% (Preferred) Work Location: In person

We Are: At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation. You Are: You are an accomplished analog IC design engineer with a proven track record of delivering high-performance, high-speed circuits in advanced technology nodes. With over a decade of hands-on experience, you possess deep technical expertise in transistor-level circuit design, particularly in FinFET and cutting-edge process nodes. You thrive in fast-paced, collaborative environments and enjoy working on challenging projects that push the boundaries of what’s possible in analog and mixed-signal design. Your passion for innovation is matched by a meticulous attention to detail and a strong commitment to quality. You are comfortable navigating complex SerDes architectures, from initial concept through to silicon validation, and you approach problem-solving with creativity and a data-driven mindset. You value teamwork and diversity, and you communicate your ideas clearly to colleagues from a variety of backgrounds, including digital designers, CAD engineers, and customers. What You’ll Be Doing: Review and interpret SerDes standards to develop innovative transceiver architectures and detailed sub-block specifications. Investigate, propose, and design novel circuit architectures that overcome performance bottlenecks, achieving significant improvements in power, area, and speed. Collaborate with cross-functional teams to streamline design and verification methodologies, ensuring efficiency and design quality. Oversee physical layout processes, minimizing the impact of parasitics, device stress, and process variation for optimal silicon performance. Present and review simulation results within the team and externally at industry panels or customer reviews, articulating complex technical concepts clearly. Document design features, methodologies, and test plans to ensure knowledge transfer and reproducibility. Consult on electrical characterization of SerDes IP, analyze customer silicon data, and propose solutions for post-silicon enhancements. The Impact You Will Have: Drive innovation in high-speed analog and mixed-signal design, directly contributing to Synopsys’ leadership in SERDES IP. Enable customers to achieve cutting-edge performance, power, and area metrics in their next-generation silicon products. Advance the adoption of the latest FinFET and gate-all-around technologies through robust, reliable analog solutions. Raise the bar for design quality and efficiency by introducing best practices in architecture, verification, and layout. Mentor and inspire a diverse team of engineers, fostering a culture of learning and continuous improvement. Strengthen Synopsys’ reputation by representing the company at industry events and delivering high-impact technical presentations. What You’ll Need: MTech/MS (4+ years) or BTech/BS (5+ years) in Electrical Engineering, Computer Engineering, or related field. Extensive analog IC design experience, especially with FinFET technologies and advanced process nodes. Expertise in transistor-level CMOS design, including successful CMOS tape-outs. Deep understanding of high-speed designs (Multi-Gbps), especially PAM4 SerDes architectures and sub-circuits (TX, RX, equalizers, PLL, DLL, regulators, oscillators, ADC/DAC). Proficiency with analog/digital interaction techniques for circuit optimization, calibration, and adaptation. Familiarity with ESD, custom digital design, design for reliability, layout effects, and signal integrity issues. Hands-on experience with schematic entry, physical layout, design verification tools, and SPICE simulation. Knowledge of scripting languages (TCL, PERL, MATLAB) for simulation post-processing. Excellent communication and documentation skills. Who You Are: An analytical thinker with a passion for solving complex technical challenges. A collaborative team player who values input from diverse perspectives. An effective communicator, able to convey technical details to both experts and non-experts. Detail-oriented, organized, and committed to quality and continuous improvement. Adaptable to changing priorities and eager to learn new technologies. Proactive in mentoring and supporting the professional growth of others. The Team You’ll Be A Part Of: You’ll join a world-class analog and mixed-signal R&D team based in Hyderabad, focused on developing high-speed SERDES IP for the latest process technologies. Our team brings together experts in analog, digital, and CAD, fostering an environment of innovation, knowledge sharing, and technical excellence. We work closely with global teams and customers to deliver industry-leading solutions that shape the future of connectivity. Rewards and Benefits: We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non-monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process.

About Us Vandana Global Limited has been empowering India Since 1996. Registered in Mumbai and working from Raipur Chhattisgarh. The group has positioned itself today to create high value across diverse domains with four key differentiators are state of the art manufacturing technology, efficient quality management, on-time delivery, and commitment to consumer satisfaction and support. Vandana Global today boasts of successes in a range of domains including Manufacturing of Sponge Iron, branded TMT bars as TMTNEXT, Wire rods, Pig Iron, Billet, branded Ferro Alloys as FEROTON, and Power (Thermal, Solar, and Wind). A company deeply rooted in sustainable development and bold progressive ideas; We support a Self - Sufficient Developing nation with its core Technology and Work Ethics. Position Overview We are looking for an experienced and detail-oriented Chemist to manage and monitor the chemical analysis of raw materials, intermediates, and finished products in our Sponge Iron and Steel Melting Shop (SMS) unit. The ideal candidate will ensure quality control through timely and accurate analysis and contribute to process optimization in a steel manufacturing setup. Key Responsibilities: Conduct chemical analysis of raw materials (iron ore, coal, dolomite, etc.), DRI, molten metal, slag, and finished steel products Monitor and control chemical composition in sponge iron and liquid steel to meet quality standards Operate and maintain lab equipment including Spectrometer, Carbon-Sulfur Analyzer, Muffle Furnace, pH meter, etc. Prepare daily test reports and maintain proper lab documentation and calibration logs Support process control by giving timely inputs to production teams based on chemical analysis Implement and follow quality management systems (QMS) and safety protocols Assist in root cause analysis of chemical-related issues in process deviation or product quality Coordinate with internal departments like production, QA/QC, and maintenance Ensure adherence to BIS, ISO, and customer specifications Required Skills and Qualifications: B.Sc. / M.Sc. in Chemistry (Inorganic / Analytical Chemistry preferred) 2 to 6 years of experience as a chemist in sponge iron and/or steel melting shop (SMS) Proficient in wet chemical and instrumental analysis methods Experience working in NABL-accredited labs or ISO-certified environments is a plus Sound understanding of metallurgical processes and quality standards in steel production Strong documentation and report writing skills Intrested Candidates can contact me on - 9109183990 Job Type: Full-time Schedule: Rotational shift Work Location: In person

