Company Description Imaging Techniques is a leading solution provider for various labeling and printing requirements across industries. With a state-of-the-art manufacturing facility in Mumbai, we deliver high-quality outputs and meet the volume requirements of our customers. Our printing and tamper-evident labeling solutions add significant value to the products and packaging of our clients. Role Description This is a full-time hybrid role for a Business Development Executive based in Thane/Mumbai, with some work from home flexibility. The Business Development Executive will be responsible for identifying new business opportunities, generating leads, managing accounts, and fostering strong client relationships. Day-to-day tasks include conducting market research, developing business strategies, and achieving sales targets. Qualifications New Business Development and Lead Generation skills Strong Business acumen and strategic thinking Excellent Communication and interpersonal skills Proficiency in Account Management Proven track record in achieving sales targets Bachelor's degree in Business Administration, Marketing, or related field Relevant experience in the labeling and printing industry is a plus Show more Show less

Job Title: Manufacturing Executive - Reagent Manufacturing Location: Bangalore Company Overview: Cambrian designs and manufactures automated medical devices for precision diagnostics. We are dedicated to innovation, quality, and compliance in all aspects of our operations. Key Responsibilities: Prepare buffers and solutions according to pre-approved standard operating procedures (SOPs) and batch production records. Measure and weigh chemicals with precision using calibrated equipment. Accurately measure, mix, and prepare reagents according to standardized Formulation, procedures, and specifications. Perform Buffer Filtration. Monitor and adjust pH levels, as required, ensuring compliance with batch specifications. Assist in investigations and deviations related to buffer preparation processes. Operate within a classified cleanroom environment while adhering to proper aseptic techniques and gowning procedures. Maintain cleanliness of the workspace, ensuring compliance with GMP, GLP and ISO standards Perform manufacturing operations, such as automation machine setup & functional checks, periodic inspection of filling, and packaging, in a controlled clean room environment following standard work instructions. Adhere to strict gowning and de-gowning procedures to maintain cleanliness and prevent contamination of the clean room environmen t. Handle and transport materials, components, and finished products within the clean room environment, following proper procedures to prevent contamination and maintain product integrity Ensuring that the manufactured products meet quality standards by conducting visual inspections, measurements, and other quality checks as per SOP throughout the manufacturing process. I dentifying and addressing any issues that arise during the manufacturing process, such as equipment malfunctions or deviations from quality standards Performing routine maintenance and cleaning of production equipment to ensure optimal performance. Accurately complete manufacturing documentation, including batch records, log sheets, and inspection reports, to ensure traceability and compliance with regulatory requirements. Contributing to continuous improvement efforts by suggesting process enhancements, participating in problem-solving initiatives Adhere to safety protocols, clean room procedures, and regulatory guidelines, including Good Manufacturing Practices (GMP), Good documentation practices (GDP) and ISO standards, to ensure a safe working environment and product quality. Cleanroom Awareness and Knowledge Requirements: Comprehensive understanding of cleanroom classifications and respective standards. Adherence to aseptic techniques and sterile gowning procedures to maintain environmental integrity. Awareness of contamination sources (e.g., particulates, microbes) and methods to prevent them. Awareness of chemical handling procedures, including storage, labeling, and disposal within a controlled environment. Understanding of cleanroom behavior, such as minimizing movement, avoiding unnecessary contact, and following approved workflows. Compliance with entry and exit procedures, including airlock systems and gowning requirements. Commitment to ensuring that all processes within the cleanroom meet the highest standards for product hygiene and integrity. Execution of environmental monitoring and in-process quality checks to verify cleanliness and compliance. Awareness of the impact of personal and procedural hygiene on product safety and customer trust. QUALIFICATION: Bachelors in Biotechnology/Biochemistry or equivalent is typically required. F amiliarity with clean room protocols, gowning procedures, and cleanliness standards. 2-3 yrs of Experience in IVD or other related field Previous experience in buffer preparation, cleanroom operations is mandatory. Pr ior experience in manufacturing, Automated filling machinery. Experience in the medical device industry will be preferred. Physical requirements: · M anufacturing executives may need to stand for extended periods, lift heavy objects, and perform repetitive tasks. Languages required: · Kannada · English Benefits: Competitive salary commensurate with experience. Comprehensive benefits package including medical, dental, and vision coverage. 401(k) retirement plan with company match. Paid time off and holidays. Opportunities for professional development and advancement within the company. Show more Show less

Home Collection Technician – Job Description Company: QnQ Healthcare Pvt Ltd Location: Tirunelveli Job Type: Full-time Contact No: 7305013107 About Us: QnQ Healthcare is a leading healthcare provider with multiple business verticals, including QnQ Diagnostics , which operates across Tamil Nadu. Our diagnostics services are integrated with QnQ Pharmacy , ensuring convenient and quality healthcare for our customers. Responsibilities: Collect blood, urine, and other lab samples from patients’ homes. Ensure proper labeling, packaging, and safe transport to the lab. Maintain hygiene and follow safety protocols. Verify patient details and complete documentation. Provide excellent patient care and address queries. Requirements: Qualification: DMLT/BMLT or relevant certification. Experience: 1-2 years in phlebotomy/home sample collection (Freshers with training can apply). Skills: Venipuncture expertise, and customer handling. Other: Two-wheeler preferred, willingness to work flexible hours. Benefits: Competitive salary, Career growth opportunities To Apply: Send your resume to [balaji_hre@qnqhealthcare.in] or contact [8925362121]. Job Type: Full-time Pay: ₹15,000.00 - ₹18,000.00 per month Schedule: Day shift Education: Diploma (Preferred) Experience: Basic computer: 1 year (Preferred) total work: 1 year (Preferred) Pharmacist: 1 year (Preferred) Work Location: In person

