2562 Labeling Jobs - Page 11

Job Title: Inventory / Warehouse Executive Location: Mohali, Punjab Company: Whispering Homes Pvt. Ltd. Job Type: Full-Time Experience Required: 1–3 years (experience with Zoho Inventory is mandatory) Working Days & Hours: Monday to Saturday | 09:00 AM to 06:00 PM About the Role: Whispering Homes Pvt. Ltd. is seeking a detail-oriented and proactive Inventory/Warehouse Executive to oversee daily warehouse operations and maintain accurate inventory records. The ideal candidate must have prior hands-on experience using Zoho Inventory and a good understanding of dispatch and logistics processes. This role is critical to ensuring smooth backend operations and timely order fulfillment. Key Responsibilities: Manage and monitor all incoming and outgoing stock activities. Maintain real-time and accurate inventory data using Zoho Inventory. Coordinate with procurement, sales, and dispatch teams to align inventory levels with business needs. Supervise packaging, labeling, and timely dispatch of customer orders. Conduct periodic stock audits and reconcile any discrepancies. Ensure proper storage, organization, and safety of inventory items. Prepare and share regular inventory reports with the management. Track damaged, returned, or misplaced items and report accordingly. Monitor warehouse cleanliness and ensure adherence to safety protocols. Candidate Requirements: Graduate in B.Com, BBA, or a relevant field. Minimum 1 year of hands-on experience using Zoho Inventory (must). Strong command over MS Excel and basic inventory reporting. Good knowledge of logistics and courier platforms (e.g., Shiprocket, Delhivery). Ability to manage warehouse operations independently and efficiently. Strong attention to detail, organization, and problem-solving skills. Preferred Background: Candidates with prior experience in e-commerce, retail, home décor, or logistics sectors will be preferred. Compensation & Benefits: Salary: ₹18,000 – ₹22,000 per month (based on experience and skills) Benefits: PF, ESI, Paid Leave, Employee Discount Reporting To: Operations Manager How to Apply: Email your updated resume to hr@whisperinghomes.com Call/WhatsApp us at 82649 49048 Note: Only candidates with proven experience in Zoho Inventory will be considered. Please do not apply if you do not meet this requirement. Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹25,000.00 per month Benefits: Provident Fund Schedule: Day shift Work Location: In person

Export Sales & Marketing Manager – Oil Location: Bandra, Mumbai | Salary: Up to ₹20 LPA | Experience: 10–25 yrs in oil exports (mandatory) | Qualification: Graduate + MBA (Marketing) Role Overview Drive global exports of Base Oil, White Oil, Liquid Paraffin, and Transformer Oil across Latin America, MENA, Europe, Africa & Asia. As an individual contributor reporting to the Sr. VP Sales / CMD, you’ll lead strategy, business development, and execution. Key Responsibilities Develop and implement export sales plans; generate leads through brokers, trade shows, and direct outreach.Identify and enter new markets; negotiate pricing, contracts, and terms.Define technical specs with engineering; ensure export regulatory compliance (documentation, labeling, transport, payments).Work with supply chain and logistics to control costs and ensure timely shipments. Candidate Profile Extensive export experience in Base Oil/Paraffin/Transformer Oil.Knowledge of international trade laws, export documentation, incoterms.Strong negotiation, analytical, and communication skills.Global mindset and ability to work independently. Skills: marketing,sales,oil based company,negotiation,export,business development,incoterms,communication skills,export sales,export documentation,analytical skills,knowledge of international trade laws,b2b

Job Title: Store Keeper – Food Industry Location: Calicut, Kerala Experience Required: Minimum 1 year (specifically in the food industry) Gender Preference: Male Salary Range: ₹15,000 – ₹22,000 per month Industry: Food & Beverage / Food Processing / Hospitality Key Responsibilities: Receive, inspect, and store food items and supplies in compliance with hygiene and safety standards. Maintain accurate inventory records and update stock levels regularly. Follow FIFO (First-In, First-Out) and FEFO (First-Expired, First-Out) principles in stock rotation. Ensure proper labeling, packaging, and storage of perishable and non-perishable items. Monitor temperature and storage conditions as per food safety norms. Coordinate with procurement and kitchen/production teams for timely stock issuance and replenishment. Conduct daily/weekly stock audits and report discrepancies. Maintain cleanliness and orderliness of the storage area as per food safety regulations. Candidate Requirements: Minimum 1 year of experience as a Store Keeper in the food industry . Knowledge of inventory and stock management practices specific to food items. Familiarity with basic food safety and hygiene standards (FSSAI guidelines preferred). Good organizational and communication skills. Physically fit and capable of handling stock movement. Education: SSLC / Plus Two / Diploma. Preference for candidates based in or around Calicut . Interested candidates are requested to share your updated resumes to mdjinitha@gmail.com Job Type: Full-time Pay: ₹15,000.00 - ₹22,000.00 per month Schedule: Day shift Work Location: On the road

