6282 Calibration Jobs - Page 36

We're Hiring: Business Development Manager Location: Hyderabad Company: Phoenix Live Industry: Experiential Events | Brand Experiences | Corporate Engagements Apply at: people@phoenixlive.in About Phoenix Live We’re not your average events agency — we’re a high-octane, creatively wired, hyper-collaborative squad trusted by brands like Microsoft, Apple, Amazon, Deloitte, and Google. We turn event ideas into extraordinary brand experiences — immersive, seamless, unforgettable. Our vibe? Think big agency capabilities with a start-up heart. Hustle meets heart. Deadlines meet dopamine. And every project? A playground for brilliance. The Role: Business Development Manager This is a dual-wield role for a sharp thinker and smooth talker. You'll be the bridge between brands and our bold ideas — converting leads, nurturing relationships, and driving serious revenue growth. We need someone who’s just as comfortable crunching numbers and hitting targets as they are building trust, pitching creative ideas, and leading seamless execution. If you thrive in high-energy environments, love people as much as performance, and bring a no-excuses attitude to your game — we want you. Key Responsibilities Business Development Own and execute smart sales strategies to drive growth & meet targets Hunt down new leads, close key accounts, and develop high-value partnerships Be the face of Phoenix Live in new rooms — pitch with power, and win trust fast Monitor market trends, spot emerging sectors, and pivot to stay ahead of the game Client Servicing Be the go-to for clients — understand their brand, needs, and business like it’s your own Collaborate closely with creative, design, and production teams to deliver wow-worthy events Maximize value — upsell, cross-sell, and deep-sell to existing clients with flair Solve problems, make processes seamless, and ensure every client feels like our only one Strategic Leadership Mentor and guide the servicing team — coach them into client whisperers Use data + instincts to forecast, report, and refine strategy Align cross-functional teams to ensure delivery matches promise Who You Are Keen interest in client servicing, BD, or account management, preferably in events, media, or marketing Requirement of closing deals, scaling client relationships, and hitting revenue goals A master of communication, negotiation, and stakeholder management Comfortable juggling chaos with a calm mind — you own timelines and targets Relentlessly positive, solution-first thinker with a sharp eye for opportunity Not a ‘yes person’ — you bring ideas, perspectives, and the fire to grow What You’ll Love About Us 💥 Work with global giants & cutting-edge brands 💥 Freedom to run your own show, with full support 💥 Team that's more tribe than workplace — fun, fast, and fiercely collaborative 💥 No red tape, just bold dreams and hard hustle 💥 Performance gets celebrated. Loudly. Ready to Join the Hustle? 📧 Send us your CV at people@phoenixlive.in 📎 Attach a short note on what makes you the right fit. Let’s build epic experiences together — ones that don’t just impress clients but make them rave. About Company: At Phoenix Live, we are driven by a singular mission: to make every event stress-free and unforgettable. As a leading creative event agency, we blend art, culture, and technology to deliver experiences that captivate audiences and bring brands to life. From intimate gatherings to large-scale productions, our team ensures flawless execution, fuelled by precise planning and boundless creativity. Innovation is at the heart of Phoenix Live. We leverage cutting-edge technology, such as AI-driven audio calibration and automated lighting systems, to elevate the event experience. Our obsession with creativity is matched by our attention to detail, ensuring each moment leaves a lasting impression. From our collaborations with some of the world's biggest brands like Microsoft, Apple, Amazon and Deloitte to our deep commitment to art, culture, and sustainability, Phoenix Live is shaping the future of the events industry.

