159 Labels Jobs - Page 3

Diploma / Graduate/ PG with 5 to 10 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.E. (Mechanical Preferred) / + Certificate course of IIP with 10 to 12 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Responsible for Cost of production, 24 hours for the plant. Required Candidate profile 5 years of experience as Senior Production Manager in an established / renowned printing-packaging plant. Handle a team of 20-25 executive & 100-120 workers. Production planning, Inventory management. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ PG with 5 to 10 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.E. (Mechanical Preferred) / + Certificate course of IIP with 10 to 12 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Responsible for Cost of production, 24 hours for the plant. Required Candidate profile 5 years of experience as Senior Production Manager in an established / renowned printing-packaging plant. Handle a team of 20-25 executive & 100-120 workers. Production planning, Inventory management. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ PG with 5 to 10 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Diploma / Graduate/ ITI with 3 to 5 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. In process Inspection / Final QC Inspection. Proper record keeping. Detect non-conformities. Required Candidate profile To check the material as per the standard procedure & as per the time frequency. Check the root cause of the non-conformity and take corrective and preventive action. Should have own vehicle. Perks and benefits Negotiable - Depending Upon Candidate & Experience

B.E. (Mechanical Preferred) / + Certificate course of IIP with 10 to 12 Years of experience in Printing Packing Industries – Mono Carton, Paper Printing, Corrugation & Self Adhesive labels. Responsible for Cost of production, 24 hours for the plant. Required Candidate profile 5 years of experience as Senior Production Manager in an established / renowned printing-packaging plant. Handle a team of 20-25 executive & 100-120 workers. Production planning, Inventory management. Perks and benefits Negotiable - Depending Upon Candidate & Experience

- Expereince in Sourcing, Purchase, Procurement, Vendor Development, Supply Chain Management - Logistics/supply chain management - Products: Labelling/ Printing/ Packaging/Textiles/Garments/Apparels Required Candidate profile Any Graduate Excellent Communication Products: Labelling/ Printing/ Packaging/Textiles/Garments/Apparels Kindly reach us Gokuladevi 8668041213 adducoindia@gmail.com

We are looking for a Packaging and Development Specialist to join our team at Sri Krishna Pharma The ideal candidate will have experience in the pharmaceutical industry and will be responsible for ensuring that all products meet the highest quality standards. The QC, Regulatory Affairs, Packaging and Development Specialist will be responsible for: Developing and implementing quality control processes and procedures Ensuring that all products meet the required regulatory standards Working with the packaging team to ensure that all products are properly packaged and labelled Working with the development team to ensure that all products are developed to the highest standards Conducting regular quality checks and inspections Investigating and resolving any quality issues Maintaining accurate records and documentation The ideal candidate will have: A degree in a relevant field such as pharmaceuticals, chemistry, or engineering At least 3 years of experience in the pharmaceutical industry Knowledge of quality control processes and procedures Knowledge of regulatory standards and requirements Excellent problem-solving and communication skills Attention to detail and accuracy . If interested please share your resume to jayakishore.gollapalli@srirkishnapharma.com

Responsibilities and Impact Accurately annotate and label data to support the development and enhancement of data products across Commodity Insights. Collaborate with business subject matter experts, product managers and developers to ensure annotations align with the requirements of various commodity data products. Utilize custom tools and workflows to efficiently process and annotate data at speed, minimizing manual input where possible. Participate in training sessions to enhance annotation techniques and deepen understanding of commodity insights products. Contribute to the continuous improvement of annotation guidelines and processes, ensuring they meet the evolving needs across Commodity Insights. What Were Looking For: Basic Required Qualifications Bachelor's degree or equivalent experience in a relevant field. Strong attention to detail and ability to work with complex data sets. Familiarity with data annotation tools and processes. Excellent communication skills to collaborate effectively with team members. Ability to work independently and manage time efficiently in a fast-paced environment. Additional Preferred Qualifications Experience or knowledge in commodity markets or related fields. Proficiency in using data management and annotation software. Demonstrated ability to adapt to new technologies and processes. Strong analytical skills and problem-solving abilities.

