741 Quality Documentation Jobs - Page 22

Job Title: QMS Specialist # Salary: As per Industry Standards (Depend on Experience/Knowledge) # Job Summary: We are seeking a highly skilled and experienced QMS Specialist to join our team in the plastic molding industry. The successful candidate will be responsible for implementing, maintaining, and continuously improving our QMS, ensuring compliance with international standards and regulations. # Key Responsibilities: 1. Develop, implement, and maintain QMS in accordance with international standards (e.g., ISO 9001, IATF 16949). 2. Ensure compliance with regulatory requirements, industry standards, and customer-specific requirements. 3. Conduct internal audits to ensure the effectiveness ...

Role & responsibilities 1) SOP Preparation 2) Daily/ Weekly/ Monthly/ Yearly Audit preparation 3) Internal Audit 4) ISO Audit Preparation 5) Daily MIS preparation 6) Monthly PPT submission and collection from department 7) All department documentation checking Preferred candidate profile

Education : UG: B Tech in Mechanical, BSc, B. Tech Medical Science, M sc. Key skills: Regulatory Submissions : 510(k), CE Marking, EU MDR 2017/745, US FDA, Indian MDR 2017 Clinical Evaluation Reports (CER) : Development, Literature Reviews, Clinical Data Analysis Risk Management : ISO 14971, Risk Assessments, Risk Mitigation Strategies Post Market Surveillance (PMS) : Data Collection, Reporting, Device Performance Monitoring Post Market Clinical Follow-up (PMCF) : Study Design, Data Analysis, Reporting Regulatory Compliance : US FDA, EU MDR, Indian MDR, ISO 13485 Communication : Cross-functional collaboration, technical writing, regulatory guidance Desired Candidate Profile: Regulatory Affai...

Role & responsibilities : Maintain , upgrade and implement the Quality Management System (QMS) / MR and Quality Assurance throughout organisation. Ensure zero customer complaints by introducting quality gate cocept. Ensure inprocess rejection and rework is within target set by the management, Assure the reliability and consistency of production by ensuring inprocess control by having internal process and product audits. Communicate and interaction with customer for QAP (Quality Assurance Plan) & Customer Complaints. To develop and implement the Quality Assurance & Quality Management Strategy in conjunction with Senior management to satisfy quality requirements defined by customers, applicabl...

Quality Planning: Develop and implement quality plans, procedures, and standards for solar power projects. Inspection and Testing: Conduct inspections and testing of solar Knowledge of solar systems, quality engineering principles.

Responsibilities: * Conduct QA/QC inspections onsite & offsite * Enforce quality standards throughout project lifecycle * Ensure compliance with IS codes & material specs * Prepare quality documentation accurately

Vacancy for Unit Manager Quality. Join us as a Unit Manager based in Pune to be responsible for the inspection of all incoming parts from supply chain and in-house produced components to meet the quality standards and systems required.. Provide clear leadership for the development of an environment focused on Quality. Develop quality-process links with customers in line with the Quality Management system. Quality Manager is directly responsible for product and equipment quality & their compliances.. About The Company. In Alfa Laval, we are every single day contributing to a more sustainable future for our planet through engineering innovation. Our global team designs and implements the refin...

Key Requirements: Hands-on experience with CEMILAC or DGQA -certified project. Experience in re-surveillance or recertification audits related to industry standards. In-depth knowledge of ISO 9001 and AS9100D standards. Proficiency in Quality Control tools and quality documentation practices. Experience with internal and external audits , including audit checklist preparation and process verification. Familiarity with ESS testing processes in the aerospace sector. Knowledge of incoming goods inspection procedures. Understanding of PCB and mechanical inspection , including related documentation. Proficiency in MS Office , especially Excel, is an added advantage. Knowledge of IPC-A-610 and its...

Site Inspection, Material Testing, Defects reporting & rectification, ensure compliance with relevant codes, standards & regulations, Maintain accurate record of inspections, test & defects, Preparation of QAP, WIR, Methodology statement, checklist Required Candidate profile 03 to 05 years experience in Industrial Civil Construction project from contractor firm site. Proactive, team player, Ability to handle work pressure, documentation skill, Good communication Perks and benefits Free bachelor accommodation, food ,transportation

Role & responsibilities Highly motivated knowledgeable Engineers with experience in Quality assurance of incoming items, bought outs, raw materials, maintenance of ISO 9001 documentation, QA inspection online and onsite of vendors materials, leading the inspection team during customer inspections at factory, establish and maintain SOPs as per company rules. Preferred candidate profile Graduate in Mechanical Engineering. The candidates should speak fluently in English/Hindi fluently. Age /Sex/Religion no bar.

Role & responsibilities Responsible for following activities: a. Verify cGMP, GDP, GLP and data integrity practices, compliance in Quality Control and microbiology laboratory. b. Review of Specification, Standard test procedures and test data sheet for adequacy and accuracy. c. Review Validation and calibrations of all Instruments. d. Review of AMV, AMT Protocols and reports. e. Handling of Lab incidents, Deviations, OOS, OOC, OOT etc. f. Handling of reserved sample of finished products and its visual inspection. g. Review of trend data of environmental monitoring, water analysis. h. Participation in audit the contract testing laboratory. Preferred candidate profile ERP/ QMS/QC software syst...

1. Create and maintain company quality documentation, such as manuals, procedures, etc. 2. Continuously improve QA processes and procedures. 3. Preparation of QA reports. 4. Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012

Must have Excellent Understanding of Organizational Structure, Accurately record & report data, Completes documentation relating to material analysis & enters data into database/software system Required Candidate profile Extensive knowledge of QC Tools required, Knowledge of IATF/IMS.