Skills: Quality Assurance, Quality Control, pharma, Documentation, Microsoft Excel, Statistical Process Control, ISO Standards, Process Improvement, Job Title: Quality Check (QC) and Quality Ana (QA) Location: [AMHEDABAD] Job Type: [Full-time]Job Location: Pirana, Ahmedabad Joining: Immediate Salary: 20 to 25 K p.m./ Qualificaiton: B/Sc/M.Sc/ B Pharm/ M/ Pharm Job Overview We are seeking a detail-oriented and proactive Quality Check (QC) and Quality Assurance (QA) Specialist to join our team. This role is responsible for ensuring the highest standards of quality in our products and services, overseeing the quality control processes, and implementing assurance protocols to meet industry standards and company requirements. Qc Key Responsibilities: Responsibilities of Quality Control Laboratory including Instrumental Lab, Chemical Lab. To ensure the compliance of current Good Laboratory Practices and Standard Operating Procedures in the Q.C. Laboratory. To prepare the working standards as per the guidelines and pharmacopoeias. Review of QC documents, test protocols and analytical reports. To carry out the sampling and testing of raw material and packing material according to approved procedure. Responsibilities for testing and approval or rejection of packaging materials after discussion with QC Head. To recommend the release of Raw Material and Packing Material in standard format To intimate the Officer Stores and QC Head for the failure of any packing material, however, if the QC Head is absent then intimate the status of the same to G.M Technical/Director. To record all the data related to the testing on line on day-to-day basis and ensuring the traceability of it. To ensure the status tag on the released material and transfer of such material in the released area. To review and updating of all SOPs as per requirements of GLP on regular basis. To participate in execution of all validation program like process validation, cleaning validation, analytical method validation, etc. To check the cleaning records of laboratory. To make documentation of all analysis including raw data, checking of all data and proper storage of data. To charge the product for stability and analysis of all stability samples, and compilation of stability data. To provide response to queries received from regulatory / marketing departments. To maintain the calibration record and annual maintenance contract records of all the instruments in QC Laboratory. To ensure the timely review and updating of all standard test procedures and specifications of raw materials and packaging materials on regular basis to meet regulatory requirements. To ensure the standardization of volumetric solution, preparation of reagents as per schedule and verification of its documentation. To develop the new analytical method and Standard Testing Procedures (STPs) for in-house or pharmacopoeia methods and prepare the method validation report. To maintain the record of retain sample by means of their inventory, their periodic check and their disposal. To train and develop all QC staff on GLP & advanced analytical techniques and their evaluation on periodical basis. To evaluate the requirements of HPLC/GC columns, reference standards, chemicals, reagents, etc and raise PR for procurement of the same. In absence of QC Head take care of the day to day activities of QC department, including approval of documents and release of material. If you take leave, your work responsibility handover to other QC Executive / Officer. Authority To carry out all the necessary test and recording their result thereof for all the material. To check the stores and ensure the implementation of GMP norms in the stores. Not to allow any material inside the plant if material is not from the approved vendor or if it is not as per the specified standards. 6.1 Over all responsibility of Quality Assurance Department. 6.2 Vendors approval for RM & PM. 6.3 Periodical Quality Audit. 6.4 Activities related to Drug Control Authorities. 6.5 Evaluation of Product Complaints & Product Recall. 6.6 Validation and Qualification. 6.7 GMP Training to Staff. 6.8 GMP Implementation in the factory. 6.9 Co-ordination with various departments to implement cGMP in Plant 6.10 Market Authorization of Products. 6.11 Release of batches for Sale. 6.12 Evaluation of change control and Deviation in system and process. 6.13 Assure the operation as per Quality Policy. 6.14 Execution and review of QMS in plant. 6.15 Other jobs, assigned by seniors as and when required. EXPERINCES: Minimum 2+year. Salary range : 20 to 25 k.

Prescience Calibration Pvt Ltd, an ISO/IEC 17025 NABL-accredited laboratory, is hiring a young, dynamic, and experienced Sales Executive to promote calibration services in Survey, Torque, and Dimensional fields. The candidate will execute sales strategies, build brand visibility, and drive business growth across industrial segments. Key responsibilities include client outreach, quotation handling, documentation coordination, target achievement and lead generation. A technical qualification in Mechanical, Instrumentation, or Electronics along with prior sales experience in calibration services is preferred. strong communication skills, and proficiency in MS Office are essential. Candidates must own a two-wheeler for field travel. Competitive salary, sales incentives are given.

· Install and commission car detailing machines (steamers, vacuum cleaners, pressure washers, polishers, etc.). · Set up lighting systems, electrical panels, and workstations as per studio layout. · Conduct routine preventive maintenance of studio equipment to avoid downtime. · Diagnose and troubleshoot machinery or infrastructure issues during or after setup. · Ensure correct calibration and safety compliance of machines. · Maintain tools, spares, and documentation for each site visit. · Train on-ground staff or franchise partners on basic operation and care of machines. · Submit visit reports and equipment status updates to the central team. · Support AMC (Annual Maintenance Contract) and service requests post-installation.

Key Responsibilities: 1. Raw Material Testing: Conduct routine quality checks of incoming raw materials including phenols, aldehydes, catalysts, fillers, etc. Approve or reject materials based on test results and specifications. Maintain records of raw material inspection and communicate deviations. 2. In-Process Monitoring: Perform real-time testing and analysis during resin synthesis and processing. Coordinate closely with production team to communicate test results effectively. 3. Finished Goods Testing: Conduct final product testing as per defined product specifications (e.g., viscosity, flow, moisture content, solid content, curing time, etc.). Issue certificates of analysis (COA) as required. 4. Documentation & Compliance: Maintain accurate records of all test data, batch histories, and calibration logs. Ensure compliance with ISO standards and internal SOPs. Participate in internal and external audits. 5. Laboratory Upkeep: Calibrate and maintain laboratory instruments and equipment. Maintain cleanliness, safety, and good laboratory practices (GLP). Maintain adequate inventory of lab chemicals and consumables. Note: Rotational Shift job, so the candidate might need to do night shift if required

