10945 Qc Jobs - Page 4

Job Title: Quality Control Manager – Radiator Manufacturing (Transformer Industry) Department: Quality Assurance / Quality Control Location: [Insert Plant Location] Reports To: Plant Head / Director – Quality / Operations Head Experience Required: 8 years in transformer component manufacturing or heavy fabrication industry, with at least 3–5 years in a QC managerial role Job Objective To lead the Quality Control department for transformer radiator manufacturing by ensuring that all incoming materials, in-process operations, and final products meet stringent quality standards, regulatory requirements, and customer specifications. The role demands a strong background in sheet metal fabrication, welding inspection, pressure testing, and painting quality control. Key Responsibilities Quality Control – Raw Materials & In-Process Supervise inspection of incoming raw materials (CRCA sheets, headers, fins, welding consumables). Monitor in-process quality checks during cutting, forming, welding (MIG/TIG/spot), and painting. Verify compliance of welding parameters, bead quality, and dimensional tolerances. Final Inspection & Testing Conduct and supervise pressure/leak tests for radiator panels and assemblies. Ensure all radiators meet specified customer requirements, including visual, dimensional, and functional parameters. Validate painting finish, coating thickness, and corrosion resistance as per standard. Quality Systems & Documentation Maintain and implement ISO-compliant quality systems and documentation (inspection reports, test certificates, NCRs). Ensure traceability of components and compliance with QMS/IMS requirements. Prepare quality documentation for customer approvals and audits. Corrective & Preventive Action (CAPA) Lead cross-functional teams to implement CAPA and monitor effectiveness. Reduce internal rejection rates and customer returns through proactive quality planning. Team Management & Training Lead and mentor a team of inspectors, weld quality technicians, and lab staff. Conduct training for shop-floor teams on quality standards, defect identification, and basic troubleshooting. Promote a zero-defect culture and continuous improvement mindset. Coordination with Other Functions Work closely with design and production teams to ensure manufacturability and quality of new radiator designs. Support SCM in vendor quality evaluations and audits. Interface with customers for pre-dispatch inspections (PDI) and technical clarifications. Calibration & Equipment Management Ensure timely calibration and upkeep of all measuring instruments (pressure gauges, vernier calipers, weld gauges, DFT meters). Maintain and operate QA equipment for testing welds, pressure holding, and paint adhesion. Key Skills & Competencies Strong knowledge of welding standards (WPS, PQR), NDT (visual, dye penetrant), and sheet metal fabrication Experience in pressure testing (hydrostatic or air), paint/coating quality checks, and leak detection Familiarity with transformer industry standards (IS, IEC) Proficiency in using QC tools: 7 QC tools, FMEA, Pareto analysis, RCA Working knowledge of ERP and quality modules (SAP / Oracle preferred) Skills: radiator,pressure,manufacturing,welding,customer,quality control,transformer,testing,documentation,materials

Job Title: Senior Civil 3D Engineer Location: Vittal Rao Nagar, HITEC City, Hyderabad, Telangana Job Type: Full-Time Experience Level: 8+ Years Industry: Civil Engineering / Land Development / Infrastructure Job Summary: We are seeking a Senior Civil 3D Engineer with a minimum of 8 years of professional experience in civil drafting using Autodesk Civil 3D . The successful candidate will lead and support a variety of civil engineering projects, including land development, site planning, grading, drainage, roadways, and utility . Key Responsibilities: Lead and manage the development of detailed civil plans using AutoCAD Civil 3D Create and manage: Existing and proposed surfaces Grading and earthwork models Alignments, profiles, and corridors Pipe networks (storm, sanitary, water) Cross-sections and plan & profile sheets Collaborate with project managers, engineers, and drafters to deliver high-quality 2d documents Oversee preparation of construction drawings, reports, and permitting documents Perform checks, QA/QC, and resolve complex technical issues Coordinate with clients, agencies, and utility providers as needed Provide mentorship to junior staff and help standardize Civil 3D workflows and templates Requirements: Bachelor’s degree in Civil Engineering, Drafting Technology, or a related field Minimum 5 years of hands-on experience with Autodesk Civil 3D in a professional setting Expertise in: Grading and earthwork design Utility layout and profiles Stormwater management and drainage systems Roadway or site development In-depth knowledge of local, state, and federal design standards and permitting processes Strong technical documentation and CAD drafting skills Ability to manage multiple projects and meet deadlines

Job Opening – Senior GCMS Analyst 📍 Location: Ahmedabad | 🏢 Department: QC Department 📅 Type: Full-time | 🆕 New Position | Openings: 1 About Us Anant Fragrance Pvt. Ltd. is a leading manufacturer and exporter of Cosmetic, Soap, Fine, and Incense Stick Fragrances , offering exceptional quality and innovation to clients worldwide. Our expertise blends art and science to create captivating olfactory experiences. 🌐 Learn more: www.anantfragrance.com Position Details Designation: Senior GCMS Analyst Grade/Level: Highly Experienced Reports To: Director Direct Reportees: None Key Responsibilities Analyze Fine Fragrances using state-of-the-art GC-MS instrumentation . Develop demo formulas based on analytical data and olfactive assessments. Share valuable olfactive insights with the creative and technical teams. Collaborate in developing unique and high-quality fragrances . Requisite Skills Proven expertise in fragrance formulation and reformulation . Strong ability to interpret GC-MS data accurately. In-depth technical knowledge of perfumery raw materials . Analytical mindset with problem-solving skills in fragrance reformulation. Passion for perfumery science and creativity . Desired Qualifications Education: Bachelor’s or Master’s degree in Science (Chemistry) or equivalent. Experience: 3–5 years as a GC-MS Analyst . Exceptional olfactive skills and attention to detail. Compensation & Benefits 💰 CTC: ₹6.00–7.20 LPA 💵 Monthly Net Salary: ₹50,000 – ₹60,000 🕒 Working Hours: 9:30 AM – 7:00 PM (Monday to Saturday) 🏠 Perks: Housing & Transportation – Negotiable 📩 Apply Now Send your CV to admin@anantfragrance.com with the subject line "Application – Senior GCMS Analyst" .

