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2.0 years

0 Lacs

Hyderabad, Telangana, India

On-site

Description AI is the most transformational technology of our time, capable of tackling some of humanity’s most challenging problems. Amazon is investing in generative AI and the responsible development and deployment of large language models (LLMs) across all of our businesses. Come build the future of human-technology interaction with us. We are looking for those candidates who just don’t think out of the box, but make the box they are in ‘Bigger’. The future is now, do you want to be a part of it? Then read on! Key job responsibilities Maintain and follow strict confidentiality as customer privacy is our most important tenet Work with a range of different types of data including, but not limited to: text, speech, audio, image, and video Deliver high-quality labelled data, using guidelines provided to meet our KPIs and using in-house tools and software, as part of Amazon's commitment to developing and deploying AI responsibly. Demonstrate proficiency in generating high quality human insight data across a range of modalities, inclusive of text, image video and audio. Capable of making sound judgments and logical decisions when faced with ambiguous or incomplete information while performing tasks. Eye for detail and ability to pivot from one category of requirement to another instantaneously. Demonstrate support on daily operational deliverables for multiple task types assigned to you and the team Analyze root causes, identify error patterns, and propose solutions to enhance the quality of labeling tasks and their outputs. Responsible for identifying day-to-day process and operational issues in Standard Operating Procedure, tools and suggest changes to unblock operations Demonstrate ownership in floor support to clarify internal queries during execution on need basis A day in the life We are looking for a ML Data Associate (MLDA) to undertake the task of foundational labeling functions, such as dialogue evaluation on speech, text, audio, video data. Your ability to concentrate, multi-task and your high attention to detail helps you deliver high-quality work as well as maintaining strict confidentiality and follow all applicable Amazon policies for securing confidential information. You will be a part of a diverse team with the shared vision of improving customers’ lives with practical, useful generative AI innovations. An inner drive, individuality, and a creative mind are extremely beneficial. Basic Qualifications An Associate’s Degree or related work experience C1+ or equivalent fluency in English language Strong business writing skills with ability to create reports, proposals, and professional correspondence Advanced reading comprehension with ability to analyze complex business documents Developed analytical thinking and structured problem-solving capabilities Strong ability to interpret and implement detailed instructions across various projects Proficient research skills with experience gathering and synthesizing information from multiple sources Proven attention to detail in managing complex tasks and documents Preferred Qualifications Bachelor’s degree in a relevant field May vary in other locations like India 2+ years of professional work experience with demonstrated task execution ability Proven capacity to leverage open-source resources effectively for comprehensive research purposes Ability to adapt well to fast-paced environments with changing circumstances, direction, and strategy 1+ years project coordination or management experience Experience managing stakeholder relationships across departments Advanced proficiency in Microsoft Office Suite and common business applications. Our inclusive culture empowers Amazonians to deliver the best results for our customers. If you have a disability and need a workplace accommodation or adjustment during the application and hiring process, including support for the interview or onboarding process, please visit https://amazon.jobs/content/en/how-we-hire/accommodations for more information. If the country/region you’re applying in isn’t listed, please contact your Recruiting Partner. Company - ADCI HYD 16 SEZ - H83 Job ID: A3045588

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3.0 years

0 Lacs

Hyderabad, Telangana, India

On-site

About the Role We’re looking for a sharp, reliable, and detail-driven Assistant Cinematographer to support our video shoots across Nxtwave's central and campus productions. In this role, you’ll work closely with the Senior Cinematographer and production leads to set up and maintain camera rigs, lighting, and other equipment. You’ll play a key part in ensuring every shoot runs smoothly—from technical setup to footage handover. This is a hands-on role for someone who wants to grow within the cinematography track and understands that great visuals start with meticulous support and on-ground readiness. Key Responsibilities Camera & Lighting Setup : Assist in prepping and setting up cameras, lenses, lighting rigs, tripods, gimbals, and monitors as per shoot requirements Focus & Framing Support : Help monitor framing, focus pulls, white balance, and exposure during multi-cam or single-cam shoots Gear Management : Track batteries, memory cards, filters, and charging cycles; ensure backups are available on set Safety & Cable Management : Maintain safety standards for wiring, lighting stands, and on-ground movement Footage & Drive Handling : Assist in transferring footage, labeling folders, and handing off data to post-production and QC teams Location Prep : Support recce and on-location prep with the cinematography and production team Shoot Assistance : Be ready on-set for live adjustments, scene resets, and equipment handling Qualifications & Requirements 1–3 years of experience assisting in video shoots, film sets, branded content, or production houses Familiarity with camera systems (Sony, Canon, Blackmagic, etc.) and lighting gear (LED panels, softboxes, bounce) Strong technical curiosity and willingness to learn cinematography fundamentals Ability to lift, carry, and set up gear independently and responsibly Basic knowledge of color temperature, lighting mood, and camera terms Discipline, punctuality, and a positive on-set attitude Bonus: Interest in becoming a DoP in the long term What You’ll Gain Mentorship from senior cinematographers and creative directors On-ground learning across masterclasses, testimonials, reels, brand films, and campus shoots Exposure to professional production workflows and post-production coordination A clear career track into cinematography, camera operation, or technical direction Be part of India’s most dynamic creative education brand

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3.0 - 5.0 years

2 - 5 Lacs

Muzaffarpur

Work from Office

Key Responsibilities: Oversee daily production of snacks and namkeen items. Ensure product quality, taste, and consistency as per company standards. Coordinate with the kitchen/production team for raw material planning and usage. Monitor hygiene, food safety, and cleanliness across the production unit. Maintain stock levels of ingredients, packaging, and finished goods. Work with R&D or chefs to develop or improve products as needed. Maintain production records and ensure timely reporting. Ensure compliance with FSSAI and internal food safety norms. Support in packaging, labeling, and dispatch processes. Minimize wastage and control production costs.