Job Title: Graphic Designer –Nutraceutical Industry Location: Borivali, Mumbai Experience : 5-7 Years Salary – As per Industry Standard About Us: We're seeking a seasoned graphics designer, dedicated to creating high-quality health supplements, functional foods, and wellness products. We are seeking a creative and detail-oriented Graphic Designer to enhance our brand’s visual presence across various platforms. Job Responsibilities: Develop eye-catching packaging designs and labels for supplements, vitamins, and other nutraceutical products in compliance with regulatory guidelines. Create engaging marketing materials such as brochures, social media graphics, infographics, presentations, and advertisements. Design website banners, UI elements, and email templates to support online marketing efforts. Ensure brand consistency across all design projects, maintaining a professional and appealing aesthetic. Collaborate with the marketing, product development, and sales teams to translate ideas into compelling visuals. Stay updated on industry trends, competitor designs, and new technologies to enhance creative output. Work with printers, packaging vendors, and production teams to ensure high-quality printing and manufacturing outcomes. Qualifications & Skills: Bachelor’s degree in Graphic Design, Visual Arts, or a related field . 5+ years of experience in graphic design, preferably in the nutraceutical or food industries . Proficiency in Coreldraw, Adobe Creative Suite (Photoshop, Illustrator, InDesign, After Effects, etc.) . Strong understanding of packaging design, branding, and digital marketing materials . Ability to work on multiple projects simultaneously while meeting deadlines. Knowledge of FDA labeling requirements and industry standards is a plus. Experience with 3D rendering software (Blender, Cinema 4D, etc.) is a bonus. Why Join Us? Work in a growing industry focused on health and wellness. Opportunity to showcase creativity in a dynamic and evolving market. Competitive salary, benefits, and a positive work environment. Show more Show less

Key Responsibilities: Client Relationship Management Act as the single point of contact for assigned clients for all warehouse-related operations. Understand client business models, product categories, and order patterns. Conduct regular client meetings, calls, and reporting on performance, SLAs, and open issues. Order Management & Coordination Monitor daily order processing, pick-pack-ship operations, and ensure adherence to SLAs. Coordinate with warehouse supervisors and floor teams for priority or bulk orders. Track inventory levels, stock movements, and highlight replenishment needs to clients. Issue Resolution Manage escalations related to delayed dispatches, inventory mismatches, damages, or incorrect shipments. Collaborate with the operations team to investigate and resolve operational bottlenecks. Reporting & Analytics Share daily, weekly, and monthly reports with clients covering KPIs like order accuracy, fulfillment rate, returns, etc. Track service level agreements (SLAs) and ensure corrective actions for deviations. Process Improvement Identify gaps in warehouse processes that impact client service. Recommend improvements to enhance accuracy, speed, and client satisfaction. Documentation & Compliance Maintain updated documentation of processes, agreements, and communications with clients. Ensure compliance with client-specific packaging, labeling, or operational requirements. Job Type: Full-time Pay: ₹16,280.00 - ₹30,744.85 per month Benefits: Health insurance Provident Fund Schedule: Day shift Experience: Key account management: 1 year (Required) Location: Virgonagar, Bengaluru, Karnataka (Required) Work Location: In person Application Deadline: 28/06/2025 Expected Start Date: 01/07/2025

Company Description Raj Innotech Pvt. Ltd. is a leading company specializing in manufacturing, supplying, and exporting various water treatment projects, mineral water projects, juice turnkey projects, and carbonated soft drink turnkey projects. The company offers a range of packaging and labeling solutions for water, juice, and carbonated soft drinks. With a strong focus on quality and performance, Raj Innotech delivers equipment and services to clients worldwide. Role Description This is a full-time on-site role for a Business Development Executive located in Rajkot. The Business Development Executive will be responsible for new business development, lead generation, business communication, and account management on a day-to-day basis. Qualifications New Business Development and Lead Generation skills Strong Business Communication skills Experience in Account Management Excellent organizational and time management skills Ability to build and maintain client relationships Knowledge of the water treatment industry is a plus Bachelor's degree in Business Administration or related field Show more Show less

