247 Sop Preparation Jobs

As the Quality Assurance Manager, your primary responsibilities will include overseeing the quality assurance procedures, protocols, and standards for steel production processes at the SMS Plant. You will be responsible for ensuring compliance with national and international quality standards, industry regulations, and customer specifications. Your role will involve implementing strategies for continual improvement, defect reduction, and process optimization. Your duties will also include leading the inspection and testing of raw materials, intermediate products, and finished products in the SMS, Rolling Mill, and Bright Bar processes. You will be expected to analyze production processes, identify potential quality issues, and ensure high-quality output at every stage of production. Reviewing and approving inspection reports, test results, and product certifications will be part of your daily tasks. In case of quality-related problems, you will lead investigations and implement corrective and preventive actions to address root causes and avoid recurrence. It will be crucial for you to document all quality issues, findings, and actions taken effectively. Additionally, you will act as the main point of contact for quality-related matters with customers, vendors, and regulatory authorities. Your role will involve monitoring customer feedback and quality complaints to ensure timely resolution and customer satisfaction. By analyzing customer complaints, you will be able to identify systemic issues and take corrective actions to enhance product quality and service. Leading internal and external audits, inspections, and certification processes will also be part of your responsibilities. Ensuring regulatory compliance and maintaining documentation for industry certifications will be essential. You will be required to prepare and present regular quality reports for senior management, highlighting performance, trends, and areas for improvement. Your contribution will play a vital role in maintaining high standards of quality and customer satisfaction within the steel production processes.,

The position of Officer in the Production Department at German Remedies Pharmaceuticals Pvt Ltd.(Sanand) is currently open for applications. As an Officer, you will report directly to the Production Head and be responsible for critical tasks within the department. Key Responsibilities: - Handling the Filling Area to ensure smooth operations - Managing the Washing and Autoclave Area for equipment sterilization - Reviewing and documenting Batch Manufacturing Records (BMR) - Preparing Standard Operating Procedures (SOPs) for various processes - Conducting Dispensing Activities as needed Requirements: - Qualifications: Bachelor of Pharmacy (B. Pharma) - Total Experience: 2 to 4 years in the pharmaceutical industry - Minimum of one year of experience at Zydus - Department Eligibility: Production This role is a Level 1 Neev position and is a replacement hire. If you meet the qualifications and have the required experience, please send your CV to Prabhaker.Tiwari@zyduslife.com to be considered for this opportunity.,

The ideal candidate for this position should have 2-8 years of experience and will be responsible for various tasks including GPCB work, SOP preparation, periodic revision of EHS SOP, work permit system, documentation work, regulatory compliance, statutory audit, safety audit, risk assessment, incident investigation, hazard identification, safety training for new joiners, legal compliance, environment audit, knowledge of work permits, fire extinguisher and fire hydrant systems, EHS related training, mock drills, preparation of risk assessment reports, GPCB related work such as NOC, CCA, product mix, compliance in XGN, ETP operations, EC work, Parivesh Portal, and CGWA work.,

The role involves serving as the single point of scientific, administrative, and regulatory control for the study. You will actively participate and supervise all study activities, including animal dosing, clinical signs observation, data collection, and analysis, ensuring compliance with relevant regulations, OECD Principles of GLP, and SOPs. Additionally, you will be responsible for the operation, maintenance, and proper utilization of various equipment/instruments like centrifuges, laminar air flow systems, anesthetic machines, and syringe pumps. Your duties will also include the preparation and updating of SOPs relevant to in vivo and in vitro experiments. Moreover, you will be expected to effectively communicate important information to key study personnel, the sponsor, and other relevant scientists. You will have the authority to approve amendments and deviations to the study plan and must respond to QA findings promptly, ensuring their resolution in a timely manner. As part of this role, you will be responsible for approving study plans, amendments, and reports, as well as ensuring the timely archiving of the study in accordance with existing practices. You will also have all the responsibilities of a Study Director as outlined in the applicable SOPs.,

Discussing with process owner and drafting SOP Reviewing the process and identify inefficiencies in operational processes. Identify and evaluate operational, financial, and regulatory risks and Identify control deficiencies and suggest improvements. Timely Updating SOP with controlling version records. Verify records and process related to client transactions, compliance, and operations. Support in review of SEBI regulations, exchange rules, and internal policies. Monitor and report compliance violations. Candidates working for stock broking companies will be preferred. Exposure of Internal Audit and SOP review is must.

