Array ( [0] => qa [1] => bhopal ) QA-Quality Assurance Jobs in Bhopal,QA-Quality Assurance Job Vacancies in Bhopal Madhya Pradesh
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QA-Quality Assurance Job Vacancies in Bhopal

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Looking For Quality Control Executive

EliteHire Placement Solutions

  • 4 - 8 yrs
  • 5.5 Lac/Yr
  • Bhopal
Quality Assurance Quality Control Quality Analysis QA-quality Assurance Quality Check QC Inspection
Required Candidates from Transmission tower line ,EPC project ,Quality strengthened the Systemic approaches towards ZEROdefect /ZERO Customer Complaints , 98% Reduction in customer complaints,QA ,QMS IMS responsible for the entire QA function, SupplierQuality, Plant Quality, Process Quality, Product Quality, Outgoing Quality, Customer Quality, QMS & IMSImplementation,A structured and planned monthly meeting with the Customers. Take up the training of the Sub-ordinate employees and mentor them to enhance their performance. Production management with daily target monitoring for out-put as well as Quality. Administer the Incoming Quality, In-process Quality and outgoing quality. Handle the supplier selection, up gradation and development emphasizing on enhancing the productivity andprofitability of the organization. PPM reduction (Internal & External both) through various CFT
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Medical Device Regulatory Affairs Specialist

Fastdrive Consultancy

  • 3 - 6 yrs
  • 5.0 Lac/Yr
  • Bhopal
EU MDR ISO 13485 CDSCO Regulatory Compliance Quality Assurance and Control
Job Title:Medical Device Regulatory Affairs SpecialistBhopal LocationCompany: Intense Medical & Dental System Pvt Ltd Bhopal.Job Brief:We are looking for a skilled Regulatory Affairs Specialist to manage and coordinate regulatory compliance for our medical devices. This role requires strong communication with channel partners, collaboration with documentation teams, and ensuring all products meet regulatory standards for both domestic and international markets.______________Key Responsibilities:* Ensure medical devices comply with all applicable national and international regulatory requirements and standards* Prepare and submit regulatory submissions, including 510(k), PMA, and other global market registrations* Communicate with regulatory authorities (such as the FDA, CDSCO) to handle queries and support approval processes* Monitor and interpret changes in medical device regulations and assess their impact on the company* Provide regulatory guidance and training to cross-functional teams including R&D, QA/RA, and Product Development* Develop and implement regulatory strategies to support new product development and market expansion* Maintain organized, up-to-date documentation to demonstrate compliance and support audits* Collaborate with channel partners and internal documentation specialists to ensure consistent regulatory alignment______________Requirements:* Bachelors degree in Biomedical Engineering, or B.E electronic commination. or a related discipline* 34 years of experience in medical device regulatory affairs* Strong knowledge of domestic and international medical device regulations (FDA, EU MDR, ISO 13485, CDSCO, etc.)* Excellent verbal and written communication skills* High attention to detail, analytical thinking, and problem-solving ability* Experience working collaboratively across multiple teams______________Preferred Qualifications:* Regulatory Affairs Certification (RAC)* Experience with Class II or III medical devices* Familiarity with quality systems (e.g., ISO 13485, FDA QSR)Key Responsibilities: Quality Assurance and Control Regulatory Compliance Process Improvement Supplier Quality Management Key Documentation and Reporting
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Quality Assurance Quality Control Engineer Jobs For B.E Freshers

Manjeet Industries

  • 0 - 2 yrs
  • Govindpura Bhopal
Quality Procedures Process Documentation QC Inspection Quality Assurance Quality Control Product Quality
Designing on solidworks & Autocad. Inspection of jobs on machine. New job study & production setup. Job record of machines. Final inspection report of jobs & packaging
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Quality Assurance Quality Control Engineer

Intense Medical & Dental System Pvt. Ltd.