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0.0 - 1.0 years

0 - 0 Lacs

Bengaluru, Karnataka

On-site

Job Overview: Store Executive – We are looking for a diligent and organized Store Executive to manage the raw materials inventory for our Cosmetic Department . The candidate will be responsible for receiving, storing, and issuing raw materials used in cosmetic product manufacturing, maintaining accurate stock records, ensuring proper storage conditions, and coordinating with production and procurement teams. This role is crucial in maintaining uninterrupted production flow and ensuring material traceability and compliance with quality standards. Key Responsibilities: Receive, inspect, and verify incoming raw materials against purchase orders. Ensure proper storage of materials as per safety and quality guidelines (e.g., temperature, segregation). Maintain real-time inventory records using store management systems or ERP. Issue raw materials to the production department as per requirement and maintain issue logs. Conduct periodic physical stock verification and reconcile discrepancies. Coordinate with procurement for timely replenishment of stock based on minimum stock levels. Maintain cleanliness, labeling, and organization of the store area. Ensure compliance with GMP, safety, and regulatory requirements relevant to raw material handling. Prepare reports related to stock movement, consumption, and shelf-life tracking. Qualifications and Skills: Less than 1 years of experience in raw material store management, preferably in cosmetics, pharma, or FMCG. Strong understanding of inventory control systems and material handling procedures. Knowledge of cosmetic raw materials and basic regulatory requirements is a plus.. Detail-oriented, organized, and capable of working independently. Good coordination and communication skills with internal teams Education: Minimum Qualification: Diploma or Bachelor's Degree in Warehouse Management , Logistics , Supply Chain Management , B.Sc. Chemistry , or a related field. Candidates with a background in Cosmetics , Pharmaceuticals , or FMCG industry will be preferred. Additional certifications in Inventory Control , Material Management , or GMP practices will be an advantage. Freshers can apply too Language : English Hindi and Marathi (Hindi is Mandatory) Kannada (optional) Salary Range: ₹15,000 – ₹18,000 per month (depending on qualification and interview) Location: Site No 74-75, No .194, Hosur Rd, behind Metro wholesale, Konappana Agrahara, Electronic City, Beratena Agrahara, Bengaluru, Karnataka 560100 HR mail: hr@invisionpharma.com Phone no. 9740126668 Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹18,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Work Location: In person Application Deadline: 08/08/2025 Expected Start Date: 08/08/2025

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0 years

0 Lacs

Pune, Maharashtra, India

Remote

Overview As the Head of Product Engineering, you will be instrumental in building and leading a cross-functional team of Tech managers, Engineers, Architects, QAs, Product owners, and Scrum masters. Your focus will be on delivering the product roadmaps consisting of Web & Mobile Applications that are AI powered in a way that is user-centric, safe and reliable. You are expected to own the Engineering Budget management and optimization will also be a critical aspect of this role, ensuring resources are allocated effectively to achieve desired outcomes. Key Outcomes Team Building & Leadership : Hire, retain and Own teams aligning with various application products, that may comprise managers, engineers, architects, QAs, product owners, and scrum masters. Builds a high-performance, accountable, and collaborative engineering culture with Agile practices. You are responsible for building a team with the right mix of skillsets to deliver the outcomes. Leads by example—hands-on but knows when to delegate and scale leadership. Deliver High-Quality Products : Ensure products across different roadmaps are delivered as per agreed timelines with high quality. Budget Management : Manage budgets effectively within organizational allocations to achieve desired outcomes. AI Productization Mindset: Understands how to operationalize AI: from experimentation and model evaluation to deployment and monitoring. Familiar with feedback loops, prompt engineering (if using LLMs), data labeling strategies, etc. Automation first Approach: Ensure products across different products have devSecOps Automation to 100%. Hybrid + Agile Working Model : Implement and optimize a robust hybrid (remote/on-site) and Agile working model, continually improving systems and processes for operational excellence and cost savings. AI in Development : We are adopting a way of using AI in our development process and resulting in acceleration of development, You are expected to carry & improve development processes as per the state of the art AI Engineering practices. Reporting - Manage Trust & Status pages to keep customers updated about product uptimes & Also enable stakeholder reporting by sharing reports of developer productivity, Incidents, Production deployments, Product usage periodically Key Parameters to qualify: Strategic Thinker & Planner : Ability to think and plan strategically, preempt situations, and delegate effectively. Business Thinker : Understands business operations at an organizational level and works to drive business success. Presentation Skills : Strong presentation skills with the capability to communicate plans and projects effectively to both technical and non-technical stakeholders and customers. Problem Solving : Exceptional problem-solving abilities, able to navigate challenges and find innovative solutions. Resourcefulness : Proactive in leveraging networks and internal resources to recruit talent and achieve objectives. Writing Skills : Strong writing skills, particularly in creating compelling content related to technology and product narratives. Location: Pune / Bengaluru Work hours: Support some US Time Zone; Monday to Friday

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0.0 years

0 Lacs

Kankarbagh, Patna, Bihar

On-site

Job Title: Photo and Video Editor Location: Patna, Bihar Job Type: Full-Time Reports To: Executive Director Salary: 10,000/- to Upto 12,000/- per Month. Job Description: About the Role: We're looking for a talented Photo and Video Editor who knows how to bring stories to life through visuals. If you love crafting stunning content—balancing color, sound, and motion—this might be your next favorite job. What You’ll Do: Edit videos and photos for social media, marketing, and branded content. Adjust color, hue, saturation, and brightness to create the right mood and look. Add motion graphics, visual effects, music, and sound to elevate the final product. Clean up and mix audio for clarity and impact. Stay organized— labeling, managing, and archiving media assets properly. Work closely with creative and marketing teams to bring ideas to life. Optimize content for platforms like Instagram, YouTube, facebook, and websites. What You Bring: Proficiency in Adobe Premiere Pro, Final Cut Pro. Solid skills in Photoshop, Lightroom, and After Effects. Experience with motion graphics, visual effects, and audio editing. Strong eye for detail, color correction, and storytelling through visuals. A portfolio or reel that shows off your editing range. Good file management habits and a team-first attitude. Familiarity with trends across social platforms. Motion design or animation experience.(Nice to Have) To Apply: Send your resume and a short cover letter to hr.himalayagroup1@gmail.com/hr@himalayagroupofinstitutions.com or contact over Whatsapp:9031624659/9031624657. Job Type: Full-time Pay: From ₹10,000.00 per month Work Location: In person