Position- QC Inspector Qualification - ITI / Diploma / Any Degree Years of exp- 2 to 3 years Duration- Call off basis Location - Visakhapatnam, Andhra Pradesh Job Type: Freelance Contract length: 2 months Pay: ₹800.00 - ₹1,200.00 per day Work Location: In person

.Position: Senior QA Engineer – CNC Machine Shop Location: Talegaon Dabhade or Chinchwad MIDC Company: JK Precision and Tools About Us: JK Precision and Tools is a fast-growing leader in CNC machining, fixture manufacturing, gauges, SPMs, and hydraulic workholding solutions. We serve leading automotive and industrial manufacturers with high-precision components, maintaining stringent quality processes aligned with IATF standards. Role Overview: We are looking for an experienced Senior QA Engineer to lead our machine shop quality function. The role involves applying advanced quality tools, managing customer quality requirements, leading audits, and driving continuous improvement to achieve zero-defect deliveries. Key Responsibilities: Lead the QA department for our Machine Shop Drive Core Tools implementation: APQP, PPAP, FMEA, MSA, SPC. Apply 7 QC Tools, Six Sigma principles, and problem-solving methodologies. Handle customer complaints using 8D methodology and ensure timely closure. Conduct MSA (Gage R&R) and maintain calibration systems for all measuring instruments. Establish and monitor SPC charts for critical processes. Lead internal, customer, and third-party audits (ISO 9001 / IATF 16949). Train the QA team on In-process inspection, quality standards, GD&T, and inspection techniques. Develop quality plans, control plans, and inspection check sheets. Conduct root cause analysis and implement corrective/preventive actions. Ensure compliance to customer-specific requirements (CSR). Work with production to drive continuous improvement and defect prevention. Required Skills & Qualifications: Diploma/Degree in Mechanical/Production Engineering. 5 years of QA experience in CNC precision machining. Expert in GD&T, CMM inspection, and advanced measurement techniques. Hands-on experience in PPAP documentation, MSA, SPC, and FMEA. Certified Six Sigma Green Belt / Black Belt (preferred). Strong communication and customer-handling skills. Proficient in preparing and presenting quality reports to management and customers. Employment Type: Full-time Job Types: Full-time, Permanent, Fresher Pay: ₹35,000.00 - ₹55,000.00 per month Benefits: Commuter assistance Food provided Health insurance Leave encashment Paid sick time Paid time off Provident Fund Ability to commute/relocate: Talegaon Dabhade, Pune, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Education: Diploma (Preferred) Experience: total work: 5 years (Preferred) Work Location: In person

Date: 7 Aug 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Discovery Services Job Location: Bangalore Department: Medical Writing About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Role Medical Writer Key Responsibilities Independently develop and finalize clinical and scientific documents for different regulatory submissions such as (but not limited to) Bioanalytical reports, Clinical Study Reports (CSRs), part of Electronic Common Technical Document (eCTD) modules, covering various therapeutic areas, and phases of clinical research Collaborates with internal and external clients to support and enable effective communication resulting in operational excellence Effectively manages medical writing and review processes to deliver quality projects in agreed timelines Ensure compliance to applicable regulatory guidelines, department SOPs, client style guides, conventions as applicable Ensures that appropriate documented quality control (QC) checks are performed on medical writing deliverables and responds to findings Follow any other instructions and perform any other related duties, as assigned by the supervisor. Performs literature search/review as necessary to obtain background information for developing scientific content Educational Qualification Graduate in Life Sciences Masters in Life Science Experience 2-4 Years Behavioural Skills Good communication Quick learner Adapt to change Time management Professionalism Technical/functional Skills Ability to comprehend scientific information Good understanding of clinical research. Knowledge of working on MS word, PPT etc. Attend training on environment, health, and safety (EHS) measures imparted company Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Position: GRN Executive (Goods Receipt Note) Location: Kalamboli Warehouse Department: Operations / Stores Role Objective: Accurately record all incoming materials in the GRN system, ensuring correct specifications, quantities, and documentation for smooth inventory management. Key Responsibilities: Create GRNs in Tally / ERP for all incoming goods. Match supplier delivery challans and invoices with physical receipts. Coordinate with QC for inspection before GRN entry. Tag and label materials as per warehouse system. Report shortages, damages, or mismatches immediately to purchase and QC teams. Maintain GRN logs for audit and reporting purposes. Requirements: 1–3 years’ experience in storekeeping, GRN, or inventory documentation. Basic knowledge of steel grades, pipe/tube sizes preferred. Familiarity with Tally ERP and MS Excel. Strong attention to detail and ability to work in warehouse environment. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Application Question(s): Have you created GRNs in Tally ERP or any other inventory system before? How do you match supplier challans/invoices with actual received goods? What steps do you take if goods are short, damaged, or mismatched? Can you maintain a clear GRN log for audit and reporting? Location: Kalamboli, Navi Mumbai, Maharashtra (Required) Work Location: In person Speak with the employer +91 9594962477

Position: Packing List Executive Location: Kalamboli Warehouse Department: Operations / Dispatch Role Objective: Prepare accurate packing lists for all outgoing shipments, ensuring correct material details, quantities, and customer requirements are met for smooth dispatch. Key Responsibilities: Prepare packing lists with correct heat numbers, sizes, weights, and quantities. Coordinate with warehouse team to verify materials before dispatch. Ensure packing lists match invoices, delivery challans, and dispatch instructions. Maintain packing list records physically and in Tally / ERP. Share packing lists with dispatch, QC, and accounts teams as required. Assist in resolving discrepancies in quantity or description before loading. Requirements: 1–3 years’ experience in warehouse/dispatch documentation. Basic knowledge of steel products (pipes, tubes, sizes, grades) preferred. Proficiency in MS Excel and Tally ERP. Detail-oriented and accurate in documentation. Job Type: Full-time Pay: ₹15,000.00 - ₹25,000.00 per month Application Question(s): Have you prepared packing lists for shipments before? Which products? How do you ensure the packing list matches the invoice, delivery challan, and dispatch instructions? Are you familiar with including details like heat number, OD, thickness, length, and grade in the packing list? What software have you used for preparing packing lists (Excel, Tally ERP, other)? Location: Kalamboli, Navi Mumbai, Maharashtra (Required) Work Location: In person