Location: Shahad, Ulhasnagar, Maharashtra (On-site) Type: Full-time | 12-hour shift (8:00 AM – 8:00 PM) Weekly Off: Fridays Salary: ₹14,000 – ₹20,000/month (based on experience & performance) Apply via: Email: ankita@maxnarrowfabrics.com WhatsApp: 9930256979 About Us Max Narrow Fabrics is an MSME manufacturing unit specializing in precision-engineered elastic narrow fabrics for leading industries across India. As we scale our operations, we are actively building robust systems, and we’re looking for team players who are hands-on, adaptable, and ready to grow with us. Role Overview: Factory Stock Executive We are hiring a Factory Stock Executive who will be fully responsible for the stock management of our factory —including raw materials, finished goods, machine parts, packaging materials, and spares . This role is central to ensuring smooth operations across production, storage, and dispatch. The ideal candidate is energetic, responsible, and not afraid to get involved in day-to-day physical and operational work . This is a ground-level yet growth-oriented role for someone who wants to be part of building something meaningful. Key Responsibilities Oversee inward and outward stock movement of all factory materials. Maintain accurate manual and system-based stock records (raw materials, packaging, finished goods, machine parts). Manage stock entry, exit logs, and daily bookkeeping . Coordinate with the production and dispatch teams to ensure timely material availability. Monitor stock levels and raise alerts for low inventory or overstock situations. Ensure proper stacking, labeling, and cleanliness in the store area. Handle documentation: delivery challans, gate passes, GRNs, e-waybills (where required). Assist with monthly and quarterly physical stock audits . Report daily stock status to management. Candidate Requirements 1–3 years of relevant experience in inventory, factory storekeeping, or warehouse roles. Freshers can apply - (3 month on job training (Salary will be fixed accordingly)) Basic working knowledge of stock registers or inventory tools (Excel/Vyapar preferred; training will be provided). Physically fit and comfortable with on-ground, hands-on work . Good organizational and record-keeping skills. Punctual, responsible, and willing to work independently. Minimum education: SSC / HSC / ITI / Diploma (preferred). Shift & Benefits Shift Timing: 8:00 AM to 8:00 PM (12 hours) Weekly Off: Every Friday Salary on full 30-day month basis (no deductions for company-declared holidays) Yearly salary hike based on performance Yearly bonus Overtime pay when applicable Opportunity to grow with a fast-growing MSME manufacturing unit What We’re Looking For This is not a desk-only role. We're building a strong operational foundation, and we need someone who: Is dynamic, proactive, and ready to take charge Doesn’t shy away from work , whether it's physical or process-driven Wants to grow long-term with a company that values contribution and accountability To Apply Email your CV to: ankita@maxnarrowfabrics.com Or WhatsApp: 9930256979 Job Types: Full-time, Permanent Pay: ₹14,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Commuter assistance Internet reimbursement Schedule: Day shift Fixed shift Supplemental Pay: Overtime pay Yearly bonus Ability to commute/relocate: Ulhasnagar, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Location: Ulhasnagar, Maharashtra Job Types: Full-time, Permanent, Fresher Pay: ₹14,000.00 - ₹20,000.00 per month Benefits: Cell phone reimbursement Commuter assistance Internet reimbursement Ability to commute/relocate: Shahad, Thane, Maharashtra: Reliably commute or planning to relocate before starting work (Preferred) Location: Shahad, Thane, Maharashtra (Preferred) Work Location: In person

Master of Marketplace Panels? We Want You! Location:- Marol, Andheri. About the Role:- Oversee end-to-end order processing across multiple marketplaces, ensuring timely invoicing, labeling, and dispatch coordination with the warehouse. Manage marketplace seller panels like Amazon and Flipkart for order tracking, cancellations, and status updates. Coordinate daily pickups with courier partners and handle any delivery exceptions. Monitor stock levels, reconcile inventory, and support audits. Handle returns and RTOs by ensuring timely inspection, restocking, and maintaining logs for damages and complaints. Role & Responsibilities:- 1. Order Processing & Fulfillment Monitor and process daily orders received from various marketplaces. Ensure timely creation of shipping labels and invoices. Coordinate with the warehouse team to prioritize order picking, packing, and dispatch. 2. Marketplace Panel Operations Operate seller panels like Amazon Seller Central, Flipkart Seller Hub, etc., for order management. Track shipment status, update dispatches, and handle cancellations or hold orders. 3. Coordination with Courier Partners Schedule daily pickups with courier partners. Share pickup manifests and confirm handover of shipments. Follow up with logistics partners in case of missed pickups or delays. 4. Stock & Inventory Monitoring Regularly reconcile inventory on marketplaces with physical stock. Notify the supply or purchase team in case of low stock alerts. Assist in basic warehouse audits if needed. 5. Returns & RTO Handling Track return orders and RTOs (Return to Origin) for each marketplace. Coordinate with the warehouse team for inspection and restocking of returned products. Maintain proper logs for damages and customer complaints related to returns. Skills:- 1. Basic Knowledge of E-commerce Logistics 2. Excel & Google Sheets Proficiency 3. Marketplace Panel Navigation 4. Data Entry & Documentation 5. Coordination & Teamwork

Prepare, compile, and review CTD/eCTD dossiers for submissions (e.g., ANDA /NDA /MAA). Coordinate with cross-functional teams (QA, QC, R&D, Manufacturing, Packaging) for accurate documentation. Submit applications to US FDA, EMA, and other authorities in compliance with regional requirements. Compile and validate submissions using tools such as Extedo, Lorenz docuBridge, or equivalent. Ensure completeness and technical accuracy of eCTD sequences. Troubleshoot validation issues before final submission. Prepare and manage post-approval changes (CMC variations, labeling updates, packaging changes). Submit supplements, amendments, and variations in accordance with regulatory guidelines (FDA’s PAS, EMA's Type IA/IB/II). Collaborate with internal departments to gather data and draft scientifically sound responses. Stay updated with changes in FDA, EMA, and ICH guidelines. Maintain regulatory databases, submission trackers, and approval records. Participate in audits and support regulatory inspections. Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Paid sick time Paid time off Schedule: Day shift UK shift Application Question(s): Product registration and post licence changes experience in Regulated market must required. Experience: Regulated Market : 3 years (Required) Location: Gota, Ahmedabad, Gujarat (Required) Work Location: In person

