3047 Labeling Jobs - Page 50

Responsibilities: Support warehouse operations by managing receiving, storage, dispatch, and maintenance activities in line with company policies and FMCG food product standards. Perform accurate in-bound and out-bound checking of FMCG food products to ensure correct quantities and quality. Assist in setting up warehouse layout for efficient space utilization and smooth workflow. Follow and help enforce operational policies and procedures to maintain warehouse efficiency and compliance. Ensure all warehousing, handling, and shipping activities comply with relevant legislation, particularly food safety and hygiene regulations. Maintain high standards of health, safety, hygiene, and security within the warehouse environment. Manage stock control activities, reconcile physical inventory with the data storage system, and report discrepancies promptly. Assist in packing, labeling, and tagging FMCG food products accurately for easy identification and compliance with food safety standards. Coordinate with suppliers, transport companies, and internal teams to ensure timely receipt and dispatch of products. Plan and organize daily tasks, monitor workflow , and support supervisors with team coordination. Produce regular reports and statistics such as stock in/out status and expired or damaged goods reports. Receive and act on feedback to continuously improve service quality and operational efficiency. Requirements & Skills: 1 to 3 years of experience in warehouse operations, preferably in FMCG food products or retail. Good understanding of inventory control, stock reconciliation, and FIFO (First In, First Out) principles. Experience in inbound and outbound checking, packing, and labeling of food products. Familiarity with warehouse management systems (WMS), barcode scanning, and basic MS Excel . Knowledge of food safety, hygiene, and storage compliance standards. Strong organizational skills and attention to detail. Ability to work in a fast-paced warehouse environment and handle physical tasks. Good communication skills and ability to coordinate with teams and external partners . Willingness to learn, follow instructions, and contribute to process improvements. Immediate joiners preferred. Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift Work Location: In person

Urgently Required Warehouse Manager The Warehouse Manager is responsible for overseeing end-to-end warehouse operations, including inventory control, logistics, staff supervision, and adherence to safety standards. This role ensures smooth functioning of receiving, storage, and dispatch processes across various product categories, with a focus on efficiency, accuracy, and compliance. Key Responsibilities: 1. Warehouse Operations Management Supervise daily activities including receiving, storing, packing, and dispatching goods. Monitor and maintain Stock based on product categories (e.g., Ready to eat, frozen, ambient, perishable). 2. Inventory Control Maintain accurate stock records using inventory management software. Implement and oversee FIFO (First In, First Out) and FEFO (First Expiry, First Out) methods. Conduct regular cycle counts and stock audits to ensure inventory accuracy. 3. Order Fulfilment & Dispatch Collaborate with sales and logistics teams to ensure timely and precise dispatch of orders. Prepare and manage dispatch schedules for online, retail, B2B, and export channels. 4. Team Supervision Oversee warehouse personnel, including supervisors, helpers, pickers, packers, and other operators. Allocate daily tasks and ensure team efficiency, discipline, and adherence to SOPs. 5. Technical Proficiency Operate and manage Warehouse Management Systems (WMS) and other logistics/inventory software. Apply principles of supply chain, warehousing, and inventory best practices. 6. Reporting & Coordination Generate and maintain daily MIS reports covering inward/outward movements and inventory status. Coordinate effectively with procurement, product development, QA, and finance departments. 7. Space and Layout Optimization Design and organize shelf layouts and racking systems to maximize warehouse space. Ensure proper SKU labeling, zoning, and product segregation to avoid mix-ups. 8. Vendor & Transport Coordination Coordinate with transport partners for inbound and outbound deliveries. Manage reverse logistics, including returns and handling of damaged goods. 9. Knowledge of Safety Regulations Ensure compliance with health and safety laws and warehouse safety standards. Implement and enforce protocols to maintain a safe and hazard-free working environment. Job Type: Full-time Pay: ₹22,000.00 - ₹25,000.00 per month Schedule: Day shift Night shift Education: Bachelor's (Preferred) Experience: WMS: 3 years (Preferred) Work Location: In person Application Deadline: 15/07/2025

Title: Executive - Regulatory Affairs Date: Jul 4, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Preparation and reviewing of labeling for ANDA and/or NDA applications and labeling query responses in accordance with the USFDA regulations. Preparation of Structured Product Labeling (SPL) for drug listing in accordance with the associated applications and USFDA regulations. Preparation, reviewing, timely submission and coordination of implementation of labeling based on FDA notifications and/or RLD labeling updates. Coordination of labeling related activities with cross functional teams for timely launch of products. Regulatory submission and filings, coordinating final labeling implementation and maintaining labeling artworks using various softwares. Communication with third parties or private label distributors to gather needs and requirements of changes/labeling development. Evaluation and coordinating with departments for REMS requirement for applications.