We're a growing brand that take great pride in the unique artistic, and aesthetic experiences our brands offer to our customers! We're looking for a qualified designer/artist who loves creating beautiful things and taking them to completion. This individual would need to be passionate about art and designing, about uniqueness, and about delivering a flawless experience to our customers when it comes to branding. Responsibilities include: Be responsible for/maintain the aesthetics of the brand in all creative collateral Responsible for Social Media Ads, ideating and creating video content - How To, products, explainers, short films, performance videos, GIFs, social media posts, etc. Responsible for creating short 30-60sec videos for social media, etc. in different video formats for Instagram, Facebook, Pinterest, YouTube, and other marketing platforms Ability to create content using existing/ stock footage to create films for campaigns, marketing assets, and social media Come up with new ideas and techniques to enhance the premium look and feel of the brand and maintain it consistently across platforms. Proficient in shooting and editing videos and coming up with interesting video content in- house Work with scriptwriters for the process of idea generation, character development, visualization, and storyboarding Design storyboards using advanced graphics and animation tools and techniques, video and film shoots, stock imagery, and photography Work with internal teams and external vendors to ensure brand values are protected and projected consistently as far as the design and philosophy of the brand are concerned. Collaborate with various stakeholders like campaign managers, creative team, and designers Work with vendors to achieve a low rejection rate in QC. Ability to innovate and think out of the box Ability to work hard and long in an intense, ambitious environment Qualifications/abilities we're looking for: Complete expertise in software such as Adobe After Effects, Adobe Premiere Pro, Final Cut Pro X, etc. Ability to draw/paint/create some form of art that will help them resonate with the aesthetics of the brand Strong conceptual & visual design skills leading to thoughtful and creative executions Undergrad or Master’s degree in Art, design, motion graphics, or a related discipline will be preferred 2 to 4 years of professional experience in creating video content Ability to create content using existing/stock footage. We are a hardcore, fast-growth focused environment and a place where only dedicated, stable, dependable individuals who are willing to immerse themselves completely to this cause can thrive.

Positions : 1. QC Chemical Section Experienced candidates required Location - Derabassi Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Health insurance Provident Fund Ability to commute/relocate: Panchkula, Haryana: Reliably commute or planning to relocate before starting work (Required) Application Question(s): Notice period? Current Salary? Expected Salary How much experience in Chemical Section? Current Location? Experience: total work: 1 year (Required) Work Location: In person

Interested candidates, kindly mail to enpcareers.hr@ril.com Job Accountabilities: An experienced geophysicist responsible for seismic reservoir characterization and seismic interpretation projects for integrated reservoir study and well placement. Should possess advanced expertise in geophysics with a deep understanding and working experience of seismic data analysis and inversion techniques to provide insights into subsurface reservoir properties. Adheres to RIL business plan with 100% compliance on HSE and core V&Bs of RIL. Seismic Inversion and reservoir characterization: Utilize cutting edge geophysical techniques and software for generating inversion products and attributes for characterizing reservoir; Identify Rock Physics Modelling (RPM) strategy, Generate RPM/RPT; Perform/review well to seismic tie & extract wavelets for seismic inversion; Perform fluid and lithology substitution; Perform cross plot and EI analysis; Select attribute for fluid/ lithology; Perform synthetic modelling - Prepare Zero-offset & offset Synthetics in both in-situ and what-if situations; Compare Synthetics with Seismic data; Identify processing requirements for seismic reservoir characterization; Provide inputs on Inversion strategy (post-stack, pre-stack, elastic, coloured, GI etc); Perform Seismic Inversion; Generate net to gross, porosity, lithology etc. volume as required; Generate AVO/DHI attributes; check consistency of attributes with RPM; Risk-uncertainty analysis of seismic inversion and reservoir characterization. Seismic Interpretation and Integration: Perform seismic interpretation and integration of well and associated data; Perform/review surgical interpretation of horizon and faults; Perform well-seismic tie, Synthetic Seismogram generation; Review/generate maps to understand structural and stratigraphic aspects; Collaborate with multi-disciplinary teams to integrate seismic data with geological and petrophysical information; Perform attribute analyses; Perform seismic blueing to enhance data; Perform/Review quantitative interpretation using Seismic Inversion, AVO attributes; Perform velocity modelling for depth conversion; Compute volumetric estimation; Capture Risk elements; QC seismic acquisition, processing/reprocessing projects in association with functional team; Provide inputs and interface with key stakeholders for static model building. Well placement and planning: Plan and Optimize well placement; perform Appraisal, development and In-fill well planning using the appropriate seismic attribute volumes; Prepare well prognosis, targets & trajectory; Analyze for shallow hazards; characterization of overburden for well placement; Provide inputs to well planning and interact with drilling/operations; Recommend data acquisition requirements during drilling. Provide inputs for DoC/ Appraisal Plan/ Field Development Plan(FDP): Provide inputs for Integrated Sub-Surface Description; Provide inputs for Appraisal Program; Execute Appraisal Activities including seismic API and well; Perform Resource Assessment; Provide inputs for appraisal and ML areas; Provide inputs for preparation of Declaration of Commerciality (DoC); Perform reservoir connectivity analysis to identify connectivity between sands, perm barriers & their impact on reservoir depletion scheme; Interact with Exploration, Projects and FC&A for Techno-economic analysis; Provide inputs for preparation and implementation of FDP in consultation with key stakeholders. Stakeholder & People Management: Prepare stage gate documents; Conduct Knowledge sharing sessions; Present to management, JV partners, regulatory authorities as required; Capture key learnings, Ensure safety as per HSE guidelines; Comply with PSC/JOA and statutory requirements. Skill & Competencies: Knowledge and working experience of Seismic Inversion and AVO analysis; Generation of rock physical model; Fluid substitution analysis and synthetic modelling; Working knowledge/ Hands-on experience in interpretation/Reservoir Characterization software like Landmark, Petrel, HRS, Jason Geoscience Workbench, RockDoc etc Capable of coding in any one of the following programming language (Python/Matlab/C); skilled in Data Science, Machine Learning, Artificial Intelligence Experience in Geophysical Interpretation; Experience with well to seismic tie, synthetic generation, wavelet extraction, horizon and fault interpretation using 2D and 3D seismic and other suitable attribute volumes, Velocity modelling and depth conversion, 3D visualization and interpretation; Seismic data enhancement- spectral blueing; Working experience in data analytics Knowledge of identifying and capturing uncertainties and risk in the geophysical interpretations. Well placement, planning and prognosis. To work in multi-disciplinary team consisting of Geologists, Geophysicists and Petrophysicist and be able to deliver as per the business plan requirement. Education Required: Minimum 8 years experience in E&P with working experience as seismic interpreter/ seismic reservoir characterization Geophysicist. Extensive experience in Prospect/ field Evaluation, Seismic attributes & Inversion, Velocity Modelling, Risk & Uncertainty assessment, Techno-Commerciality Analysis and exploration/ appraisal/development well placement Interested candidates, kindly mail to enpcareers.hr@ril.com

