86 Labels Jobs - Page 3

Responsibilities: * Manage packing process from label creation to dispatch * Collaborate with warehouse team on inventory management * Oversee packaging operations and quality control

Meet Sales targets as per the Budget assigned by HOD Technical demonstrations on how our product will meet client needs, in assigned territory. Increase client base for geographical area assigned Attending International Various Seminars, Exhibitions Required Candidate profile Experience in international market either of Middle East and Africa, Egypt, Tunisia and MENA Countries. Generate clients for Track n trace , vision inspection products for Pharmaceutical clients.

Job Responsibilities Prospect and Generate Leads: Identify and target potential clients through market research, networking, and industry events. Client Relationship Management: Build and maintain strong, long-term relationships with clients by understanding their business objectives and providing customised label printing solutions. Consultative Sales: Conduct thorough needs assessments with clients to determine their label printing requirements and recommend the most suitable products and services. Quotation and Proposal Preparation: Prepare accurate and competitive quotes and proposals for clients, ensuring all details are clear and comprehensive. Sales Presentations: Deliver compelling presentations and demonstrations of our label printing capabilities, highlighting the benefits and advantages of our products and services. Sales Targets: Meet and exceed monthly and quarterly sales targets, driving revenue growth for the company. Market Research: Stay up to date with industry trends, competitive products, and emerging technologies to provide valuable insights to clients. Collaboration: Work closely with the internal sales support and production teams to ensure smooth order processing and fulfilment. Reporting: Maintain detailed records of sales activities, leads, and customer interactions in CRM system. Desired Candidate Profile 5+ years of successful B2B sales experience, preferably in the printing or packaging industry. Knowledge of key consumer & industrial good segments and its unique label printing requirements Excellent communication and presentation skills. Strong negotiation and closing skills. Self-motivated, results-oriented, and able to work independently. Willingness to travel within the designated sales territory.

We are a screen printing company looking for a qualified individual to join our team as a full-time quality systems specialist. The ideal candidate will have a background in engineering or quality management, along with a minimum of 3-4 years of experience in automotive or printing field. The primary responsibility will be managing the quality systems for screen printed automotive parts. Knowledge of ISO and other quality certifications is a must. Role & responsibilities Oversee quality operations and supervise the QA team Document and review all QMS activities, 5S, 8D, Fishbone diagrams, Rootcause analysis deviations, change controls, CAPAs, PPAP, PSW. Compile and manage SOPs and master documents Approve and manage suppliers Coordinate and execute internal and external audits Review production/batch documents Compile quality reports and conduct quality reviews for presentation to management Preferred candidate profile The ideal candidate will have a background in engineering or quality management, along with a minimum of 3-4 years of experience in the automotive or printing field.

Jr. Officer - Plant Maintenance: Educational Qualification - D.E.E / D.M.E (Only diploma holders must apply.) Experience - 02 - 04 years in pharmaceutical manufacturing machine maintenance Job Responsibilities - 1. Day-to-day maintenance of manufacturing filling and Packaging machines used in formulation facility. troubleshooting, and repair of pharmaceuticals plant machinery, preferably hands on experience about ointment tube filling machines, liquid filling, labelling with OCR system and other packing machines like cartonators, check weighing machines, blister & strip packing machines etc. 2. Manufacturing machines like O intment Manufacturing vessels, Bottom entry agitators, RMG, FBD Compression machines and allied manufacturing machines like metal detectors dust extractors de - dusters counting machines washing machines and slat conveyor belts. 3. Diagnose and troubleshoot equipment malfunctions effectively and efficiently. 4. Optimize equipment performance to maximize output and minimize downtime. 5. P reventive and predictive maintenance on assigned equipment, recording data in log books and planners and schedules. 6. In addition to this added knowledge about utilities like boiler and AHU systems will be preferable.

We are looking for fresher candidates with no prior job experience to train for a period of 6 months in data annotation. Post training we will offer them full time job opportunities as Associate Experienced candidates NEED NOT APPLY

Strides Pharma is conducting walk in interview on 23rd Mar 2025 (Sunday) in Bangalore for below positions. Department: Packing Qualification: B.Pharm/M.Pharm Work Location: Bangalore Experience: 2-5 years in Oral Solid Dosage Key Responsibilities Planning and execution of batch packing activities such as Dispensing & Line clearance. Expertise in handling Blister, Bottle and Sachet packing machineries like BQS, CAM, Maspack, Auto Cartonator etc. Handling of QMS activities like Change Control, Deviation, OOS, OOT, CAPA etc. Department: Maintenance Engineering Qualification: Diploma/B.E/B.Tech (Mechanical/Electrical/Instrumentation) Work Location: Bangalore Experience: 2-7 years Key Responsibilities Responsible to conduct Preventive Maintenance and Breakdown Maintenance of production and packing equipment's like Fluid bed driers (FBD), Compression machines, Coating machines, Blenders, Rapid mixture grinders (RMG), Capsule filling machines, Blister packaging, Bulk counting lines, Sachet filling lines, Serialization equipment's, inspection systems. Troubleshooting knowledge of PLC, HMI, IPCs, SCADA systems. Knowledge on Digital platform SAP & TrackWise to handle PM/BD and QMS documents. Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