Requirements Experience: Minimum of 3 to 4 years in store/inventory management, preferably in a Metal Components manufacturing company. Technical Skills: Proficiency in ERP software and MS Office is required. Education: Any Graduate. Key Responsibilities Monitor and maintain stock levels to ensure the availability of required materials. Conduct regular stock checks and reconciliations and and ensure accurate record-keeping. Use ERP software to update inventory records, generate reports, and manage stock movements. Receive, inspect, and store incoming materials as per company standards. Ensure proper labeling and storage of items to maintain traceability. Issue materials to production and other departments as needed. Maintain accurate documentation for all inventory transactions. Generate regular reports on stock status, consumption, and replenishment needs. Ensure compliance with company policies and procedures related to inventory management. Maintain the store area in an organized and clean manner. Follow safety protocols to prevent damage to materials and ensure workplace safety. Job Type: Full-time Pay: Up to ₹30,000.00 per month Schedule: Day shift Supplemental Pay: Yearly bonus Education: Bachelor's (Required) Experience: Inventory control: 3 years (Required) Store management: 3 years (Required) Microsoft Office: 3 years (Required) Location: Jamnagar, Gujarat (Required) Work Location: In person

Job Type: Full-Time Location: St. John's Medical College Hospital at Brigade Meadows, Salahunase Village, Kanakapura Main Rd, Bangalore Experience: Minimum 3 years experience as a mid or senior level staff in a hospital preferred Key Responsibilities: Receive, inspect, and issue materials as per requisition Maintain inventory records and conduct regular audits Monitor stock movement and maintain optimal stock levels Ensure proper storage and labeling of all items Coordinate with purchase, accounts, and user departments Eligibility Criteria: Diploma or Graduate in Materials Management or similar fields preferred Minimum 3 years of experience in hospital/medical store operations Strong knowledge of inventory control systems Good computer and documentation skills Send your updated resume to: careers.bm@stjohns.in / sjmch.recruitment@stjohns.in

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control #LI-PFE

We are seeking a highly motivated and technically adept Sales Representative to drive sales and market growth in the Coding & Marking and Industrial Automation sectors. This role involves selling solutions such as industrial inkjet printers, laser coders, labeling systems to manufacturing companies. Key Responsibilities: Identify and pursue new business opportunities within the manufacturing and industrial sectors. Promote and sell coding & marking systems (e.g., CIJ, Laser) and automation solutions (e.g., software, conveyors, vision systems). Build strong relationships with plant engineers, maintenance managers, production managers, and procurement teams. Conduct site visits to assess customer needs and recommend appropriate solutions. Prepare and deliver customized sales presentations and product demos. Collaborate with technical support and engineering teams to design and implement integrated solutions. Develop proposals, quotations, and negotiate pricing and contracts. Meet or exceed monthly and quarterly sales targets. Maintain CRM entries for all sales activities and pipeline tracking. Job Qualifications: 2–5+ years of sales experience in coding & marking, packaging machinery, or industrial Products Familiarity with products such as CIJ/TIJ printers, laser coders, conveyors, Stackers, Re-winder, Vision inspection, or robotics . Skills & Competencies: Strong technical aptitude and ability to understand and communicate engineering concepts. Excellent communication and presentation skills. Proven negotiation and deal-closing skills. Proficient in CRM tools and Microsoft Office. Highly self-driven with a proactive sales approach. Strong organizational skills and ability to manage a sales territory independently. Willingness to travel locally or regionally for client visits and product demonstrations.