The key responsibility is to ensure business development & operational support for FTWZ activities. You will be reviewing pre-alerts and checking shipment documents as required for inward into FTWZ. It will be your responsibility to share clearance documents with the EDI team for BoE. You will need to review SOPs and prepare the requirements accordingly. Checking ETA and contacting all stakeholders such as forwarder, carrier, custodian, and billing party will also be part of your duties. You will be required to review the Checklist prepared by the EDI team, ensure BoE is filed, and share it with operations to carry out customs clearance formalities at Nhava Sheva and FTWZ. Securing delivery orders from the shipping line and sharing them with the FTWZ team will be essential. Monitoring the pickup from the port and arrival at FTWZ, providing offloading instructions, and information to FTWZ operations will also fall under your purview. Your tasks will include tallying all inward items as per documents, reporting any damages, and maintaining stock inventory in excel. You will need to review the invoices received for outward shipments, check inventory stock for the items on the invoice, and issue picking instructions. Coordinating with DPW on the pick list, sharing the inbound BoE of items picked, and securing the revised final invoice with inward BoE will be part of your responsibilities. You will be required to be physically involved in custom clearance at the FTWZ custom office, assess inbound and outbound shipments, handle ADC clearance when necessary, manage custom examinations, and submit required custom documents at the FTWZ main gate. Coordinating and supporting clients for VAS activities, outbound picking activities, and outbound activities will also be your tasks. Additionally, you will need to share documents with the EDI team for BoE, share checklists with clients, and obtain approvals. Coordinating for BoE filing, customs assessment, and OOC once duty is paid, placing vehicles for loading, giving loading instructions to FTWZ operations, and sending monthly invoices for storage will be part of your daily routine. You will also need to maintain PODs in a file, update DSR and FTWZ stock inventory reports, attend client meetings for reviews, compare FTWZ and DSV stock inventory, provide operational support for FTWZ activities, and discuss with DP World for any development plans. You will be responsible for keeping the Head of Department informed of any daily issues or concerns for clearance process improvement requirements, coordinate with corporate finance for the Annual Performance Report (APR) preparation, approval, and submission to SEEPZ as per SEZ Rules. Having functional knowledge in FTWZ activities, understanding business processes and interdependencies, staying updated on SEZ Rules and Regulations, conducting and managing investigations, and providing pragmatic solutions will be crucial. You are expected to have effective oral and written communication skills, sound management and organizational skills, understanding of the importance of documents, compliance, and legalities. A minimum of 5 years of FTWZ coordination experience, at least 2 years in the logistics industry, and a preference for a graduation degree are required. Computer literacy in SEZ system and other vendor systems, MS Office skills (especially in Word & Excel), good knowledge of IT systems, and experience with SAP or similar ERP systems will be advantageous.,

The role entails the analysis of samples, preparation of reagents, and maintenance of the chemical data book, stock of Acids, chemicals, and glassware, among others. You will be responsible for accurate and impartial reporting as per QMS standards. Proper handling and maintenance of instruments and equipment are also crucial aspects of the role. Additionally, ensuring QHSE procedures are implemented and followed in the laboratory is a key responsibility. Your main accountabilities will include preparing SOPs for testing procedures, verifying goods" descriptions, ensuring compliance with SOP and FIM instructions, and preparing MIS reports for management. Standardization and preparation of solutions of different normalities, as well as creating lab reports, quality reports, worksheets, registers, and laboratory charts will also be part of your responsibilities. Effective communication with office personnel and clients on testing-related matters is essential. Ensuring proper storage of samples, chemicals, and records as per QMS standards and handling testing equipment while maintaining and calibrating them as required by the system are also important tasks. Performance indicators for this role will include monitoring the percentage of testing errors, verifying errors, the number of tests undertaken, the number of different items tested, cost and time savings, and the results of training tests and annual technical assessments. Qualifications required for this position include a B.Sc in Chemistry (inorganic division) or a related field of Science based on business requirements. Freshers with excellent academic records are welcome for entry-level positions, while candidates with 1-2 years of experience as a Chemist are preferred for autonomous roles. Specific training or experience in testing particular products like coal, iron ore, or manganese will be considered advantageous. This is a full-time position that offers benefits such as commuter assistance and a performance bonus. The work schedule is in the morning shift, and a Bachelor's degree is preferred. The work location is in person.,