*Sr. Calibration Engineer :- 2Nos. Basic requirement :- Qualification :-BSC/ITI(fitter)/DME/B.E. Experience:- Having experience of min 2yr. (In Dimension metrology calibration Lab / Standard Room) Knowledge required :- 1)hands-on in calibration of mechanical instruments & gauges (Caliper ,Micro-meters, gauge block etc as per attached scope ) a) should have system knowledge as per international standard ISO/IEC 10725 :2017 b) should have familiar with NABL Documentation ,uncertainty of measurements etc. c) candidate who had faced NABL Audit in previous experience is most Preferable. d) Should have managerial skill to handle calibration manpower (min.7-10 personel). e)hands-on in calibration of mechanical instruments & gauges (Caliper ,Micro-meters, gauge block etc as per attached scope ) f) Computer literacy (Ms. Word, Excel, PowerPoint ) Interested candidates direct attend walkin interview Job Location Waluj MIDC Thanks Job.Com Placement and Services 8888572037 8888572020 Office - X-340 Mahavir Chauk waluj MIDC Bajajnagar Aurangabad Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Provident Fund Work Location: In person Expected Start Date: 28/07/2025

Job Summary: This is a cross-functional role responsible for managing document control in line with ISO 17025:2017 and NABL requirements, supporting implementation and continual improvement of the Quality Management System (QMS), and providing administrative and HR support. The role ensures regulatory compliance, document traceability, personnel record management, and seamless internal communication across departments. Key Responsibilities: A. Document Control Responsibilities Maintain the Master List of Controlled Documents as per ISO 17025:2017. Manage issuing, revision, archiving, and withdrawal of documents in both physical and ERP formats. Ensure version control and timely updates to SOPs, Quality Manuals, Work Instructions, and Test Methods. Coordinate interdepartmental approvals and record training on document revisions. Track and file calibration certificates, validation records, audit reports, and uncertainty data sheets. Support technical team by maintaining all method validation and traceability records. B. ISO 17025/NABL Implementation Responsibilities Assist in implementation and upkeep of ISO 17025:2017 Quality System requirements. Coordinate internal audits, manage non-conformity records, and track corrective/preventive actions. Help conduct Management Review Meetings and monitor quality objectives. Liaise with NABL assessors during surveillance or renewal assessments. Facilitate staff training programs on ISO standards and QMS awareness. C. Administrative Responsibilities Maintain office records, vendor agreements, licenses, and general administration registers. Coordinate procurement requests with the purchase and inventory teams. Ensure proper upkeep of office utilities, documentation stations, and visitor logs. Schedule meetings, manage calendars, and circulate internal communication. D. HR Support Responsibilities Maintain and update employee files, leave records, and appraisal trackers. Track attendance using TRUFIL_HRMS and support payroll coordination. Coordinate recruitment documentation and onboarding formalities. Manage statutory compliance documentation (ESI, PF, ID proofs, policies acknowledgment). Organize employee trainings, ID cards, and internal welfare communications. E. ERP & Digital System Handling Work on TRUFIL_HRMS, ERP modules for Quality, Admin, HR. Ensure all documents and forms are digitally stored and traceable. Generate reports for document expiry, audit compliance, and HR metrics Required Skills & Competencies: Document Management Tools: MS Office, ERP Systems, Excel-based trackers QMS & ISO Skills: Working knowledge of ISO 17025:2017, NABL documentation HRMS Handling: Basic HRMS usage for attendance, leave, and payroll support Soft Skills: Organized, detail-oriented, confidential handling, interpersonal communication Language Skills: English and Hindi proficiency (Marathi is a plus) Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Schedule: Day shift Work Location: In person

preferred plastic industries Key Responsibilities: 1. Production Planning & Execution : o Develop and monitor daily, weekly, and monthly production schedules o Balance raw material usage, machine availability, and workforce 2. Process Optimization : o Improve assembly line efficiency o Apply Lean, Kaizen, or Six Sigma to minimize waste 3. Machine & Tool Handling o Operate and maintain CNC routers, edge banding, panel saws, etc. o Tool calibration and preventive maintenance scheduling 4. Quality Assurance o Ensure adherence to finish, durability, and dimensional tolerances o Use of gauges, measurement tools, and quality checklists 5. Material Management o Coordinate with the store and purchase departments o Optimize inventory for MDF, plywood, laminates, adhesives, etc. 6. Health, Safety & Compliance o Enforce EHS protocols in the shopfloor o Comply with fire safety, chemical handling, and ergonomic guidelines 7. Team Coordination o Supervise operators, fitters, carpenters, and helpers o Conduct daily toolbox talks and shift handovers https://www.plasto.in/ Please Note: Please share your resume on Mail Id jobs@plasto.in Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹40,000.00 per month Benefits: Leave encashment Provident Fund Schedule: Rotational shift Supplemental Pay: Yearly bonus Work Location: In person