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Company Description Raj Innotech Pvt. Ltd., established in 2004, is a leading manufacturer, supplier, and exporter of various water treatment projects, mineral water projects, RTS juice turnkey projects, synthetic juice projects, and carbonated soft drink turnkey projects. Our products are manufactured to industry standards, thoroughly tested for quality, and include solutions for rinsing, filling, capping, packaging, and labeling. With our advanced manufacturing unit located in Rajkot, Gujarat, we cater to a global clientele, ensuring high satisfaction and delivering our equipment and services across India and to international markets, including the Indian Subcontinent, East Asia, and South/West Europe. Role Description This is a full-time on-site role located in Rajkot for an AutoCAD Designer - Mechanical. The AutoCAD Designer will be responsible for creating detailed mechanical designs and drawings using AutoCAD software, collaborating with engineering and production teams, and ensuring that designs meet project specifications and standards. Daily tasks will include drafting, revising, and finalizing mechanical plans, updating and maintaining design documents, and performing quality checks on all drawings. Qualifications Proficiency in AutoCAD, Mechanical Drafting, and Design Experience with CAD software and creating detailed mechanical drawings Ability to collaborate with engineering and production teams Strong understanding of mechanical design principles and standards Excellent communication and teamwork skills Attention to detail and ability to perform quality checks on designs Bachelor's degree in Mechanical Engineering, Design Engineering, or related field Experience in water treatment or related industry is a plus

Walk in at GHC Hospital, Mumbra Time: 11am to 4pm (Monday to Saturday) Report Transcription: Type sonography reports as dictated by the radiologist/sonologist. Ensure all medical terms, anatomical descriptions, and clinical details are correctly spelled and structured. Coordination with Radiologists: Seek clarifications from the radiologist for unclear dictations or handwritten notes. Ensure daily reports are completed and printed on time. System Entry: Enter final reports into the Hospital Information System (HIS) or relevant software. Ensure backup and proper labeling of digital reports. Report Handling: Print, verify, and file reports for patient handover. Maintain patient report records in both physical and electronic format. Confidentiality & Compliance: Maintain strict confidentiality of all patient data and sonography findings. Follow hospital policies for data privacy and SOP compliance. Administrative Support: Assist with daily scheduling of sonography patients if required. Maintain adequate stock of report paper, stationery, and consumables. Best Regards, Ms. Kaisar Shikalgar Assistant Manager - HR Mobile: 7400151259 E-mail: hr@ghchospitals.com GHC Hospitals Thane Shil Road, Kausa, Mumbra, Thane, Maharashtra 400612 Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Provident Fund Schedule: Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Work Location: In person

Job Title: E-commerce & Operations Executive (Full-Time, In-Office – East Delhi) Working Hours: Monday to Saturday, 10:00 AM to 7:00 PM Monthly Salary: INR 18,000 – 22,000 per month Preferred Candidate: Male candidate preferred (due to nature of operational and coordination work) Roles & Responsibilities: Marketplace Operations (Amazon, Flipkart, Meesho, etc.) Daily processing of orders across all portals. Coordinate FBA/FBM shipments, packaging, dispatches. Raise and track support cases for: Delayed shipments Blocked/broken listings Missing “Buy Now” button Missed pickups Ensure seller panels are clean, with active listings and correct inventory reflected. Product Listings & Ads Upload, update & optimize listings (titles, descriptions, pricing). Coordinate product bundles (Pack of 2, 3, etc.) and ensure they go live on time. Track and run ads (Amazon, Flipkart, Meesho). Maintain performance logs and pause/adjust campaigns as needed based on ROI. Label & Packaging Coordination Liaise with multiple vendors/designers for label and carton design. Review and finalize files, ensuring correct sizing, content, and quality. Compare rates and quality between vendors for cost-effective solutions. Ensure print orders are completed in time and shared with internal teams. Vendor & Logistics Coordination Follow up with printers, label designers, carton vendors, photographers, and logistics partners. Book porters/couriers as required. Manage sample coordination for shoots or vendor evaluation. Inventory & Admin Reporting Maintain real-time inventory data across SKUs and platforms. Share daily/weekly EOD reports with order counts, pending items, and issues resolved. Maintain payment logs, pending approvals, and shared trackers. Photoshoot & Visual Coordination Coordinate with photographers for clean product shoots. Review image quality and share improvements. Ensure correct labeling of products being sent for shoot. Portal Onboarding & Documentation Work on new seller onboarding on portals like Blinkit, Tata 1mg, Myntra, etc. Handle document submissions like GST certificates, brand authorization, etc. Review Management Coordinate review activities across portals (Amazon, Flipkart, Meesho). Maintain logs of buyers assigned for reviews, completed tasks, and SKUs covered. Office Infrastructure & Bills Track and manage internet issues, service requests, and power backup needs. Ensure timely submission of electricity bills and other utilities for multiple units. Interview Scheduling & Candidate Follow-ups Follow up with operations and design candidates for in-person interviews. Maintain call status, confirmations, and drop-off reports. To Apply: Email your resume to info@mlspl.co.in Job Types: Full-time, Permanent, Fresher Pay: ₹17,000.00 - ₹22,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Application Question(s): Weather you can join Immediately at our Delhi office ? Would you be available for in personal interview at Delhi Office Experience: Operations: 1 year (Preferred) total work: 1 year (Preferred) Work Location: In person Application Deadline: 14/04/2025