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5.0 years

0 Lacs

Dhanbad, Jharkhand, India

On-site

Company Description MADHULIKA FOODS PRIVATE LIMITED is a leading food production company based in Dhanbad, Jharkhand, India. We specialize in crafting high-quality sweets and a diverse range of food products. Our manufacturing facility is located on Hirak Road, Bhelatand, P.O. Nagnagar, P.S. Barwadda. With a deep commitment to excellence, we uphold the highest standards of quality, hygiene, and customer satisfaction across all our products. Role: Factory Manager (Madhulika Sweets) Location: On-site, Dhanbad, Jharkhand Job Type: Full-Time Role Description We are seeking an experienced and dedicated Factory Manager to lead our sweets production facility in Dhanbad. The ideal candidate will be responsible for overseeing the entire production process, ensuring timely manufacturing, quality control, regulatory compliance, and smooth day-to-day operations. Key Responsibilities: Production Management: Plan and execute production schedules for sweets and food items, ensuring timely and high-quality output. Quality Control: Establish and maintain a basic lab setup for sensory checks, recipe accuracy, portion control, and packaging verification. Hygiene and Safety: Ensure cleanliness and hygiene standards are strictly maintained across the factory premises. Regulatory Compliance: Adhere to and manage compliance with basic food safety regulations, including FOSTAC certification (mandatory to maintain). Inventory & Asset Management: Maintain up-to-date records of raw materials, packaging items, assets, and factory supplies. Staff Management: Supervise production staff, maintain attendance records, and ensure efficient workforce management. Operations Coordination: Collaborate with procurement, logistics, and quality departments to ensure seamless operations. Dispatch Management: Oversee timely and accurate dispatch of finished goods. Documentation & Recordkeeping: Maintain detailed logs for batch production, labeling, pest control, maintenance visits, and other operational activities. Qualifications: Bachelor's degree in food technology, Industrial Engineering, Business Administration, or a related field. Proven experience in food production management, preferably in the sweets or snacks industry. Strong skills in production planning, quality assurance, and operations management. Sound knowledge of FSSAI standards and FOSTAC certification. Leadership qualities with effective team management and organizational skills. Attention to detail and problem-solving ability in a fast-paced environment. Preferred Experience: Minimum 3–5 years in a similar role within the food production industry. Hands-on experience with traditional and modern sweets manufacturing. Familiarity with regulatory and hygiene audits. This position offers an exciting opportunity to be part of a growing company with a strong commitment to quality and innovation in traditional Indian sweets.

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0.0 years

0 - 0 Lacs

Patiala, Punjab

On-site

Job Title: Packer Company: Manvi International Courier Location: Gaushalla Road, near shere punjab market Work Timing: 10:00 PM to 8:00 PM Salary: ₹10,000 to ₹13,000 (Based on skills & experience) Experience: Freshers/ Minimum 6 months preferred Joining: Immediate Job Responsibilities: Packing parcels securely and accurately as per company guidelines Labeling and organizing packages for dispatch Ensuring packaging quality and minimizing damage during transit Maintaining cleanliness and order in the packing area Assisting in loading/unloading shipments when needed Requirements: Basic understanding of packaging techniques Ability to handle materials carefully and efficiently Physically fit and able to work properly Attention to detail and a responsible attitude Previous experience in a courier or logistics company is a plus Apply Now: hr@manvicourier.com Contact: 9220032489 Job Type: Full-time Pay: ₹10,000.00 - ₹13,000.00 per month Work Location: In person

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8.0 years

0 Lacs

Bengaluru, Karnataka, India

On-site

The Opportunity: The Manager is responsible for the supervision, critical review, and approval of established US Gx labeling documents filed under an ANDA/505(b)(2) by US and Mumbai/Bangalore (India locations) members while adhering to federal regulations, internal processes, and meeting timelines driven by company goals. The Manager will also be responsible for their own assignments, when needed, and working closely with other Managers surrounding the review and approval of labeling documents established for these projects. Additionally, the Manager will oversee all team databases and trackers and will update them when changes are required. The candidate must possess a firm knowledge of FDA US labeling regulations and guidances for products filed under an ANDA/505(b)(2). They should be a Subject Matter Expert (SME) in all facets of US labeling, including, but not limited to, SPL, PADERs, and AR compilation, in order to provide direction to direct reports. Finally, the candidate will be responsible for ensuring all required FDA reporting obligations are met in accordance with business objectives and regulations, maintaining compliance. Roles & Responsibilities: Hands-on leader in regard to daily workload; in addition to managerial responsibilities, this position could have independent work assignments to manage, when needed, as well as participate in the preparation of labeling submission documents. SME in the development, review, and electronic compilation of labeling documents to align with the RLD, FDA-solicited safety changes, company goals, and submission requirements for assigned ANDAs/505(b)(2)s per internal processes and prior to final disposition. Responsible for ensuring projects are assigned to direct reports and/or external team members in the US and Mumbai. Communicate, plan, prioritize, and perform training to ensure labeling documents meet all legal and regulatory requirements. Maintain the labeling tracker, ensuring all assigned projects remain on track by direct reports. SME in the development/review of Structured Product Labeling (SPL) documents (content and data elements) ensuring alignment with applicable FDA regulations and guidances. Work closely with Regulatory Operations to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Work closely with external departments to align with product/device strategy impacting the approved portfolio. Attend meetings relevant to the area of responsibility. Train and develop respective team members in the US and Mumbai. Create, revise, and/or train on SOPs/WIs, as appropriate. Maintain a metric of all team projects for reporting purposes. Maintain knowledge of US regulations, guidelines, and SOPs/WIs applicable to US Gx labeling. Experience in developing labeling content that requires carve-outs due to protected language associated with patents/exclusivities is preferred. Perform all other job-related duties as required by management. Experience & Qualification: M.Pharm/B.Pharm with a scientific or regulatory background, or an equivalent combination of education and experience. Total years of experience required for the role: Minimum 8+ years of US labeling experience and at least 1 year of supervisory experience preferred. Relevant years of experience: Minimum 6 to 7 years of pharmaceutical industry experience required, specifically in Regulatory Affairs and US ANDA/505(b)(2) labeling. Overall pharma industry experience: 6 to 7 years of US labeling experience.

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0 years

0 Lacs

Jaipur, Rajasthan, India

On-site

Job Title: Showroom Sample Executive – Jewelry Manufacturing Location Jaipur Mahapura Job Summary: We are seeking a dedicated and detail-oriented Sample Executive to manage the jewelry sample inventory, coordinate with buyers, and present sample pieces during buyer visits or exhibitions. The ideal candidate should have good communication skills, knowledge of jewelry products, and experience in handling samples and inventory. Key Responsibilities: Present jewelry sample pieces to buyers during meetings, visits, or trade shows. Understand buyer preferences and ensure appropriate samples are prepared and available in advance. Coordinate with the production and design teams for the development of sample pieces. Maintain and manage the entire sample inventory with proper labeling and tracking. Keep accurate records of sample movement (inward/outward). Ensure safe handling and secure storage of all sample jewelry items. Prepare sample kits for buyer presentations or exports. Handle any buyer requests related to samples and ensure timely follow-up. Assist in documentation related to sample approvals or rejections. Coordinate with the merchandising team for updates related to sample status. Ensure cleanliness and display aesthetics of the sample room/showcase. Strong organizational and communication skills. Attention to detail and ability to handle valuable items responsibly. Immediate Joiner will be preferable interested candidates share their resume at recruitment@pinkcityindia.com, WhatsApp – 7300081857