Job Title: Senior Manager – Quality Assurance and R&D – Activated Carbon Plant Location: Ponnapuram Village, Dharapuram Taluk, Tirupur District, Tamil Nadu Company Overview: Carbonmax Advantech Pvt Ltd is a leading manufacturer of coconut shell-based steam activated carbon with integrated infrastructure for granulation, rotary kiln-based activation, post-activation processes, and advanced value addition plants. These include acid-washed carbon, powdered activated carbon, impregnated carbon, pelletized carbon, and catalytic carbon. Carbonmax is rapidly expanding into custom and specialty carbon applications , including supercapacitors, gas filtration, gold recovery , and other high-performance material domains. Position Summary: We are looking for a Senior Manager – Quality Assurance, R&D and Value-Added Carbon Products to lead end-to-end QA, QC, and product innovation efforts across all divisions of the plant. The role includes oversight of production QA/QC labs, value-added carbon labs, and R&D studio; implementation of international testing protocols (ASTM, AWWA, JIS, EN); team management; compliance leadership; and new product development for global carbon applications. This role demands deep domain expertise in activated carbon quality, laboratory instrumentation, documentation, and lean quality management systems , and will play a key role in transitioning the company from commodity to specialty carbon manufacturing. Key Responsibilities: Quality Assurance & Quality Control: Oversee QA/QC of: Raw material (charcoal, chemicals) In-process material Finished activated carbon (steam activated, acid washed, PAC, impregnated, pelletized, catalytic) Implement global test methods: ASTM Standards : D4607 (Iodine), D2854 (Ash), D2867 (Moisture), D3838 (Density), D3467 (CTC), D5158 (Hardness) AWWA B600 (Water treatment carbon) JIS Methods (MB adsorption, pH, volatile content) Gold Recovery Testing (K value, R value, cyanide adsorption) BET surface area , pore distribution , acid/base leaching VOC & gas phase testing using GC/FID, if applicable Approve and issue Certificate of Analysis (COA) with batch data Conduct inter-lab validation , retain sample reviews, and audit trails Laboratory Operations & Equipment: Supervise operations across: Production QA/QC Lab Value-Added Carbon Lab R&D Studio Lab Maintain, calibrate and utilize: BET Analyzer , Malvern Particle Size Analyzer UV-VIS Spectrophotometer , Turbidity Meter Atomic Absorption Spectrophotometer (AAS) Moisture Analyzer , Muffle Furnace , Crushers TGA/DSC , Zeta Potential , GC-MS (if deployed) Ensure GLP, safety, chemical handling, calibration logs, and SOPs New Product Development & R&D: Lead formulation and testing of specialty carbon products for: Supercapacitor cathodes – high surface area, electrical conductivity VOC and gas phase filtration Gold recovery and metal adsorption Pharma and food grade carbon – low leachable impurities Coordinate: Bench-scale trials, scale-up validations, application benchmarking Lab-to-production integration and performance testing Technical datasheet development Team Management & Capability Development: Build and supervise team of: Lab chemists, QA/QC officers, R&D executives, documentation staff Define KRAs, skill matrix, SOP adherence Conduct training programs in: Test methods, documentation, root cause analysis International QA/QC standards, instrumentation usage ISO 9001, ISO 14001, ISO 45001, REACH, FSSAI (if applicable) Systems, Documentation & Compliance: Implement and maintain: COAs, Batch sheets, NCR logs, Deviation Reports, Lab notebooks ISO documentation and internal audits Drive compliance with: TNPCB, ISO, FSSAI, ROHS, REACH, Electrical/Boiler Inspectorate Coordinate third-party inspections, customer audits, and validations Continuous Improvement & Lean QA: Promote 5S, Lean Lab, and Kaizen culture Conduct RCA for non-conformances and implement CAPAs Improve: Test cycle time COA dispatch reliability Equipment downtime and lab utility efficiency Eligibility Criteria:Qualification: M.Sc. / B.E. in Chemistry, Chemical Engineering, Material Science or Industrial Chemistry Additional training in QA systems or analytical chemistry preferred Experience: 10–18 years in QA/QC or R&D roles, preferably in: Activated Carbon / Specialty Chemicals / Battery Materials / Water & Air Filtration Media Hands-on experience in advanced lab instruments and international testing protocols Technical Skills: Global test standards: ASTM, AWWA, JIS, EN Advanced instrumentation and lab data interpretation Quality systems, audit handling, team leadership ERP or LIMS for quality and traceability Language: Tamil (mandatory), English (working), Hindi (preferred) Software Skills: ERP systems, MS Excel, QA reports, instrument software Key Competencies: Lab and QA team leadership Global test method application Documentation and audit readiness Product development and application benchmarking Structured execution and problem-solving Commitment to innovation in carbon materials Reporting To: Director – Technical & Operations Employment Type: Full-time | On-site (Ponnapuram Plant) Compensation & Benefits: Competitive salary based on experience Performance-based incentives Statutory benefits and medical insurance On-site accommodation and canteen facility Exposure to advanced carbon materials segment Learning and development support Schedule: Day Shift Monday to Saturday (occasional weekend availability) Supplemental Pay: Performance bonus Annual bonus Overtime pay (where applicable) Ability to Commute/Relocate: Ponnapuram, Dharapuram Taluk: Must be able to relocate or commute reliably. On-site factory accommodation available if required. How to Apply: Send your updated CV to: hr.factory@carbonmaxtech.com Subject: “Application – Senior Manager – QA & R&D – Activated Carbon” Speak with us: +91 99434 99855 Job Types: Full-time, Permanent Pay: ₹50,000.00 - ₹75,000.00 per month Benefits: Commuter assistance Food provided Health insurance Provident Fund Schedule: Day shift Monday to Friday Weekend availability Supplemental Pay: Overtime pay Performance bonus Yearly bonus Ability to commute/relocate: Dharapuram, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver. We believe Vantive will not only build our leadership in the kidney care space, it will also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous and don’t settle for the mediocre. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities. Essential Duties and Responsibilities: Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management. Assist in decision making for process improvement efforts. Provide quality role in assisting with generating Design Plans, reviewing design inputs, outputs, verification, validation and design transfer strategies. Ensures that activities within the Product Development elements are performed in a manner consistent with the Design and Development Plan, Change Plan and Quality Planning. Support Risk Management activities for sustaining engineering projects. Support post market activities such as complaint investigation, complaint trending, CAPA, and FA Support global manufacturing facilities and associated manufacturing and supplier changes. Preside as key quality participant in compliance audits and FDA/ministry of health (MOH) inquiries. Lead and Support global procedure implementations at site for laboratory process and Analytical Studies. Perform CAPA reviews and provide input to management reviews. Support Supplier quality activities and assist to maintain Approved Entity List for the Site. Support CRO OOL, OOS and insight to the ongoing studies and SCAR. Responsible for Quality Assurance of the Product Development and Lifecycle Management process. Responsible for the compliance and approval of PDLM records to Vantive procedures throughout the product lifecycle. Collaborate with regulatory affairs as needed to guide teams in meeting quality/regulatory requirements based on the regulatory plan/strategy or assessment. Collaborate with teams to provide strategy and guidance for meeting Vantive Requirements and External Quality Standards as appropriate. Qualifications: Good interpersonal/communication/influencing/negotiation skills. Good analytical and problem solving skills. Working knowledge of FDA Regulations. Demonstrated ability to lead others within small project or investigational environments. Good technical overview of medical device verification, validation and test automation. Good understanding of 21 CFR Part 820, ISO 13485, EU MDD / EU MDR. Broad working knowledge of Medical Device Software Development Lifecycle and IEC 62304. Good understanding of medical device manufacturing process. Good Understanding of requirements for Calibration and Qualification of Test & Measurement equipment in labs used for Verification and Validation. Education and/or Experience: BS engineering and 12 + years in related Quality or Engineering field in the medical products industry. ASQ (e.g., CQE, CMQ/OE, etc.) and/or Six Sigma certification highly preferred. Reasonable Accommodation Vantive is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information. Form Link Recruitment Fraud Notice Vantive has discovered incidents of employment scams, where fraudulent parties pose as Vantive employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our Recruitment Fraud Notice.