Company Profile: is a fresh dog food company with its head office in Model Town, Delhi. Benny’s Bowl is the same food that you would cook in your own kitchen or eat yourself, but our experts have ensured that it has the right nutrition and avoids the hassle of cooking yourself. Our food is cooked fresh, using whole and real ingredients, only fresh meat & fresh vegetables without any preservatives or additives at any stage. It is packed in sophisticated retort technology used to pack food for astronauts which allows shelf life of two years. Role Overview: We are looking for a passionate and innovative Product Manager to lead the development and launch of new products in the pet food category. You will play a critical role in identifying pet nutrition trends, creating differentiated offerings, and ensuring successful product launches that meet both pet and pet parent expectations. This role requires a deep understanding of consumer needs, nutrition science, and cross-functional collaboration. Key Responsibilities (KRAs): Market & Consumer Insights Conduct in-depth research on pet food trends, consumer behavior, and nutritional requirements. Gather insights from vets, pet parents, and channel partners to identify new product opportunities. Benchmark global pet food innovations and adapt them to local markets. Product Strategy & Development Own the full lifecycle of new product development — from concept to commercialization. Define product positioning, nutritional goals, ingredient selection, packaging type, and pricing. Collaborate with R&D, nutritionists, procurement, and manufacturing teams to develop high-quality formulations. Go-to-Market Execution Develop GTM strategies including packaging design, channel launch plans, and promotional ideas. Work with marketing and sales teams to build launch campaigns and product training decks. Track performance post-launch and suggest iterations based on feedback and data. Cross-functional Coordination Act as the single point of contact between product, marketing, production, and supply chain. Ensure timely sampling, testing, regulatory checks, and vendor coordination for smooth execution. Maintain launch calendars, budgets, and project timelines. Compliance & Quality Focus Ensure all new products comply with FSSAI and other relevant food safety guidelines. Maintain documentation for labeling, nutrition facts, claims, and certifications. Qualifications: Bachelor’s/Master’s in Food Technology, Animal Nutrition, Veterinary Science, Business, or related fields. 3–6 years of experience in product management, preferably in FMCG, pet food, or health/nutrition sectors. Strong understanding of pet food categories – dry, wet, treats, supplements, etc. Experience in launching new food or pet-related products across multiple formats. Excellent project management, communication, and analytical skills. Nice to Have: Passion for pets and prior experience working in the pet care ecosystem. Exposure to D2C brands and digital-first product launches. Familiarity with nutritional labeling, ingredient sourcing, and packaging trends. Pet Lover Location : Panchsheel Park, Delhi (5 minutes walk from Metro Station) Employment Type : Full Time, Work from Office, 6 Days Working CTC: Based on experience and profile Joining : Immediate preferred Job Type: Full-time Pay: From ₹25,000.00 per month Benefits: Health insurance Schedule: Morning shift Work Location: In person