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2.0 - 6.0 years

0 Lacs

maharashtra

On-site

You will be responsible for ensuring proper storage of scrap and surplus generated in the hospital which has salvage value or can be used later on. It is crucial to make sure that the allocated scrap area is properly arranged and labelled. In case it is not, you will need to coordinate with the user department. Your duties will also include maintaining places or godowns outside the hospital that are required to store these materials in proper condition in terms of cleanliness and safety. This involves gathering scrap materials from designated areas and, with the help of mathadis/scrap vendors, loading them into vehicles and transporting them to the disposal site. You will be in charge of separating different types of scrap such as metals, plastics, paper, etc., and preparing them for recycling or disposal with the assistance of mathadis/scrap vendors. Keeping accurate records of materials received, processed, and disposed of, including quantities and types, will be part of your responsibilities. Ensuring that all activities comply with safety regulations and environmental policies is essential. You will also need to maintain a database of scrap vendors and update it periodically, as well as call for competitive bids from scrap vendors for various scrap materials. Another aspect of your role will involve carrying out proper checks of scrap items, filling in the Scrap Sale Check List, and obtaining the signature of respective representatives on the form. You will also be responsible for the actual selling of scrap after obtaining necessary approvals for regular scrap items and scrapped capital assets as per standard operating procedures (SOP). Additionally, you will be tasked with preparing Non-Revenue Generating Purchase (NRGP) for the sale of scrap items along with recording notes against an approved list and submitting them to the purchase department for further processing, while maintaining records of the same. Providing Mathadi manpower to any department of the hospital for heavy physical movement activities and supervising and maintaining items involved in legal disputes will also fall under your purview. Interacting with clients and the public, addressing inquiries, and ensuring smooth operations will be part of your regular tasks. For Capital Expenditure (Capex) items, you will be responsible for checking items against ASSET SCRAP PROPOSAL FORM in locations specified on the note, tagging them, along with Matadi workers, and shifting items to the allocated area against Material Transfer Note.,

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0 years

0 Lacs

India

Remote

Job Title: AI Data Annotation Employment Type : Full-Time | Entry-Intermediate Level Domain : Artificial Intelligence | Machine Learning | Data Annotation Languages: French German Spanish Polish Finnish Arabic Hebrew Turkish About the Role Step into the future of work with us! We’re hiring AI Data Operations Associates — fresh graduates who are eager to start their careers in the fast-growing field of AI. In this role, you'll contribute to training the next generation of intelligent systems by labeling and curating high-quality data. Key Responsibilities Annotate, label, and tag various types of data (text, image, audio, video) following project guidelines. Ensure accuracy, consistency, and attention to detail in annotation tasks. Collaborate with team leads and QA specialists to deliver high-quality datasets. Meet daily productivity and quality benchmarks. Provide insights and feedback to enhance internal tools and processes. Eligibility Criteria Education : Minimum Bachelor’s Degree (any stream). No prior work experience required – fresh graduates are encouraged to apply . Proficiency in reading and writing English . Tech-savvy and comfortable working with digital tools and web-based platforms. Strong attention to detail, patience, and problem-solving mindset. What We Offer Comprehensive training on tools, annotation methods, and AI workflows. PAN India roles with remote-first flexibility . Clear growth paths into QA, project coordination, and AI operations roles. Be part of global AI projects and work with cutting-edge datasets. Collaborative, inclusive, and future-focused work culture.

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2.0 years

0 Lacs

Hyderabad, Telangana, India

On-site

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. Job Description Job Summary We are seeking an individual to test samples and release results within Turnaround Time (TAT) for commercial and stability batches, adhering to GMP (Good Manufacturing Practices). This role involves calibrating and maintaining assigned equipment within departmental and organizational guidelines, processes, and procedures. The primary objective is to ensure accuracy in results provided within timelines. Roles & Responsibilities • Your responsibilities encompass testing assigned samples and releasing data within defined timelines, ensuring absence of executional errors against established procedures. You will be responsible for preparing required reagents and buffers in alignment with the testing plan and ensuring the availability of equipment for analysis. • Your role involves documenting activities contemporaneously, adhering to Good Documentation Practices and compliance expectations, and conducting self-checks post-analysis to ensure accuracy. • You will promptly inform the supervisor about risk actions, providing necessary data and analysis to support the investigation process. You will adhere to QMS (Quality Management systems) and closure timelines, actively participate in laboratory investigations and discrepancy closures, fulfilling defined roles in audits. • Your responsibilities also include ensuring lab cleanliness, proper sample storage, chemical labeling, removal of expired material, usage of calibrated equipment, equipment calibration, maintenance, and qualification. • You will address instrument-related issues and conduct root cause analyses (RCAs) for unknown problems, and play a crucial role in training new team members on analytical techniques. Qualifications Educational qualification: An M.Sc., M.Tech. or B.Tech. in Microbiology, Biochemistry, or Biotechnology Minimum work experience: 2 years Skills & attributes: Technical Skills • Basic understanding of the Biologics/Biosimilar industry, including processes, regulations, and trends. • Hands-on experience in High-Performance Liquid Chromatography (HPLC) techniques, including Size Exclusion, Reverse Phase, Ion Exchange chromatography, and Peptide mapping analysis, especially within the context of Analytics. • Hands-on experience in Biochemical analysis techniques, specifically Electrophoresis, Enzyme-Linked Immunosorbent Assay (ELISA), and Polymerase Chain Reaction (PCR), with a focus on Analytics. • Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). • Basic knowledge in protein chemistry, including an understanding of protein structure, function, and relevant analytical techniques. • Basic knowledge and hands-on exposure to Microbiology techniques, particularly relevant for individuals working in Microbiology Labs. • Basic knowledge and hands-on exposure to cell culture techniques, specifically for working in Bioassay (BA) Labs. Behavioural skills • Prioritizes effective communication and demonstrates a performance-oriented mind-set. • Effective verbal and written communication skills. • Performance-oriented approach, consistently striving for high standards. • Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