Role Purpose To conduct raw materials, stage wise and final inspection of the product in accordance with quality plan and customer requirement. To review MTC as per relevant standard. To look all NDT (DP, UT & RT) & Testing (Hydro, Pneumatic & Helium Leak Test) activity. To look all the activity of IMT Equipment like Preservation, calibration etc. To qualify the welder as per standard. Responsibility conduct stage wise and final inspection of raw materials Product as per Quality requirements. To conduct NDT (DP, UT & RT) Inspection and make reports as per standard requirement. To conduct Pressure testing (Hydro, Pneumatic & Helium Leak Test) Inspection and make report as per standard requirement. To identify non conforming products / components To ensure and maintain records for calibration of inspection and test equipments. To conduct and assist customer and IIIparty inspection To fulfil the quality department objectives of ISO 9001 2015 system Knowledge of ASME/TEMA.. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per year Work Location: In person

We are seeking a skilled and motivated Service Engineer for three locations Lucknow, Varanasi and Kanpur to manage the Annual Maintenance Contracts (AMC) and Comprehensive Maintenance Contracts (CMC) of Samsung ultrasound machines. The candidate will be responsible for preventive maintenance, breakdown support, installation, calibration, and technical troubleshooting of ultrasound systems. This role requires field visits, client interaction, and technical excellence in diagnostic imaging equipment. Contact Details phone number- 8866710087 email- anmedicalsystems01@gmail.com Job Type: Full-time Pay: ₹15,000.00 - ₹35,000.00 per month Schedule: Day shift Work Location: In person Expected Start Date: 28/07/2025

About the Role: We are looking for a detail-oriented and quality-focused individual to join our team as a QC and Lab Executive. This role is crucial in ensuring that all GFRP rebars produced meet internal standards, customer specifications, and relevant ASTM/ISO requirements. The candidate will be responsible for conducting lab tests, maintaining records, and ensuring consistent product quality throughout the manufacturing process. Key Responsibilities: Raw Material Testing: Inspect and verify quality of incoming raw materials such as resin, roving, catalyst, and fillers. Test resin for viscosity, gel time, specific gravity, and shelf life. In-process Quality Checks: Monitor GFRP production process to ensure compliance with process parameters. Perform visual and dimensional inspections on in-process bars. Ensure fiber alignment and impregnation quality. Finished Product Testing: Conduct tests such as: Weight per meter Bar diameter and straightness Tensile strength (using UTM) Tensile modulus Bond strength Glass content / mass fraction Glass transition temperature (Tg) Maintain product traceability through batch documentation. Documentation & Reporting: Maintain proper documentation of all tests, calibrations, and inspections. Prepare batch-wise quality reports and submit to management. Ensure compliance with ISO 9001:2015 documentation standards. Equipment Handling & Calibration: Operate lab equipment like UTM, Micrometer, Muffle Furnace, DSC Machine, and other relevant tools. Ensure timely calibration of testing instruments. Quality Assurance: Participate in internal quality audits and corrective actions. Assist in third-party testing coordination and result verification. Maintain lab cleanliness and safety protocols. Qualifications & Experience: B.Sc. / Diploma / B.Tech in Chemistry, Polymer Science, or Mechanical Engineering. 1-3 years of experience in a similar QC role, preferably in composites or GFRP industry. Familiarity with ASTM standards like D7205, D7957, and ISO quality systems. Skills Required: Strong understanding of material testing procedures. Knowledge of composite materials and resin chemistry. Attention to detail and accuracy in reporting. Ability to interpret technical data and make quality decisions. Proficiency in MS Excel and report preparation. Why Join Us: At Fibretron Composites Pvt. Ltd., we’re redefining sustainable construction with advanced GFRP technologies. Join a growing team dedicated to quality, innovation, and engineering excellence. Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹30,000.00 per month Application Question(s): What is current CTC? What is your expected CTC, job location would be Dasna Experience: total work: 5 years (Required) Work Location: In person