Require Male candidate as Warehouse Supervisor age 20-40 years. Job details: Coordinate pick up and deliveries, arrange transport vehicles, load unload cargo, Packing cargo, labeling them appropriately, Inspecting packages to ensure they are not damaged; Collecting/Delivering/Loading/Unloading of Packages; Perform other duties as assigned

Maintain accurate records of incoming and outgoing materials. Perform daily, weekly, and monthly stock reconciliation. Monitor stock levels and initiate reordering of items when necessary. Receive, inspect, and store materials in designated storage areas. Ensure proper stacking, labeling, and preservation of materials. Issue raw materials, consumables, or spares against approved requisitions. Maintain Issue Slips, and other inventory records. Update stock in ERP system regularly. Prepare periodic reports for consumption, damage, and movement of stock. Coordinate with purchase, production, and accounts departments for smooth flow of materials.

We're Hiring! Our company is looking for Helpers to join our team in Agamaly. Salary: ₹11,000 to ₹16,000 Shifts Available for Male Candidates: 6:00 AM to 2:00 PM 2:00 PM to 10:00 PM 10:00 PM to 6:00 AM females have day shift available 9 to 6 Job Duties: General helper tasks Labeling work Other assigned duties

Search by Keyword Search by Location Show More Options Loading... Location All Select How Often (in Days) To Receive An Alert: Create Alert Select How Often (in Days) To Receive An Alert: Apply Now » Apply Now Start applying with LinkedIn Please wait... Title: Executive - Regulatory Affairs Date: Jul 4, 2025 Location: Tandalja - R&D Company: Sun Pharmaceutical Industries Ltd Preparation and reviewing of labeling for ANDA and/or NDA applications and labeling query responses in accordance with the USFDA regulations. Preparation of Structured Product Labeling (SPL) for drug listing in accordance with the associated applications and USFDA regulations. Preparation, reviewing, timely submission and coordination of implementation of labeling based on FDA notifications and/or RLD labeling updates. Coordination of labeling related activities with cross functional teams for timely launch of products. Regulatory submission and filings, coordinating final labeling implementation and maintaining labeling artworks using various softwares. Communication with third parties or private label distributors to gather needs and requirements of changes/labeling development. Evaluation and coordinating with departments for REMS requirement for applications. Apply Now » Apply Now Start applying with LinkedIn Please wait...

As an AI Research Apprentice you'll push the frontiers of generative and multimodal learning that power our autonomous robots. You will prototype diffusion-based vision models, vision-language architectures (VLAs/VLMs) and automated data-annotation pipelines that turn raw site footage into training gold. Key Responsibilities Design and train diffusion-based generative models for realistic, high-resolution synthetic data Build compact Vision-Language Models (VLMs) to caption, query and retrieve job-site scenes for downstream perception tasks Develop Vision-Language Alignment (VLA) objectives that link textual work-orders with pixel-level segmentation masks Architect large-scale auto-annotation pipelines that transform unlabeled images / point-clouds into high-quality labels with minimal human input Benchmark model performance on accuracy, latency and memory for deployment on Jetson-class hardware; compress with distillation or LoRA Collaborate with perception and robotics teams to integrate research prototypes into live ROS 2 stacks Qualifications & Skills Strong foundation in deep learning, probabilistic modeling and computer vision (coursework or research projects) Hands-on experience with diffusion models (e.g., DDPM, Latent Diffusion) in PyTorch or JAX Familiarity with multimodal transformers / VLMs (CLIP, BLIP, Flamingo, LLaVA, etc.) and contrastive pre-training objectives Working knowledge of data-centric AI: active learning, self-training, pseudo-labeling and large-scale annotation pipelines Solid coding skills in Python, PyTorch / Lightning, plus git-driven workflows; bonus for C++ and CUDA kernels Bonus: experience with on-device inference (TensorRT, ONNX Runtime) & synthetic data tools (Isaac Sim) Why Join Us Research bleeding-edge generative & multimodal tech and watch it land on real construction robots Publish, patent and open-source: we encourage conference submissions and community engagement Help build a company from the ground up—your experiments can become flagship product features Requirements PyTorch or JAX C++ CUDA kernels ONNX Runtime TensorRT Isaac Sim Latent Diffusion