Job Summary: The Room Service Staff is responsible for the timely and hygienic delivery of meals to patients as per prescribed diets and schedules. This role ensures accurate meal distribution, maintains food safety standards, and provides courteous service to patients and hospital staff. Key Responsibilities: Deliver meals to patient rooms in accordance with dietary instructions and scheduled meal times. Verify patient details and diet orders before delivering food. Assist patients with meal tray setup if needed. Coordinate with the dietitian or kitchen staff for any special dietary needs, allergies, or changes in orders. Ensure food is served at the correct temperature and presented neatly. Retrieve used trays and utensils after meal times and return them to the canteen promptly. Maintain cleanliness and hygiene during food transport and service. Record meal delivery logs and report any discrepancies or patient feedback. Follow all infection control, food safety, and hospital hygiene protocols. Assist in packing and labeling meal trays accurately. Requirements: Minimum Higher Secondary / Diploma or equivalent. 1+ year of experience in food service, preferably in a hospital or healthcare environment. Knowledge of basic hygiene and food handling practices. Good interpersonal and communication skills. Physically fit and able to walk/stand for long periods. Polite, patient, and service-oriented attitude. Willing to work in shifts, including weekends and public holidays. Job Type: Full-time Pay: ₹10,000.00 - ₹13,000.00 per month Benefits: Food provided Schedule: Day shift Rotational shift Education: Diploma (Preferred) Experience: F&B: 1 year (Preferred) Location: Calicut, Kerala (Preferred) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Willingness to travel: 50% (Preferred) Work Location: In person Expected Start Date: 12/06/2025

Intercorp Biotech Group is a reputed manufacturer of high-quality products in Human Food Fortification, Personal & Home Care, and Animal Feed Supplements. We are committed to innovation, efficiency, and delivering impactful solutions to our customers. Job Summary: We are seeking an experienced and driven Sales Manager – Veterinary Products to lead our sales efforts in Animal Feed Supplements and Ingredients. The ideal candidate will bring a strong network within the poultry, cattle, and aquaculture feed sectors and a proven ability to build, manage, and grow key accounts across India. Key Responsibilities: Drive sales and expand the customer base for animal feed supplements across regions Build and maintain relationships with manufacturers of poultry, cattle, and aquaculture feed Develop and manage distributor/dealer networks and regional sales teams Conduct field visits with sales personnel and channel partners Formulate and execute marketing campaigns, sales schemes, trade offers, and product promotions Oversee design of packaging, labeling, marketing collaterals, and digital campaigns Conduct competitor analysis and gather market intelligence Manage product lifecycle including R&D coordination, market surveys, cost & pricing strategy, and new product introductions Stay updated on regulatory standards for veterinary products Travel 15–20 days/month as required to maintain field presence Preferred Experience: · Sales experience with feed supplements/ingredients targeted to poultry, cattle, and fish/aquaculture feed manufacturers · Familiarity with government e-procurement platforms like GEM and international procurement channels · Product management and marketing experience in animal nutrition or veterinary products Qualifications: · Bachelor’s degree in Business, Marketing, Animal Nutrition, Veterinary Science, or related field · 5+ years of relevant sales experience in animal feed or veterinary sector · Strong knowledge of animal nutrition, feed ingredients, and industry trends · Excellent communication, negotiation, and leadership skills · Ability to work independently and as part of a team · Strong problem-solving and analytical skills · Willingness to travel frequently Job Location- Tamil Nadu, Andhra & Telangana, Karnataka Job Type: Permanent Pay: ₹30,480.07 - ₹50,196.12 per month Benefits: Provident Fund Schedule: Day shift Language: English (Preferred) Work Location: In person

Intercorp Biotech Group is a reputed manufacturer of high-quality products in Human Food Fortification, Personal & Home Care, and Animal Feed Supplements. We are committed to innovation, efficiency, and delivering impactful solutions to our customers. Job Summary: We are seeking an experienced and driven Sales Manager – Veterinary Products to lead our sales efforts in Animal Feed Supplements and Ingredients. The ideal candidate will bring a strong network within the poultry, cattle, and aquaculture feed sectors and a proven ability to build, manage, and grow key accounts across India. Key Responsibilities: Drive sales and expand the customer base for animal feed supplements across regions Build and maintain relationships with manufacturers of poultry, cattle, and aquaculture feed Develop and manage distributor/dealer networks and regional sales teams Conduct field visits with sales personnel and channel partners Formulate and execute marketing campaigns, sales schemes, trade offers, and product promotions Oversee design of packaging, labeling, marketing collaterals, and digital campaigns Conduct competitor analysis and gather market intelligence Manage product lifecycle including R&D coordination, market surveys, cost & pricing strategy, and new product introductions Stay updated on regulatory standards for veterinary products Travel 15–20 days/month as required to maintain field presence Preferred Experience: · Sales experience with feed supplements/ingredients targeted to poultry, cattle, and fish/aquaculture feed manufacturers · Familiarity with government e-procurement platforms like GEM and international procurement channels · Product management and marketing experience in animal nutrition or veterinary products Qualifications: · Bachelor’s degree in Business, Marketing, Animal Nutrition, Veterinary Science, or related field · 5+ years of relevant sales experience in animal feed or veterinary sector · Strong knowledge of animal nutrition, feed ingredients, and industry trends · Excellent communication, negotiation, and leadership skills · Ability to work independently and as part of a team · Strong problem-solving and analytical skills · Willingness to travel frequently Job Location- Punjab & Haryana/ UP/ Rajasthan/ MP & Chhattisgarh Job Type: Permanent Pay: ₹30,480.07 - ₹50,196.12 per month Benefits: Provident Fund Schedule: Day shift Language: English (Preferred) Work Location: In person