Goods Receipt & Dispatch Receive incoming materials (raw materials, packaging, spares, etc.) and verify against PO/invoice. Inspect goods for damages or discrepancies and report promptly. Prepare and coordinate dispatches as per sales or production requirements. Ensure proper packaging and labeling before dispatch. Maintain all store-related documentation: GRN, DC, Gate Pass, Stock Register. Logistics Coordination Liaise with transporters, courier services, and vendors for delivery arrangements. Follow up on transit delays, shortages, or damage claims. Ensure timely data entry in ERP/Tally/Inventory software. Generate daily/weekly stock and movement reports Housekeeping & Safety Maintain store area cleanliness and organization. Ensure proper storage conditions (e.g., chemical safety norms). Comply with fire and safety norms and ensure all items are stored safely. Job Types: Full-time, Permanent Pay: ₹23,000.00 - ₹30,000.00 per month Benefits: Provident Fund Schedule: Day shift Education: Bachelor's (Required) Experience: Store management: 3 years (Required) Language: Tamil (Required) Location: Madhavaram, Chennai, Tamil Nadu (Required) Work Location: In person

Additional Information Job Number 25116723 Job Category Food and Beverage & Culinary Location Marriott Executive Apartments Bengaluru UB City, 24 Vittal Mallya Road UB City, Bengaluru, Karnataka, India, 560001 Schedule Full Time Located Remotely? N Position Type Non-Management POSITION SUMMARY Supervise and coordinate operations are in compliance with hygiene and food safety standards. Advises on proper food handling practices and provides food hygiene training for all new hires and trainees. Identifies key areas of risk in various food operations and takes preemptive remedial action. Provides technical advice on product labeling issues for fulfilling government requirements. Assist management in hiring, training, scheduling, evaluating, counseling, disciplining, and motivating and coaching employees. Follow all company and safety and security policies and procedures; report maintenance needs, accidents, injuries, and unsafe work conditions to manager; complete safety training and certifications. Ensure uniform and personal appearance are clean and professional; maintain confidentiality of proprietary information; protect company assets. Address guests’ service needs. Speak with others using clear and professional language. Develop and maintain positive working relationships with others; support team to reach common goals; listen and respond appropriately to the concerns of other employees. Ensure adherence to quality expectations and standards. Stand, sit, or walk for an extended period of time. Reach overhead and below the knees, including bending, twisting, pulling, and stooping. Move, lift, carry, push, pull, and place objects weighing less than or equal to 25 pounds without assistance. Perform other reasonable job duties as requested by Supervisors. PREFERRED QUALIFICATION Education: Bachelor’s degree from accredited university or college in Environmental Health or Culinary. Related Work Experience: 2 to 4 years of related work experience. Supervisory Experience: At least 1 year of supervisory experience. License or Certification: None At Marriott International, we are dedicated to being an equal opportunity employer, welcoming all and providing access to opportunity. We actively foster an environment where the unique backgrounds of our associates are valued and celebrated. Our greatest strength lies in the rich blend of culture, talent, and experiences of our associates. We are committed to non-discrimination on any protected basis, including disability, veteran status, or other basis protected by applicable law. The world is a big place and Marriott Executive Apartments offers temporary housing that feels like home in the biggest and best cities for business travel across Europe, Asia, Latin America, Africa and the Middle East. Join the Marriott Executive Apartments team and help our guests adapt to a new locale and feel comfortable and cared for while living away from home. In joining Marriott Executive Apartments, you join a portfolio of brands with Marriott International. Be where you can do your best work, begin your purpose, belong to an amazing global team, and become the best version of you.