Drive the next wave of generative and multimodal intelligence that powers our autonomous drywall-finishing robots. As a core member of the AI Research team, you'll turn cutting-edge vision-language and diffusion advances into robust, real-time systems that see, reason, and act on dynamic construction sites. Key Responsibilities Research & innovate diffusion-based generative models for photorealistic wall-surface simulation, defect synthesis, and domain adaptation Architect and train Vision-Language Models (VLMs) and Vision-Language Alignment (VLA) objectives that connect textual work orders, CAD plans, and sensor data to pixel-level understanding Lead development of auto-annotation pipelines (active learning, self-training, synthetic data) that scale to millions of frames and point-clouds with minimal human effort Optimize and compress models (INT8, LoRA, distillation) for deployment on Jetson-class edge devices under ROS 2 Own the full lifecycle—problem definition, literature review, prototyping, offline/online evaluation, and production hand-off to perception & controls teams Publish internal tech reports and external conference papers; mentor interns and junior engineers Qualifications & Skills 3+ years in deep-learning R\&D or Ph.D./M.S. in CS, EE, Robotics or related field with strong publication record Demonstrated expertise in diffusion models (DDPM, LDM, ControlNet) and multimodal transformers / VLMs (CLIP, BLIP-2, LLaVA, Flamingo) Proven success building large-scale data-centric AI workflows—active learning, pseudo-labeling, weak supervision Advanced proficiency in Python, PyTorch (or JAX), experiment tracking, and scalable training (PyTorch Lightning, DeepSpeed, Ray) Familiarity with edge-AI runtimes (TensorRT, ONNX Runtime), and CUDA / C++ performance tuning Strong mathematical foundation (probability, information theory, optimization) and ability to translate theory into production code Bonus: experience with synthetic data generation in Isaac Sim, or robotics perception stacks (ROS2, Nav2, MoveIt 2, Open3D) Why join us? Own breakthrough tech from idea to autonomous robot on active job-sites—your work leaves the lab fast Collaborate cross-functionally with perception, controls, and product teams & publish at top venues with company support Shape an industry by replacing dangerous, repetitive construction labor with intelligent robots Competitive salary + equity, hardware budget, flexible hybrid work, and a culture that prizes deep work and rapid iteration Requirements Vision-Language Models Vision-Language Alignment R\&D Ph.D./M.S. in CS, EE, Robotics TensorRT, ONNX Runtime CUDA / C++

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree with microbiology and minimum of 03 years of experience, Demonstrated technical skills in method validation and microbiology testing's Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

We’re looking for an experienced AI Engineer to join our mission at Shopper.com - where millions of users rely on our technology to save money, discover deals, and shop smarter every day. If you’re excited about applying AI to real-world problems in finance and shopping, we’d love to hear from you. About Shopper.com At Shopper.com, we are redefining how people save money while shopping online. Our platform helps creators and communities share the best deals, while our browser extensions and AI tools deliver personalized, real-time couponing experiences. We're backed by a passionate team, and we’re looking for an AI Engineer to help us take our products to the next level. Why This Role Matters This is a hands-on, high-ownership role. You'll work directly with the founding team to shape how we process, model, and deliver shopping intelligence through language models and structured data. What You'll Do Design, fine-tune, and deploy GPT-based agents and tools to process, normalize, and explain messy data. Integrate with large language models (OpenAI, Claude, Mistral, etc.) to build conversational interfaces. Work with embeddings, vector search, retrieval augmentation, and few-shot prompts for precision. Optimize performance, latency, and cost tradeoffs for real-time query responses. Work across our AI infra and backend, including using tools like LangChain, LlamaIndex, Weaviate, or custom RAG pipelines. Collaborate on data labeling strategies, synthetic data generation, and evaluation loops. Influence the product roadmap with AI-first features and user interactions. What We're Looking For Strong experience with LLMs (GPT-4, Claude, etc.) and applied NLP/ML techniques. Hands-on experience with LangChain, OpenAI API, Pinecone/Weaviate, Hugging Face, or similar tools. Experience working with structured data (JSON, tabular), particularly in financial or tabular domains. Startup mindset: bias for action, ownership, and comfort with ambiguity. Bonus Points For Built or contributed to a production AI/ML product. Background in fintech, accounting systems (QuickBooks/Xero), or business intelligence tools. Shipped AI features as a solo builder or in a 0→1 environment. How to Apply Respond here on Linkedin with your GitHub, resume, and 1–2 lines about what excites you about Shopper. We’re open to exploratory conversations too.