Senior Associate, Receivable & Inventory Controls Location: Bangalore WHAT YOU WILL DO Key deliverable will be receivable and inventory controls including reconciliation between our book of accounts and customer books. RESPONSIBILITIES Receivable & Inventory Control Receivable and Inventory reconciliation between our books and customers at order level on a continuous basis. Process improvement and automation of the reporting process of Inventory and Debtors Resolving operational challenges in inventory financial reporting through partnering with warehouse and SCM teams. Dispute ticket raising process implementation in marketplace/ Payment Gateway/ Currier partners/ warehouse operators and realisation of disputed amount Ensure that correct weighted average cost at style code level should reflect in the financial accounting system including coordination with technology team if required. Tracking absorption of the direct and indirect overheads and maintaining tracker/ audit trail of the adjustments to the product cost and closing stock (if any). Ensure review of the internal processes and inventory health periodically, identify risks and highlight the same to the regional and corporate management through standard and exception reports Coordination for internal audit including bank and stock audit. Ensuring the corrections if any should be incorporated in the warehouse management system Coordination for statutory compliances and maintaining the tracker. SOP preparation, periodic review and to ensure that these are adequate and operating effectively related to warehousing and manufacturing. IDEAL CANDIDATE ATTRIBUTES A self-starter who needs minimal supervisory control Strong on laying down systems and processes and ability to adhere to it Highly focused on cost accounting and controls High on integrity & energy Collaboratively working with other business RELEVANT EXPERIENCE Chartered Accountant with 8-10 years of relevant experience Experience of working in E-Commerce ecosystem is mandatory Efficient in managing and processing large data Ability to work in an unstructured environment and setting up system & processes from scratch is must Good communication skills and ability to represent the organization externally. A candidate with ability to efficiently manage Stakeholders (Internal & External) Show more Show less

Agivant Technologies is looking for Software Technical Writer (Lucknow) to join our dynamic team and embark on a rewarding career journeyWriting, editing, and proofreading technical documentation, including user manuals, product specifications, and process documentation.Collaborating with cross-functional teams, to gather information and ensure accuracy of technical documentation.Conducting research and gathering information from subject matter experts to develop technical documentation and other materials.Organizing and managing documentation, including updating and maintaining document libraries and version control systems.Creating and maintaining templates, style guides, and other documentation standards to ensure consistency and clarity of technical documentation.Ensuring technical documentation meets regulatory and compliance requirements.Publishing technical documentation in various formats, including online help, PDFs, and printed materials.Should have excellent writing and editing skills, as well as strong attention to detail and the ability to explain complex technical concepts in clear and concise language.Strong research and analytical skills.

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 02.08.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D Candidates also eligible Position : Executive / Senior Executive Qualification : M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 02.08.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

You will be responsible for ensuring the completion of experiments and generating accurate and reproducible data. This will involve developing relevant models, validating them, and supervising laboratory/pilot plant experiments within the research area. Your duties will include sample preparation, characterization, and evaluation, as well as organizing facilities and resources for experiments. Additionally, you will participate in pilot plant operations/studies and use the results as boundary conditions for model development. Supporting plant operations, collecting data, conducting analysis, uploading reports, and preparing Internal Technical Reports are also part of your responsibilities. To qualify for this role, you must have a PhD in Biology/Chemistry/Chemical Engineering with specialization in the relevant research area. A minimum of 2-3 years of research experience is required. Your skills and competencies should include conducting literature surveys, compiling information for analysis, developing work methods, and preparing SOPs for experiments. You should be able to design and plan experiments, use simulation models, study technology offers, and process engineering documents. Familiarity with process engineering design activities, relevant tools, and applicable guidelines, codes, standards, and legislations in the field of research is essential.,