Greetings from TATA Consultancy Services Job Openings at TCS Skill :BACKUP ADMIN Exp range :12 to 18 years+ YEARS Role : Permanent Role Job location :CHENNAI/HYDERABAD/BANGALORE Current location : Anywhere In India Interview date :11th Jun 25(FRIDAY)10:00 AM to 12:00 PM IST/ 30 MINS Interview mode : MS Teams Pls find the Job Description below. Architecture & Design Commvault Environment & Data center Administration • Planning & Design the Backup Network architecture (for Cloud and/or on prim) • Planning and provided the Backup solution for New Customer • Backup DR setup for New customer • Tape Library Implementation • Tape Drive setup • Tape Labeling Setup for Different Customer • Iron Mountain Account setup for All the region • SAN configuration from Commvault depends upon FRONT END DATA • Commvault License Procurement • Commvault Vendor Setup with different Regions • Migrate Backed up Data from One Storage to Another Storage from Commvault • Migrate De-duplication data from one Disk to other Disks • Physical Hardware Implementation (Network, Storage, Compute etc.) • RACK implementation • DC Cabling and Patch Panel Implementation Backup Operation Activity • COMM server Installation with Different Customers with DR SETUP (Stand-BY COMM server) • Setup Global Deduplication Policies & Storage Policies • Client Module installation and configuration and scheduling as per Customer requirement. • Building Media agent as per requirement from Customer • Managing User Access to Different Customers • Monitoring Backups and Performance from Commvault • Troubleshooting the performance issues • Disk space management on the media agent and handling dedup backup • Retention policy management via Primary/secondary copy policy. • Vault tracker policy management (tape handling) • Tape Library & Drive configuration • Drive Slot Assigning • Setting Up (Installation and configuration) and managing DB Backups (RMAN, SQL, SYBASE, Exchange) and NDMP Backup. • Setting up Backup in SQL Cluster Environment. • Setting Up and maintain Backup In Oracle RAC Server. • Setting Up VMWARE snapshot backup On Commvault. • Managing VMWARE Snapshot Backups and Restore operations. • Backup using Snap-Protect operations In VNX/Clarion. • Media resource management (Media Agent, Disk and Tape Library, Media) • Managing Firewall and communication issues efficiently. • Managing capacity license and troubleshooting license issues • Monitoring Drives and Devices. • Configuration/de-activation of backup policies for new and de-commissioned clients. • Configuring tape drives/ tape drive cleaning and stuck media removal. • Troubleshooting failed backups within SLA timeline and re- run the backups • Perform the restores for System state, Exchange servers, databases and File System restores for Windows and UNIX servers. · Perform 1 Touch Restores • Upgrading service pack for all the clients in a timely manner. • Commvault Version upgrade for backup server and clients in timely manner • Handling various backup failures and logging case with Commvault vendor • DR plan execution • Troubleshooting Deduplication database issues • Pro-actively monitor for the slow backups, Hung jobs, long queued Jobs in the environment and take necessary action. • Strive for customer satisfaction while doing the restores. Keeping the tickets with updated status of with all the activities, take care of SLA of all the tickets and Update the customer regularly about the work we are doing on the respective restore tickets. • Collaborating with other teams, users, clients onsite/offsite facilities and vendors like Iron Mountain, Symantec, HP etc. • Send reports to top management after analyzing the performance of critical servers Thanks & Regards Priyanka Talent Acquisition Group Tata Consultancy Services Show more Show less

Work location: Mumbai & Bangalore Role & responsibilities Develop US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s, if required, and for early development projects requiring a human factor or comparative analysis study to ensure labeling meets all legal and regulatory requirements. This includes QC, proofing, editing, and formatting of documents, and coordinating the review and approval of final submission documents documents with all relevant departments. Develop labeling content that requires carve-outs due to protected language associated with patents/exclusivities. Serve as a Subject Matter Expert (SME) in all facets of SPL/drug listing, including but not limited to finished product, bulk, and manufacturer under contract. The SME must be able to provide guidance to other team members related to established SPL documents (content and data elements) to ensure alignment with associated applications and applicable FDA regulations and guidance, as well as troubleshoot any validation errors received. Work closely with the SPL Vendor, as well as the FDA Drug Listing team, on any drug listing issues, ensuring a rapid resolution. Prepare and electronically compile full responses to the FDA via the appropriate filing mode. This includes but is not limited to the development of side-by-side comparisons, SPL, and other required submission materials, as necessary. Perform quality reviews of labeling and submission documents by proofreading established files for content accuracy, either manually or by utilizing the electronic proofreading tool TVT. Work closely with external departments, including the CMC and Device teams, to align with internal product/device strategy and processes. Work closely with Regulatory Operations, as well as in Teva’s publishing software, to ensure assigned projects are submitted on time following the eCTD requirements related to labeling. Support products falling under Business Development deals, if required, from a labeling/artwork and drug listing perspective. Attend assigned project meetings to ensure labeling timelines are met. Maintain an accurate project tracker of all assigned projects with identified due date priorities and timelines of initial assignment, initiation, and completion of projects. Provide support to the Manager, as needed, in completing the year-end FDA Mandated Blanket No Change certification. This ensures all drug product listings remain active within the agency's National Drug Code (NDC) Directory, preventing potential issues such as disruptions in the market, Medicaid rebates, and other regulatory complications. Assist in the training of new labeling personnel. Maintain knowledge of US regulations, guidelines, and standard operating procedures applicable to US Gx labeling and drug listing. Work in a team environment. Perform all other job-related duties as required by management and dictated by process changes. Experience & Qualification: 7-9 years experience in the Pharmaceutical Industry. Min 6+ years of RA experience will be preferred in the respective Markets. Bachelors in Pharmacy/Master in Pharmacy/Master in science & Life sciences Be able to multi-task in a fast-paced work environment. Possess in-depth knowledge of US FDA regulations and guidance documents related to US Gx labeling and drug listing. Possess in-depth knowledge of US FDA eCTD submission standards and demonstrate experience in applying these requirements to routine labeling submissions. Proficiency with PC and Microsoft Office Suite, including Microsoft Word and Microsoft Excel. Thorough knowledge of Structured Product Labeling software. Proficiency in Adobe Acrobat Professional is a must. Interested candidate can share their CV to ankita.sonawane@teva.co.in Show more Show less