Company Description ChillFill Foods, presented by Bizz Corporation, has been a leading name in the frozen snack industry for two decades. Known for supreme quality products, longer shelf life, and equal portion servings, the company boasts sustainable practices and the adoption of the latest technologies. Serving major brands in HoReCa, QSRs, Catering, and Private Labeling industries, ChillFill Foods also engages in contract manufacturing for MNCs. We specialize in customizing products to meet customer demands. Role Description This is a full-time on-site role for a Business Development Executive located in South West Delhi. The Business Development Executive will be responsible for identifying new business opportunities, generating leads, managing client accounts, and facilitating communication between the company and its clients. The role involves developing strategies to enter new markets and expanding the company's reach within existing markets. Day-to-day tasks include conducting market research, negotiating contracts, and maintaining strong relationships with clients. Qualifications New Business Development and Lead Generation skills Experience in Business and Account Management Excellent Communication skills Ability to work independently and as part of a team Strong analytical and problem-solving skills Experience in the food industry is a plus Bachelor's degree in Business, Marketing, or related field 📩 mail on CV - shakti@chillfillfoods.com Experience - 3+ years HoReCa Sales only Horeca sales preferred location:- West Delhi

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Responsible for issuance of raw material from warehouse as per production requirement. Storage and labeling as per applicable procedure Assisting the Team leader in ensuring proper storage of raw materials, intermediates and finished goods in designated areas and labeling as per applicable procedures Carrying out dispensing activities as per applicable procedure & carrying out process and sampling activities during the production of Intermediate/API’s according to the approved batch cards Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card Ensure verification of weigh balances and all daily documents as per applicable procedures & carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures Follow Standard operating procedure (SOP), Safety and cGMP guideline Ensure housekeeping of plant and cleanliness of the equipment/area, update the equipment status board, use logbook, other documents as per applicable procedure Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements & expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others Preparation of batch card, qualification protocol, report & other GMP related documents and adding batch details in ERP system Preparation of safety work permits to carry out maintenance activities in shift & report accidents and irregularities at the workstation to the Shift Officer Your Experience And Qualifications B.Sc./M.Sc./Diploma (Chemical)/B.Tech (Chemical)/B.E (Chemical) Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Who We Are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How You’ll Spend Your Day Responsible for processing and oversight of changes through the generation, justification, impact assessment, modification, review, approval, and implementation workflow. This includes but is not limited to SOPs, production records, test methods, specifications, protocols, reports, equipment, processes, material suppliers, facilities, computer systems etc. Responsible for review and approval of all continual improvement projects affecting quality at a site Responsible for processing of documents through the generation, modification, review, and approval workflow. This includes but is not limited to SOPs, production records, test methods, protocols, reports, labeling, etc. also, archival of records Responsible for Review of regulatory and quality compliance requirements and divisional policy, performance of gap assessments, and establishment or improvement of SOPs covering all areas of applicability. Development and monitoring of corrective action plans where needed Ensuring quality support to regulatory affairs as it relates to updates/changes to market authorizations Review of all documentation (i.e. LIR, OOS, Change Controls, etc.) Ensuring quality interface with internal and external customers when dealing with activities such as service requests, issue resolution, complaints, product information, or for movement of materials, products, or process from site to site Responsible for management of regulatory authority and other external compliance audits (e.g. Customer audits) including communication, tracking and resolution of observations. Management of communications with regulatory agencies including required reporting and resolution of any actions required by the agencies Responsible for Performing, reporting of observations and verification of compliance reports of internal audit Your Experience And Qualifications M.Sc. or B.tech chemical Minimum 10 Years of experience required Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.