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Key Responsibilities Labeling Variations Implementation: Responsible for the execution of all related activities for worldwide labeling variations for the BMS portfolio. Project Management: Lead weekly or bi-weekly meetings with relevant stakeholders and issue trackers/minutes. Act as a point of contact for all labeling variations for the assigned products. Develop and build detailed switch planning for each labeling change. Perform labeling variations tasks and follow-up each job in our Artworks Management System until Master Artwork approval. Initiate and follow-up Artwork Requests in BMS systems. Quality and Compliance: Record all activities in the BMS Artwork Management System. Complete assigned training to ensure compliance with BMS and global regulatory requirements. Problem Solving and Escalation: Anticipate problems, keep team members informed, and escalate potential/major issues. Identify business needs where needed and propose solutions. Cross-functional Collaboration: Work cross-functionally provide partnership and support to Artwork Designer, Artwork Proofreader, regulatory markets, packaging sites (internal or CMO), print vendors, Quality, Global Supply Chain Planning, Demand Planning, Market partners, and other operations departments. Skills and Knowledge required Prerequisites: Strong experience in pharmaceutical supply chain and artwork launch/labeling variation. Experience in project management and continuous improvement efforts. Educational Qualifications: Advanced professional certificate/BS degree in a graphical industry profession or graduate degree in science, preferably with a focus on Packaging, Operations, and Supply Chain. Experience: A minimum of 5+ years of related experience in Pharmaceutical Supply Chain, with Artwork launch and Artwork labeling variation. Technical Skills: Strong knowledge of the current Good Manufacturing Practice (cGMP)/Good Distribution Practice (cGDP) and its application in a pharmaceutical company. In-depth knowledge of manufacturing/packaging processes/regulatory environment. Proficiency in common MS Office software. Knowledge of MS Project and/or Visio and other relevant project management/continuous improvement software is a plus. Interpersonal Skills: Strong interpersonal skills with the ability to work with independently, or to work effectively with teams in different geographical locations and with other functions at global level. Be a good team player and work in an international environment. Ability to challenge status quo, is comfortable with the unknown, results oriented. Strong problem-solving skills. Ability to lead project teams and timelines successfully. Communication/Language Skills: Strong written and verbal communication skills. Fluent in English; additional languages are a plus. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Responsibilities BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . Key Responsibilities Artwork Creation and Revision: Create and revise artwork for printed packaging materials by utilizing provided regulatory text content, graphics, branding elements, and technical drawing structures. Artwork Technical Verification: Perform technical verification of artwork to ensure compliance with packaging sites (internal or CMO) and/or print vendors. Artwork Deployment: Distribute approved artwork to the packaging sites (internal or CMO) and/or print vendors for implementation. Vendor Proof Approval: Review and approve vendor proofs provided by the packaging sites (internal or CMO) and/or print vendors. Quality and Compliance: Establish color standards for complex graphics and other required elements. Record all activities in the BMS Artwork Management System. Complete assigned training to ensure compliance with BMS and global regulatory requirements. Documentation: Review and complete all associated cGMP documentation. Collaboration: Provide partnership and support to Artwork Coordinator, Artwork Proofreader, regulatory markets packaging sites (internal or CMO), and print vendors. Skills and Knowledge required Prerequisites: Strong experience in a graphical industry and pharmaceutical environment. Experience in artwork labeling and packaging design. Educational Qualifications: Advanced professional certificate or BS degree in a graphical industry profession. Experience: A minimum of 3-5 years in artwork labeling and package design. Technical Skills: Strong knowledge of the current Good Manufacturing Practice (cGMP) and its application in a pharmaceutical company. Proficiency in Adobe Creative Suite and other relevant graphical design software. Knowledge of GlobalVision and/or TVT and other relevant comparison software is a plus. Good knowledge of common MS Office software. Language Skills: Fluent in English; additional languages are a plus. If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as Transforming patients' lives through science™ , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Responsibilities BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role: Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/ Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Job Description Report this job Collect blood, urine, stool, and other body fluid samples from patients. Perform routine laboratory tests including hematology, biochemistry, microbiology, and pathology. Prepare specimens for examination and ensure proper labeling and storage. Operate and maintain laboratory instruments and equipment. Record and analyze test results accurately and report to the concerned physician or department. Maintain inventory of laboratory supplies and reagents. Ensure proper disposal of biohazardous waste following safety protocols. Adhere to standard operating procedures (SOPs), infection control, and quality control guidelines. Enter patient data into the Laboratory Information System (LIS). Assist in preparing diagnostic reports and documentation. Maintain cleanliness and hygiene of the laboratory at all times. Key Details Job Function: Doctors/Nurses/Medical Professional Industry: Healthcare Specialization:Lab/Medical Technician Role: Lab/ Medical Technician Qualification: Other School/ Graduation - Bsc(MLT) Employment Type: Full Time Vacancies: 2 Key Skills Lab Procedures Lab Testing Lab Technician medical lab technician Hospital BMLT DMLT About Company Company:Platinum Hospital - Vasai Platinum Hospital Vasai is an Unit Of Platinum Hospital Group which is one of the Largest Chain of Multi Speciality Hospital in Mumbai. This hospital is the first Cardiac Super Speciality Hospital of Palghar District. Job Posted by Company Platinum Hospitals Private Limited Platinum Hospital Vasai is an Unit Of Platinum Hospital Group which is one of the Largest Chain of M... Moreulti Speciality Hospital in Mumbai. This hospital is the first Cardiac Super Speciality Hospital of Palghar District. Less Job Id: 71574566

Job Title: QC Technician (Mobile, Laptop & MacBook) cum Office Assistant Location: Bangalore Job Summary: We are looking for a QC Technician cum Office Assistant (fresher or experienced) to support quality checking of mobile phones, laptops, and MacBooks, assist in office work, and travel to other states for device inspection as per company requirement. This is a field + office-based role suitable for candidates willing to learn and grow in the electronics and IT hardware industry. Key Responsibilities: QC Duties (Training will be provided for freshers):Perform quality checks of used mobile phones, laptops, and MacBooks. Check device functionality (hardware/software), cosmetic condition, and accessories. Identify defects and mark grading based on QC checklist. Maintain records and prepare QC reports. Office Assistant Duties: Assist in packaging, labeling, and inventory handling. Support in data entry, Excel updates, and courier coordination. Help maintain cleanliness and organization in the office. Outstation QC Visit: Travel to different states for physical QC inspection of bulk devices. Coordinate with vendors and submit proper QC visit reports to the head office. Travel expenses will be reimbursed as per company policy. Required Skills: Basic knowledge of mobile/laptop hardware preferred (training will be given to freshers). Must know Basic Excel, Basic English, and Hindi. Willingness to travel outside the city/state frequently. Good observation, discipline, and ability to follow instructions. Eligibility: Freshers and Experienced both can apply. Minimum Qualification: 12th Pass / ITI / Diploma / Any Graduate. Must be comfortable with field visits and outstation inspections. Job Type: Full-time | On-site + Field Travel Salary: ₹12,000 – ₹18,000 (depending on experience and skills) Joining: Immediate preferred