Hi, We are looking for an Support Engineer( Security and Compliance ) Skills: Exchange Online supporting email hygiene, labels, policies or Audit logs ,DKIM Exp:4 to 6 yrs Location:Bangalore,Hyderabad NP:Immediate within 15 days Interested candidate send resume to sreeram.sekhar@thakralone.in

Hi, We are looking for an Support Engineer( Security and Compliance ) Skills: Exchange Online supporting email hygiene, labels, policies or Audit logs ,DKIM Exp:4 to 6 yrs Location:Bangalore,Hyderabad NP:Immediate within 15 days Interested candidate send resume to sreeram.sekhar@thakralone.in

Hi, We are looking for an Support Engineer( Security and Compliance ) Skills: Exchange Online supporting email hygiene, labels, policies or Audit logs ,DKIM Exp:4 to 6 yrs Location:Bangalore,Hyderabad NP:Immediate within 15 days Interested candidate send resume to sreeram.sekhar@thakralone.in

- Audit preparation - SOP making & updating - Preparation of NPD & update as per progress - Periodic training on topics - Handling customer complaints - Maintaining rules & regulation as per advanced regulatory norms - Ensure all product Quality . Required Candidate profile - B.Sc/M.Sc full time degree - 1+ years experience in Pharma company

Target potential & existing customers for HP indigo digital label printing systems sales Assess customer needs & suggest suitable products Presentations & demos Participate in social media industry events, sales & trades shows exhibitions New leads Required Candidate profile MBA Sales & Marketing B.E. Printing/relevant Exp 10-15 yrs Exp in selling capital equipment -label printing industry, digital presses, consumables like Label substrates, Inks Tamil,Telugu, Eng & Hindi

Data Annotator: Data Annotators play a critical role in the development of our machine learning models. You will be working closely with our data scientists and engineers where you will be responsible for labeling and annotating large datasets, ensuring that our models are trained on high-quality data. You will also be responsible for identifying and resolving any data quality issues, ensuring that our models are robust and reliable. Data Annotator job responsibilities: Annotate and label various types of data according to project guidelines and specifications. Review annotated data for accuracy and completeness, making adjustments as needed. Work collaboratively with data scientists and engineers to ensure high-quality annotated data for machine learning models. Maintain organized and detailed records of annotated data and any changes made during the annotation process. Continuously learn and apply new annotation techniques and tools to improve efficiency and accuracy. Communicate any issues or challenges with data annotation to project leads in a timely and professional manner. Adhere to project deadlines and deliver annotated data within predetermined timelines. Data Annotator job requirements: Ability to accurately and efficiently label datasets for machine learning models Strong attention to detail and ability to maintain data quality standards Ability to work in a fast-paced environment and meet tight deadlines Comfortable working with complex and large-scale datasets Strong problem-solving skills and ability to troubleshoot annotation challenges Communication skills, both written and verbal, are of paramount importance for data annotators. Clear and concise communication allows annotators to understand project goals, requirements, and expectations. ( Contact or Mail: muthu.r@handigital.com)

Only Male Candidates Roles & Responsibility • Checking Product name • Checking Manufacturing date • Checking Expiry date Shift Timings:- Day - 09:00 AM To 06:00 PM Night - 08:00 PM To 05:00 AM 4 weekly off

Role & responsibilities 1. All Licenses, Labels, Products, PM etc. to comply with FSSAI, LMA, PCB regulations for all 3 plants. Represent CF on regulatory forums. Legal notices closure. Regulatory document filing, tracking and completion for all 3 plants 2. Tracking, CAPA, Complaint resolution communication to relevant stakeholders, Timely resolution/closure of quality related customer complaints 3. Giving regulatory inputs for all NPD/NPI for Label, Ingredients and PM compliance. 100% compliance on all Labels 4. Creating and conducting various Food safety trainings according to BRC requirement to all employees. Food Regulatory training module preparation and training for quality and other relevant stake-holders. 5. Complete at least 3 regulatory related trainings. Preferred candidate profile 5-10 years in Quality Assurance, with 2+ years in a managerial role . Degree in Food Tech, Microbiology, Engineering, or related field . Strong knowledge of QMS, audits, risk management, and compliance . Regulatory & Compliance Process Management Knowledge on Licenses, Factory Compliances Perks and benefits Gratuity Group Mediclaim Policy Group Accidental Policy Performance based Incentives

