Average salary: Rs623,571 /yearly
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- ...Key Responsibilities # Documentation and Compliance : # Prepare and verify shipping documents (e.g., invoices, packing lists, certificates... ...: # Calculate tariffs, taxes, and duties for imports and exports. # Stay updated on changes in customs regulations and tariff...SuggestedFull time
- Documentation Executive Start Date Starts Immediately CTC (ANNUAL) Competitive salary Competitive salary Experience...SuggestedImmediate start
- ...Ingredients (APIs). We are a part of 50+ year-old group, currently exporting to 70 countries worldwide. The company has received global FDA... ...submissions, renewals, and variations. • Review technical documentation: PDR, DMF, AMV, BMR/BPR, Specifications, Stability Reports, BE...SuggestedPermanent employmentFull timeWorldwide
- ...planning Monitor inventory levels and help optimize stock carrying costs Maintain accurate purchase records, MIS reports, and documentation Evaluate vendor performance on quality, cost, and delivery Ensure compliance with company policies and statutory...SuggestedImmediate startRelocation
- ...integrity. Address audit observations, prepare responses, and ensure timely closure. Maintain inspection readiness and validation documentation as per regulatory expectations. Engineering & Cross‑Functional Support Coordinate with Quality Assurance, IT, Production, QC...Suggested
- ...activities. Line clearance for aseptic filling, compounding, filtration, and packing. Review BMR/BPR, logbooks, and batch related documents. Monitor compliance with GMP, GDP, SOP requirements. Handle deviation, change control, CAPA documentation. Ensure data...Suggested
- ...testing, endotoxin testing, MLT. Preparation and handling of culture media. Maintain aseptic conditions in microbiology lab. Documentation of test results and analytical reports. Calibration and maintenance of microbiology instruments. Investigation of OOT, OOS...Suggested
- ...quality standards. Coordinate with QA, QC, Engineering, and Warehouse departments for smooth production flow. Ensure proper documentation and compliance with USFDA, MHRA, and other regulatory guidelines. Train and guide operators and technicians on GMP practices and...Suggested
- ...Disable / Re-activation of User Account(s) and assigning of privileges for application. To prepare, review configuration specification documents. To prepare and review standard operating procedures associated with the planning, development and operation of IT related...Suggested
- Job Description Job Title: Senior Executive - Unit Supply Chain About The Role Role Responsibilities: Purchase Prepare, Check and review purchase order requests Monitor the receipt and control of the Daily Purchase Receipt/Production Receipt of material ...SuggestedFlexible hours
- ...years of experience in the medical device / IVD industry. The candidate will support regulatory submissions, maintenance of technical documentation, and compliance with applicable global regulatory requirements, including EU IVDR, WHO Prequalification, Brazil ANVISA, and other...Suggested
- Location: [Valsad/Gujarat] Experience: 4–8 Years Reports To: Supply Chain Manager / Operations Head Role Objective We are looking for a proactive SCM Executive to lead the procurement and expediting of high-value materials. In this role, you will be the ...SuggestedFull time
- ...instruments. Customer complaint redressal Suggestion Assist to Team Leader for Implementation of ISO System Update test results in documentation of all Quality records and online Sample manager. Testing equipment trouble shooting and reporting. Color correction to meet...SuggestedShift work
- ...roles and responsibilities specified in SQRE plan. Outline activities in the unit Stewardship and Reliability and quality plans. Document in SOP's, rounds, checklist, etc. Monitor process and equipment for anomalies. Make adjustments & minor repairs along with...SuggestedShift work
- ...Performance evaluation of Technologists & other operators. 14. Maintain High Level Of Cleanliness in the plant. Maintain records and documents. Manpower management Awareness of ISO 28000/SCSMS. 18. Awareness of ISO 9001 and IATF. Develop the team and work with cross...SuggestedFor contractorsShift work
- ...Promote a strong quality mindset across the site. Drive the site's quality goals in alignment with global and regional strategies. 2.Documentation & Compliance: Oversee the creation, control, and maintenance of quality documents and policies. Ensure compliance with global...Local areaRelocation
- ...guidelines. Select appropriate animal models that mimic human neurovascular anatomy and pathology. 2. Regulatory Compliance & Documentation Ensure adherence to FDA guidance on animal studies, including proper study design, monitoring, and reporting. Oversee...Contract work
Rs 1.5 - 2.5 lakhs p.a.
...Validation o SCADA Validation o Computer System Validation (CSV) o Building Management System (BMS) Validation o Camera System Validation o Excel Sheet Validation o Risk Assessment · Maintaining accuracy, documentation integrity, and compliance standards....- Some careers open more doors than others. If you’re looking for a career that will unlock new opportunities, join HSBC and experience the possibilities. Whether you want a career that could take you to the top, or simply take you in an exciting new direction, HSBC offers...Permanent employmentLocal areaWorldwideFlexible hours
- ..., China, Japan, Brazil, India, Australia, Russia, South Korea, and more. The role involves preparing and submitting the necessary documentation to regulatory agencies, ensuring compliance with local regulations, and facilitating timely market access. Key Responsibilities...Full timeLocal area
- ...basic working knowledge of GST and TDS, including calculations and entries.- Prepare invoices, vouchers, and supporting accounting documents.- Ensure timely posting and reconciliation of transactions.- Assist during audits by providing necessary accounting data and reports...Work at office
- ...cause analysis. Maintaining statistical and financial records. Creation, development and amendment of the requisites SOPs and other documents.Maintain and update QMS records. Preparation and implementation of technical training programs for workmen and staff. Updating critical...Long term contractFull time
- ...To support and execute clinical studies, trials, and observational research activities while developing high-quality clinical documentation, scientific outputs, and regulatory-ready evidence. The role contributes to patient safety, product credibility, and scientific excellence...
- Company Description Megaplast India Pvt. Ltd. is a leading manufacturer of Geomembranes, Films, and Carrier Bags (HDPE/LLDPE/PE), operating for over a decade with a reputation for innovation, quality, and reliability. Certified as an ISO 9001:2008 company, Megaplast leverages...Full time
- ...counts and annual wall-to-wall audits to ensure physical stock matches system records. • Traceability: Maintain rigorous documentation for material heat numbers and batch codes to ensure full traceability throughout the production process. • Consumable...Full time
- ...Job Title: Executive – Regulatory & Technical Documentation Department: Quality Assurance & Regulatory Affairs (QA / RA) – Women’s Health & Fertility Location: Vapi, Gujarat Reports To: Manager / Senior Manager – QA / RA Job Purpose: To prepare,...
Rs 2.16 lakh p.a.
...and ad-hoc duties Core Responsibilities Data Management: Entering, updating, and maintaining records in systems (Excel, etc.) Documentation: Preparing, organizing, and verifying invoices, reports, and official documents Process Support: Assisting in daily operational...Full timeImmediate start- ...performance and safety. Regulatory Compliance : Ensuring all studies follow GLP (Good Laboratory Practice) guidelines and generating documentation for FDA or regulatory submissions. Data Analysis & Reporting : Analyzing experimental data, interpreting results, and writing...Work at office
- ...Assurance system for surgical robotic products by ensuring compliance with ISO 13485, internal SOPs, and regulatory requirements through documentation control, process adherence, non-conformance handling, and coordination with cross-functional teams. Key Responsibilities: 1...
- ...○ Oversee equipment changeovers, cleaning, and preparation for new batches in compliance with SOPs. ○ Ensure all procedures are documented and followed meticulously. 10. Continuous Improvement: ○ Actively participate in continuous improvement programs, like Lean Manufacturing...Shift work