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0.0 - 1.0 years

0 - 0 Lacs

Tiruchchirappalli, Tamil Nadu

On-site

Role: Process Associate Location: Cantonment & K.K.Nagar,Trichy Mode: Fulltime Experience: 0 to 1+ Years (Freshers can also apply for this Job) Job Description: · Bachelor’s degree or equivalent · Excellent Communication Skills · System Handling Responsibilities: · Will work as a Data Annotator with our Axximum team · This process known as Text Annotation, Data annotation, involves labeling the objects in the scene, such as cars, pedestrians, and traffic signs. · Annotation heavily relies on machine learning models to provide real-time interpretations of point cloud data. · Image, Video, and text annotators contribute to the development of AI and machine learning systems by providing accurately labeled datasets, enabling the training and evaluation of algorithms for various applications such as object detection, image classification, semantic segmentation, and more. · Collaborate with team members, project managers, or stakeholders to address any questions, concerns, or issues related to the annotation process. Effective communication is essential for ensuring consistent and accurate annotations. · Should have good communication skills in English with MS office Knowledge. Thanks & Regards Irfaan Basha A Executive Human Resource Axximum.Inc Ph.no: +91 9442800761 / +91 9843342426 Email: hr@axximum.in Job Types: Full-time, Permanent, Fresher Pay: ₹10,000.00 - ₹12,000.00 per month Schedule: Night shift Rotational shift US shift Ability to commute/relocate: Trichy, Tamil Nadu: Reliably commute or planning to relocate before starting work (Required) Experience: total work: 1 year (Preferred) Location: Trichy, Tamil Nadu (Required) Work Location: In person

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0.0 - 2.0 years

0 Lacs

Mumbai, Maharashtra

Remote

Additional Information Job Number 25122664 Job Category Food and Beverage & Culinary Location The Westin Mumbai Garden City, Goregaon East, Mumbai, Maharashtra, India, 400063 Schedule Full Time Located Remotely? N Position Type Management JOB SUMMARY Responsible verifying that operations are in compliance with hygiene and food safety standards. Advises on proper food handling practices and provides food hygiene training for all new hires and trainees. Identifies key areas of risk in various food operations and takes preemptive remedial action. Provides technical advice on product labeling issues for fulfilling government requriements. CANDIDATE PROFILE Education and Experience High school diploma or GED; 2 years experience in the food and beverage, culinary, or related professional area. OR 2-year degree from an accredited university in Hotel and Restaurant Management, Hospitality, Business Administration, or related major. Preferred: Environmental Health Degree or Culinary Degree CORE WORK ACTIVITIES Managing Hygience and Food Safety Operations Verifies compliance with Brand Standard Audit (BSA) requriements of Marriott International throughout the operations. Advises and monitors food handlers on the proper good handling practices and verifies their observance. Identifies key areas of risk in various food operations and takes preemptive remedial action. Verifies complianace with food and hygiene regulations, licensing conditions and codes of practice relating to food operations. Provides technical advice on product labeling issues for fulfilling government requirements. Provides in-house food hygiene training for all good handlers, (e.g. new hires and trainees). Handles complaints or enquiries from customers and local food sategey and health departments on food hygiene matters. Conducts and records daily kitchen inspections on the personal, environmental and food hygiene condictions and provides corrective action plans as necessary. Conducts regular vendor inspections in partnership with purchasing and culinary leadership. Conducts regular internal BSA inspections with culinary leadership and kitchen cleaning staff. Conducts regular inspections on the kitchen of kitchen equipment and verifies defects and non-conformities are remedied by the appropriate parties. Coordinates cleaning program in all F&B areas (e.g., General clean), identifying trends and making recommendation for improvements. Establishes and maintains open, collaborative relationships with employees. Liases with pest control company for any pest issues and monitors pest control performance. Maintains and makes improvements to hygiene standards. Regularly reviews and refreshes the food safety standards of all food handlers withing the property. Maintains documentation on all hygiene and food safety stadards throughout the operation. At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non-discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law. At Westin, we are committed to empowering guests to regain control and enhance their well-being when they need it most while traveling, ensuring they can be the best version of themselves. To achieve the brand mission of becoming the preeminent wellness brand in hospitality, we need passionate and engaged associates to bring the brand’s unique programming to life. We want our associates to embrace their own well-being practices both on and off property. You are the ideal Westin candidate if you are passionate; you are active and take pride in how you maintain your well-being; you are optimistic; you are adventurous. Be where you can do your best work, begin your purpose, belong to an amazing globalteam, and become the best version of you.

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0.0 - 4.0 years

0 Lacs

coimbatore, tamil nadu

On-site

Job Description: As a Packer at Sathyam International Consulting Services in Coimbatore, you will play a crucial role in the packing process. Your primary responsibilities will include packing goods, preparing packages for shipment, labeling boxes, and ensuring the quality of packed items. In addition to this, you will also support inventory management tasks and contribute to maintaining a clean and organized workspace. To excel in this role, you should have prior experience in packing, labeling, and shipping goods. Attention to detail and a keen eye for quality control are essential traits for this position. The ability to work efficiently in a fast-paced environment, coupled with physical stamina to lift heavy objects, will be key to your success. Basic math and communication skills are necessary to carry out the tasks effectively. Being a team player with a positive attitude is highly valued in our work environment. Any prior experience in a warehouse or packing role will be advantageous. A High School diploma or an equivalent qualification is required to be considered for this position. If you are looking for a challenging yet rewarding opportunity in the field of packing and logistics, we invite you to join our team at Sathyam International Consulting Services and contribute to our commitment to excellence in service.,

