QA-Quality Assurance Job Vacancies in Madhya Pradesh

Key Responsibility:- Perform routine chemical and physical analysis on incoming raw materials, in-process batches, and final finished goods. Maintain and track control/retention samples of finished products and raw materials. Write down test results and keep detailed logs following Good Documentation Practices. Operate and maintain key analytical laboratory instruments Execute and document timely calibration and standardization of laboratory instruments to ensure Measurement accuracy. Ensure strict adherence to chemical handling, waste disposal guidelines, and the usage of Personal Protective Equipment (PPE)Qualification & Skills: 2 to 3 years of working experience in a Quality Control laboratory of a Chemical, Understanding of chemical properties, wet chemistry, and analytical methods. Hands-on experience with handling hazardous chemicals safely. Proficient in Microsoft Excel for compiling test data.Share Resume :- palak.hitech@gmail.com

We are looking for a Pharmaceutical Quality Assurance Executive to ensure that our products meet the highest standards of quality and safety. This role is ideal for recent graduates or those with up to five years of experience in the pharmaceutical industry.Key Responsibilities:1. Quality Audits: Conduct routine inspections and audits of production processes to ensure compliance with quality standards and regulatory requirements.2. Document Control: Manage and maintain quality documentation, including standard operating procedures (SOPs) and quality manuals, ensuring all records are up to date and accurate.3. Product Testing: Collaborate with laboratory teams to perform sample testing and analyze results, guaranteeing that products meet established quality specifications before release.4. Problem Resolution: Identify quality issues, investigate root causes, and recommend corrective actions to prevent recurrence and enhance overall product quality.5. Training and Support: Assist in training staff on quality assurance processes and regulatory requirements, fostering a quality-first culture within the organization.Required Skills and Expectations:Candidates must possess a relevant graduate degree. Strong attention to detail and excellent analytical skills are essential for identifying and resolving quality issues. Clear communication abilities are necessary to effectively collaborate with various teams. A proactive attitude, along with a willingness to learn and adapt in a fast-paced environment, is crucial for success in this role. Familiarity with quality assurance principles and regulatory guidelines in the pharmaceutical sector is a plus.

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

Designing on solidworks & Autocad. Inspection of jobs on machine. New job study & production setup. Job record of machines. Final inspection report of jobs & packaging

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

. 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.

QA Manager / Asst QA Manager Responsibilities:-To handle calibration & validation activities at site.Preparation & review of Technical Documents like Site Master File, Validation Master Plan, Qualifications & Validation Protocols, Validation Reports, Master Formulas, Batch Manufacturing & Packing Records, Policies, Manuals Work Instructions, general and standard specifications and testing procedures & Standard Operating Procedures.To prepare, review & report annual product reviews & product stability reports.To investigate complaints, deviations, quality incidents and non-conformances and ensure implementation of CAPA.To control IPQC activities in production and packing of finished products.To handled external audits like regulatory audits and vendor audits.To indent QA requirements.To approve (sanction) leaves of QA department personnel..To conduct internal audits as per current Good Manufacturing Practices (cGMP) requirements.To issue Corrective Action & Preventive Action and to do follow up for effective implementation of Corrective Action & Preventive Action.To review and approve out of specification, quality incident, deviation, change control, validation documents.To Review and Release manufactured batch.Revision of SOPs & it's integration with Corporate Documents.Act as the pollution prevention, waste minimization and energy team member where applicable.Implementation of Quality Management System & Environment Management System requirements as applicable to IPQC function.To conduct training on Good Manufacturing Practices/Good Laboratory Practices in coordination with Human Resources department.Vendor development, evaluation & assessment of suppliers through auditsTo review Batch Manufacturing Records.To perform gap & risk analysis.To handle change controls.