Focus on QMS IMPLEMENTATION, QUALITY MANUALS, PLANT INTERNAL AUDIT SYSTEM, conduct QUALITY SYSTEM AUDITS, QMS TRAINING, CONTINUOUS IMPROVEMENT INITIATIVES, EXTERNAL AUDIT COORDINATION, MR ACTIVITIES, Plan SOPs, QA CERTIFICATIONS, OEMs HNANDLING etc Required Candidate profile BE 5+yrs exp into QMS/ SYSTEM QUALITY with EMS/AUTO/ENGG Unit with strong exp in ISO, IATF, APQP, PPAP, FMEA, QA AUDITS, MR TASKS, ACCREDITATIONS, INTERNAL QA AUDITS, SIX SIGMA, LEAN et Work at TADA Perks and benefits Excellent perks. Send CV to cv.ch1@adonisstaff.in

To assist the Quality Assurance function as technical support in issues affecting manufacturing. To support and drive corrective action efforts. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Ensure capability studies are performed on critical processes. Perform first article inspection and review visual aids. Perform defect analysis reporting. Perform MRB on sustained products. Participate in CAC meetings support continuous improvement. Perform line and product audits. Assist Quality Engineering in APQP. Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor. Comply and follow all procedur...

SUMMARY To assist the Quality Assurance function as technical support in issues affecting manufacturing. To support and drive corrective action efforts. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Ensure capability studies are performed on critical processes. Perform first article inspection and review visual aids. Perform defect analysis reporting. Perform MRB on sustained products. Participate in CAC meetings support continuous improvement. Perform line and product audits. Assist Quality Engineering in APQP. Adhere to all safety and health rules and regulations associated with this position and as directed by supervisor. Comply and follow all ...

Conduct inspections of MCC-PCC-LT-PLC panel manufacturing processes to ensure compliance with design specifications,customer requirements,preparing QMS document,perform visual inspection,ISO 9001,Such as UL-IEC, including implementation, verification

Role & responsibilities Quality System Implementation (ISO 9001:2015) Production Quality Monitoring (inspections, testing) Problem-Solving & Non-Conformance (RCA, CAPA) Process Control & Improvement (Kaizen, 5S) Supplier Quality Management Preferred candidate profile ISO 9001:2015 knowledge Quality tools (7 QC tools, RCA, CAPA, FMEA) Certified internal auditor for ISO 9001:2015 (preferred) QA experience from plastic drum or any packaging industry

Developing & implementing quality control system, Monitoring Quality Performance, Material Testing, Quality Check, Develop Corrective Action, Quality Process, Coordination with departments to improve the quality, Process comply with safety measures.

Experienced QA Manager to oversee&manage QA operations our pharmaceutical manufacturing unit.Ideal candidate will ensure compliance with GMP, WHO other regulatory standard,while developing &maintaining QMS Share your Resume to hrd@stedmanpharma.com

Role & responsibilities Role :QC engineer As a QA/QC Engineer, you will be responsible for implementing and managing quality assurance and control systems to ensure our mechanical products meet customer, industry, and regulatory standards. You will work closely with our manufacturing, design, and service teams to drive continuous improvement and ensure product excellence. Key Responsibilities Include: Developing and maintaining QA/QC procedures and inspection plans. Reviewing drawings, specifications, and manufacturing processes for compliance. Conducting inspections of mechanical parts and assemblies. Leading root cause analyses and corrective/preventive action activities. Preparing quality...

Whats the roleWe are looking for customer-focused Specification Consultants to kick-start their careers in a rewarding, high-performing, multinational company. Who is HiltiHilti is where innovation is improving productivity, safety and sustainability in the global construction industry, and beyond. Where strong customer relationships are creating solutions that build a better future. Where there is pride and a sense of belonging across our 120 locations, carrying right into our lives and homes. Where people are exploring possibilities, leveraging their potential, owning their personal development and growing lasting careers. What does the role involveAs a Specification Consultant, you will b...

Conduct field inspections and audits to assess internal field quality standards and procedures Monitor key process quality throughout the production activities, from source lot purity check to final harvest seed, ensuring the standard critical to processes Identify quality issues, deviations, and non-conformities, and initiate corrective and preventive actions. Strong knowledge in digitalization of processes and soft skills in improving the applications for field scoring systems Monitor and assess crop health, identifying and addressing issues related to pests, diseases, nutrient deficiencies, and environmental factors which affect Seed Quality. Monitor and analyze field data and metrics to ...

Role Summary: A quality control Manager is responsible for ensuring that products or services meet established quality standards by developing and implementing quality control procedures, conducting inspections, and analyzing data to identify areas for improvement. Key Responsibilities: Performs verification on Incoming, In-Process, and Outgoing products. Assists and/or trains operators on part visual acceptability, and measurement and process procedures as required. Internal Customer complaint handling , Record keeping and CAPA/Closure . Creating and maintaining the Companys Quality Standards; develop, implement and maintain the Companys quality documentation, such as quality procedures, re...

Understanding the market dynamics competitive environment in Vegetable markets of scope countries To devise strategies implement business strategies based on the market study competitor analysis to tap the markets. Design and execute the trial plan as per the requirements of the region , collect trial data for evaluation and report to the crop teams Coordinating with state and central universities and other organizations, understanding the requirement of the licensing, organize the trials for variety registration Provide Technical support to customers internal team. Work closely with internal stakeholders Viz., Supply Chain, R D, Bio Tech etc. Gather the knowledge of the distributors in the ...