Group Company ACGE Primary Responsibilities Functional- Quality Assurance Expertise: Demonstrate a comprehensive understanding of quality assurance (QA) processes, ensuring all FAT activities align with company standards, customer requirements, and regulatory norms. FTR (First Time Right) Implementation: Collaboratively lead the FAT team to achieve First Time Right execution across each stage of inspection and testing, minimizing rework and enhancing process efficiency. Execution & Problem Solving: Plan and execute FAT activities in accordance with project timelines. Identify operational challenges during FAT and inspection and proactively develop and implement effective solutions. Customer & Third-Party Handling: Serve as a subject matter expert for handling customers, Third Party Inspectors (TPI), and internal stakeholders during FATs, ensuring clarity, confidence, and satisfaction throughout the inspection process. Customer Complaint Analysis & CAPA Support: Lead the analysis of customer complaints, contribute to root cause analysis (RCA), and support the development and implementation of Corrective and Preventive Actions (CAPA) to ensure continuous product improvement. Continuous Improvement Initiatives: Drive and contribute to continuous improvement efforts by identifying process gaps and implementing changes that enhance FAT quality, reduce testing time, and ensure operational excellence. Technical Clarifications: Consult with Managers or Project, Engineering, Automation Heads for clarification on discrepancies related to part specifications, drawings, or documentation to ensure issues are resolved before FAT execution. Documentation & Compliance Knowledge: Maintain sound knowledge of qualification protocols, certifications, calibration procedures, and regulatory documentation required for successful FAT execution in a pharma environment. Pharma Equipment & Testing Expertise: Possess deep understanding of pharmaceutical machinery and their standard functional testing procedures, including compliance with cGMP, GAMP, and 21 CFR Part 11 requirements. Audit & Compliance Standards: Be familiar with standard auditing methodologies (e.g., ISO, ASME) and apply non-destructive testing (NDT) procedures as required during inspection. Cross-functional FAT Collaboration: Collaborate with cross-functional teams to highlight and resolve issues that may affect on-site installation and commissioning, ensuring all concerns are addressed prior to dispatch. Site Readiness Optimization (I-FAT): Ensure installation readiness by executing effective Internal FATs (I-FAT) at the factory, thus minimizing site installation time and reducing resource wastage. Validation Document Review: Review and verify all validation and qualification documentation during I-FAT, ensuring alignment with customer expectations and regulatory compliance. Mechanical BOM Review: Validate the Mechanical Bill of Materials (BOM) to confirm inclusion of all installation-critical parts, ensuring nothing essential is omitted from dispatch. Site Learning Integration: Integrate learnings from site installations into factory FAT protocols to continuously improve pre-dispatch testing, especially for electrical and mechanical components. Software Integrity Pre-Installation: Develop robust methodologies to minimize or eliminate the need for software modifications during site installation, thereby reducing commissioning time and risk. Packing Process Enhancement: Re-structure the packing slip format to include equipment Tag Numbers and standardize packing slip generation for better traceability and error reduction. Site Issue Resolution Coordination: Act as the central point of coordination for resolving factory-originated issues identified at the site, enabling immediate corrective actions. Key Result Areas Cross-Functional Collaboration & Quality At Source: Objective: Develop and maintain strong, trust-based relationships with Cross-Functional Team (CFT) members—including Engineering, Manufacturing, Procurement, Quality Assurance, and Project Management—to drive a shared responsibility for quality from the very first stage of the product lifecycle. Key Results: Reduction in quality issues detected during FAT due to upstream corrections. Timely resolution of inter-departmental issues affecting FAT readiness. Active participation in CFT meetings, design reviews, and root cause investigations. Implementation of design/process feedback from FAT into product development Quality Compliance & Standardization: Objective: Ensure full compliance with internal quality standards, regulatory requirements (ISO, GMP, etc.), and customer-specific URS and documentation expectations during FAT. Key Results: Zero non-conformities in internal audits and customer FATs. 100% adherence to SOPs, checklists, calibration protocols, and document validation. Reduction in post-dispatch NCs (non-conformities) due to strict in-process adherence. Maintenance of up-to-date records and traceability for all FAT-related activities. Process Improvement & Efficiency Optimization: Objective: Continuously identify and implement improvements in FAT processes, workflows, and testing methods that enhance product quality, reduce inspection time, and streamline communication—without compromising safety, compliance, or customer satisfaction. Key Results: Measurable reduction in FAT cycle time through lean process enhancements. Implementation of automation or standardization tools in testing and reporting. Documented process improvements with quantifiable impact on quality and efficiency. Increased number of tests shifted from site to factory (I-FAT effectiveness). Customer Expectation Alignment: Objective: Consistently align FAT activities and deliverables with customer-specific requirements and expectations by ensuring transparent communication, effective documentation, and readiness to handle audits or custom protocols. Key Results: Positive customer feedback and satisfaction scores during and after FAT. Reduction in post-FAT changes or rework requested by customers. Increased rate of "First Pass" customer approvals during FAT. Safety and Risk Management: Objective: Maintain a high standard of safety in all FAT activities, ensuring both team members and machinery are protected during testing, inspection, and pre-dispatch operations. Key Results: Zero incidents or safety violations during FAT execution. Timely implementation of safety recommendations or audit observations. Team trained and compliant with updated safety protocols and practices. Key Interfaces Internal Interfaces- AE PRD NPD A&C PSC PPC & Project External Interfaces- Supplier Customer External Auditors (If any) Third party inspector ISO Auditors Competencies Plant QA understanding Communication Problem Solving Delivering Consistent Results Knowledge of Regulatory Compliance

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.,