  • 1 - 7 yrs
  • 3.8 Lac/Yr
  • Bhopal
Quality Assurance Quality Control ISO Audit ISO Documentation Quality Check Quality Procedures Quality Analysis
Key ResponsibilitiesQuality AssuranceDevelop, implement, and maintain Quality Management Systems (QMS) in compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable standards.Conduct internal audits, CAPA (Corrective & Preventive Action), and risk assessments to ensure ongoing compliance.Monitor production processes and verify adherence to SOPs, specifications, and quality standards.Quality ControlPerform in-process inspections, final product testing, and release of products.Review and approve batch records, test reports, and other QC documentation.Manage calibration and preventive maintenance schedules for testing and measuring instruments.Investigate non-conformities and implement corrective actions.Regulatory ComplianceEnsure compliance with national and international medical device regulations (FDA, CDSCO, CE, ISO).Support preparation of regulatory submissions (510(k), PMA, CE Marking, etc.).Communicate with regulatory authorities to resolve compliance issues.Process ImprovementIdentify areas of process improvement to enhance product quality and operational efficiency.Implement Lean Six Sigma/continuous improvement methodologies to reduce defects and improve productivity.Supplier Quality ManagementConduct supplier audits and ensure raw material/component quality.Collaborate with vendors for corrective actions and quality improvement initiatives.Documentation & ReportingPrepare and maintain technical files, Device Master Records (DMR), and Device History Records (DHR).Maintain up-to-date documentation to support internal audits, external inspections, and certifications.Generate quality reports and present trends to management for decision-making.Required Skills & KnowledgeStrong understanding of QA/QC principles in the medical device industry.Knowledge of ISO 13485, ISO 14971, GMP, and FDA 21 CFR Part 820.Hands-on experience with quality audits, validation, and verification processes.Familiarity with regulatory submissions and compliance requirements.Excellent documentation, analytical, and problem-solving skills.Ability to train and guide cross-functional teams on quality and compliance. WhatsApp: +91 9266682964
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Jobs by Related Category

Quality Assurance Quality Control Engineer

Right Way Solution

  • 2 - 4 yrs
  • 3.0 Lac/Yr
  • Govindpura Bhopal
Quality Check Product Quality QA-quality Assurance Quality Assurance Inprocess Inspection UPCOMING Final Inspection VT Industrial Designer Cost Estimator
Candidates should be relevant experience in sheet metal fabrication industry Should be good in English languages
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Opening For Quality Head

Global Talent Pool

  • 10 - 14 yrs
  • Bhopal
QA-quality Assurance QMS Implementation Product Quality Quality Control
. Quality Management System (QMS):- Develop, implement, and maintain an effective Quality Management System (QMS) in compliance with regulatory requirements.- Continuously assess and improve the QMS to enhance efficiency and effectiveness.2. Regulatory Compliance:- Stay abreast of relevant regulatory requirements and ensure the plant's compliance with local and international quality standards.- Interface with regulatory authorities as needed for inspections and approvals.3. Quality Assurance:- Establish and maintain quality policies and procedures.- Conduct internal audits to ensure adherence to established quality standards.- Oversee the documentation and review of batch records, specifications, and other relevant documents.4. Quality Control:- Develop and implement robust quality control processes for incoming raw materials, in-process production, and finished products.- Supervise the testing and inspection of materials and products to ensure compliance with specifications.5. Continuous Improvement:- Lead and promote a culture of continuous improvement in quality processes and systems.- Analyze quality data to identify trends and areas for improvement.6. Team Leadership:- Train, and develop a high-performing QA and QC team.- Provide leadership and guidance to ensure a culture of quality and compliance.
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Quality Control Engineer

Bend Joints Pvt. Ltd.

  • 2 - 8 yrs
  • Bhopal
Microsoft Office QA-Quality Assurance AutoCAD Quality Control Quality Control Management Quality Engineer
Role & Responsibility:1. Prepares reports by collecting, analyzing, and summarizing data; making recommendations.2. Familiar with ASME Codes and all welding processes (GTAW, GMAW, SAW, SMAW etc).3. Monitoring manufacturing progress and coordinate with customers.4. Review of customer contracts, specifications, determines testing and fabrication methods required.
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Relationship Manager

Workforce Recruitment and Placement

Corporate Banking Banking Good English Communication Good Personality Quality Assurance Leader
Hiring for 15 Relationship Manager Jobs in Indore, Madhya Pradesh, Bhopal, Madhya Pradesh, Seoni, Madhya Pradesh, Jabalpur, Madhya Pradesh, Chhindwara, Madhya Pradesh, Betul, Madhya Pradesh, Hoshangabad, Madhya Pradesh, Vidisha, Madhya Pradesh, Sagar, Madhya Pradesh, Good English Communication, Good Personality, Quality Assurance Leader, for Freshers, Required Educational Qualification is : Higher Secondary, Secondary School, Professional Degree, other Bachelor Degree, B.a, B.c.a, B.com, B.pharma, B.tech/b.e, Md/medicinae Doctor, Post Graduate Diploma, M.a, M.arch, M.c.a, M.b.a/pgdm, M.com, Ms/master of Surgery, M.sc, M.tech with Good Knowledge in Corporate Banking, Good English Communication, Good Personality, Quality Assurance Leader Etc.,
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Quality Analyst