Apply Now Locations: Mumbai - India Key Responsibilities Should have sound marine background in vessels of Oil tankers, Bulk carriers OSV. The Candidate must have hands on working experience of following systems: ME Manuvering system (Pneumatic / electro-pneumatic) CPP controls ME Safety systems Auxiliary engine safety systems OWS 15PPM monitors FI-FI systems ME auxiliary system automation ODMCS Oil fired Boiler automation / Composite Boiler automation Cargo pump automation / safety Calibration experience for Pressure / Temperature / Level of Pneumatic / Electric sensors is must. Engineers should have sound knowledge of class requirements. Should have leadership quality to handle team of instrumentation engineers / technicians. The job demands extensive traveling in Indian ports. Education: Degree/Diploma in Electrical Engineering. Experience: 5 to 10 years. Marine/Offshore/Power Generation Industry knowledge with 2 stroke & 4 stroke engines is essential. Working with Engine Makers and sailing experience with Seaman book will be added advantage. Should have similar type of experience with ship repair and marine industry exposure. Technological: Adequate Computer literacy is essential. CAD operating skill will be added advantage. General Fluent in English speaking and report writing. Ability to work well under pressure Demonstrate ability to handle work professionally, independently and efficiently Continuous improvement mindset. Analytical, planning, execution and problem-solving skills Excellent managerial and mentorship skills Excellent interpersonal and communication skills. Good team player with good attitude, integrity, interpersonal, organization and time management skills. Apply below Full Name* Email* Resume* Accepted file types: doc, docx, pdf, Max. file size: 50 MB. Additional Information Name This field is for validation purposes and should be left unchanged.

Job Title: Senior Manager – Quality Assurance and R&D – Activated Carbon Plant Location: Ponnapuram Village, Dharapuram Taluk, Tirupur District, Tamil Nadu Company Overview: Carbonmax Advantech Pvt Ltd is a leading manufacturer of coconut shell-based steam activated carbon with integrated infrastructure for granulation, rotary kiln-based activation, post-activation processes, and advanced value addition plants. These include acid-washed carbon, powdered activated carbon, impregnated carbon, pelletized carbon, and catalytic carbon. Carbonmax is rapidly expanding into custom and specialty carbon applications , including supercapacitors, gas filtration, gold recovery , and other high-performance material domains. Position Summary: We are looking for a Senior Manager – Quality Assurance, R&D and Value-Added Carbon Products to lead end-to-end QA, QC, and product innovation efforts across all divisions of the plant. The role includes oversight of production QA/QC labs, value-added carbon labs, and R&D studio; implementation of international testing protocols (ASTM, AWWA, JIS, EN); team management; compliance leadership; and new product development for global carbon applications. This role demands deep domain expertise in activated carbon quality, laboratory instrumentation, documentation, and lean quality management systems , and will play a key role in transitioning the company from commodity to specialty carbon manufacturing. Key Responsibilities: Quality Assurance & Quality Control: Oversee QA/QC of: Raw material (charcoal, chemicals) In-process material Finished activated carbon (steam activated, acid washed, PAC, impregnated, pelletized, catalytic) Implement global test methods: ASTM Standards : D4607 (Iodine), D2854 (Ash), D2867 (Moisture), D3838 (Density), D3467 (CTC), D5158 (Hardness) AWWA B600 (Water treatment carbon) JIS Methods (MB adsorption, pH, volatile content) Gold Recovery Testing (K value, R value, cyanide adsorption) BET surface area , pore distribution , acid/base leaching VOC & gas phase testing using GC/FID, if applicable Approve and issue Certificate of Analysis (COA) with batch data Conduct inter-lab validation , retain sample reviews, and audit trails Laboratory Operations & Equipment: Supervise operations across: Production QA/QC Lab Value-Added Carbon Lab R&D Studio Lab Maintain, calibrate and utilize: BET Analyzer , Malvern Particle Size Analyzer UV-VIS Spectrophotometer , Turbidity Meter Atomic Absorption Spectrophotometer (AAS) Moisture Analyzer , Muffle Furnace , Crushers TGA/DSC , Zeta Potential , GC-MS (if deployed) Ensure GLP, safety, chemical handling, calibration logs, and SOPs New Product Development & R&D: Lead formulation and testing of specialty carbon products for: Supercapacitor cathodes – high surface area, electrical conductivity VOC and gas phase filtration Gold recovery and metal adsorption Pharma and food grade carbon – low leachable impurities Coordinate: Bench-scale trials, scale-up validations, application benchmarking Lab-to-production integration and performance testing Technical datasheet development Team Management & Capability Development: Build and supervise team of: Lab chemists, QA/QC officers, R&D executives, documentation staff Define KRAs, skill matrix, SOP adherence Conduct training programs in: Test methods, documentation, root cause analysis International QA/QC standards, instrumentation usage ISO 9001, ISO 14001, ISO 45001, REACH, FSSAI (if applicable) Systems, Documentation & Compliance: Implement and maintain: COAs, Batch sheets, NCR logs, Deviation Reports, Lab notebooks ISO documentation and internal audits Drive compliance with: TNPCB, ISO, FSSAI, ROHS, REACH, Electrical/Boiler Inspectorate Coordinate third-party inspections, customer audits, and validations Continuous Improvement & Lean QA: Promote 5S, Lean Lab, and Kaizen culture Conduct RCA for non-conformances and implement CAPAs Improve: Test cycle time COA dispatch reliability Equipment downtime and lab utility efficiency Eligibility Criteria:Qualification: M.Sc. / B.E. in Chemistry, Chemical Engineering, Material Science or Industrial Chemistry Additional training in QA systems or analytical chemistry preferred Experience: 10–18 years in QA/QC or R&D roles, preferably in: Activated Carbon / Specialty Chemicals / Battery Materials / Water & Air Filtration Media Hands-on experience in advanced lab instruments and international testing protocols Technical Skills: Global test standards: ASTM, AWWA, JIS, EN Advanced instrumentation and lab data interpretation Quality systems, audit handling, team leadership ERP or LIMS for quality and traceability Language: Tamil (mandatory), English (working), Hindi (preferred) Software Skills: ERP systems, MS Excel, QA reports, instrument software Key Competencies: Lab and QA team leadership Global test method application Documentation and audit readiness Product development and application benchmarking Structured execution and problem-solving Commitment to innovation in carbon materials Reporting To: Director – Technical & Operations Employment Type: Full-time | On-site (Ponnapuram Plant) Compensation & Benefits: Competitive salary based on experience Performance-based incentives Statutory benefits and medical insurance On-site accommodation and canteen facility Exposure to advanced carbon materials segment Learning and development support Schedule: Day Shift Monday to Saturday (occasional weekend availability) Supplemental Pay: Performance bonus Annual bonus Overtime pay (where applicable) Ability to Commute/Relocate: Ponnapuram, Dharapuram Taluk: Must be able to relocate or commute reliably. On-site factory accommodation available if required. How to Apply: Send your updated CV to: hr.factory@carbonmaxtech.com Subject: “Application – Senior Manager – QA & R&D – Activated Carbon” Speak with us: +91 99434 99855 Job Types: Full-time, Permanent Pay: ₹50,000.00 - ₹75,000.00 per month Benefits: Commuter assistance Food provided Health insurance Provident Fund Schedule: Day shift Monday to Friday Weekend availability Supplemental Pay: Overtime pay Performance bonus Yearly bonus Ability to commute/relocate: Dharapuram, Tamil Nadu: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