Accountabilities: Responsible for preparation, review, filling and timely launch of labeling for new submissions and Life cycle management for Rx/OTC products in US and Canada. Role & responsibilities :- New Submissions: 1. Review and timely completion of Labeling for ANDA/ANDS dossiers for submissions and prepare and review response to Labeling deficiencies to secure approval. 2. Provide necessary feedback to team developing drug products using regulatory guidelines and communication with agencies that has impact on product labeling. Life-Cycle Management 3. Routinely tracking of RLD/CRP labeling updates from Agencys website and timely notifying concerned stakeholders for the same. Completion and coordinating commercial launch activities for new/existing approved Rx products for Sun Pharma/Acquired products, and Customers. To initiate/provide approval for Artwork Approval Sheets for commercialization of artworks through Artwork Management System (AMS). 6. Providing timely information of Artwork approvals through approval package upon receipt of approval and update the same based on renewals and variations. 7. Coordination with various departments for preparation of variation packages (specifically w.r.t labeling part) and submit the same to regional offices. 8. To raise Change Controls for approved drug products in Track wise for labeling supplements and to ensure completion of variation proposal/management in a timely manner. 9. To provide labeling inputs to MACR for PSUR. 10. To prepare Annual reports 11. Review regulatory filing impact of variations, change controls, deviations (wrt to Labeling) etc. Ensure reposition of comprehensive product information into repository.

HIRING FOR ASSOCIATE PROCESS EXECUTIVE Please fill the google form without fail https://forms.gle/XrVeSE4LACdiU8ec8 Mode : Work From Home (WFH) Candidate Should have Mandatory Own Laptop or Desktop with (i5 processor, 2.0GHZ, 8GB RAM, windows 10) Internet or Wi-Fi Speed Should be there at least 60 Mbps Role :Contract (Third Party Payroll -Randstad India Pvt ltd) Qualification (Mandatory) : BCA (CS), BSc (Computers), BE/BTech (Computer Science, ECE, EEE, ), MSc (Computers), MCA (Computers). Role & responsibilities with 0-1 year Exp required with Degree certificate required For Autonomous Cars technology: Validating, Video Labeling for Autonomous cars /Chassis control Systems in Automated cars and trucks. Infrastructure for video sequences of a camera mounted autonomous capable Cars. Synchronizing recorded video files to master database, annotation of images It deals with finding Road signs, Lane, Lights, Pedestrians, Vehicles, Infrastructure in video sequences of a camera mounted on the front of a car. Supporting team members with issues while labeling video.

Job description Note : 6 months contract (project) based on performance contract will be extended. Position Summary: The Audio Annotation Specialist is responsible for reviewing, labeling, and annotating audio files to prepare them for use in research, machine learning models, or other applications. This role requires a keen attention to detail, familiarity with audio tools, and a strong understanding of the context in which audio is being used (e.g., speech recognition, sound event detection, etc.). Role & responsibilities Hiring Audio annotation @ Koramangala, Bangalore (3 months project) LabourNet3.9346 Reviews 0 - 2 years50,000-3 Lacs P.A.Hosur, Bengaluru( Koramangala ) Women candidates preferredSend me jobs like this Posted: 30+ days ago Openings: 200 Applicants: 607Register to applyLogin to apply Hiring Audio annotation @ Koramangala, Bangalore (3 months project)LabourNet3.9346 ReviewsSend me jobs like thisApply Job description Note : 3 months contract (project) based on performance contract will be extended. Position Summary: The Audio Annotation Specialist is responsible for reviewing, labeling, and annotating audio files to prepare them for use in research, machine learning models, or other applications. This role requires a keen attention to detail, familiarity with audio tools, and a strong understanding of the context in which audio is being used (e.g., speech recognition, sound event detection, etc.). Role & responsibilities Audio Transcription: Convert audio recordings into accurate text, ensuring correct punctuation, grammar, and speaker identification. Speaker Labeling: Identify and label different speakers in multi-speaker environments, ensuring proper segmentation. Emotion & Sentiment Annotation: Label and categorize the emotional tone or sentiment of the speaker's voice (e.g., happy, angry, neutral). Noise and Event Labeling: Annotate non-speech sounds (e.g., background noises, environmental sounds) and tag key events within the audio. Phonetic or Linguistic Annotation: Mark phonetic features or annotate linguistic structures (such as syllables or intonation) for more advanced analysis. Quality Control: Ensure the quality and accuracy of annotated data by reviewing and verifying previous annotations. Collaboration: Work with cross-functional teams (such as data scientists, developers, or linguists) to ensure that annotations align with project goals. Use of Annotation Tools: Familiarity with audio annotation software such as Audacity, ELAN, Praat, or custom platforms used by your employer. Preferred candidate profile Attention to Detail: Ability to listen to audio recordings carefully and make accurate annotations. Proficiency with Audio Tools: Experience with audio editing and annotation software. Strong Communication: Clear, concise communication skills for transcribing and tagging spoken content. Knowledge of multiple languages, especially in multilingual projects. Experience with transcription or captioning. Understanding of audio formats and audio processing techniques. Education and Experience: Education: Bachelors degree in Linguistics, Computer Science, Data Science, Communications, or a related field is often preferred. Experience: Prior experience in audio-related fields, transcription, or data annotation. Interview Process: Face-to-face or Virtual interview Working Days: 6 days a week Daily Lineup: 20 candidates Contract Type: 6 months Designation: Audio Annotator Salary: Up to 35K CTC Role: Data Science & Machine Learning - Other Industry Type: Analytics / KPO / Research Department: Data Science & Analytics Employment Type: Full Time, Permanent Role Category: Data Science & Machine Learning Education UG: Graduation Not Required Key Skills highlighted with are preferred key skills Transcription Annotation Generics

