Quality Control Job Vacancies in Madhya Pradesh

Need FARO CMM Operator for indore pithampur location

We are seeking a Finishing Supervisor to oversee the final stages of production in Indore, India. Your key responsibilities will include inspecting finished products for quality, ensuring all finishing processes are completed correctly, and supervising a team of finishing workers.You will be responsible for ensuring that all finishing work meets company standards and customer specifications. This includes coordinating with other departments to ensure timely completion of projects, maintaining accurate records of production data, and troubleshooting any issues that may arise during the finishing process.The ideal candidate will have strong attention to detail, excellent communication skills, and the ability to work well under pressure. Prior experience in a supervisory role and knowledge of finishing techniques and equipment are preferred. A 12th pass education level is required for this position, and candidates with 0-3 years of experience will be considered. This is a full-time, work-from-home position that offers the opportunity for growth and advancement within the company.

Designation :- QC Officer/Senior OfficerQualification:- MSc/B. Pharma Experience :- 4 Years To 8 YearsSalary:- As Per Interview Gender:- MaleJob Responsibilities:- i)RM (Raw Material) Analysisii) FG (Finished Goods) Analysisiii) AMT / AMV Analysisiv)Strong knowledge of QC proceduresJob Location:- Indore,MPIndustry:- Reputed Manufacturing Industry

We req manufacturing ex to oversee manufacturing activities for our plant manufacturing machining components and fabricated assemblies

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

Candidates should be relevant experience in sheet metal fabrication industry Should be good in English languages

Location: D-8, Sector 63, Noida Position: Project Engineer / Project Manager Salary: 30,000 60,000 per month (Negotiable based on experience) Job Description:We are looking for motivated and detail-oriented individuals to join our team as Project Engineers or Project Managers, who will manage and oversee technical projects from planning to execution in the field of robotics, automation, and engineering solutions. Roles & Responsibilities:Plan, coordinate, and execute technical projectsSupervise on-site work and ensure project timelines are metHandle client communication and progress reportingCollaborate with design, R&D, and field teamsOversee material and manpower management on project sitesEnsure compliance with safety and quality standards Qualifications:B.Tech / Diploma in Civil, Electrical, Mechanical, Mechatronics, or related fieldsFreshers and experienced both can applyCandidates with MBA (Civil/Project Management) preferred for managerial roles Key Skills:Strong communication and project coordination skillsBasic technical knowledge of robotics, automation, or construction processesAbility to handle documentation and reportingTeam management & leadership (for PM roles)

. 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.

Officer/SrOfficer Quality ControlAMV, HPLCAnalysis, FP/RM/PM Analysis & GLP

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.

QC Analyst required for quality control department

We are looking for 30 Quality Engineer Posts in Delhi NCR,Pune, Chakan Pune, Mahalunge, Pune, Bihta, Patna,Muzaffarpur, Gaya, Sitamarhi, Bihar, Pithampur Industrial Area, Dhar,Indore,Quality Analyst,Quality Implementation,5s,7 QC Tool,8D Report,Inspection Engineer,Quality Lead, with deep knowledge in Quality Analyst,Quality Implementation,5s,7 QC Tool,8D Report,Inspection Engineer,Quality Lead and Required Educational Qualification is : Secondary School, Diploma, Advanced/Higher Diploma, Professional Degree

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.

- Monitor and oversee the finishing processes: The finishing supervisor is responsible for supervising and ensuring that all finishing processes are carried out efficiently and according to standards.- Train and guide finishing team members: It is the duty of the finishing supervisor to train new team members on finishing techniques and procedures, as well as to provide guidance and support to existing staff.- Inspect finished products for quality: The finishing supervisor must conduct regular inspections of finished products to ensure they meet quality standards and specifications before further processing or shipping.- Maintain records and reports: Keeping track of production records, quality assurance reports, and other relevant documentation is essential for the finishing supervisor to maintain smooth operations.- Coordinate with other departments: Collaboration with different departments, such as production, quality control, and logistics, is crucial for the finishing supervisor to ensure a seamless workflow.The ideal candidate for the finishing supervisor position should have a high school diploma or equivalent, with 0-3 years of experience in a similar role. They should have strong attention to detail, excellent communication skills, and the ability to work independently. A good understanding of finishing techniques and processes is required, as well as the ability to multitask and prioritize tasks effectively. Additionally, proficiency in basic computer skills for data entry and reporting purposes is necessary.

Hiring for 10 Analytical Chemist Jobs in Indore, for Freshers, Required Educational Qualification is : Diploma, Professional Degree, Other Bachelor Degree, B.Pharma, B.Sc, Post Graduate Diploma, M.Pharma, M.Sc with Good knowledge in Analytical Chemistry, Quality Control, HPLC, Chemical Analysis, Analytical Method Development, Numerical, well qualified etc.,

We are looking for a part-time Data Encoder to join our team, ideally suited for freshers who have completed at least the 10th grade. This role allows you to work from home and is perfect for those looking to gain experience in data management.**Key Responsibilities:**- **Data Entry:** Accurately input data from various sources into the computer system. This ensures that all information is current and easily accessible.- **Data Verification:** Check and verify the accuracy of data entered into the system. This is important to maintain data integrity and prevent errors.- **Organizing Files:** Arrange and maintain digital files systematically. Keeping files organized helps in easy retrieval and improves workflow efficiency.- **Report Generation:** Create reports based on the data collected. This can include summaries and statistics that help the team make informed decisions.- **Communication:** Respond promptly to any queries regarding data entry and processing. Effective communication keeps the workflow smooth and addresses any misunderstandings.**Required Skills and Expectations:**- Basic computer skills are essential, including familiarity with word processing and spreadsheet software.- Strong attention to detail is necessary to ensure data accuracy and prevent mistakes.- Good time management skills to meet deadlines while working from home.- Ability to work independently and stay motivated under minimal supervision.- Basic understanding of data privacy and security practices is a plus. If you are diligent, reliable, and eager to learn, this role could be an excellent opportunity for you.