1. Sales & Marketing of Heat Pump, Scroll Chiller & Solar System.2. Maintain relationships with Consultants, Architects, Builders, Contractors & End-user by Providing support, information, and guidance.3. Establishing a new business, negotiating contracts & packages, and booking the job.4. Attending exhibitions, conferences, and meetings.5. Reviewing sales performance & aiming to achieve quarterly targets.6. Prepare design-based BOQ & price estimate.7. Project Planning, Execution & Supervision.8. Invoice submission, payment follow up & payment collection.9. Co-ordination between Sales & Service and Branch & HO.10. Co-ordinate with the transporter and arrange to do loading-unloading work.11. Willing to travel East & North

Anand Group is a dynamic and growing Dealership of Tata Motors dedicated to delivering exceptional products/services to our valued customers. We are seeking an experienced and results-driven General Manager - Sales & Service to lead our team and drive revenue growth.Position Summary:As the General Manager - Sales & service you will be responsible for developing and executing effective sales/Service strategies, leading a high-performing team, and achieving revenue targets. The ideal candidate will have a proven track record of successful leadership, excellent communication skills, and a strategic mindset.Key Responsibilities:Develop and implement strategic Sales/Service plans to achieve company objectives.Lead and motivate the team to meet and exceed targets.Build and maintain strong relationships with key clients and partners.Analyze market trends, competitor activities, and customer needs.Provide regular reports on performance and market trends to senior management.Collaborate with cross-functional teams to ensure a unified organizational approach.Conduct regular training and development programs for the team.Stay updated on industry trends and implement innovative sales/Service approaches.Negotiate contracts and agreements with clients.Qualifications:Bachelor's degree in Business Administration or related field (MBA preferred).Proven experience in a senior sales leadership role.Strong track record of achieving and exceeding sales targets.Excellent communication, negotiation, and interpersonal skills.Strategic thinking and analytical abilities.Ability to inspire and lead a diverse sales team.Familiarity with Sales and market dynamics.Results-driven with a focus on customer satisfaction.

Hiring for 20 Quality Inspector Jobs in Delhi NCR,Pune,Bengaluru,Pithampur Industrial Area, Dhar,Delhi Road, Rewari,Faridabad,IMT, Faridabad,IMT Manesar,5s,Quality Analyst,Inspection Engineer,Quality Assurance Leader, for Freshers,Required Educational Qualification is : Diploma, Advanced/Higher Diploma, B.Tech/B.E with Good knowledge in 5s,Quality Analyst,Inspection Engineer,Quality Assurance Leader etc.

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.

Job DescriptionWe are looking for Manager Application, Process & Quality Assurance (For AAI) Reporting to Plant HeadLocation-Pithampur, India (Near Indore, Madhya Pradesh)What to expect / your job purpose / ContextWe are looking for a highly experienced technical specialised manager in the field of application, Process and Quality Assurance strengthen our Quality Assurance and New Product development team.As part of the team who will manage the application, process and quality assurance & controls of New Product. You will directly be involved in this unique opportunity. After define the process of application & product, you will ensure SOP without any failure and facilitate production ramp up. Thereafter you will be incharge of the product development, quality of the product and of its continuous improvement.Your team will consist of 04 direct reportees in the beginning who are basically electrical engineers and technicians. You will be based in Pithampur, at our site dedicated to Clad products. With a community of 250 employees in 2024, our subsidiary company Innovative Clad Solutions Pvt. Ltd. & Aperam Alloys India Pvt. Ltd. which is situated in the Pithampur, Madhya Pradesh region in India and produces high added value products for the domestic and international market in the field of electronics, automotive, electrical OEMs, etc.What you will doIn new projects, (project refers to Definition, Verification, Installation and Commissioning of single equipment or set of multiple equipment) Assist the global head of Quality and define key tasks in order to achieve the Product process & Development. Define the equipment specifications for developing the Quality Lab.in close coordination with Electrical, operational and safety heads Monitor the installation and commissioning of the equipment in close collaboration with outside (third party) suppliers Extend support to Production department to establish the new process & product.