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5.0 - 9.0 years

0 Lacs

karnataka

On-site

Our Senior Regulatory Affairs Specialist position is primarily focused on supporting regulatory sustaining activities within the SM organization, including providing support for change control activities and continued compliance with postmarket MDR and IVDR regulatory requirements. The ideal candidate will be energetic, possess strong regulatory technical knowledge (particularly in the area of change control), have experience supporting MDR and IVDR requirements, and perform well independently and as part of a team. Be part of something bigger! BD is one of the largest global medical technology companies in the world and is advancing the world of health by improving medical discovery, diagnostics and the delivery of care. We have over 65,000 employees and a presence in virtually every country around the world to address some of the most challenging global health issues. In BD Specimen Management (SM), we develop some of the most widely used products in the field of specimen collection including acquisition of the sample, collection into an appropriate container, and also emerging point-of-care applications. Our team has the unique opportunity to be involved with both medical devices and in vitro diagnostics, allowing you to broaden your expertise and grow in your career. Our Senior Regulatory Affairs Specialist position is primarily focused on supporting regulatory sustaining activities within the SM organization, including providing support for change control activities and continued compliance with postmarket MDR and IVDR regulatory requirements. The ideal candidate will be energetic, possess strong regulatory technical knowledge (particularly in the area of change control), have experience supporting MDR and IVDR requirements, and perform well independently and as part of a team. Our people make all the difference in our success. Join us in our mission to advance the world of health. Support the Regulatory Affairs function on Product Lifecycle Management (PLM)/Sustaining project teams and liaise with Regulatory Affairs subject matter experts (SMEs) to fulfill US FDA and EU CE requirements. Assist in compiling, drafting and submitting the required submission documents to support 510(k) and/or CE Technical File Documentation, (eg STeD ) to obtain clearances and/or approvals to established timelines. Assist and manage Notification of Change (NOC)/International Regulatory Affairs assessments of PLM/Sustaining activities to ensure regional/country requirements of US, EU and Rest of World (ROW) are captured in Regulatory strategy development. Develop regulatory strategies for Change Controls (CC) and establish Regulatory Requirements. Monitor completion of all CC task requirements recorded in the PEGA CC system and verify completion of requirements before Engineering Change Release ECRO release. Monitor and assess the impact of existing, modified and new standards pertaining to BD products for the US and EU markets and maintenance of related regulatory documentation. Support regulatory efforts to maintain and /or simplify technical documentation maintenance, labeling changes/remediations projects and UDI assessments. Review and approve labeling and promotional material for compliance to FDA and EU regulations. Support completion of EU Substantial Change Notifications and Substantial Change Applications for approval. Prepare responses to notified body inquiries. Prepare EU CE re-certification applications following notified body templates with supporting evidence from cross functional teams. Provide training or deliver presentations to cross-functional groups across TCI and SM on salient regulatory topics. Recognize potential compliance problems areas or associate ambiguity and make recommendations to resolve. Work independently and carries out the above tasks with minimal supervision. Education and Experience: B.S. degree in a scientific, health sciences or technical discipline (e.g., engineering, bioengineering, biology, chemistry). Minimum 5 years regulatory experience and working knowledge in regulated medical device or in vitro diagnostic device companies or an equivalence combination of experience with an advanced degree. Experience in preparing, approving and maintaining Technical Documentation and other submissions compliant with US, EU and global regulations. Experience in supporting product development projects for product and process changes. Demonstrated ability to participate on cross-functional team to consistently to meet regulatory requirements and project timelines. Proficient in using Microsoft Word, Excel, PowerPoint, and Project. Strong communication (written, oral) and project management skills. Able to handle multiple competing tasks with great attention to detail. Able to work independently to achieve objectives on or before schedule. Demonstrated cross-functional collaboration and teamwork skills including influencing without authority. Comprehensive knowledge of medical device regulations and standards. Current knowledge of European quality system standards, and requirements under EU MDR and IVDR preferred. Ability to navigate ambiguous regulatory requirements and standards interpretation.,

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0 years

0 Lacs

Mumbai Metropolitan Region

Remote

About the Role We're looking for a detail-oriented Data Labeling Associate to support our recruiting operations by researching, verifying, and enriching candidate profiles. You'll receive basic candidate details such as a name and LinkedIn link, and your job is to confirm the information and add missing data such as location, email, or company details. This is a highly detail-focused role, ideal for someone who enjoys online research, structured work, and has a knack for spotting inconsistencies. Key Responsibilities Review candidate profiles using LinkedIn and other online sources. Verify that the provided LinkedIn profile matches the correct individual. Correct inaccurate data (e.g., mismatched names, incorrect profiles). Add missing information such as: Current location (city, state, country) Email address (when publicly available) Company name and title Additional social or professional links, if applicable Tag or label data accurately based on provided instructions. Meet daily productivity and accuracy goals. Flag ambiguous or hard-to-resolve cases for further review. Requirements Strong attention to detail and high standards for accuracy. Ability to follow structured instructions and research guidelines. Comfortable conducting web-based research using LinkedIn, Google, and other tools. Good written English communication skills. Prior experience with data entry, lead generation, sourcing, or similar roles is a plus. Familiarity with spreadsheets (e.g., Excel or Google Sheets). Nice-to-Have Experience in recruiting, sourcing, or research operations. Familiarity with tools like Hunter.io, ContactOut, Apollo, or People Data Labs. Comfortable working in a fast-paced, metrics-driven environment. What We Offer Competitive compensation Fully remote and flexible work schedule

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0.0 - 31.0 years

2 - 3 Lacs

Peenya, Bengaluru/Bangalore

On-site

Job Summary: The Assembly Technician is responsible for assembling lithium battery packs, inverters, energy storage systems (ESS), and related electrical/mechanical components according to company standards. The technician will ensure high-quality builds, follow standard operating procedures (SOPs), and support testing and troubleshooting of systems. Key Responsibilities: Assemble lithium battery packs (including LiFePO₄ cells, BMS, wiring, connectors, enclosures). Work with inverters, circuit boards, power cables, DC/AC connections, and cooling systems. Read and follow wiring diagrams, mechanical drawings, and SOPs accurately. Use hand tools, crimping tools, multimeters, torque wrenches, and other basic equipment. Perform insulation, polarity, voltage checks, and basic electrical testing post-assembly. Assist in quality checks, labeling, and packing of finished products. Maintain a clean and organized workspace to ensure safety and efficiency. Record production data, serial numbers, and defects in job sheets or digital logs. Collaborate with engineers and R&D for new product development or improvements. Follow safety guidelines and adhere to ESD protection and PPE compliance. Assist in inventory checks for raw materials and sub-assemblies.

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0 years

0 Lacs

India

Remote

Ready to embark on a journey where your growth is intertwined with our commitment to making a positive impact? Join the Delphi family - where Growth Meets Values. At Delphi Consulting Pvt. Ltd. , we foster a thriving environment with a hybrid work model that lets you prioritize what matters most. Interviews and onboarding are conducted virtually, reflecting our digital-first mindset . We specialize in Data, Advanced Analytics, AI, Infrastructure, Cloud Security , and Application Modernization , delivering impactful solutions that drive smarter, efficient futures for our clients. About the Role: The Azure Data Governance Specialist with define and enforce data policies, ownerships, lineage, cataloging, and quality management aligned with client’s regulatory and data management needs. What you'll do: Define, data classification, quality, ownership models Implement governance policies using Microsoft Purview Create golden record processed with MDM Work closely with stakeholders to understand and recommend approaches for data governance implementation of all required data sources What you'll bring: Proven experience in implementing end-to-end data governance using Microsoft Purview Define metadata, business glossary, data stewards, owner etc. Set up automated data quality checks. Manage cataloging and discoverability of internal and external data fields Identify and implement critical and key data elements Develop automated data classification and labeling mechanisms using MS Purview Knowledge of data governance lifecycle and frameworks such as DAMA-DMBOK Exposure to regulatory frameworks like GDPR, ISO 8000 What We Offer: At Delphi, we are dedicated to creating an environment where you can thrive, both professionally and personally. Our competitive compensation package, performance-based incentives, and health benefits are designed to ensure you're well-supported. We believe in your continuous growth and offer company-sponsored certifications, training programs , and skill-building opportunities to help you succeed. We foster a culture of inclusivity and support, with remote work options and a fully supported work-from-home setup to ensure your comfort and productivity. Our positive and inclusive culture includes team activities, wellness and mental health programs to ensure you feel supported.