We are hiring a SHIFT INCHARGE to supervise First Mile Operations for Meesho under our 3PL organization. This position is ideal for individuals who are proactive, process-driven, and want to build a long-term career in warehouse operations with a structured and rapidly growing organization. What We Offer: Absolute clarity on work expectations and number based appraisal system. Company is growing 10X in next 4 years, so a superb growth opportunity for people contributing towards growth of company. Stable company with clear laid down procedures, and a great track record of growth. Pan India operations so scope of moving across India to gain multiple experience in various geographies. Job Security with cash rich , well funded company listed on NSE with market cap of 600 Crores. Professional work culture and learning environment, where the only pressure is of upgrading your skillset and growing along with organization. Key Responsibilities: Supervise daily First Mile warehouse operations during allocated shift. Ensure smooth handling of inbound, sorting, QC, packaging, and dispatch as per SOP. Manage ground-level staff and resources to achieve shift targets efficiently. Maintain shift-wise productivity and track performance of team members. Ensure adherence to TAT, SLAs, and client-specific operational requirements. Resolve on-ground challenges and escalate key issues for timely resolution. Ensure cleanliness, safety, and discipline within the warehouse during shift hours. Coordinate with internal teams and client representatives to meet real-time operational needs. Requirements: 2-5 years of experience in warehouse operations, preferably with e-commerce clients. Prior experience working under 3PL model with structured SOPs. Should have handled shift operations in medium to high throughput environments. Good team handling capability and comfort in working with contractual manpower. Strong understanding of floor processes like sorting, scanning, labeling, and dispatch. Comfortable using system tools such as WMS or handheld devices (scanners, apps, etc.). Process-oriented approach with attention to detail and execution discipline. Flexible with shift timings and working hours as per operational requirements.

Role & responsibilities: 1. Act as Study Director for various Pre-Clinical studies as per guidelines 2. Conduct, schedule & report toxicological studies for various products in pre-clinical studies 3. Conduct Pharmacological evaluation of various pharmaceutical products 4. Preparation of SOP & documentation as per guidelines 5. Ensuring facility readiness as per regulatory guidelines & audits Preferred candidate profile: Local candidates

We are looking for a dynamic, organized, and confident female Executive Assistant / Secretary to support our Managing Director (MD). Whether you're a fresh graduate or someone with experience, this is a great opportunity to work closely with leadership in a fast-paced and professional environment. Key Responsibilities : Provide end-to-end administrative and secretarial support to the MD Manage calendars, meetings, travel bookings, and daily coordination Create and manage business reports, presentations, and MIS documents Maintain filing systems both digital and physical Assist with HR coordination, internal communication & admin tasks Handle professional communication with clients and external stakeholders Maintain confidentiality and professionalism at all times Contribute to overall office support and operations Candidate Profile : Female Graduates from any discipline Freshers with good communication and learning attitude are welcome Excellent command over English (spoken & written); Kannada is a plus Proficiency in MS Office (Word, Excel, PowerPoint, Outlook) Strong interpersonal skills, time management, and coordination ability Confident, proactive, and reliable personality Preference for candidates who can join immediately What You Will Get : Direct mentorship from senior leadership High learning exposure in client communication, reporting & coordination Professional and inclusive work environment Opportunity to grow within the organization Performance-based recognition and rewards Interested candidates may please share their updated resumes to hr@tyagroup.co.in at the earliest.