We have Vacant of 10 Sales Officer Jobs in Balaghat, Madhya Pradesh, Mandla, Madhya Pradesh, Betul, Madhya Pradesh, Chhindwara, Madhya Pradesh, Gondiya, Maharashtra, Sales Coordinator, Market Executive, Quality Assurance Leader, Experience Required : 1 Year Educational Qualification : Higher Secondary, Secondary School, B.a, B.c.a, B.b.a, B.com Skill Sales Coordinator, Market Executive, Quality Assurance Leader Etc.,

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.

Please Contact/Send your CV The person should have complete understanding and hands-on experience of the following activities which are carried out at the project site :RCC road Work (from Excavation, Murram filling, Gsb bed, DLC to PQC layer)Boundary Wall of the complete siteWater Supply network: Drainage Line, Storm Line and Water LineSTP: Sewage Treatment PlantOHT : Overhead Tank with sizes varying from 1Kl to 5KLSump well TankLandscaping / Gardening : from Rcc structure to Plant belt developmentPlot beam & Garden beamChembersPaver BlocksMain Gate & Site GateManage, design, develop, create and maintain construction projects in a cost effective, timely and sustainable mannerAssess potential risks, materials and costs.Complete material managementOversee and mentor staff and other employees.Monitor progress and compile reports on project status.Manage budget and purchase equipment/materials.Effective and quick decision making

Designation:- Quality AnalystExeperience :- 6 months to 1 yearSkills:- Good communication, knowledge of Quality parameters.Roles and Responsibilities:-Responsibility of Quality Analyst : Audit Calls, Emails, Chats, Etc.1)To Conduct Regular Feedback Sessions.2)To Conduct Calibration Sessions With Operations, Consulting, And Technical Team.3) Generating Daily, Weekly & Monthly Quality Reports. 4)Should Have Knowledge Of 7 Tools Of Quality. 5)Assistance For Continual Improvement RegardsHr AnjaliMake My HouseIndore

QUALITY CONTROL MANAGER WITH BASIC ENGINEERING KNOWLEDGE AND CAN USE MS EXCEL, WORD, ETC.

Job Description:You are required to check quality of application forms provided to you (online). After checking a bunch of applications, you need to create a batch of all the application. Editing of Photo and Signature will be a part of this process. You need to send all the batches via mail to the concerned department. Candidates need to have good computer skills Typing speed must be above 25wpm Candidate must have basic excel knowledge Internet skills are required for this job position There will be 1 year bond for those who gets selected for the position Working of Minimum 8 hours is mandatory Salary will be based on per application. You will be given 1/- (Rs.1) per quality check of application Freshers can also apply

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.

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.,

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

We are looking for a Software Quality Engineer to ensure the highest quality standards in our software products. This role is suitable for candidates with 0 to 6 years of experience and offers an opportunity to work in a dynamic team environment.Key Responsibilities:1. Test Planning and Design: Create and review test plans and test cases to ensure comprehensive coverage of software requirements. This involves understanding the application and designing tests to verify functionality.2. Manual and Automated Testing: Execute both manual and automated tests to find defects. This includes running test scripts and validating that the software functions as intended, identifying bugs, and reporting issues.3. Defect Tracking and Reporting: Use tracking tools to document defects and monitor their resolution. Communicating the status of defects to development teams is crucial for prompting quick fixes.4. Collaboration with Development Teams: Work closely with developers and other team members to understand the software development process. This collaboration helps in identifying and addressing quality issues early in the development lifecycle.5. Continuous Improvement: Contribute to the improvement of the testing process and methodologies. Sharing insights and suggesting enhancements can lead to improved product quality and more efficient testing.Required Skills and Expectations: Candidates should have a graduate degree and a keen interest in software quality assurance. Strong problem-solving skills, attention to detail, and the ability to work within a team are essential. Familiarity with testing tools and methodologies will be an added advantage. Strong communication skills are important for effective collaboration with the development team.