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25.0 years

0 Lacs

Gurgaon, Haryana, India

Remote

Welo Data works with technology companies to provide datasets that are high-quality, ethically sourced, relevant, diverse, and scalable to supercharge their AI models. As a Welocalize brand, WeloData leverages over 25 years of experience in partnering with the world’s most innovative companies and brings together a curated global community of over 500,000 AI training and domain experts to offer services that span: ANNOTATION & LABELLING: Transcription, summarization, image and video classification and labeling. ENHANCING LLMs: Prompt engineering, SFT, RLHF, red teaming and adversarial model training, model output ranking. DATA COLLECTION & GENERATION: From institutional languages to remote field audio collection. RELEVANCE & INTENT: Culturally nuanced and aware, ranking, relevance, and evaluation to train models for search, ads, and LLM output. Want to join our Welo Data team? We bring practical, applied AI expertise to projects. We have both strong academic experience and a deep working knowledge of state-of-the-art AI tools, frameworks, and best practices. Help us elevate our clients' Data at Welo Data. MAIN PURPOSE OF JOB As an Operations Specialist, you will play a pivotal role in the day-to-day operations of the company, driving revenue and ensuring that customer commitments are met on time while maintaining the highest quality standards. This position will require a hands-on approach, strategic thinking, and exceptional organizational skills. You will be an early member of our operations team and have the opportunity to shape our most critical operational processes. MAIN DUTIES: Build and drive operational processes to ensure day-to-day delivery of customer commitments. Manage and oversee various aspects of daily operations including inventory, procurement, logistics, billing/invoicing, ticketing, timekeeping, project management, and customer service. Assist Project teams with planning, scoping, requirements gathering and validation with client. Create an effective feedback loop between the front line, product, strategy, and customers. Collaborate with cross-functional teams, including Customer Operations, Product Operations, Data Analytics, HR, Finance, Talent/Procurement, Product Managers, and more to achieve company objectives and KPIs. Conduct periodic audits to ensure compliance with standards and regulations. Provide support in the onboarding and training of new employees. Analyze operational data and metrics to identify areas for improvement. Participate in process optimization projects and come up with creative solutions to bottlenecks. Assist in financial budgeting and reporting. Support multiple squads on rotation asneeded. REQUIREMENTS Advanced English skills. Bachelor’s degree in an analytics-heavy major (e.g., Engineering or Economics) and/or a graduate degree in Operations, Engineering, Economics, or Business. Minimum of 2-4 years of experience in an operations role and/or a top-tier consulting firm. Excellent communication skills, both verbal and written. Strong organizational and multitasking skills. An action-oriented mindset that balances creative problem-solving with the scrappiness to ultimately deliver results. Proficiency in Microsoft Office Suite, with strong Excel skills. Analytical, planning, and process improvement capability. Other relevant skills Experience with reading SQL or demonstrated analytical skills Experience with resource management tools (e.g. Workday) Analytical Thinking Time Management Attention to Detail Team Collaboration Process Improvement Flexibility & Adaptability

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8.0 years

0 Lacs

Bengaluru, Karnataka, India

On-site

Job Title Regulatory Affairs Excellence Specialist Job Description Job Title : Regulatory Affairs Excellence Specialist Job Responsibilities Implements global regulatory strategies and roadmaps by leveraging a comprehensive understanding of the competitive market landscape and product marketing strategy to ensure alignment with organizational objectives. Works under general supervision and broad guidelines, consistently exercising independent judgment on matters of significance, ensuring adherence to company policies and regulatory requirements while maintaining high standards of performance and accountability. Demonstrates substantial understanding of regulator's role in the Quality System with good awareness of product lines, disease states, and customers, possessing general knowledge of business developed through education or past experience. Executes, manages, and prepares U.S. FDA 510(k) pre-market notification submissions—defining regulatory pathways, compiling technical dossiers, coordinating cross-functional inputs, and driving the process through clearance. Prepares and coordinates FDA Pre-Submissions (Q-Subs) when strategic feedback is required, drafting meeting requests and briefing packages, leading interactions with the Agency, and ensuring follow-up actions are completed. Resolves a wide range of moderate complexity requests in creative ways, leads comprehensive safety risk assessments to identify potential safety incidents and regulatory non-compliance, managing these incidents in Trackwise and ensuring corrective actions are effectively implemented. Monitors and handles potential regulatory impacts on product safety, implementing continuous improvement processes within the regulatory framework and engaging with cross-functional teams to proactively manage regulatory risks. Collaborates with central and regional Regulatory Affairs teams to support establishment registration and listing, and UDI/Global Trade Identification Number (GTIN) related activities, maintaining processes for regulatory filings/ licenses and developing technical contribution. Coordinates and facilitates witness testing to ensure products comply with safety regulations, maintaining direct contact with certification bodies, test houses, and regulatory personnel in local sales organizations. Takes ownership of regulatory planning for new product introductions and product changes, assisting in the maintenance of regulatory compliance throughout the product lifecycle. Supports the development of the regulatory plan, offering guidance on risk assessment and necessary corrective actions to meet regulatory requirements, including product registrations such as CE Marking and clinical evaluations. Develops and facilitates regulatory submissions for both new and existing products/solutions, ensuring accuracy and completeness to expedite regulatory approval processes effectively, preparing regulatory justifications to support submission filing decisions. Creates, reviews, and validates marketing and labeling materials, providing support to projects and other key regulatory initiatives while ensuring compliance with regulatory guidelines and standards. Recommends enhancements in systems and processes to solve problems or improve effectiveness of job area by collaborating with other functions, making periodic or ad-hoc revisions to Regulatory SOPs and templates. Implements safety and compliance requirements for product development projects and OEM/ODM products, communicating and integrating regulatory standards into the I&D organization through memos, training sessions, and deployment strategies. Administers the compliance protocol process within PDLM and MLD, overseeing safety certifications and country-specific approvals to ensure products meet international regulatory standards. Minimum required Education: Bachelor's / Master's Degree in Biomedical Engineering, Business Administration, Health Sciences, Pharmaceutical, Law or equivalent. Minimum required Experience: Minimum 8-10 years of experience with Bachelor's in areas such as Regulatory Affairs, Quality Compliance, Product Development in Medical Devices Industry or equivalent About Philips We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose. How We Work At Philips Our newly-adopted hybrid work concept fuses flexibility with collaboration to deliver great outcomes for our people and our customers. We are embracing an approach wherein we spend more time together than apart Our commitment to inclusion and diversity At Philips, we provide equal opportunities to all our employees and to all eligible applicants for employment in our company , irrespective of age, color, disability, nationality, race, religion, gender, sexual orientation (LGBTQ +), and all aspects that make individuals unique. Encouraging diversity and fostering inclusion are key to our mission of improving the lives of 2.5 billion people a year by 2030 through meaningful innovation. We have fair, transparent, and clear employee policies which promote diversity and equality, in accordance with currently applicable law. For, we believe that life is better when #youareyou. Our hybrid working model is defined in 3 ways: We believe in the importance of impactful collaboration: There's a certain energy when everyone’s in the same room that can heighten idea generation and creative friction needed for problem-solving. We embrace flexibility: Choosing where, when and how to work can vary according to task and team schedules. Flexibility isn’t office or online, it means choosing the space that works best for you, your teams and our customers on a case-by-case basis. We want to be at our best: The way we work and our workspaces are designed to support our well-being, offer career advancement opportunities, and enable us to be at our best. Why should you join Philips? Working at Philips is more than a job. It’s a calling to create a healthier society through meaningful work, focused on innovative, customer-first health technology solutions. Help us improve the health and well-being of billions of people, every year. Ultimately creating a career that no one could have planned for. Even you.