URGENT OPENING Currently We required Manager - regulatory Affairs for Medical Device company. JD-Manager- Regulatory Affairs Plant office - Medical devices 52-54,63&64, Roz ka meo , Industrial Area, Nuh , District. Mewat ( Haryana), India Company will provide you the cab facility from Fix point of Gurugram & Faridabad Working Daya - 6 days in a week The candidate Profile and the job description is as follows - · The Company has state of art manufacturing facility and its own R & D facility with 10,000 and 1,00,000 Class room specifications with continuous innovations and thereby offering customized products as per the requirements of various markets in India and abroad. · The Company is accredited with the following standards – a) ISO 9001 : 2008 b) ISO 13485 : 2003 ( EN) c) Directive 93/42/EEC (CE) d) Registration certificate with Dept of Health & Human Services, USA e) GMP Certificate as per schedule M. f) DGQA registered · The Company is having strong presence in almost all the Corporate Hospitals across India besides Trade, Military, Para-Military forces and in prestigious Government institutions. · The Company markets under its own brand name in International markets like UAE, Oman, Sri Lanka, Nepal and Bangladesh and besides being an OEM supplier to various MNCs for the entire Europe, Australia, New Zealand, South Africa etc. · Company’s product range includes various types of high quality gauze and bandage products besides some unique products in the Advance Wound Care segment which are being exported to major companies in Europe as well as to Australia, New Zealand, Middle & Far East and South Africa. Key responsibilities: Spearheaded regulatory submission strategy for CE marking under EU MDR for Class IIa, IIb & III devices. Authored and maintained FDA 510 (K) submission, including predicate device comparison and labeling review. Developed and maintained Technical Files and Design Dossier for European markets. Coordinated Clinical Evaluation Reports (CER) and Periodic Safety Update Reports (PSUR). Acted as point-of-contact for notified bodies and regulatory authorities during audits and inspections. Implemented and maintained ISO 13485:2016-Compliant QMS, prepared company for successful MDSAP audit. Developed and maintained company-wide QMS in compliance with ISO 13485:2016 AND 21 CFR 820. Conducted risk management activities as per ISO 14971:2019 and ISO/TR 24971:2020, including, AFAP, FMEA and Hazard Analysis. Led PMS activity (Plan, Report and arrange the feedback, sales data and other regulatory requirements from Marketing team). Prepare documents related to the Post Market Surveillance, General Safety and Performance Requirement (GSPR) Risk Management process of Class III medical devices as per MDR 2017. Plz Mention your Current CTC - Expected CTC - Notice period- Date of Birth- And ready for relocate - Regards, Khushi Asthana HR Manager Pratham Search Job Types: Full-time, Permanent Pay: ₹70,000.00 - ₹100,000.00 per month Benefits: Cell phone reimbursement Food provided Health insurance Provident Fund Work Location: In person

Company Description Cosmetify, one of the top 5 Cosmetic manufacturers in India, specializes in third-party contract manufacturing for skincare, haircare, and personal care products. We offer private labeling and custom formulations, with years of experience and a dedicated team of professionals committed to ensuring the success of your brand. Role Description This is a full-time on-site role for a Business Development Manager at Cosmetify.in in Panchkula. The Business Development Manager will be responsible for identifying new business opportunities, building and maintaining customer relationships, and developing growth strategies to expand the company's market presence. Qualifications Strong sales, negotiation, and business development skills Experience in the cosmetic industry or related field Ability to understand customer needs and build productive relationships Excellent communication and presentation skills Knowledge of market research and analysis Ability to work with targets Ability to handle a Team Bachelors/Masters degree in Business Administration, Marketing, or related field P.S- Prior experience in cosmetic third party manufacturing will be Preferred. Job Types: Full-time, Permanent Pay: ₹50,000.00 - ₹60,000.00 per month Benefits: Paid sick time Paid time off Schedule: Morning shift Supplemental Pay: Commission pay Experience: Cosmetic Third party Manufacturing: 2 years (Required) Language: English (Required) Location: Panchkula, Haryana (Required) Work Location: In person