Nurse JD Location: Ultrahuman Performance Center, 100 feet road, Indiranagar, Bangalore Reports To: Wellness Director About Ultrahuman Ultrahuman is on a mission to help people understand and optimize their health through cutting-edge wearable technology and personalized insights. With products like the Ultrahuman Ring AIR, Ultrahuman M1 (continuous glucose monitoring), and Blood Vision, were helping people connect their lifestyle data with internal biomarkers to make smarter health decisions.The Ultrahuman Performance Center extends this missionbringing together advanced diagnostics (Advanced blood panels, Longevity testing, Genetics, Nutrition), recovery modalities (Cryotherapy, HBOT, Contrast therapies, IV therapy). This will also include Ultrahumans first experience center, designed to help users understand preventive health through Ultrahumans multi-device ecosystem. What Youll Do Conduct clinical diagnostics, including blood draws, vitals, ECGs, and IV therapy for recovery and wellness treatments. Prioritize safety and compliance across all procedures, including infection control, safety SOPs and emergency protocols. Educate and comfort clients on test preparation, results, and recovery processes. Collaborate with clinicians, technicians, and nutritionists to connect findings with personalized action plans. Support client understanding of insights from Ultrahuman tools like Ring AIR, Home, Blood Vision and M1. Maintaining log recordsExplaining the test and recovery procedures, taking informed consent Recognize signs of medical distress and initiate emergency response protocols, including activating EMS when required. What We’re Looking For Registered Nurse (valid BLS Certification) with 2+ years in diagnostics, wellness, or critical care.Experience with IV administration and recovery protocols. Experience in recognizing and managing medical emergencies Safety-first mindset, excellent communicator, and calm under pressure. Passion for health, wellness, and performance science.Working knowledge or proven experience of integrating nutrigenomics and other related information in assessments and developing plans Experience in advising people across different geographies and food habits.

Maintain media stock and reconcile records of media used in analysis. Perform water sampling and analysis following defined SOPs/protocols and ensure proper documentation. Report and log OOS (Out of Specification), OOT (Out of Trend), and EM (Environmental Monitoring) excursions. Conduct environmental monitoring of the laboratory. Perform analytical validation, culture maintenance, and growth promotion testing (GPT) of media; record observations and generate reports. Carry out microbiology laboratory tests such as Bioburden Analysis, MLT (Microbial Limit Test), Sterility Testing, BET (Bacterial Endotoxin Test), etc., in compliance with approved procedures. Skills and Proficiency: Microbiology Instrumentation Handling Expert Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner BET & Sterility testing expertise and evaluation skills Expert Interpretation of Resulting Data Trend Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Writing compelling personal statements, supplemental essays, and scholarship applications unique narrative angles, Craft stories that authentically represent students while meeting specific university requirements

Role & responsibilities We are looking for highly skilled and process-driven professionals to join our Quality Assurance (QA) team at a cutting-edge surgical gloves manufacturing facility. The ideal candidate will play a key role in ensuring that every aspect of production especially raw material evaluation , packing material testing , process validation , and regulatory compliance meets stringent national and international standards for Class B, C and D medical devices. Quality Management System (QMS): Design, implement, and monitor QMS as per ISO 13485 and MDR 2017 . Maintain SOPs, work instructions, and controlled documents. Regulatory Compliance: Ensure adherence to CDSCO regulations , BIS 13422 (Surgical Gloves), BIS 15354 (Examination Gloves), and GMP guidelines. Support during audits (internal, external, and regulatory). Validation & Process Control: Oversee validation protocols including cleaning, packaging, and sterilisation (ETO/Gamma). Conduct risk assessments , change control , and CAPA implementation. Batch Records Review: Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) . Ensure traceability from raw materials to finished goods using batch/lot numbers. Packaging Material Testing & Traceability: Verify and test all packaging materials against relevant standards. Maintain Certificates of Analysis (COA) for inward materials, including packing components. Ensure complete traceability for raw materials , packaging , and finished gloves . Training & Documentation: Conduct training on QA procedures, GMP, and regulatory updates. Manage deviation reports and QA documentation flow across production and QC. Mandatory Requirements: Prior experience in a CDSCO-approved manufacturing facility handling Class B, C & D medical devices. Strong understanding of: ISO 13485 MDR 2017 BIS 13422 / BIS 15354 GMP/QMS documentation Hands-on with internal audits, regulatory inspections, and validation processes. Inward Raw Material Testing: Evaluate incoming latex and other input materials using lab instruments such as viscometers, tensile testers, hardness testers, etc. Test and verify packaging materials as per standard requirements. Attach and maintain Certificates of Analysis (COA) for all inward materials, including packaging materials. Sample Preparation: Prepare glove samples for technical evaluation, customer trials, and tender submissions. In-Process Quality Checks: Monitor ongoing production to ensure compliance with defined AQL levels and physical parameters. Identify and classify critical defects during manufacturing. Packaging & Sterilization Checks: Conduct QC checks at all packing stages: Valeting, Pouching, and Sterilization (ETO/Gamma). Verify packaging integrity and labeling accuracy. Final Product Inspection: Perform thorough inspections of finished goods, including Pre-Dispatch Inspections (PDI) . Traceability & Documentation: Maintain batch and lot numbers for raw materials, packing materials, and finished goods to ensure full traceability. Generate daily QC reports, maintain batch records, and ensure proper documentation flow. Preferred candidate profile Education: B.Sc / M.Sc in Chemistry, Microbiology, or Polymer Science OR B.Tech in Chemical Engineering, Rubber Technology, or Biomedical Engineering Experience: 37 years in QA roles within the medical devices industry (gloves manufacturing preferred) Skills: Proficiency in QA documentation , process audits , and compliance systems Experience with ERP tools (SAP or equivalent), Excel , and root cause analysis Familiarity with AQL standards , though not primary in QA, is a plus Proficiency in using QC lab instruments and interpreting test results Familiarity with Excel , ERP systems (SAP or equivalent) Knowledge of internal audits , root cause analysis , and process validation