🔧 Hiring: Junior Biomedical Engineer – Bombay Hospital, Jaipur 🧑‍💼 Position: Junior Biomedical Engineer 📍 Location: Jaipur 🧑‍🤝‍🧑 Vacancy: 1 post 🎓 Qualifications: · B.E. / B.Tech in Biomedical Engineering · Minimum 2+ years of hands-on industry experience 🛠️ Key Responsibilities: · Maintenance, calibration, troubleshooting of biomedical equipment (e.g., MRI, CT, ventilators) · Coordination with clinical teams for timely equipment servicing and downtime management · Documentation of repairs, part replacements, and compliance with hospital safety standards · Adherence to NABH standards for biomedical equipment management and patient safety · Participation in internal audits and quality improvement initiatives related to biomedical engineering · Training hospital staff on the proper and safe use of equipment to improve patient care outcomes · Liaison with vendors for procurement, servicing, and AMC (Annual Maintenance Contract) management 📅 Joining Date: Immediate – July–August 📧 To Apply: Send your resume & cover letter to bme.bhjaipur@gmail.com

The Project Controller position at our company in Chengalpattu is a full-time, on-site role where you will be responsible for overseeing and managing project controls, including process control, instrumentation, and calibration. Your day-to-day tasks will involve troubleshooting issues, maintaining and optimizing electrical systems, and ensuring accurate reporting and documentation of project progress. To excel in this role, you should have proficiency in Process Control and Instrumentation, skills in Troubleshooting and Electrical Engineering, experience with Calibration techniques, strong analytical and problem-solving skills, excellent organizational and time management abilities, and the ability to work both independently and as part of a team. A Bachelor's degree in Electrical Engineering or a related field is required, and any relevant certification or training in project control would be a plus.,

The General Manager INSTRUMENTATION role at Krishna Tissues Pvt. Ltd. in Burdwan is a full-time on-site position that entails overseeing the instrumentation department. As the General Manager INSTRUMENTATION, your primary responsibilities will include ensuring the proper installation, calibration, and maintenance of all instruments. You will be tasked with managing the team, troubleshooting technical issues, optimizing processes, and ensuring compliance with safety and regulatory standards. Collaboration with other departments to facilitate smooth operations and active participation in continuous improvement initiatives are also key aspects of this role. To excel in this position, you should possess experience in Instrumentation, Calibration, and Maintenance, along with technical proficiency in troubleshooting and problem-solving. Strong leadership and team management skills are essential, as well as a good understanding of safety and regulatory compliance standards. Effective communication and coordination abilities are crucial for successful performance in this role. The capacity to work independently, handle multiple tasks simultaneously, and a Bachelor's degree in Engineering, Instrumentation, or a related field are also required qualifications. Additionally, experience in the paper industry would be considered advantageous for candidates interested in this position at Krishna Tissues Pvt. Ltd.,