5-10 year good experience required in Illustrator & Photoshop Should have working knowledge of : Custom Tags, Printed Labels, Stickers, Boxes, Sensomatic Tags, Wooven Tags,Price Tickets, Plastic Seals, Jwellery Cards,Books Location-Manesar,Gurgaon Required Candidate profile Diploma related to required field. 5-10 year good experience required in Illustrator & Photoshop Perks and benefits 30k to 35k Depends on candidate

Responsible for procurement of brought-out parts/items used in assembly Sourcing & procuring, corrugated boxes, stickers, labels, inserts, tapes, and other packaging consumables. Identify and develop reliable vendors for packaging and outsourced components. Negotiate prices, payment terms, and delivery schedules with suppliers. Raise purchase orders and coordinate deliveries in alignment with production schedules. Collaborate with production, planning, and stores departments to understand material requirements. Monitor inventory levels and ensure optimum stock of packaging and bought-out items. Track supplier performance in terms of quality, cost, and delivery timelines. Maintain accurate records of purchases, pricing, and supplier information. Ensure compliance with quality and packaging specifications defined by the organization.

Job Summary: We are seeking a detail-oriented and quality-driven Artwork Proofreader to join our pharmaceutical packaging/artwork team. The ideal candidate will have 1-3 years of experience in proofreading pharmaceutical artworks, ensuring accuracy, compliance, and consistency across all packaging materials. Key Responsibilities: Review and proofread pharmaceutical packaging artwork files including labels, cartons, leaflets, and inserts. Verify all textual content against reference documents such as approved product information (PI), summary of product characteristics (SmPC), and regulatory texts. Ensure consistency in font, spacing, grammar, punctuation, regulatory symbols, and artwork layout. Cross-check barcodes, braille (if applicable), batch numbers, expiry dates, and other variable data. Collaborate with regulatory, artwork development, quality, and packaging teams to ensure accuracy and timely delivery of artworks. Mark errors and provide clear and structured feedback to the design team or external vendors. Maintain accurate records of revisions, approvals, and version control for each artwork. Ensure that all materials meet internal quality standards as well as regulatory and market-specific requirements (e.g., ROW, EMA, MHRA). Required Skills & Qualifications: Bachelors degree in Life Sciences, Pharmacy, English, Communications, or a related field. 1-3 years of experience in proofreading pharma artwork or regulatory labeling content. Strong command of written English with excellent grammar and attention to detail. Familiarity with regulatory guidelines for pharmaceutical packaging and labeling. Proficiency in using proofreading tools, PDF annotation software (e.g., Adobe Acrobat), and basic Microsoft Office applications. Understanding of pharma artwork lifecycle and artwork management systems (e.g., Esko, Veeva Vault, or similar) is a plus. Ability to manage multiple projects under tight deadlines while maintaining quality. Team player with good communication and collaboration skills. Preferred Qualifications: Experience working in a GMP or regulatory-controlled environment. Knowledge of regional labeling requirements (e.g., EU, APAC). Exposure to braille validation or barcode verification tools is an advantage.

Generate Sales thru aggressive business development,lead generation,cold calling, networking,prospecting database leads. Derive sales from education publishing,key , book publications, Co. annual reports, magazines, marketing leaflets,catalogs etc. Required Candidate profile 8 years B2B Sales & Business Development experience in commercial printing industry, including digital and offset printing technologies.Hunter approach.