Designation: Phlebotomist Role: Field Ops Department: Collection Ops Location: Gurugram About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is tomakehealthcare understandable, accessible, and affordable for all Indians. Over the past three years, we'veworked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities– And we’re just getting started. Leading the chart as one of thetopconsumer health platforms through e Pharmacy, e Diagnostics, e-consult, and offline stores, Tata1mghas delivered over 15M e Pharmacy orders, 2M e Diagnostics orders & 1M+ organic users/day in2022and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver onourmission consistently. Know more about us: https://www.1mg.com/aboutUs Brief about the Team i. Tata 1mg labs is a state-of-art facility offering the highest quality diagnostic services at the convenience of your doorstep. ii. We pride ourselves on three things; Assured Quality, Best Prices, Excellent Turn Around Time. iii. We believe in providing the highest level of transparency to our customers. iv. Our entire team is dedicated to providing the best customer experience and continuously strives to come up with solutions to remain in line with the needs of our customers. What will you do  Sample collection of customer/patients and rapid testing of samples  Maintaining specimen integrity by using aseptic technique and following standard operating procedures.  Identifying patients and their personal information by reviewing their identity documents  Extracting blood from patients through venipuncture or finger-sticks.  Analyzing blood specimens using the correct testing equipment, when necessary.  Preparing specimens for transportation, including labeling vials accurately and matching blood specimens to patients.  Keeping and maintaining records of patient names, volume of blood drawn, and diagnostic findings.  Cleaning, maintaining, and calibrating laboratory equipment used in the drawing and testing of blood specimens.  Collect and tag specimens exactly as outlined in each medical requisition.  Properly package each specimen What we are looking for  Candidates should have a work experience of 3 year to 10 year in the relevant Phlebotomy domain.  Phlebotomy experience is a mandate, experience in sample collection, knowledge of test, ableto handle patient’s, preparing specimens for transportation including labeling vials accuratelyand matching blood specimens to patients and also have knowledge about Waste management.  Education: DMLT/BMLT  Candidate must have good verbal and written communication skills and knowledge of basic computer.  Candidate must have good knowledge of testing protocols and the use of testing equipment'sand also deliver excellent patient service, answer patient questions, act as a resource for patient information and strengthen the relationship between the patient and our entire medical facility.  Candidate should be ready to travel.

🧾 Job Description: Warehouse Executive Position: Warehouse Executive Location: Pan India (Initial training in Jamalpur, Gurgaon – 7 days) Relocation: Candidate must be ready to relocate anywhere in India Food & Stay: Provided by the company Salary: ₹15,000 to ₹18,000 per month Eligibility: 10th / 12th pass or above Experience: Fresher or experienced both can apply --- Roles & Responsibilities: Receive, store, and dispatch goods in a timely and accurate manner Maintain inventory records and manage stock levels Ensure proper labeling and storage of materials Perform daily warehouse inspections for cleanliness and safety Coordinate with transport and logistics teams for timely dispatch Follow all standard operating procedures (SOPs) of the warehouse Operate basic warehouse equipment if required (training will be provided) Support team members and supervisors in daily warehouse operations --- Key Skills Required: Basic understanding of warehouse and logistics operations Good physical stamina and willingness to work in shifts if required Ability to follow instructions and company policies Basic computer knowledge is a plus Teamwork and time management skills

Supervise daily packing activities to meet production and dispatch schedules. Monitor staff performance, provide guidance, and ensure adherence to quality and safety standards. Allocate work duties to packing staff based on priority and capacity. Ensure that packaging materials are available and properly used. Inspect finished packages for accuracy, labeling, and proper sealing. Maintain cleanliness and order in the packing area. Train new employees on packing procedures and safety protocols. Record production data and generate reports for management. Coordinate with inventory, quality control, and dispatch teams.

•Job profile : * Attend Walk in Customers • Alterations * Display Management * Inventory Management * Labeling & Folding & Packing * Handle Social Media * Should be camera friendly * Participate in Promotional activities such as Youtube and Insta Reels etc. * keeping records * Sales Support etc. * ⁠Good English Speaking * ⁠Must wear western outfits

We are hiring two female staff members for our eCommerce godown. The role involves product packing, labeling, and preparing orders for dispatch. Candidates should be detail-oriented, punctual, and able to work in a fast-paced environment. Basic training will be provided. Location: Saniya Hemad, Surat. Full-time position with a supportive team.

📌 Job Vacancy: Store Keeper Company Name: Vinyork Leather Works Location: Ranipet Website: www.vinyork.com Industry: Premium Leather Furniture Manufacturing Job Type: Full-time Experience: 1-3 years preferred 🧰 Roles and Responsibilities: Maintain accurate records of inventory and stock levels. Receive, inspect, and store incoming materials and supplies. Issue raw materials, tools, and components to the production team as per requirement. Ensure proper labeling, storage, and safety of all goods. Keep the store clean, organized, and well-managed. Coordinate with purchase and production teams for stock planning. Perform regular stock audits and physical inventory checks. Maintain stock register (manual or software-based). Raise alerts for low stock or shortages. Ensure dispatch readiness of finished goods when required. Follow FIFO (First In, First Out) and other inventory best practices. ✅ Requirements: Prior experience in storekeeping/inventory management (preferably in manufacturing). Basic computer knowledge (Excel, Inventory software preferred). Strong attention to detail and organizational skills. Trustworthy and responsible. Able to lift and move goods when required.

We are looking for a dedicated and responsible Packing Boy to manage daily order packing for our e-commerce business. The job involves packing orders for platforms like Meesho, Amazon, and Flipkart, mainly dealing with anime merchandise (figurines, t-shirts, posters, accessories, etc.). 🔧 Key Responsibilities: Pack daily e-commerce orders carefully and efficiently. Ensure proper labeling, taping, and safety of products before dispatch. Maintain cleanliness and organization of the packing area. Coordinate with the dispatch/logistics team for timely pickup. Handle fragile or unique anime merchandise with care.