As a key member of ReNew, you will be responsible for overseeing CPK, DOE, and establishing as well as monitoring the processes and process parameters across all production stages. Your role will involve ensuring the timely calibration of primary and secondary modules utilized in the IV tester. Additionally, you will play a crucial part in creating new recipes and process parameters whenever there are changes in raw materials, products, or machinery. In this position, it will be your duty to monitor process parameters consistently throughout all stages of production across three shifts. You will also be involved in evaluating the development of new or alternate Bills of Materials (BOM). Furthermore, you will be responsible for conducting Statistical Process Control (SPC) and analyzing process capability to ensure optimal performance and quality standards are maintained. Your contributions will be instrumental in driving efficiency, quality, and innovation within our production processes. By focusing on continuous improvement and adherence to set parameters, you will play a vital role in upholding our commitment to sustainability and excellence.,

Must have minimum 2+ years of relevant experience with good analytical skill having experience in Implementation and Support projects In-depth knowledge in below mentioned areas – Master Data: - Functional Location, Equipment Master, Class & Characteristics, Work center, Task List, Revision, Measuring Points etc. Notification Management: - Configuration and Process Flow, Integration with Maintenance Order Preventive Maintenance: -Single Cycle Plan, Strategy Based Maintenance Plan, Task List, Maintenance Plan Scheduling Parameter, Maintenance Strategy, Deadline Monitoring Maintenance Order Management: - Breakdown Maintenance Process & Corrective Maintenance Process, Calibration Maintenance Should have worked on Status Management in Notification and Maintenance Order. Must have experience in SAP PM integration with third party tool Experience in writing Functional Specification (FS), co-ordination with ABAP team and testing of new functionality or enhancement A day in the life of an Infoscion As part of the Infosys consulting team, your primary role would be to actively aid the consulting team in different phases of the project including problem definition, effort estimation, diagnosis, solution generation and design and deployment You will explore the alternatives to the recommended solutions based on research that includes literature surveys, information available in public domains, vendor evaluation information, etc. and build POCs You will create requirement specifications from the business needs, define the to-be-processes and detailed functional designs based on requirements. You will support configuring solution requirements on the products; understand if any issues, diagnose the root-cause of such issues, seek clarifications, and then identify and shortlist solution alternatives You will also contribute to unit-level and organizational initiatives with an objective of providing high quality value adding solutions to customers. If you think you fit right in to help our clients navigate their next in their digital transformation journey, this is the place for you! Ability to work with clients to identify business challenges and contribute to client deliverables by refining, analyzing, and structuring relevant data Awareness of latest technologies and trends Logical thinking and problem-solving skills along with an ability to collaborate Ability to assess the current processes, identify improvement areas and suggest the technology solutions One or two industry domain knowledge Infosys Ltd. is committed to ensuring you have the best experience throughout your journey with us. We currently have open positions in a number of locations across India - Bangalore, Pune, Hyderabad, Chennai, Chandigarh, Trivandrum, Indore, Nagpur, Mangalore, Noida, Bhubaneswar, Kolkata, Coimbatore, Mumbai, Jaipur, Mysore, Hubli. While we work in accordance with business requirements, we shall strive to offer you the location of your choice, where possible

The role offers you the opportunity to complete product quality checks under close supervision. You will be responsible for conducting routine testing and analysis of production work, ensuring accuracy in quality checks and documenting quality control issues as needed. Your essential functions will include timely analysis of samples under test, coordinating with production for quality-related issues, sampling and analyzing RM/Intermediate/Finished Goods, ensuring compliance of ATR, assisting in ISO implementation, and possessing knowledge of calibration, standard preparation, standardization, and relevant documentation. Furthermore, you will need to have expertise in handling HPLC, GC, and wet analysis. As part of your department-specific and ongoing functions, you will be required to provide timely reports to SAP for result recording, fill and update all relevant documents, maintain zero accidents in quality operations, achieve batch-wise timelines, quantity, and quality, train and supervise operators in your department, participate in the Emergency response team, and maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality systems. To qualify for this position, you must hold an M. Sc. in Chemistry and have 3-4 years of experience in Quality, including cGMP, ISO, and regulatory audits, as well as laboratory safety. Preferred skills and qualifications include knowledge of Quality Control in Fine Chemicals and pharmaceutical companies and experience of cGMP. Desired skills and competencies for this role include willingness to learn, being a team player, and possessing good communication skills. Please note that the above statements are a general description of the nature of work performed in this classification and are not exhaustive. Avantor is an equal opportunity employer committed to diversity and inclusion. Join our global team of 14,000+ associates at Avantor and make a difference in people's lives through life-changing science. Dare to go further in your career, contribute your talents, learn new skills, and grow with us. Apply today and be part of a culture that supports your career growth and success. If you require a reasonable accommodation during the employment process, please contact us at recruiting@avantorsciences.com to discuss your needs. Requests for accommodation will be considered on a case-by-case basis. By submitting candidates without a formal assignment or contract from Avantor, you forfeit any fee, as per our 3rd Party Non-solicitation Policy. Avantor engages with recruitment agencies based on its needs and does not accept unsolicited solicitations.,