Backend/Annotator International Process Salary-: - 25 K CTC / Experience - 20 K CTC/ Fresher Perks and Benifits-: -Both side Cabs -5 Day working -Salary Increament after every 6 Months -Incentive Required Candidate profile -Immediate Joiners -Knowledge of Data Annotation preffered -Graduate can only apply(no result awaied) -Confortable working Rotational shifts -Team Player -Confortable in Reloaction -BCA/MCA Preffered

Annotator International Process Salary-: - 25 K CTC / Experience - 20 K CTC/ Fresher Assessment:- Data Annotation assessment Operations Round Perks and Benifits-: -Both side Cabs -5 Day working -Salary Increament after every 6 Months -Incentive Required Candidate profile -Immediate Joiners -Good Knowledge of Data Annotation -Graduate can only apply(no result awaied) -Confortable working Rotational shifts -Team Player -Confortable in Reloaction -BCA/MCA Preffered

International Process Salary - 22-23,000 In-Hand / Experience - 17,000 Fresher Assessment :- Data Annotation assessment Operations Round Graduate only Both side Cabs 5 Day working / Rotational shift / 2 day Rotational week off

Team Leader Quality - Private Label FMCG (Non-Food: Home Care, Personal Care, Baby Care Products) Location: Bangalore Job Summary: Team leader 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

Salary - 22,000 / Experience 17,000 / Fresher Assessment :- Data Annotation assessment Operations Round Graduate only 5 Day working / Rotational shift / 2 day Rotational week off

International Process Salary - 22,000 In-Hand / Experience - 17,000 In-Hand/ Fresher Assessment :- Data Annotation assessment Operations Round Graduate only Both side Cabs 5 Day working / Rotational shift / 2 day Rotational week off

Walk-In Drive For Regulatory Affairs - FML Department in FML Division - MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 27-06-2025. Regulatory Affairs FML Department in FML Division , Job Description: ( Regulatory Affairs - FML Division ) Should have minimum of 08 to 13 years of experience in FML Regulatory Affairs Job Title : Asst. Manager / Deputy Manager / Manager / Sr Manager Experience : 08 to 13 years in FML RA field Education: B Pharm \ MSc \ M Pharm Department : Regulatory Affairs - FML Roles & Responsibilities : Collect documents from various departments to prepare regulatory submissions. Prepare regulatory submissions to relevant authorities. Prepare amendments, updates, and revisions to submissions. Conduct meetings with cross-functional teams (CFT) to address deficiencies received from regulatory authorities and customers. Draft responses to regulatory deficiencies and review comments. Update the database as per requirements. Prepare the applicant and restricted parts for Abbreviated New Drug Applications (ANDAs). Compile dossiers in electronic Common Technical Document (eCTD) and Common Technical Document (CTD) formats for all relevant countries. Guide the CFT based on current requirements from regulatory authorities. Plan and allocate projects within the team. Assess proposed changes for approved products and finalize the submission category. Review and clear specifications, protocols, stability data, bio-waivers, etc. Key Performance Indicators: Demonstrate in-depth knowledge of regulatory guidelines and requirements for each market. Ensure all submissions are cleared within the stipulated timeline. Provide actionable items to address regulatory queries and dossiers. Required skills : Knowledge of RA Guidelines and Requirements Action Item for RA deficiency. Cross-Functional Team Work Represent regulatory affairs at cross functional meetings and coordinate with R&D, Production, Plant QA/QC and Marketing to efficiently and successfully complete regulatory activities Support plant teams in regulatory audits, liaison with domestic & export regulatory authority. Assess and approve change controls and update files accordingly Interview Date : 27-05-2025 Department : Regulatory Affairs - FML Dept. Experience : 08 to 13 Years Position: Asst. Manager / Deputy Manager / Manager / Sr Manager Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue: MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 27-06-2025.

Must to have experience Supervise the packaging team, ensuring proper handling and packaging of finished products. Coordinate with production, quality assurance, warehouse teams to ensure the timely availability of approved materials and products.

- Job profile : Data Annotator - 5 Days working and 2 week offs - Rotational shifts and offs - Both side cabs as per international process - Salary : Freshers - 21k ctc, Experienced - 25k ctc - Rounds : Ops, Assessment Required Candidate profile - Decent english speaking candidates required - Graduation is mandatory to apply