Magnum Group

  • 1 - 2 yrs
  • 3.5 Lac/Yr
  • Bhopal
Manual Testing Quality Monitoring QA-Quality Assurance Medical Transcription Call Monitoring Quality Analysis Cset MS-EXCEL Quality Analyst
Roles and Responsibilities:Closely work with Account Management team and OPS leaders to ensure Customer centricity of assigned accounts Contractual compliance, meet CSAT target, other customer asks/ action items, proactively identify potential escalationOperation Excellence E2E process mapping, identify & agreement on RACI, FMEA, propose controlsProcess Improvement Identify and lead potential improvement projects following Lean/ Six Sigma/ Kaizen/ AutomationHelp team to meet the SLA/ KPI TargetAssurance - Periodic audit on the Service Delivery model and identify opportunity of improvement, ensure compliance with CMS/ ISO/ CMMI standardQualifications:GraduateLeanMandatory Skills:Hands on Operational Management experience - Service Delivery model, Forecasting, Work Planning, Work monitoring & control, Quality Audit/ VOCLean principleOthers - Process documentation, metrics/ SLA-KPI frameworkAdditional Skills:Excellent verbal and written communication skills, email etiquette, interpersonal skills, corporate etiquette and knowledge of escalation procedures.
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Opening For QA QC Manager

Global Talent Pool

  • 8 - 11 yrs
  • 15.0 Lac/Yr
  • Bhopal
QA-Quality Assurance QC Inspection
Quality Management System (QMS):- Develop, implement, and maintain an effective Quality Management System (QMS) in compliance with regulatory requirements.- Continuously assess and improve the QMS to enhance efficiency and effectiveness.Regulatory Compliance:- Stay abreast of relevant regulatory requirements and ensure the plant's compliance with local and international quality standards.- Interface with regulatory authorities as needed for inspections and approvals.Quality Assurance:- Establish and maintain quality policies and procedures.- Conduct internal audits to ensure adherence to established quality standards.- Oversee the documentation and review of batch records, specifications, and other relevant documents.Quality Control:- Develop and implement robust quality control processes for incoming raw materials, in-process production, and finished products.- Supervise the testing and inspection of materials and products to ensure compliance with specifications.5.Collaboration:- Collaborate with cross-functional teams, including production, R&D, and supply chain, to drive quality improvements throughout the product life cycle.Quality Metrics:- Develop and report key performance indicators (KPIs) related to quality, providing regular updates to senior management.Qualifications:- Bachelor's or Master's degree in a relevant scientific or engineering discipline.- 8+ years of experience in quality assurance and quality control within the empty capsules, or related industry.
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Regulatory Affairs Executive

Intense Medical & Dental System Pvt. Ltd.

  • 10 - 11 yrs
  • 4.8 Lac/Yr
  • Bhopal
Software Quality Assurance Quality Assurance Executive
Key Responsibilities: Ensure medical devices comply with all applicable national and international regulatory requirements and standards Prepare and submit regulatory submissions, including 510(k), PMA, and other global market registrations Communicate with regulatory authorities (such as the FDA, CDSCO) to handle queries and support approval processes Monitor and interpret changes in medical device regulations and assess their impact on the company Provide regulatory guidance and training to cross-functional teams including R&D, QA/RA, and Product Development Develop and implement regulatory strategies to support new product development and market expansion Maintain organized, up-to-date documentation to demonstrate compliance and support audits Collaborate with channel partners and internal documentation specialists to ensure consistent regulatory alignment________________________________________Requirements: Bachelors degree in Biomedical Engineering, or B.E electronic commination. or a related discipline 3 - 4 years of experience in medical device regulatory affairs Strong knowledge of domestic and international medical device regulations (FDA, EU MDR, ISO 13485, CDSCO, etc.) Excellent verbal and written communication skills High attention to detail, analytical thinking, and problem-solving ability Experience working collaboratively across multiple tea
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