Job Description : Home Collection Phlebotomist Role: Field Ops Department: Collection Ops Location: Various locations What will you do:  Sample collection of customer/patients and rapid testing of samples  Maintaining specimen integrity by using aseptic technique and following standard operating procedures.  Identifying patients and their personal information by reviewing their identity documents  Extracting blood from patients through venipuncture or finger-sticks.  Analyzing blood specimens using the correct testing equipment, when necessary.  Preparing specimens for transportation, including labeling vials accurately and matching blood specimens to patients.  Keeping and maintaining records of patient names, volume of blood drawn, and diagnostic findings.  Cleaning, maintaining, and calibrating laboratory equipment used in the drawing and testing of blood specimens.  Collect and tag specimens exactly as outlined in each medical requisition.  Properly package each specimen What we are looking for   Candidates should have a work experience of 1 year to 10 year in the relevant Phlebotomy domain.  Phlebotomy experience is a mandate, experience in sample collection, knowledge of test, able to Assist patients, preparing specimens for transportation including labeling vials accurately and matching blood specimens to patients and also have knowledge about Biomedical waste management.  Education: DMLT/BMLT  Candidate must have good verbal and written communication skills and knowledge of basic computer.  Candidate must have good knowledge of testing protocols and the use of testing equipment's and also deliver excellent patient service, answer patient questions, act as a resource for patient information and strengthen the relationship between the patient and our entire medical facility.  Candidate should be Willingness to travel for home collections is required. Education: MLT/DMLT/BMLT Experience: both fresher and experince Requirements: 2-wheeler Mandatory with a valid Driving License CTC: Up to ₹3.6 LPA + ₹3.5/km Duty Timings: 6:00 AM – 3:00 PM rotational shifts

Rhombus Power is purposefully transforming defense and global security enterprises with Guardian, our Artificial Intelligence platform for strategic, operational, and tactical decision-making at the speed of relevance. We provide relevant, actionable, and AI-powered insights at each step in the defense decision-making cycle. Equipped with Guardian's AI-powered tools-- from infrastructure to data to insights -- our clients are able to solve their most complex, interconnected challenges and achieve decision and operational superiority. Come join our cross-disciplinary and world-class team that is delivering game-changing solutions to transform global security. Learn more about Rhombus and watch a demonstration of Guardian, our AI Platform here -- https://youtube.com/watch?v=3PxY6su1Q-Q See the following articles to learn more about what we do: https://foreignpolicy.com/2023/06/19/ai-artificial-intelligence-national-security-foreign-policy-threats-prediction/ https://federalnewsnetwork.com/air-force/2023/12/new-decision-advantage-tool-will-change-how-air-force-makes-investment-decisions/ https://apnews.com/article/us-intelligence-services-ai-models-9471e8c5703306eb29f6c971b6923187 RHOMBUS IS ONLY CONSIDERING CANDIDATES CURRENTLY BASED IN INDIA. NO OTHER LOCATIONS WILL BE CONSIDERED, PLEASE DO NO APPLY IF YOU DO NOT MEET THIS REQUIREMENT. Location India (Remote) Job Description We are a cutting-edge defense technology firm that is renown for building next-generation AI systems for national security applications. We seek highly motivated, execution-focused individuals in India to join our remote team as Data Labeling Specialists for an urgent and high-priority client deliverable involving overhead imagery analysis. As a Data Labeling Specialist , you will play a critical role in training object detection AI by accurately labeling image data. You’ll work within a tightly focused and collaborative team, operating at a high tempo to meet tight deadlines and stringent quality standards. This is an ideal role for individuals who are extremely detail-oriented, analytical, and excited to contribute to impactful defense-related AI work. We will rely on you to produce high-accuracy actions under demanding timelines, over several months. We only seek those that will sustain this work ethic and enthusiasm, and like the rest of us, find ways to exceed expectations. We are considering transitioning select Data Labelling team members into a full-time roles as we scale our work. Responsibilities Accurately Identify, analyze, and label objects in satellite or aerial imagery. Apply sound logic on edge cases and don’t assume when you’re not sure. Communicate! Proactively communicate with project leadership and technical teams to provide updates, transparently reporting on progress, flagging and raising issues about labeling and data workflows. Don’t wait for guidance, test and suggest an improvement! Cultivate expertise and leadership in the imagery analysis domain and gain basic machine learning knowledge to better understand how labels are utilized by our ML algorithms. Qualifications Preference for those that have completed an undergraduate degree; please list your GPA in your CV. Prior experience with imagery analysis, GIS, and labeling is preferred, but not required. Strong command over Microsoft Suite and Google tools such as Excel, Word, Sheets, etc. You must be well versed in file management- we want those who are highly organized! The perfect candidate for this role is someone who is adaptable, highly dependable, and can apply logic to multiple different scenarios concurrently. We’re seeking candidates with proven analytical skills, and are excited to solve complex problems. This position is a remote role, however, candidates must be able to reliably produce, at a high degree of accuracy, over sustained timelines. You must be extremely quality focused, a self-starter with bias for action, and able to work in a fast-paced environment. You must be able to learn quickly and have a baseline of strong computer skills. Benefits Full medical, dental, vision coverage for employee and dependents 401k matching program PTO and Holidays Bonus and other incentive programs Access to mental health program Access to Flexible Spending Accounts for Health Care, Dependent and Commuter About Rhombus Rhombus Power Inc. (Rhombus) is a startup located in the heart of Silicon Valley at Stanford Research Park in Palo Alto. We use cutting-edge cross-disciplinary approaches to solve pressing Big Data and Sensing problems in security, energy, and healthcare. Our advisory board includes two Nobel Laureates and a Draper Prize winner. Rhombus compensates, motivates, and develops employees, who are trusted, empowered, and involved. Employees have clear roles and expectations – and their roles are flexible enough to move at the speed of innovation in order to meet and exceed client expectations. We have a unique culture of global purpose, rooted in the innovation and progress of Silicon Valley. Rhombus knows that diversity is a condition for success. We are committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity/Affirmative Action Employer.