Conduct induction for new joines, ensure continuous training for all plant employees. Perform daily safety walk paths, coordinate work permits with engineering, health check. Handle factory inspections, lead safety audits, emergency plan effectively. Perks and benefits Accommodation Transportation, Mediclaim

KPMG India is looking for Executive - Adobe QA to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

Job Title: Global Content & Research Expert Job Location: Ahmedabad (Work From Office) Salary Range: No bar for right candidate Education: Any Graduate Position Overview: We are seeking a talented and creative Content Writer to join our Winny immigration company. The successful candidate will play a critical role in developing, writing, and editing content that helps potential clients understand our immigration services. You will also be responsible for writing and reviewing visa letters, ensuring clarity, accuracy, and compliance with legal and visa requirements. About Company: Winny Immigration and Education Services Ltd. is an established company with expertise in several verticals of travel, visas , immigration, international education, career counselling and coaching. Winny, as it is popularly known, has consistently been delivering quality and reliable services for the past 43+ years. Trust, strong work ethics, professionalism, and commitment are the main pillars of our organization. Website: https://winnyimmigration.com/ Roles & Responsibilities: Content Writing & Research: Create personalized and professional resumes, visa letters, and support documents. Draft clear, logical case representations that align with visa requirements and client objectives. Ensure all written materials meet quality, accuracy, and compliance standards. Client Profiling & Advisory: Assess client backgrounds to identify suitable visa categories and career opportunities. Analyze client goals and recommend tailored pathways with a high probability of visa approval. Offer strategic suggestions aligned with immigration rules and career alignment. Visa Process Management: Manage and coordinate the end-to-end visa process for employment-related visas across various countries. Liaise with clients for documentation, follow-ups, and clarification on requirements. Keep up-to-date with visa regulations and documentation standards for multiple destinations Client Communication & Coordination: Serve as the primary point of contact for clients throughout their visa journey. Maintain clear, professional communication and ensure timely updates. Collaborate with internal teams to ensure a seamless client experience. Required Skills Knowledge of AI tools and Prompts Content Writing & Editing Expertise Immigration Knowledge & Compliance Research Skills Adaptability & Problem-Solving Team Player Ability to understand and communicate MS Office Why Join Winny? Prestigious Brand: Be part of a legacy spanning four decades, trusted by millions. Impactful Role: Play a pivotal part in our ambitious growth journey. Innovative Environment: Work with cutting-edge technology, including proprietary CRM systems and mobile applications designed for seamless service delivery. Ethical Work Culture: Thrive in an organization that values integrity, teamwork, and operational excellence. Leadership Opportunities: Develop your career in a leadership role where your expertise will shape the future of the regions business. Accelerated Growth Trajectory: Join an organization poised for exponential growth, offering unparalleled opportunities to contribute, innovate, and thrive as we scale new heights. Flexible and Open Culture: Experience a supportive and transparent work environment that encourages creativity, collaboration, and work-life balance.