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0 years

0 Lacs

Rajkot, Gujarat, India

On-site

Company Description Raj Water Technology (Guj.) Pvt. Ltd. is a leading company specializing in the manufacturing, supplying, and exporting of water treatment projects, mineral water projects, natural mineral water projects, RTS juice turnkey projects, synthetic juice projects, and carbonated soft drink turnkey projects. Located in Rajkot, Gujarat, we offer comprehensive solutions for rinsing, filling, capping, packaging, and labeling across various packaging formats (PET bottle, pouch, PET can, tin can, glass, pouch). Our products conform to industry standards and undergo rigorous quality testing. Established in 2004, we have garnered a global clientele including regions like the Indian Subcontinent, East Asia, and South/West Europe. The company holds ISO 9001:2008 certification. Role Description This is a full-time on-site role for a Brewery Plant Designer, based in Rajkot. The Brewery Plant Designer will be responsible for designing brewery plant layouts, developing process flow diagrams, creating detailed engineering drawings, and collaborating with cross-functional teams to ensure design feasibility. The role includes overseeing installation and commissioning processes, ensuring compliance with industry standards, and providing technical support throughout the project lifecycle. Qualifications Proficiency in designing brewery plants and creating engineering drawings Experience in developing process flow diagrams and plant layouts Knowledge of industry standards and compliance requirements Strong collaboration and teamwork abilities Ability to oversee installation and commissioning processes Bachelor's degree in Mechanical Engineering, Chemical Engineering, or related field Excellent problem-solving and analytical skills Relevant industry experience is a plus

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100.0 years

0 Lacs

Chennai, Tamil Nadu, India

On-site

Company Description Dehgamwala & Sons is a pioneering company in the pipe, fittings, valves, and fasteners industry with over 100 years of experience, having started in 1916. We are committed to providing best-in-class quality and services, founded on the pillars of trust and quality. We deal with renowned brands like Jindal, Sivananda, TVS, and more, and are equipped for Hot Dip Galvanising & Zinc Plating. Our clientele spans various industries including Chemical, Agriculture, Construction, Pharmaceuticals, Water treatment, and Petrochemicals. Role Description This is a full-time on-site role located in Chennai for a Packing and Dispatch team member at Dehgamwala & Sons. The candidate will be responsible for organizing, packing, and dispatching STEEL products according to specified guidelines. Daily tasks include coordinating with the inventory team, ensuring accurate labeling, maintaining records of dispatched goods, and complying with safety standards. The role also involves timely communication with logistics partners to ensure prompt delivery of products. Qualifications Experience in packing and dispatch operations in STEEL INDUSTRY Strong organizational and time-management skills Attention to detail for accurate labeling and record-keeping Ability to work collaboratively with inventory and logistics teams Knowledge of safety protocols and compliance standards Good communication skills Prior experience in a similar role within manufacturing or logistics sectors is a plus High school diploma or equivalent education

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2.0 years

2 - 2 Lacs

Panaji

On-site

About Xpanse Coffee: At Xpanse Coffee, we blend the art of great coffee and continental cuisine with the precision of technology. As a tech-driven coffee chain, we’re redefining the café experience to meet the needs of today’s fast-paced world delivering quality, consistency, and efficiency at every touchpoint. Join us as we build a seamless and elevated café culture across our expanding network. Job Overview: As a Commis I , you will be a key part of our kitchen brigade, responsible for preparing high-quality food in accordance with our recipes and presentation standards. You will work closely with the culinary team to ensure a smooth, clean, and efficient kitchen operation that supports our commitment to excellence. Key Responsibilities: Assist in the preparation, cooking, and presentation of food items under the guidance of senior kitchen staff. Maintain consistency in taste, quality, and presentation as per Xpanse Coffee’s standards. Ensure all ingredients, tools, and stations are properly prepared and organized before each service. Follow food hygiene and safety standards strictly. Coordinate with the service team for timely delivery of food orders. Maintain cleanliness and organization of the kitchen work area. Receive and store kitchen supplies, checking for quality and freshness. Support inventory control by properly labeling and storing food items. Adhere to standard operating procedures and participate in training sessions. Qualifications & Skills: Diploma or certificate in Culinary Arts or relevant training. Minimum 2 years of kitchen experience in a café, restaurant, or hotel environment. Strong passion for food preparation and learning. Basic knowledge of kitchen equipment and food safety practices. Ability to work in a fast-paced, high-volume environment. Good communication skills and a team-oriented attitude. What We Offer: A dynamic and modern work environment. Opportunities for growth and skill development. Staff meals Being part of a forward-thinking and expanding brand. Accommodation Provided Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Work Location: In person

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