Job Overview Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assume accountability of quality of the deliverables and implementation of quality processes with minimal support from the Manager. Function as a Point of Contact for the delivery team for regulatory updates, quality concepts, applicable procedures, practices, and conventions on the assigned projects. Act as the process and quality expert for the Client. Work with other team members to analyze Quality findings and help develop action plans. Ownership of responding to and addressing periodic client quality reviews and other ad-hoc client quality findings. Perform ongoing review of a sample of various cases or safety reports for global regulatory submissions, labeling / regulatory documents for Fortrea clients e.g., Annual Reports (IND and other), PSURs, PADERs, Clinical Study Reports, Core Data Sheets, USPI, centralized SPC’s, Med Guides etc. Assist with the overall functional quality operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Provide adequate oversight to ongoing sample case reviews and perform reviews as required. Publish quality metrics based on this review and use it to ensure deliverables meet agreed quality targets. Identify, report quality trends to internal and external stakeholders, suggest corrective actions and monitor the execution and closure. Assume ownership of quality of reports and CAPAs as assigned. Ensure that CAPAs are implemented for the assigned project. Conduct process review in coordination with Project Manager and Quality Manager to identify process gaps and proactively coordinate with the delivery team to develop process standards and suggest process improvements. Measure and track audit readiness for assigned projects. Lead authoring, reviews, training and distribution of SOPs, project specific Work Instructions / convention documents etc. Work with individuals in identifying training needs based on quality review findings. Assist in designing sign-off criteria, development and tracking of training schedule and training material for new hires and existing team. Ensure that periodic feedback is provided to the team based on review findings. Initiate discussion forums on Quality errors within assigned project and identify process improvements, share best practices across projects. Communicate with internal Subject Matter experts to get clarification on case-processing queries and providing feedback to team. Responsible to coordinate and handle queries during the client or external audits of the assigned projects. Assume accountability of supporting the client during regulatory inspections and ensuring quality and timely completion of inspection requests. Responsible for developing Quality Management Plan and / or contributing to the Quality Agreement for assigned projects. Support Computer System Validation related activities as required. To respond/review to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Review recorded information that may be received over the telephone call, email, fax etc. Execute drug safety data management processes - a combination of call intake review, call dialogue documentation review and case follow-up. Guide safety associates in managing voice calls (as required). Perform any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources. Coordinate with the project team to support the Client during regulatory inspections at client sites with support from Quality Manager. Perform Analysis of data and if required, suggest strategies for process improvement/excellence. Perform and Review of analysis of data performed and drive strategies for process improvement/excellence. All other duties as needed or assigned. Qualifications (Minimum Required) Bachelors/Masters/PhD degree in Medicine or Alternative medicine, Medical Science, Pharmaceutical science, Nursing, Life Sciences, or related area. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) Five years of overall work experience in the pharmaceutical industry, biotechnology, or CRO industry primarily in Pharmacovigilance / Safety writing with at least Two years’ experience in Peer review/Quality review. Knowledge of regulatory requirements viz. GPV and applicable EU and FDA guidelines. In-depth understanding of case processing and assessment. Knowledge of Quality Assurance. Awareness of lean methodology concepts. Technical proficiency with Microsoft Office suite of applications. Preferred Qualifications Include Experience in generating quality metrics with trend analysis, authoring, and coordinating Corrective and Preventive Action Reports is preferred. Experience in assessing quality of a case/safety report from a medical, scientific and documentation perspective is preferred. Physical Demands/Work Environment Office Environment . Available for travel 10% of the time including overnight stays as necessary consistent with project needs and office location. Learn more about our EEO & Accommodations request here.

Job Overview Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary Of Responsibilities Undertake primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review. Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. Provide training and guidance to the case processing team on medical aspects of case processing, only after a tenure of 1 year. Performs secondary medical review (QC role) and retrospective review of cases reviewed (QA role), as required for measuring quality of deliverables, identifying error trends, training needs and areas of improvement only after a tenure of greater than 1year. Performs aggregate medical review and signal detection/analysis activities, as required. Enhances existing client relationships whenever possible. Creates, maintains, and assumes accountability for a culture of high customer service. Participates in process improvement activities across Company. Qualifications (Minimum Required) Bachelor’s degree in medical science or MD or DO or equivalent degree. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Language Skills: Speaking: English at ILR level 3+ or higher. Writing / Reading: English at ILR level 4+ or higher. Experience (Minimum Required) Working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures. Knowledge and understanding of regulatory requirements for Clinical Research. Knowledge and understanding of ICH-GCP guidelines. Preferred Qualifications Include Good understanding of regulatory requirements relating to Pharmacovigilance. Up to 1 year of pharmaceutical industry experience, including pharmacovigilance (case processing, medical review) and / clinical research. 1 to 2 years of Clinical practice experience. Physical Demands/Work Environment Office or home-based environment, as requested by the line manager. Learn more about our EEO & Accommodations request here.