Company Description At Color Theory, creativity defines our essence in the color-cosmetics industry, we are a leading color cosmetics manufacturing company that celebrates innovative beauty. We collaborate with global brands to craft bespoke makeup products using premium-quality formulations. Our 140,000 sq. ft. plant in India is equipped with fully automatic machines, clean room operations, and in-house R&D labs, all certified by GMP and FDA. We specialize in contract manufacturing and private labeling, transforming client ideas into reality while championing sustainable and eco-conscious practices. Role Description This is a full-time, on-site role for a Senior R&D Manager Color Cosmetics - Formulations, based in Vadodara. The role involves leading the R&D team to develop new cosmetic formulations, overseeing research projects, managing team activities, and ensuring projects are completed within deadlines. The manager will foster innovation, maintain high product quality, and keep up with industry trends. Qualifications Experience in Research and Development (R&D) and conducting Research Strong Team Management and Team Leadership skills Proficiency in Project Management Excellent problem-solving skills and attention to detail Bachelor's or Master's degree in Chemistry, Cosmetic Science, or related field Previous experience in the cosmetics industry Ability to work collaboratively in a fast-paced environment Show more Show less

Location: CHENNAI, Chhattisgarh, IN, 602106 Req ID: 88417 Facility: Chennai-470 Department: Production Team A Division: Global APS Production Technician Basic Function Be responsible for activities include line start up, product verification, labeling, weighing stitching and stacking Continuously improve performance on safety, quality and productivity Roles & Responsibilities Assure daily operation is in line with HSE requirement. Keep good housekeeping in Shop floor to maintain workplace in a required basic condition. Manage the day to day activities include line start up, changeovers, Weighing scale verification, labeling, weighing sealing and Stacking with quality of product. Ensure Zero error in weighing of FG & reduce pellet loss. Responsible for recording to verify each and every finished bags such as cross contamination, stitching and stacking of finished Goods with zero defect in Quality of product. Recording data as per audit requirements of ISO : 9001 : 2015, IATF 16949 : 2016, EMS 14001 : 2015 and MIS reporting (daily, weekly and monthly). Performs the duties of the handover in the production department Min. Qualifications Diploma in any Engineering stream from reputed college. Work Experience 1 - 2 years' experience of relevant industries. Critical Competencies/Behaviors Prudent and enthusiastic. Physical and mental health-You should be physically and mentally fit to perform your job responsibility. Colour blindness- you should not have colour blindness. Competencies Build Partnerships Deliver Results Drive Innovation Grow Capabilities Promote Inclusion Motivational Fit Technical Skills

NOTE : Candidates with only Telangana PCI can apply. Key Responsibilities: Dispense medications accurately based on prescriptions. Review and interpret prescriptions from doctors. Counsel customers on dosage, usage, and possible side effects of medications. Maintain records of prescriptions, stock, and controlled drugs. Ensure proper storage and labeling of all medications. Maintain cleanliness and organization in the pharmacy. Support pharmacy billing and inventory management systems.

Key Responsibilities: Inventory Management: Maintaining accurate records of stock levels, ensuring optimal stock levels to avoid overstocking or shortages. Receipt and Storage: Receiving, inspecting, and verifying pharmaceutical shipments, ensuring proper storage and labeling, and maintaining a clean and organized storage area. Dispatch and Issue of Goods: Facilitating the dispatch of finished products and ensuring materials are issued efficiently. Record Keeping: Maintaining accurate records of all received and dispatched goods, as well as inventory movement. Compliance and Audits: Ensuring compliance with all relevant regulations (e.g., GMP, GHP) and maintaining readiness for audits. Coordination: Coordinating with other departments (e.g., procurement, accounts) for smooth operations. Team Management: (If applicable) Training and supervising store staff, ensuring efficient workflow. Material Handling: Overseeing the receipt, inspection, storage, and issue of materials. FIFO/FEFO: Ensuring the implementation of FIFO (First In, First Out) or FEFO (First Expire, First Out) principles for inventory management. Additional Skills: Strong organizational and communication skills: Essential for managing inventory, coordinating with other departments, and communicating with staff. Attention to detail: Required for accurate record keeping and inventory management. Knowledge of relevant regulations: (e.g., GMP, GHP). Basic understanding of ERP systems: (if applicable). Good people management skills: (if supervising staff).

The Packaging Supervisor oversees and manages all packaging activities for 3D printing filament products, ensuring efficiency, quality, and timely dispatch. This role requires strong attention to detail, knowledge of packaging standards for technical products, and team leadership abilities. Key Responsibilities:Supervise and coordinate day-to-day packaging operations of 3D printing filament spools. Ensure accurate labeling, spooling, sealing, and boxing in compliance with product specifications and quality standards. Monitor packaging line efficiency and minimize downtime. Manage and train packaging staff to meet productivity and safety goals. Implement standard operating procedures (SOPs) and ensure compliance with ISO, QC, and safety guidelines. Collaborate with quality control and production departments to address defects or inconsistencies. Maintain inventory of packaging materials and request timely replenishment. Keep detailed records of production output, material usage, and shift reports. Coordinate with dispatch/logistics for shipment scheduling and documentation. Drive continuous improvement initiatives in packaging design, waste reduction, and process automation.