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd.! We're hiring a Document Controller - Food Manufacturing for our client. Location: Hyderabad Department: Quality Assurance / Operations / Compliance Experience Required: Minimum 5 years in Document Control, preferably in the food manufacturing, FMCG, Pharma and manufacturing Industry only. Job Summary: We are looking for an experienced Document Controller to manage and maintain all controlled documents and records in compliance with internal standards and regulatory requirements. The role involves overseeing documentation workflows, ensuring version control, supporting audits, and coordinating across departments to ensure timely access to accurate information. Key Responsibilities: Maintain and organize all company-controlled documents including SOPs, specifications, audit records, and quality manuals. Ensure version control, proper labeling, and secure storage of all documents. Support internal and external audits by providing relevant records promptly. Coordinate document approvals and revisions across departments. Implement and improve document control systems and procedures. Train and support staff on document management processes. Track document changes and maintain a master document list. Ensure compliance with applicable industry and regulatory standards. Requirements: Bachelor's degree in Business Administration, Quality Management, or a related field. At least 5 years of experience in a document control or quality systems role. Proficiency with document control software and Microsoft Office tools. Strong attention to detail and organizational skills. Excellent communication and coordination abilities. Familiarity with quality systems and compliance standards. (Interested candidates can share their CV to aradhana@hungrybird.in or call on 9959417171) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: RAHUL, MARKETING MANAGER, 8 YEARS, 60 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards, Aradhana +91 9959417171

Title: Instrumentation and Automation Engineer Qualification: B.E in Electrical & Instrumentation Primary Responsibilities: 1. To attend /or supervise all jobs related to Instrumentation Engineering activities in site. 2. Timely execution of all calibrations of equipments/instruments as per schedule coordination with user. 3. To attend emergency breakdowns of all plant wide machines round the clock as and when required. 4. Maintain the Spare parts of all critical Instruments in site. 5. Timely execution and completion of Validation activities to be done in site. 6. Execution of all In-house Projects in instrumentation and automation in site. 7. Maintain the calibration logs, area /equipment logbooks, preventive maintenance schedule of all the activities. Audit readiness Secondary Responsibilities: 1. Preparation and Review of all documents related to engineering. Timely execution and completion of Performance verification of the equipments. Interested candidates can share your resume to [ Careers@curateqbio.com, hasumitha.chitti@curateqbio.com] with relevant subject line.

Envirocoats is looking for Quality Control Engineer to join our dynamic team and embark on a rewarding career journey Analyzing customer needs to determine appropriate solutions for complex technical issues Creating technical diagrams, flowcharts, formulas, and other written documentation to support projects Providing guidance to junior engineers on projects within their areas of expertise Conducting research on new technologies and products in order to recommend improvements to current processes Developing designs for new products or systems based on customer specifications Researching existing technologies to determine how they could be applied in new ways to solve problems Reviewing existing products or concepts to ensure compliance with industry standards, regulations, and company policies Preparing proposals for new projects, identifying potential problems, and proposing solutions Estimating costs and scheduling requirements for projects and evaluating results

Role & responsibilities Manage end-to-end recruitment: sourcing, screening, interviewing, onboarding Maintain employee database, personal files, and HR documentation Handle monthly payroll processing, attendance, and leave management Update employee data in HRIS/ERP systems Oversee probation tracking and issue confirmation letters Ensure statutory compliance (PF, ESI, PT, LWF, Gratuity) Conduct HR inductions, support training programs Assist in performance management process Manage exit process: interviews, full & final settlements, relieving formalities Maintain job descriptions and organization charts Address employee queries and grievances Support employee engagement initiatives Draft HR policies, SOPs and ensure implementation Coordinate with QA team for internal audits and ISO/GMP documentation Preferred candidate profile MBA/PGDM in HR preferred Preferably manufacturing unit experience Hands-on experience in payroll, compliance (PF, ESI, PT), and HRIS/ERP systems Good knowledge of labour laws and HR documentation Good communication skills Knowledge on HRMS software Fluent in English