As the LEAD– BIM, you will lead the strategic implementation and management of BIM technologies across all projects. You’ll oversee BIM teams, drive innovation, ensure compliance with global standards, and collaborate with stakeholders to optimize digital construction workflows. Strategic Leadership Develop and execute BIM strategies aligned with organizational goals. Lead digital transformation initiatives in design and construction workflows. Manage BIM teams including managers, coordinators, and modelers. Oversee BIM execution plans and ensure timely delivery of digital models. Technology & Standards Implement and maintain BIM protocols, standards, and QA/QC processes. Ensure integration of BIM with other platforms (e.g., ERP, project management tools). Stakeholder Collaboration Coordinate with architects, engineers & contractors Facilitate BIM coordination meetings and resolve model-related issues. Training & Development Mentor BIM professionals and conduct training programs. Stay updated on emerging BIM technologies and trends. 📚 Qualifications Bachelor’s or Master’s in Architecture or Civil Engineering Minimum 15 years of experience in BIM roles Proficiency in BIM software: Revit, Navisworks, AutoCAD, BIM 360. Strong understanding of ISO 19650 and other BIM standards. Excellent leadership, communication, and project management skills.

ROLE DEFINITION Responsible for Quality Inspection and Records REPORTING To GM –Operations &Senior Engineer QA/QC REPORTEES - RESPONSIBILITIES Inward inspection at stores In process / stage inspection and Quality control as per requirements Final inspection as per Requirement Measuring Instrument and welding machine Calibration External inspection at supplier place and site as per schedule Documentation as per Drawing and customer requirements Implementing ISO 9001:2015 & Other systems as per requirement Maintaining the documents with traceability for easy retrieval Quality improvement at supplier place KEY RESULT AREAS Inspection completion as per schedule Zero complaints on inspection No Gaps in Calibration due Timely submission of Documents to customer Quality improvement at in house / supplier place Monitor the effective implementation of procedures in accordance with Quality Management system No Major Nonconformance in Internal / External Audit EDUCATIONAL QUALIFICATION BE / B.TECH – Mechanical Engineering with min 1 years experience DME with 2 years experience Behavioral · Planning and organizing · Attention to detail · Oral and written communication skills · Interpersonal relationship Functional · Optional-Knowledge and experience in Codes and standards such as ASME / IS / EN of welding and equipment fabrication. · Knowledge of inspection and testing methods · Knowledge of QA /QC documentation /Dossier · Optional- Good Knowledge and experience in Welding process and Qualifications · MS –office · Experience in NDT methods and reports · Experience in Customer /TPI coordination Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Ability to commute/relocate: Coimbatore, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required) Work Location: In person

Job Title: Good Manufacturing Practices (GMP) Trainer Location: Peenya, Bangalore, Karnataka Job Type: Part-Time / Contract / Guest Faculty Duration: 30 Hours (Flexible Schedule) About the Role: We are looking for an experienced Good Manufacturing Practices (GMP) Trainer to deliver high-quality training to undergraduate students (BSc – Pharma) at our partnered college in Peenya, Bangalore . This training will be part of their academic curriculum to bridge classroom learning with industry practices. Responsibilities: Conduct engaging sessions on GMP as per industry and regulatory guidelines. Share training content, presentations, and real-world examples. Evaluate student learning through activities and Q&A sessions. Ensure training meets both academic and industry standards. Requirements: Bachelor’s/Master’s degree in Pharmacy, Biotechnology, Microbiology, Life Sciences, or related discipline. Minimum 2–3 years of industry or training experience in GMP-compliant environments. Strong knowledge of FDA, WHO, and ISO standards related to manufacturing practices. Excellent communication and presentation skills. Preferred: Prior experience as a corporate/academic trainer. Hands-on exposure to pharma manufacturing, QA/QC, or regulatory affairs. Session Details: Batch: College students (BSc level) Total Hours: 30 hours (schedule will be discussed) Mode: On-campus (Peenya, Bangalore) How to Apply: Send your updated CV and availability details to hr@netcraftz.in with the subject line “GMP Trainer – Peenya” or contact to 9686022805 Job Type: Freelance Contract length: 15 days Pay: ₹9,292.97 - ₹20,000.00 per month Work Location: In person