Position: Store Helper Location: Arcadia sector 49 Job Timing : 9:00AM to PM 9:00 Employment Type: Full-Time Salary: 12000 to 17000 per month Reports To: Store Owner Role Overview : The Store Helper supports daily retail operations by assisting with stocking, organizing, and maintaining the store environment. This role ensures a positive shopping experience for customers and contributes to the store's overall efficiency. Key Responsibilities Customer Assistance: Greet and assist customers in locating products, providing information, and answering queries. Stock Management: Restock shelves, organize products, and ensure proper labeling and pricing. Inventory Support: Assist in inventory counts, report discrepancies, and help with stock replenishment. Store Maintenance: Maintain cleanliness and orderliness of the store, including sweeping, mopping, and organizing displays. Product Handling: Unpack and arrange new stock deliveries, ensuring products are stored appropriately. Checkout Assistance: Support cashiers during peak hours by packing items and assisting with transactions. Safety Compliance: Ensure adherence to safety protocols and report any hazards or issues Qualifications Education: Minimum 10th grade Experience: Previous experience in retail or customer service is advantageous but not mandatory. Skills: Basic math skills, attention to detail, and ability to operate basic point-of-sale (POS) systems. Physical Requirements: Ability to stand for extended periods and lift moderate weights. Personal Attributes Customer-Oriented: Friendly and approachable demeanor with a focus on customer satisfaction. Team Player: Collaborative attitude and willingness to assist colleagues. Adaptable: Ability to handle varying tasks and work in a dynamic retail environment. Reliable: Punctual and dependable with a strong work ethic. BenefitsCompensation: Competitive salary with performance-based incentives. Work Schedule: Flexible hours, including weekends and holidays as required. Growth Opportunities: Potential for advancement within the retail organization. Employee Discounts: Discounts on store products and services. Health & Safety: Adherence to health and safety regulations to ensure a safe working environment.

Job Title: AI/ML Developer Location: Bangalore Experience: 4+ Years CTC: Up to 30 LPA Industry: AI Product Key Responsibilities: -Design and deploy ML models focused on NLP and Computer Vision. -Handle data labeling, preprocessing, and model validation. -Assist in API development to integrate ML models into apps. -Fine-tune and train models to improve performance. -Collaborate with teams to deliver practical AI-driven solutions. -Maintain documentation of model processes and outcomes. Required Skills & Qualification: -4+ years in AI/ML development with hands-on work in NLP or CV. -Strong Python skills with libraries like TensorFlow, PyTorch, scikit-learn. -Experience in data preprocessing and model deployment. -Exposure to cloud platforms (AWS/GCP/Azure) is a plus. -Familiarity with MLOps and API integration is desirable. -Degree in Computer Science, Data Science, or related field. -Knowledge of big data tools (Spark/Hadoop) or other languages (R/Java/C++) is an advantage. Show more Show less

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description: Objective / Purpose : This is a key position in GI2 TAU clinical science to accelerate the drug development in India, and belongs to organization of RnD China & APAC. This role is the local clinical lead to drive the drug development from clinical development strategy establishment to local registration in India as member of China Asia Development Team, with close collaboration with cross function team members of CADT, India Development Lead, India business operation and other relevant global and local stakeholders. In some cases, the scope may be extended to other Asia countries/regions besides India based on the business needs. Leads and drives local strategy and clinical development plan taking into consideration the medical, scientific, regulatory and commercial issues for the assigned Takeda pipeline compound(s) in GI2. Interacts with and influences Takeda’s senior leadership decision-making by setting strategic direction locally. Cultivates and manage relationships with local KOLs and investigators. Play a crucial role as the local clinical lead for the assigned studies, including the development of study concept, synopsis, protocol, booster enrollment engagement activities, study conduction, databased lock, data interpretation, and etc. Applies clinical expertise as the local clinical lead for the CTA, NDA, and the interaction with local Health Authorities. Accountabilities : Clinical Development team participation and leadership: Leads and drives local clinical development strategy and deliverables for GI2 pipeline assets, including the Development Strategy, Clinical Development Plan and Clinical Protocols. Provides continual critical evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans to meet regulatory submission and approval goals locally. Leads or supports high impact decisions based on strong clinical/scientific expertise as well as leadership monitors and interprets data from ongoing internal and external studies, assessing the medical and scientific implications, and making recommendations that impact local and global development such as “go/no go” decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling. Synopsis / Protocol Development, Study Execution & Study Interpretation: Drives clinical science activities relating to the preparation / approval of synopsis, protocols and the conduct of clinical studies. Accountable for the successful design and interpretation of clinical studies. Presents study conclusions to Management and determine how individual study results impact the overall compound strategy. Interprets data from an overall scientific standpoint as well as within the context of the medical significance to individual patients. Booster enrollment activities and: Trial Medical Monitoring: Provides strong supports to the local booster enrollment activities from clinical perspective Responsible for medical monitoring activities, assessing issues related to protocol conduct and/or individual subject safety. Assesses safety information for studies and compound in conjunction with Pharmacovigilance. External Interactions: Directs activities involved in interactions with local regulatory authorities / agencies and clinical development activities undertaken to establish and maintain strong relationships with local key opinion leaders. Leads collaboration with academia, local development network to advance drug development in India. Lead roles will also be taken on the incorporation of advice / recommendations received into the design of clinical studies/programs as appropriate, and ensuring these activities are aligned with the RnD China&APAC region and global strategy .: : Due Diligence, Business Development and Alliance Projects: May participate in due diligence evaluations, and development and negotiation of clinical development plans for potential alliances and or in-licensing opportunities. Assesses scientific, medical, and development feasibility, evaluating complete or ongoing clinical trials, assessing local regulatory interactions and future development plans, and representing clinical science on internal assessment teams in conjunction with other parts of the organization. Leadership, Influence, Leading Capability Development: , Communication and Collaboration Capability Development,: and M: ultidisciplinary Task Force: Demonstrates strong leadership and clinical/scientific expertise to influent key internal stakeholders from RnD China & APAC and global about pipeline/compound strategy and decision making. Proactively leads TA capability development by coaching and mentoring to local team members; advocates and creates share-learning and growth supportive environment. Proactively leads and contributes in multidisciplinary task forces on across divisions representing clinical science to increase local team/organization capability and efficiency. Embraces innovation, diversity and inclusive culture in teams/organization and leading as a local role model, brandings RnD China&APAC on behalf of GI2 Clinical Science team. Keep strong communication and collaboration capability with the team members to ensure high quality and timely deliverables. Education & Competencies : MD or internationally recognized equivalent plus minimum 15 years of clinical practice and/or research experience. Direct experience in GI2 therapy pharmaceutical development, or related field required Previous experience of influencing senior-level management and key stakeholders is a plus Previous experience successfully leading a clinical development team/matrix team with responsibility for studies in India. The experience in other Asia countries/regions is a plus. Fluent in English and Indian. NDA/MAA/Submission experience preferred Management experience Excellent communication and collaboration skills Models the Takeda Leadership Behaviors Locations: IND - Bengaluru Worker Type: Employee Worker Sub-Type: Regular Time Type: Full time Show more Show less