Preparation and reviewing of labeling for ANDA and/or NDA applications and labeling query responses in accordance with the USFDA regulations. Preparation of Structured Product Labeling (SPL) for drug listing in accordance with the associated applications and USFDA regulations. Preparation, reviewing, timely submission and coordination of implementation of labeling based on FDA notifications and/or RLD labeling updates. Coordination of labeling related activities with cross functional teams for timely launch of products. Regulatory submission and filings, coordinating final labeling implementation and maintaining labeling artworks using various softwares. Communication with third parties or private label distributors to gather needs and requirements of changes/labeling development. Evaluation and coordinating with departments for REMS requirement for applications.

Job Title: Senior Executive – Quality Assurance / Quality Control (QA/QC) Location: Vikasnagar, Uttarakhand Job Type: Full-Time, On-site About KIWI Kisan Window KIWI Kisan Window is an innovative and rapidly growing food brand committed to bringingHealthy Unique Flavours of India to every household. We connect farmers and consumersthrough sustainable sourcing, premium quality, and a mission to take handmade and authenticIndian produce to the world. Role Summary: We are looking for a detail-oriented and experienced Sr. Executive – QA/QC to ensure the highest quality standards across our fresh produce, grocery SKUs, packaging processes, and warehouse operations. The candidate will be responsible for monitoring, improving, and enforcing quality across raw materials, production, labeling, packaging, and dispatch processes, ensuring compliance with FSSAI, SOPs, and company protocols. Key Responsibilities:Quality Assurance Define and implement QA protocols for fresh, processed, and packaged food items. Ensure product quality meets internal standards and FSSAI regulations. Approve incoming raw materials by confirming specifications and conducting visual/physical checks. Conduct regular audits at vendors and internal processing units. Quality Control Perform and supervise quality checks across stages: receiving, processing, packaging, and dispatch. Monitor parameters like moisture content, microbial load (where relevant), packaging integrity, and label accuracy. Implement batch-wise QC reporting and traceability. Packaging &Label Control Check labeling compliance: MRP, date of packaging, batch no., expiry, nutritional info. Ensure correct packaging material usage as per SKU standards. Documentation & Compliance Maintain QA/QC documentation: checklists, batch records, test reports, and deviation logs. Support FSSAI, HACCP, and other regulatory audits. Drive adherence to SOPs and hygiene protocols (5S, GMP). Training & Team Coordination Train warehouse, processing, and packing staff on quality and hygiene standards. Work closely with procurement, production, and dispatch teams to resolve quality issues. Key Requirements: B.Sc./M.Sc. in Food Technology, Microbiology, or a related field. Minimum 3–5 years of hands-on experience in QA/QC in food processing, FMCG, agritech, or grocery brands. Strong knowledge of FSSAI regulations, shelf-life standards, food safety practices, and packaging QC. Experience with quality tools: checklists, RCA (Root Cause Analysis), 5 Why, and CAPA. Proficiency in MS Excel, Google Sheets, and basic data reporting. Good communication and team coordination skills. Ability to work in fast-paced, multi-SKU environments. What We Offer: Career Growth & Impact: Be part of a fast-growing brand making a mark in the food industry. Innovative Work Culture: Join a team that values creativity, collaboration, and customer-centric solutions. Performance-Based Incentives: Enjoy competitive bonuses and rewards for outstanding sales performance. Continuous Learning & Development: Gain access to mentorship, tools, and resources for career advancement. Who We Are: KIWI Kisan Window is a pioneering and innovative food brand committed to delivering the Healthy Unique Flavours of India to every household. As a bridge between farmers and consumers, we focus on sustainable practices, farmer empowerment, and offering premium, farm-fresh products that celebrate India’s diverse culinary heritage. Our journey has been fueled by a passion for redefining how people experience food—bringing fresh, authentic, and health-focused products to the forefront. Featured in Shark Tank India Season 4 , we take pride in our entrepreneurial spirit, commitment to excellence, and mission to take handmade to the world. How to Apply: Send your resume and cover letter to career@kisanwindow.com with the subject line “Application for Quality Assurance / Quality Control - KIWI Kisan Window.” We look forward to hearing from you! Job Types: Full-time, Permanent Pay: ₹14,000.00 - ₹25,000.00 per month Schedule: Day shift Morning shift Work Location: In person