As a Junior Research Associate in the Bioanalytical Research field, your responsibilities will include the operation and maintenance of various laboratory equipment. You will be required to handle biological samples, manage sample receipt and shipment, and procure biological matrix lots as needed. Additionally, you will be responsible for the operation, calibration, and maintenance of equipment such as deep freezers, refrigerators, Eurotherm, Thermo hygrometers, thermometers, centrifuge, evaporator, pH meter, balance, and pipettes. Furthermore, you will be involved in the management of biological samples including study samples, validation samples, and matrix lots. It will be crucial for you to maintain and archive relevant data in accordance with Standard Operating Procedures (SOPs) in coordination with the QC associate. The ideal candidate for this position should hold a B.Pharm or B.Sc. in Lifescience and possess 0-6 years of relevant experience. Strong attention to detail, organizational skills, and the ability to work effectively in a team are essential for success in this role.,

The main purpose of your role is to monitor the In Process against the Standard process flow and Continuously Improve the process by reducing Process rejections. As part of your responsibilities, you will frequently interact with internal teams such as R&D, Production, and Stores to ensure good Quality production. You will be responsible for creating documents for the entire product, including Process Flow, Control plan, PFMEA, etc. Additionally, you will confirm that the Line Process meets the BOM and Drawing requirements, define Inspection methods, and provide training to Process Engineers. You will also collaborate with the Supplier Quality team to communicate any deviations from the Drawing requirements using the FFF methodology. It is essential to ensure timely PDI inspection clearance and take immediate actions without stopping shipments. Supporting the QMS lead to achieve ISO 9001: 2015 requirements for the In process is also part of your role. When dealing with New Products, you will evaluate samples based on customer usage conditions and create new standards beyond Drawing requirements. Another important aspect of your role is to focus on factory-related customer complaints and take appropriate actions to address them. Proactively thinking to achieve Zero-line stoppage due to Quality incidents is crucial, as well as interacting frequently with the CFT for new model parts and sharing past failure issues to prevent reoccurrence of Quality issues. Key performance indicators for your role include the Reduction of Process Quality Rejection, Zero downtime due to Quality incidents, 100% deployment of Quality System for In-process Quality, ensuring 100% Training to engineers to achieve Quality Targets, and leading the calibration of IMTE for Factory & R&D Team. Qualifications and Education: - Education Qualification: B. Tech required - 7+ years of experience required About Eruvaka: Eruvaka Technologies serves the Aquaculture industry by designing and building advanced pond management and diagnostic systems that utilize complex algorithms, IoT, and machine learning. These systems help farmers improve profitability, protect pond ecosystems, reduce feed usage significantly, and provide valuable actionable insights. With customers in over 10 countries, Eruvaka Technologies is rapidly expanding to deploy systems across the world to achieve sustainable aquaculture. To know more about Eruvaka, visit: www.eruvaka.com To explore Eruvaka's products, visit: https://youtu.be/TjKCTJjBhUU,

As an R&D Intern at Teva Pharmaceuticals, you will be part of a team dedicated to making good health more affordable and accessible to help millions around the world enjoy healthier lives. With a presence in nearly 60 countries and a diverse mix of nationalities and backgrounds, you will work with the world's leading manufacturer of generic medicines and contribute to producing essential medicines listed by the World Health Organization. Every day, at least 200 million people worldwide benefit from our products, but we are constantly looking for new ways to make a difference and seeking new talents to join us in this mission. Your primary responsibilities will include analyzing samples received from the FRD department, which encompass in-process, finished products, pre-formulation study samples, and stability samples. You will also be tasked with developing analytical methods for APIs, in-process samples, and finished products, including methods for cleaning studies. Additionally, you will handle analytical method transfer activities, calibration, and maintenance of analytical instruments, ensuring adherence to good laboratory and documentation practices and existing quality systems. Safety protocols and EHS systems on-site will be strictly followed, and troubleshooting of analytical instruments for daily operational challenges will be part of your routine tasks. To qualify for this role, you should hold a Master's degree in pharmaceutical sciences, MSc, or M. Pharm with 0 to 1 year of relevant experience. Experience in regulated markets such as the US, EU, or Canada is preferred, along with expertise in routine analysis, chemistry, analytical method development, and instrumental methods of analysis. If you are passionate about contributing to the pharmaceutical industry's advancement, ensuring product quality, and promoting health worldwide, we invite you to apply now and be a part of our team at Teva Pharmaceuticals.,

We are seeking a Biomedical Engineer to join our 120-bed hospital in Palwal. If you have experience working in a reputable hospital, we encourage you to apply for this position. As a Biomedical Engineer, your main responsibilities will include supporting patient diagnosis and treatment through the installation, testing, calibration, and repair of biomedical equipment. You will also be responsible for training users, ensuring safe operations, and approving new equipment by conducting tests and modifications to adhere to codes. In addition, you will be involved in installing new equipment, maintaining existing equipment through preventive maintenance schedules, troubleshooting malfunctions, and coordinating special equipment services. You will play a key role in directing biomedical equipment operations, providing demonstrations, and training healthcare staff on equipment usage and care. To excel in this role, you should have at least 3-6 years of experience as a Biomedical Engineer with a focus on delivering excellent patient care. Strong communication and computer skills are essential, along with the ability to multitask effectively in a fast-paced environment. Interpersonal skills and the ability to maintain patient confidentiality are also crucial. If you are a detail-oriented individual who is passionate about improving equipment performance, conducting tests, and collaborating with manufacturers to enhance patient care, we would like to hear from you. This is a full-time position that requires in-person work at our hospital in Palwal. If you meet the preferred candidate profile and are ready to contribute to maintaining a safe and healthy working environment while upholding the highest standards of patient care, we look forward to receiving your application.,