Job Title: Quality Analysis Specialist Location: Sangli, Maharashtra Experience Level: 0-5 Years Shift: US Shift (Saturday and Sunday Off) Role and Responsibilities of Quality Analysis Specialist: As a Quality Analysis Specialist in Residential Appraisal Quality Control (QC), you will play a critical role in ensuring the accuracy, compliance, and quality of residential property appraisals. You will be responsible for reviewing, verifying, and optimizing appraisal reports to meet regulatory and industry standards. This role is essential for minimizing risks and ensuring accurate property valuations. Key Responsibilities: Reviewing and Verifying Appraisal Reports. Ensure accuracy, consistency, and completeness of appraisal reports. Cross-check property details, such as size, layout, condition, and comparable properties. Assess the appropriateness of adjustments made to comparable sales. Compliance and Regulatory Adherence. Ensure adherence to the Uniform Standards of Professional Appraisal Practice (USPAP), federal guidelines, and lender requirements. Verify compliance with internal policies and client-specific standards. Risk Assessment and Quality Control. Identify red flags such as inconsistencies, questionable comparables, or potential appraisal bias. Detect and document signs of fraud or misrepresentation. Mitigate valuation risks to protect lenders from financial losses. Collaboration with Stakeholders. Provide constructive feedback to appraisers to improve report quality. Work closely with underwriters, loan officers, and compliance teams to resolve appraisal-related issues. Documentation and Reporting. Prepare detailed reports outlining discrepancies or areas requiring clarification. Maintain QC logs and track trends to refine quality control processes. Training and Process Improvement. Deliver training sessions for appraisal teams and QC staff on best practices and regulatory updates. Identify and implement process improvements to enhance efficiency and minimize errors. Technology and Tools Usage. Use specialized appraisal QC software and databases for efficient review and data management. Leverage data analytics to identify and address recurring appraisal errors. Client Relationship Management. Prepare customized quality control reports to meet client specifications. Assist with client audits by providing relevant documentation and analysis. Core Skills and Qualities Required: Exceptional attention to detail for identifying inconsistencies or errors in reports. Strong analytical skills to critically assess data and ensure appraisal credibility. Excellent communication skills for effective interaction with appraisers, underwriters, and clients. Knowledge of USPAP, industry standards, and lending regulations. Strong problem-solving abilities for resolving appraisal discrepancies. What We Offer: Opportunity to work on cutting-edge AI-driven solutions. Exposure to the real estate and financial services industries. Professional growth and development opportunities. Collaborative and innovative work environment. Ability to commute/relocate: Sangli, Maharashtra: Reliably commute or plan to relocate before starting work (Required) Language: English (Required) Shift Availability: Night Shift (Required) Job Types: Full-time, Permanent Pay: ₹200,000.00 - ₹600,000.00 per year Benefits: Cell phone reimbursement Health insurance Internet reimbursement Paid sick time Provident Fund Work from home Application Question(s): Do you have any exposure to US Mortgage, Real Estate Valuation Process? Do you have experience in loan processing, insurance? Experience: Quality Analysis Specialist: 2 years (Required) Work Location: In person

Job Description: New Product Development Job Title: New Product Development Experience: 2 + years of experience Salary: Negotiable Based on experience Location: Kadi, Gujarat Employment Type: Full Time About Innovitoy: Innovitoy Pvt. Ltd., established in 2021 in Ahmedabad, is a pioneering toy manufacturer specializing in high-quality, innovative, and safe toys for children of all ages. Guided by core values of quality, trust, and delight, the company aims to revolutionize childhood experiences through its state-of-the-art R&D lab and ethical business practices. Innovitoy's mission is to enrich children’s lives with joy and imagination by offering exceptional toys crafted with precision and care. Job Summary: We are seeking a hands-on, detail-oriented New Product Development (NPD) Engineer to lead and execute the complete product development lifecycle — from idea generation and prototyping to tooling and mass production. The ideal candidate will have a strong understanding of toy design, materials, manufacturing processes (especially plastic injection moulding), and child safety standards. Key Responsibilities:  Drive end-to-end product development — ideation, design, prototyping, testing, validation, and mass manufacturing.  Collaborate with product designers, marketing, and production teams to refine concepts and translate them into manufacturable products.  Create and review technical drawings, BOMs (Bill of Materials), 3D CAD models, and design documentation.  Identify appropriate manufacturing methods and vendors (in-house and outsourced).  Coordinate with mold/tooling suppliers for prototype and production tooling.  Evaluate product safety, quality standards (e.g., BIS, EN71), and compliance.  Troubleshoot manufacturing challenges, quality issues, and suggest process improvements.  Ensure cost-effective designs while maintaining product safety and functionality.  Monitor pilot batches and handover to production with proper SOPs and QC parameters. Key Skills & Qualifications:  Bachelor’s degree in Mechanical Engineering, Industrial Design, Product Design, or related field.3–6 years of experience in new product development in toys, consumer products, plastics, or electronics industries.  Proficiency in CAD software (SolidWorks, Creo, AutoCAD, or similar).  Familiarity with plastic injection moulding, tooling, DFM (Design for Manufacturing), and child safety standards.  Strong project management and cross-functional communication skills.  Passion for product innovation and user-centric design. Kindly share your resume on hr1.rrmgt@gmail.com and contact on 9081819471. Job Type: Full-time Pay: ₹35,000.00 - ₹40,000.00 per month Work Location: In person Speak with the employer +91 9081819471