Position Title: Package Assistant Location: Hyderabad, India Job Type : Contract Job Summary: We are seeking a highly organized and detail-oriented Package Assistant to join our team in Hyderabad, India. Under the guidance of the Packaging Engineers, this role will work mainly in the field of packaging development and optimization. The Package Assistant will take responsibility for working as an administrator for Corteva package material database, Specright. This role involves the update, maintenance and management of the technical documentation of packaging. This role will be based in Hyderabad, India and provide support to Packaging Technology R&D teams globally (APAC, NA, LATAM and EMEA). Key Responsibilities: Upload, maintain and update comprehensive packaging documentation (drawings and technical specifications) to Corteva's Specright package material database. Perform regular updates and maintenance tasks as required. Generate and distribute regular reports on Specright database status and progress. Coordinate with global and regional teams to ensure system requirements are met. Ensure data integrity and accuracy within the system. Ensure compliance with company policies and procedures. Assist with troubleshooting and resolving Specright database-related issues and provide system admin support to global and regional teams. Provide training and guidance to users on the Spec-Right system. Develop user manuals and training materials as needed. Write test protocols and reports related to packaging. Summarize package studies with the help of the Packaging Manager. Assist the packaging team on new packaging implementation projects. Collaborate with the regional Package Engineers to implement best practices. Generate, maintain, and update MDG SAP workflow for Material code setup. Assist PS&T APAC Regional Lab Team to manage and update all databases on time and file reports properly. Provide secretarial/administrative support to leadership. Qualifications: Master or equivalent level in chemistry, material engineering or formulation science. A successful 1-2 year's experience in a packaging field would be desirable. Experience with package material systems or similar software is a plus. Flexibility to work with global teams across different time zones. Ability to adapt to changing priorities and deadlines. Ability to work independently and as part of a global team. English required, both writing and speaking.

To target and crack orders from potential customers To Co-ordinate with customers and production department Update management on daily basis on the progress and development Sent weekly reports to directors sales of various type of labels. Required Candidate profile Experience in sales & marketing of label printing industry Strong knowledge of label printing technologies, materials, and applications Should have sales experience of Africa region Ready to travel

Must be innovative with designs should be smooth and familiar with coral draw, illustrator ,experience in Label & packaging designing. label cutting, should be flexible on rotational shifts and days Note- Only female candidate residing near Panvel

Role & responsibilities Authoring Safety Data Sheets compliant with global regulations independently. Capable of collaborating with internal stakeholders for SDS pre-requisites Managing other Regulatory affairs in process Excellent record keeping of all regulatory tracksheets.

Responsibilities: Manage production packing processes from blister to bottle. Ensure accurate tracking & traceability through labels and labelling. Oversee packaging operations with focus on quality control.