Key Responsibilities: Manage daily store operations at the site including material inward/outward. Receive and inspect all incoming materials as per PO and delivery challans. Maintain stock registers (manual/digital) and update daily reports. Issue materials as per site requirements and keep track of usage. Ensure proper storage, labeling, and stacking of materials. Coordinate with the HO Store/Procurement team for replenishments and returns. Handle GRN (Goods Receipt Note), vendor bill verification, and reconciliation. Maintain documentation for audits and compliance. Manage scrap and unused materials as per company policies. Maintain safety and cleanliness at the store. Job Types: Full-time, Permanent Pay: ₹35,000.00 - ₹45,000.00 per month Benefits: Food provided Health insurance Leave encashment Provident Fund Schedule: Day shift Morning shift Supplemental Pay: Performance bonus Yearly bonus Work Location: In person

Job Title : Executive – Store Assistant Location : Gandhidham, Gujarat Industry : Manufacturing Department : Store / Inventory Management Experience : 1–2 years (Manufacturing industry – Store Department) Qualification : Graduate (Mandatory) Salary : ₹18000-25000 Per Month Key Responsibilities : Assist in receiving, storing, and issuing raw materials, spare parts, and finished goods Maintain accurate inventory records using software or manual systems Conduct physical stock verification and reconcile discrepancies Ensure proper tagging, labeling, and systematic storage of materials Prepare GRNs, issue slips, and related store documentation Coordinate with procurement, production, and accounts departments Maintain cleanliness, safety, and organization of the store area Assist in monthly/yearly stock audits Skills Required : Basic knowledge of storekeeping and inventory control Proficiency in MS Excel, ERP software (preferred) Good communication and coordination skills Accuracy in documentation and attention to detail Ability to work in a team and under supervision Contact: 9904582301 / 6358812301 Email your resume to: resume@theactivegroup.in Job Type: Full-time Pay: ₹18,000.00 - ₹26,000.00 per month Schedule: Rotational shift Language: English (Preferred) Shift availability: Day Shift (Preferred) Work Location: In person

Job Title : Packing Operator Location : Gandhidham, Gujarat Department : Packing / Production Industry : Manufacturing / FMCG / Edible Oil Salary : ₹18,000 – ₹32,000 per month Experience : 1+ Year Qualification : 10th Pass / 12th / ITI (preferred) Key Responsibilities : Operate packing machines to pack finished products as per company standards Ensure correct labeling, weighing, and sealing of packed products Maintain cleanliness and hygiene of packing area Inspect packaging materials for quality and report any issues Coordinate with production and warehouse teams for timely packing and dispatch Follow safety and quality guidelines during packing operations Record daily packing output and report to supervisor Skills Required : Basic knowledge of packing machines and operations Ability to work in a fast-paced production environment Attention to detail and quality-conscious Good teamwork and communication skills Contact: 9904582301 / 6358812301 Email your resume to: resume@theactivegroup.in Job Type: Full-time Pay: ₹18,000.00 - ₹32,000.00 per month Schedule: Day shift Work Location: In person

Company Description 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 We are seeking a highly skilled Regulatory Affairs Professional specializing in biosimilar combination products (drug-device combinations). This role will be responsible for developing and executing global regulatory strategies for combination product devices, ensuring compliance with evolving regulatory requirements from agencies such as the FDA, EMA, MHRA, and other global health authorities. Qualifications 5+ years of regulatory affairs experience in biosimilars, biologics, or combination product development. Additional Information Provide regulatory guidance on device design, human factors, risk management, and manufacturing considerations. Lead and coordinate regulatory submissions for biosimilar combination products, including IND, BLA, and EU MDR filings. Ensure accurate regulatory documentation for design control, risk assessment, usability studies, and post-market surveillance. Work closely with R&D, Quality, Clinical, and Manufacturing teams to align regulatory strategies with product development. Support design verification and validation activities, including human factors engineering (HFE) and risk management. Provide regulatory support for product lifecycle management, including manufacturing changes, labeling updates, and device modifications. Show more Show less