About Us Mosaic Wellness is building digital first, health brands for elective health concerns. Man Matters is a digital elective health platform for men, helping 2.5M men every year diagnose and solve for their hair loss, beard growth, fitness, and nutrition concerns by offering personalized treatment plans and access to expert doctors and health coaches. Be Body Wise is an online womens elective health platform, serving 4M women every year by providing personalized solutions and doctor consults across concerns for hair health, body care, sleep, and nutrition. Little Joys is an online health platform for kids, helping 2M parents every year solve for their childs physical, mental, and emotional development by offering age-appropriate solutions for nutrition, immunity, brain health, and bone health with access to expert doctors and nutritionists. We have now launched a company in the US and are now a top seller in the category there, and this role is for that. Job Summary As the Manager, New Product Development, you will convert concepts into real-life products, directing every phase of the launch cycle for evidence-based supplements and beauty products in the U.S. market. You Will Identify high-potential opportunities through rigorous market analysis and competitive benchmarking, taking full ownership of each products strategic rationale. Secure best-in-class suppliers and contract manufacturers, negotiating pricing, minimum order quantities, and lead times to safeguard margins and schedules. Design and oversee an international supply chain that delivers on time, on budget, and at scale. Your successful launches will open new revenue streams and strengthen Mosaics footprint in the US You'll Do? Analyze market data to quantify total addressable market, price corridors, and whitespaces in the market. Prepare P&L projections and scenario models that support go/no-go decisions. Identify and qualify certified partners in the United States, India, and Asian markets. Negotiate cost breaks, payment terms, and exclusivity agreements that help the business scale sustainably. Work with legal teams to confirm formula, label, and claim compliance under FDA, FTC, Prop 65, and OTC Monograph rules. Establish QC protocols including COAs, stability, micro, and heavy-metal testing and monitor first-pass yield. Design freight and warehousing flows from factory gate to 3PL, balancing cost with service level. Build live dashboards for OTIF, landed cost, and inventory cover; intervene proactively to keep targets on track. Coordinate cross-functionally with Marketing, Growth, and Creator teams on timelines, claims, and inventory drops. Lead post-launch reviews covering unit economics, supplier scorecards, and next-batch Were Looking For? 2-5 years experience delivering end-to-end launches of supplements or beauty products at a consumer/D2C startup; export experience is advantageous. Demonstrated success negotiating with raw-material vendors or CMOs, consistently reducing COGS while maintaining relationships. Supply-chain fluency across Incoterms, freight forwarding, duty optimization, and 3PL integration. Advanced analytical skills; able to build dynamic cost models and demand plans in Excel or Google Sheets. Clear, concise communicator capable of aligning cross-functional This Role? End-to-end ownership Each product you introduce carries your imprint and drives a new revenue line. Global scope Engage factories worldwide and negotiate without procurement bottlenecks. Speed of execution Concepts move to purchase orders in weeks, providing rapid, visible impact. Accelerated growth Two successive wins position you to shape the entire new-product roadmap and build the team that delivers Delhi, Type: Full-Time. (ref:iimjobs.com)

Position Summary Embark on a fulfilling career journey with BGH, where innovation meets compassion in healthcare. Join our dynamic team at the forefront of medical excellence, with a focus on Chemistry, Hematology, Transfusion Medicine, Microbiology, and Anatomical Pathology. Elevate your skills in our cutting-edge Point of Care department, where professionals like MLAs, MLTs, Senior MLTs, Charge MLTs, and PAs collaborate seamlessly. Embrace the excitement of 24/7 core lab operations, spanning days, nights, evenings, weekends, and STATs. Be part of our dedicated Microbiology and Histology teams, where your commitment to community care truly shines. At BGH, we're not just a workplace – we're a family, united by cohesiveness, professionalism, and a shared passion for making a positive impact. Join us in shaping the future of healthcare, where every day brings new opportunities for growth and success! Responsible to the Charge Technologist(s) in the Division(s) in which they are working and to the Lab Manager for performing phlebotomy and ECG tracings (site specific), as well as, preparing and organizing specimens for analysis and various duties in different divisions of the lab. Duties do not require interpretation, assessment or the exercise of independent judgment. Required EDUCATIONAL REQUIREMENTS: Successful Completion of an approved Laboratory Assistants training program and Certification with other professional organizations (i.e., CSMLS, OSMT). OR Technologist current registered with the College of Medical Laboratory Technologist of Ontario. Supervisory, verbal and written communication skills. Ability to organize, prioritize and meet deadlines. Students and new graduates actively pursuing certification are welcome to apply. Duties Blood Specimen Procurement Performs phlebotomy on Inpatients and Outpatients and BG Emergency. Implements good quality venipuncture - adult and paediatric. Implements good quality capillary collection – adult and paediatric. Maintains accurate patient identification and specimen labelling at all times. Recognizes suitability of specimens and the need for requests. Advises Technologists on Diagnosis, STATS, A.S.A.P, etc. Operates Lab computer – ordering test, logging specimen in, receiving, etc. ECGs - TMH Requires special training. Performs electrocardiograms (ECG). Responsible for good quality ECG tracings – adult and paediatric. Enters ECG into computer. Copies and dispenses ECG as required. Completes ECG process with special attention to Pre-Op ECG. Departmental Maintains pleasant and professional rapport with patients and other customers at all times. This key position has direct interaction with all the laboratories main customers, thus has a direct effect on laboratory reputation. Maintains good infection control practices. Helps with documentation and phone enquiries, as required. Assists with compiling statistics when necessary. Participates in quality assurance activities. Orientates and trains new staff/students. Assists in developing, reviewing and amending department policies and procedures. Prepare Hospital Incident Forms. Lab Tests/Set-Up – May Be Site Specific Prepares referred out specimens for appropriate outside labs for special testing and documents as required. Prepares specimens for shipment to QHC Laboratories as required. Performs inventory. Performs temperature readings. Change charts. Packaging and unpacking blood. Stocking POCT refrigerator. Maintenance (centrifuge, tachometers, timers, etc.). Sorts, centrifuges and distributes laboratory specimens entering the Laboratory. Maintains good quality sterile techniques. May place specimens on Hematology, or Biochemistry, analysers with special training. Assists with send outs. Assists with sample separating (centrifuging). Assists with worksheets. Assists with units Haematology May place specimens on analysers after special training. Chemistry Assists with aliquoting and identifying Assist with the setup of tests (eg. drugs screens, pregnancy). May place specimens on analysers after special training. Performs urinalysis (excluding microscopic). Microbiology (Site specific) Receives all microbiology samples. Answer phone calls and transfer to MLT as required. Plating microbiology samples and cultures as required. Restocking microbiology supplies. Subculture QC organisms. Equipment maintenance. Discard microbiology samples once complete. Construct Public Health kits. Equipment/Supply Procurement/Maintenance Troubleshoots problem with ECG, Holter, and Events machines and calls for service when required. Obtains weekly order from stores and organizes and puts order away. Keeps supply of Kleenex, Javex and towels, etc. in each division. Maintains and cleans blood taking room and ECG room. Assists with general maintenance and clean up of equipment and instruments. Assists with housekeeping and glassware washing. Safety Maintains a safe environment by: Following established safety, WHMIS, infection control and waste disposal policies. Maintaining a clean and organized work area. Cleaning phlebotomy trays. Keeping equipment cleaning records (eg. ECG). Weekly cleaning and minor maintenance of ECG machines. Follow infection control policies eg. Isolation, universal precautions. Working with needles and blood requires special care - all staff are to use safety equipment supplied and specified gloves, goggles, safety devices, lab coats, etc. Minimizes risks to self, other staff, patients and visitors through: Familiarity with policies and procedures regarding safety. Attendance at safety training including fire safety, back care and W.H.M.I.S. training. Reporting of hazards and incidents. Related Duties Contributes to Department by performing related tasks as required. Maintains patient confidence and protects Health Centre operations by keeping information confidential. Maintains skills/knowledge by attending educational sessions and keeping informed of Health Centre policies and procedures. Models QHC Vision and Values At Quinte Health, guided by our core values of Imagine It's You, Value Everyone, We All Make a Difference, and Stronger Together, our family of four hospitals holds a central role in the mission to enhance lives and foster healthier communities. We operate as a cohesive team, uniting all our hospitals, to deliver local and regional healthcare services. In partnership with our communities, we strive to improve access to high-quality care, right in their own neighborhoods. Our sense of fulfillment is deeply rooted in the impactful work we do, a sentiment shared by our dynamic teams of staff, dedicated physicians, and committed volunteers. They not only care passionately for our patients but also for each other, embodying our core values at every turn. We don't just serve our communities, we actively contribute to them. Quinte Health is woven into the fabric of our local landscape, with our team members residing, raising their families, and often retiring right here in the communities they cherish. We are on a constant lookout for compassionate and dedicated individuals to join our team. Our diverse array of exciting roles encompasses positions that span multiple hospitals, as well as opportunities situated within a single hospital. Join us as we live out our values in providing exceptional healthcare close to home Physical Demands Analysis Physical Requirements Able to communicate and respond clearly on the telephone and face-to-face. Able to sit 2-6 hours per day at a computer table or bench. Able to stand and/or walk 3-5 hours a day. Able to lift no greater than 28 pounds on an occasional basis. Frequent bending or leaning depending on section of Laboratory where working. Able to work at a moderate pace maintaining accurate results. Must be able to see objects close up, reading requisitions, computer screens. Must be able to distinguish between colors, depending on section of Laboratory where working. Must have good manual dexterity. Mental Requirements Able to concentrate on details despite frequent interruptions. Attention to detail is essential. Able to follow both written and oral directions and remember in detail daily requirements and routine. Able to comprehend and utilize written materials. Able to cope with a high paced, sometimes high stress, work environment. Able to interact positively with a variety of individuals from various socio-economic backgrounds. Equal Opportunity We thank all interested candidates for their response, however, only those chosen for an interview will be contacted. Quinte Health is an equal opportunity employer committed to meeting needs under the Canadian Charter of Rights and Freedom and the Ontario Human Rights Code. Our Recruitment process follows the Accessibility for Ontarians with Disabilities Act in order to provide a fair and equitable process for all candidates. Applicants requiring accommodation through the recruitment/interview process are encouraged to contact the Human Resources Department at 613-969-7400 x2577 or