Greetings from BVR People Consulting!! Position: Regulatory Affairs - Formulation Designation: Executive or Asst. Manager Division: Injectable and Solid oral products Qualification: B. Pharm, M. Pharm and M. Sc (FULL TIME) only Years of Experience: 4 to 8 Years CTC range: 5 to 13 LPA. Job Locations: Bangalore ( Electronic City ) No. of Positions: 04 Job Summary: Compilation and submission of the dossier and query responses as per the EU/UK/ANZ /Israel/Belarus and Ukraine regulatory requirements within stipulated timeframe (for Injectable and Solid oral products ). Interaction with CFTs for product specific requirements and to attend product strategy meetings. Review of final data and technical documents received towards dossier compilation from API team, RnD, IP, PV, QA, Commercial, Packaging and Plant team. Compilation of labelling documents as per current EU/UK/ANZ/Israel/Belarus and Ukraine regulatory requirements. eCTD Publishing of dossiers in DocuBridge software. Product life cycle management for approved Europe products i.e. variation, Renewal and sunset exemption filings. Maintain product database, regulatory files, records and reporting systems. Timely updation and maintenance of RIMS database. Preparation and submission of high-quality national translations for National Phase. Post Approval and Pre approval NOTE: We are looking Notice period 01 month or immediate joiner. Interested Candidates should forward their resume to " ganapathi@bvrpc.com" and also Your Current CTC, Excepted CTC and Notice period. Thanks K Ganapathi Mob. No. 9600387468

Assistant Manager Quality - Private Label FMCG (Non-Food: Home Care, Personal Care, Baby Care Products) Location: Bangalore Job Summary: Asst. Manager Quality Private Label FMCG (Non-Food) will be responsible for ensuring the highest quality standards in the development, production, and delivery of Home Care, Personal Care, and Baby Care products. The role involves collaborating with cross-functional teams, managing supplier quality, and adhering to regulatory compliance to ensure customer satisfaction and brand reputation. Key Responsibilities: Define and implement quality standards, specifications, and guidelines for Home Care, Personal Care, and Baby Care product categories. Work closely with 3P Suppliers for R&D and product development to ensure products meet safety, performance, and quality benchmarks. Conduct product evaluations, sensory testing, and performance assessments during development phases. Ensure the products comply with regulatory standards- BIS,FDA,ISO, Ayush Conduct comprehensive audits of Home Care, Personal Care, and Baby Care product Suppliers to ensure compliance with quality standards and regulatory requirements. Ensure on boarding of New FMCG suppliers with adherence to quality and regulatory criteria. Analyze quality trends and implement continuous improvement initiatives across manufacturing and supply chain processes. Identify root causes for quality issues and drive corrective and preventive actions. Provide training and support to new suppliers to help them understand and comply with company standards. Responsible for handling end-to-end quality operations in the retail supply chain. Travel to multiple 3rd party supplier locations within the city and out of the city for Quality inspections and solving the issues. Framing of Specifications and SOPs for Home Care, Personal Care, and Baby Care Products Should have good command on leading the FMCG Nonfoods Project from development to Implementation. Strong Technical Knowledge on Drug &Cosmetic, Ayush license, LM , PCB & Labeling Guidelines. Develops and implements Nonfood regulatory and quality strategic plan for Private label brands in concert with corporate strategic plan. Address and resolve customer complaints related to product quality in a timely and effective manner. Use customer feedback to drive product and process improvements. Develop supplier QA team continuously through training, knowledge sharing and follow up. Working and interacting daily with the 3 rd Party Suppliers and corporate QA Team on projects related to Quality and safety efficiencies. Guidance needs to be provided from time to time for the Supplier Quality Team. Key Skills: Ability to develop & lead the project Individually. Should have strong experience in managing stakeholders and understanding of the strategic sourcing process. Able to utilize and critically evaluate data from a variety of sources to identify root cause and lead teams towards resolution. Proven experience in NonFood Categories like Home care, Cosmetics, paper & disposables, party needs, puja articles, general merchandise etc. Process oriented with excellent communication and problem-solving skills. Strong communication skills verbal and written, ability to communicate effectively to varied audiences Self-motivated, able to perform role with minimal supervision Able to manage multiple priorities in a dynamic environment Ability to work in a team environment to consistently achieve results & achievement. Strong organizational skills Demonstrates a positive can-do excellent teamwork attitude with strong communication/ information sharing skills A self-starter capable of designing and implementing services/processes Team player who can collaborate across multiple functional areas Qualifications: Bachelors/Masters degree in Chemistry, Cosmetology Chemical Engineering Minimum 6 years in quality assurance/quality control, preferably in FMCG (Non-Food) Home Care, Personal Care, or Baby Care products. Familiarity with chemical formulations, product testing, and regulatory frameworks. Proficiency in quality management tools and techniques (e.g., FMEA, SPC, CAPA). Should have Good Knowledge on Data analysis & Excel, Word, PPT. How to Apply Interested Candidates please share your resumes at - sandhya.tiwari1_ch@external.swiggy.in