Job Overview Provide medical safety expertise, directly and indirectly, to Sponsors of drugs, devices, and combination products, in the post marketing period. Summary Of Responsibilities Undertake primary medical review of cases, including medical assessment of the case for seriousness, listed/labeling, causality, adverse event coding and narrative review. Update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs. Provide training and guidance to the case processing team on medical aspects of case processing. Performs secondary medical review (QC role) and retrospective review of cases reviewed (QA role), as required for measuring quality of deliverables, identifying error trends, training needs and areas of improvement. Performs aggregate medical review and signal detection/analysis activities, as required. Enhances existing client relationships whenever possible. Creates, maintains, and assumes accountability for a culture of high customer service. Participates in process improvement activities across Company. And all other duties as needed or assigned. Qualifications (Minimum Required) Bachelor’s degree in medical science or MD or DO or equivalent degree. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Language Skills: Speaking: English at ILR level 3+ or higher. Writing / Reading: English at ILR level 4+ or higher. Experience (Minimum Required) Working knowledge of medical sciences, diagnosis and therapeutics including drug treatments and procedures. Knowledge and understanding of regulatory requirements for Clinical Research. Knowledge and understanding of ICH-GCP guidelines. Preferred Qualifications Include Good understanding of regulatory requirements relating to Pharmacovigilance. Up to 2 years pharmaceutical industry experience, including pharmacovigilance (case processing, medical review) and/or clinical research. 1 to 2 years of clinicial practice experience. Physical Demands/Work Environment Office or home-based environment, as requested by the line manager. Learn more about our EEO & Accommodations request here.

Job Overview Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. It is the responsibility of the post holder to provide all clients, both internal and external, with the appropriate quality of service in a safe and cost effective manner. The individual will be expected to comply with the legal requirements of the Health and Safety at Work Act 1974, the COSHH regulations 1989 and the EC (European Commission) Directives 1992/3 as documented in the Company’s Health and Safety Manual. Summary Of Responsibilities Assume accountability of quality of the deliverables and implementation of quality processes with minimal support from the Manager. Function as a Point of Contact for the delivery team for regulatory updates, quality concepts, applicable procedures, practices, and conventions on the assigned projects. Act as the process and quality expert for the Client. Work with other team members to analyze Quality findings and help develop action plans. Ownership of responding to and addressing periodic client quality reviews and other ad-hoc client quality findings. Perform ongoing review of a sample of various cases or safety reports for global regulatory submissions, labeling / regulatory documents for Fortrea clients e.g., Annual Reports (IND and other), PSURs, PADERs, Clinical Study Reports, Core Data Sheets, USPI, centralized SPC’s, Med Guides etc. Assist with the overall functional quality operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage and review expeditable adverse events, product quality complaints and medical information to the required standard and submit them to the client and the regulatory agencies (if required) within the agreed/stated timelines. Provide adequate oversight to ongoing sample case reviews and perform reviews as required. Publish quality metrics based on this review and use it to ensure deliverables meet agreed quality targets. Identify, report quality trends to internal and external stakeholders, suggest corrective actions and monitor the execution and closure. Assume ownership of quality of reports and CAPAs as assigned. Ensure that CAPAs are implemented for the assigned project. Conduct process review in coordination with Project Manager and Quality Manager to identify process gaps and proactively coordinate with the delivery team to develop process standards and suggest process improvements. Measure and track audit readiness for assigned projects. Lead authoring, reviews, training and distribution of SOPs, project specific Work Instructions / convention documents etc. Work with individuals in identifying training needs based on quality review findings. Assist in designing sign-off criteria, development and tracking of training schedule and training material for new hires and existing team. Ensure that periodic feedback is provided to the team based on review findings. Initiate discussion forums on Quality errors within assigned project and identify process improvements, share best practices across projects. Communicate with internal Subject Matter experts to get clarification on case-processing queries and providing feedback to team. Responsible to coordinate and handle queries during the client or external audits of the assigned projects. Assume accountability of supporting the client during regulatory inspections and ensuring quality and timely completion of inspection requests. Responsible for developing Quality Management Plan and / or contributing to the Quality Agreement for assigned projects. Support Computer System Validation related activities as required. To respond/review to medical information queries/product quality complaints/general queries that may be received over the telephone call, email, fax etc. Review recorded information that may be received over the telephone call, email, fax etc. Execute drug safety data management processes - a combination of call intake review, call dialogue documentation review and case follow-up. Guide safety associates in managing voice calls (as required). Perform any other support activities as assigned – tracking various types of information and metrics, ongoing QC of defined process steps, training, reconciliation of data from multiple sources. Coordinate with the project team to support the Client during regulatory inspections at client sites with support from Quality Manager. Perform Analysis of data and if required, suggest strategies for process improvement/excellence. Perform and Review of analysis of data performed and drive strategies for process improvement/excellence. All other duties as needed or assigned. Qualifications (Minimum Required) Bachelors/Masters/PhD degree in Medicine or Alternative medicine, Medical Science, Pharmaceutical science, Nursing, Life Sciences, or related area. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. Experience (Minimum Required) Five years of overall work experience in the pharmaceutical industry, biotechnology, or CRO industry primarily in Pharmacovigilance / Safety writing with at least Two years’ experience in Peer review/Quality review. Knowledge of regulatory requirements viz. GPV and applicable EU and FDA guidelines. In-depth understanding of case processing and assessment. Knowledge of Quality Assurance. Awareness of lean methodology concepts. Technical proficiency with Microsoft Office suite of applications. Preferred Qualifications Include Experience in generating quality metrics with trend analysis, authoring, and coordinating Corrective and Preventive Action Reports is preferred. Experience in assessing quality of a case/safety report from a medical, scientific and documentation perspective is preferred. Physical Demands/Work Environment Office Environment . Available for travel 10% of the time including overnight stays as necessary consistent with project needs and office location. Learn more about our EEO & Accommodations request here.