Key Skills, Project Planning and management Structural Analysis and Design Site Inspection And Supervision Environment Impact Assessment Cos Estimation and Budgeting AutoCAD 2D,3D,and MS office Strong Communication and teamwork abilities Knowledge of local and international building code and regulation roles and Responsibilities of Civil Engineer (Including RMC Plant, QA/QC, Procurement, Concrete Design, 2D/3D Drawings) 1. Project Planning & Coordination Plan, schedule, and execute civil works in line with project timelines. Coordinate with architects, consultants, contractors, and vendors. Ensure compliance with drawings, technical specifications, and safety regulations. 2. RMC Plant Establishment & Operations Plan the layout and infrastructure for Ready-Mix Concrete (RMC) plant setup. Select and coordinate with machinery/equipment suppliers for batching, mixing, and material handling. Oversee installation, commissioning, and trial runs of the RMC plant. Monitor production quality, batching accuracy, and operational efficiency. 3. Quality Assurance (QA) Develop and implement QA procedures for civil works and concrete production. Ensure all materials meet relevant IS codes and project specifications. Review and approve method statements and work procedures. Maintain QA documentation and compliance records. 4. Quality Control (QC) Conduct on-site inspections to verify work quality and adherence to specifications. Perform and supervise concrete and aggregate testing (slump, cube strength, sieve analysis, etc.). Maintain site test records and initiate corrective measures when required.Verify reinforcement placement, formwork quality, and curing practices. 5. Material Procurement Identify, source, and procure raw materials (cement, aggregates, steel, admixtures, etc.) as per project needs. Maintain vendor database and evaluate supplier performance. Monitor inventory and ensure timely delivery of materials to avoid delays. Negotiate prices, prepare purchase orders, and follow up with suppliers. 6. Concrete Mix Design Prepare mix designs based on strength, workability, durability, and environmental conditions. Optimize cement content, water-cement ratio, and admixture dosage for cost-effectiveness. Conduct trial mixes and finalize designs in compliance with IS codes. Maintain records of all mix designs and test reports. 7. Drawings & Design Management Prepare and review 2D CAD drawings for structural, architectural, and site layout works. Develop 3D models for better visualization and client presentations. Check for discrepancies between drawings and actual site conditions. Ensure as-built drawings are updated and documented after project completion. 8. Site Supervision & Execution Supervise daily site activities to ensure adherence to plan and safety norms. Resolve technical issues and provide solutions on-site. Manage subcontractors and workforce to meet productivity targets. Ensure proper curing, finishing, and protection of completed work. 9. Safety & Compliance Implement safety protocols for workers and machinery. Conduct regular safety meetings and toolbox talks. Ensure compliance with environmental and labor laws. 10. Documentation & Reporting Maintain site logs, daily progress reports, and material consumption records. Prepare monthly project status and cost reports. Document QA/QC test reports, purchase records, and equipment maintenance logs.

Greetings from Khazana Jewellery! We are hiring in Bangalore (HSR Layout) Interview Date: 20th & 21st August 2025 Venue: The Krishna Grand Rooms, No.77, Hosur Road, Near Ayyappa Temple, Madiwala, Bengaluru – 560068 Time: 10 am to 5 pm Designation: Sales Executive & Cashier Eligibility : Sales: 0 - 5 Years (Freshers Eligible) Cashier: Minimum 1 Year Experience Qualification: 12th/Diploma/Any Degree Gender : Male/Female Language: Speaking Kannada Must Age : 20 to 35 Job Descriptions for Sales: 1. Presents the customer with the needed Jewellery and provide information, such as pricing 2. Expertise in handling customers 3. Sale of the products, up selling & cross-selling of products/services 4. Responsible for Counter Sales & Store operation 5. Responsible for selling the Gold, Diamond, Platinum, and silver items in Store. 6. Receive stock additions, QC and manage inventory of the counter 7. Meeting counter wise Target as per store business Plan Benefits: Competitive and on time salary Attractive monthly Incentives. PF & ESI. Salary on Time. Yearly Salary Increment (Performance Basis) Opportunity to grow to higher positions Refreshment Provided Accomodation Provided on sharing basis (Only in Banglore)

Job description Check and execute the Project- specific QA/QC Plan with Scopes of work and work procedures.  Make and maintain daily MTC reports.  Prepare daily Marking reports of materials.  Knowledge of Preparing sample inspection report and Data Sheet whenever require.  Prepare all QA/QC Related Document/records as per system required.  Keeping aware of all Kind of QC checks.  Review and process all purchase orders accordance with company policy.  Well Versed with material grade Knowledge. Knowledge of ASME Standard of Pipes Tubes Flanges Fittings Fasteners and Valves Plates

Responsibilities & Key Deliverables Hands-on experience with transmission (gearbox) assembly and testing. Experience with hydraulic assembly and testing. Knowledge of APQP, SPC, PPAP, FMEA, MSA, 7 QC tools, Poka Yoke, Kaizen, etc. Conducting process and product audits in assembly and testing areas. Preparing quality/production procedures, work instructions, and visual instructions. Knowledge about Millipore and NAS testing. Preparation, review, and control of internal technical documents. Coordination with other departments for line trials, PPAP, ECN implementation, and issue closure (ORC). Ensuring field technical reports (FTRs) and field complaint (CVL) analysis, and providing solutions. Expertise in investigating and resolving quality issues on the assembly line using root cause analysis. Ability to read drawings and knowledge about GD&T (Geometric Dimensioning & Tolerancing). Should have knowledge about the gear manufacturing process.

Identify, develop, and onboard new international customers in assigned territory. - Execute sales cycles from inquiry to dispatch in coordination with logistics, documentation, and accounts. - Ensure monthly revenue targets are met through pipeline planning and client engagement. - Maintain updated and accurate CRM records including leads, quotes, orders, and feedback. - Work closely with production, purchase, and QC teams to deliver as per customer specifications. - Proactively resolve customer issues to ensure repeat business and brand trust. - Submit weekly performance dashboards to Regional Manager and log customer meetings. - Act as front-facing representative of Sagar Polytechnik in global markets, including exhibitions, etc.

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Analyst Qualifications: Master of Pharmacy Years of Experience: 3 to 5 years Language - Ability: English(International) - Advanced About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The incumbent will perform the regulatory operations tasks of bookmarking and hyper linking for granular components (documents) of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components. Collect, collate and evaluate the scientific data gathered as part of R & D. Advise on legal and scientific restraints and requirements. Ensure the organization`s products comply with current regulations. Example; Build regulatory submission strategy, author CMC documents, and health authority packages etc. What are we looking for? Adaptable and flexible Problem-solving skills Agility for quick learning Strong analytical skills Ability to meet deadlines Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts

Job Summary: We are seeking a dedicated and detail-oriented QC Microbiologist with 2 to 4 years of experience in pharmaceutical/biotech microbiology labs. The ideal candidate will be responsible for performing microbiological testing to ensure compliance with GMP standards and regulatory requirements. Key Responsibilities: Perform routine microbiological testing including: Sterility testing Water and air sampling Environmental monitoring (EM) Bioburden and endotoxin testing Identification of microorganisms Microbial limit tests Maintain microbiological data and logbooks. Participate in media fill validations and aseptic process simulations. Prepare and review SOPs, protocols, and reports related to microbiology activities. Ensure all testing and documentation complies with GMP, USP, EP, and regulatory guidelines. Support microbiological investigations (OOS, deviations, CAPAs). Operate and maintain laboratory instruments such as autoclaves, incubators, particle counters, etc. Coordinate with production, QA, and validation teams for sample planning and testing timelines. Assist in audits and regulatory inspections as needed. Qualifications: · B.Sc. / M.Sc. in Microbiology, Biotechnology, or related life science discipline. · 2 to 7 years of hands-on experience in QC Microbiology within a regulated pharmaceutical or biotech environment. · Knowledge of cGMP, GLP, and regulatory guidelines (FDA, EMA, WHO). · Familiarity with microbiological techniques and cleanroom classifications. · Good documentation practices and understanding of data integrity principles. · Proficiency in MS Office and LIMS (Laboratory Information Management System) is a plus. Job Type: Full-time Pay: ₹10,000.00 - ₹30,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Pondicherry, Puducherry: Reliably commute or planning to relocate before starting work (Required) Work Location: In person