446 Qc Inspection Jobs - Page 18

Position: Senior Quality Assurance Manager Location: Shapar / Bhunava, Dist. Rajkot Industry: Heavy Fabrication & Machine Building Experience: 1015 Years Qualification: B.E. / Diploma in Mechanical Engineering (DME) About the Company: Singhal Power Presses Pvt. Ltd. is a reputed manufacturer of precision-engineered mechanical presses with a strong commitment to quality, innovation, and customer satisfaction. As we continue to grow, we are seeking a dedicated and highly experienced Senior Quality Assurance Manager to lead our QA function and ensure excellence across all manufacturing stages. Key Responsibilities: Lead the Quality Assurance function across Fabrication, Machine Shop, and Assembly operations . Ensure compliance with internal quality standards and customer specifications. Conduct and supervise in-process inspections , final quality audits , and pre-dispatch checks . Monitor and control Welding, Machining, Painting, and Assembly processes for quality assurance. Drive root cause analysis (RCA) and implement corrective & preventive actions (CAPA) to address quality issues. Prepare and maintain quality documentation, test reports, and inspection records as per ISO standards. Coordinate with the Design, Production, and Purchase departments to enhance product quality. Visit customer sites when required to inspect complaints, analyze defects, and ensure customer satisfaction . Conduct supplier audits and incoming quality inspections for raw materials and bought-out items. Hands-on experience and working knowledge of SAP B1 Quality modules for effective quality tracking and reporting. Champion a culture of continuous improvement through quality awareness, training, and Kaizen initiatives. Desired Candidate Profile: B.E. / Diploma in Mechanical Engineering with 1015 years of relevant experience in heavy fabrication and machine building. Proven leadership in managing a mid-to-large QA team and working across cross-functional departments. Strong understanding of GD&T, fabrication drawings, machining tolerances, welding standards, and QA tools . Experience with ISO 9001 , quality control plans, PPAP, and SPC is highly preferred. Proficiency in using measurement instruments like CMM, Vernier, Micrometer, Surface Tester, etc. Exposure to customer interaction, audits , and problem-solving at the field level . Working knowledge of SAP Business One (SAP B1) is an added advantage. Why Join Us? Work with a leading name in the mechanical press manufacturing industry. Opportunity to drive quality excellence in a high-growth, technology-driven environment. Professional development through cross-functional exposure and leadership responsibility. Competitive salary and growth opportunities for the right candidate. Interested candidates may share their CV at: hr@singhal.co.in 9376624724

Manage and oversee project quality to ensure compliance to codes, standards, regulations, specifications, and QMS requirements Coordinate inspections, audits, and quality documentation with subcontractors, vendors, and client representatives Required Candidate profile Drive cost savings, ensure safety adherence, and deliver quality assurance through effective site execution. Implement the QA/QC management system at site,

Skill : Machining & fixture Industry QMS & MR-Systems in Straight Ducts, hoods Bends Control Inward in process Quality SQA Customer Quality & Audits IATF Pre-Dispatch Inspection Client Site & Mgmt Vendors Audit & system Customer Complaints handling Required Candidate profile Candidates should have Exp. in QMS,QMS Work in Product Base Compnay ISO Certification this Pro Machining Part fixture automation Transition Pieces, Welding Fixture Pooja Pawar Contact Us 8149927268

Candidate will be responsible for our auto component warehouse to ensure compliance with quality standards, inspecting incoming and outgoing parts, analyzing defect, documentation & coordinating with suppliers & internal team to resolve quality issue

Role & responsibilities In process and final inspection, handling instruments, check sheet maintaining, data analysing & logbook maintaining. Preferred candidate profile Perks and benefits Free Uniform & Safety shoe. Food and Transport on subsidy basis.

JOB DESCRIPTION Department : Quality Control Chemical Designation : Manager – Stability Reporting To : Head – Quality Control Educational Qualification : M. Pharma / M.Sc. (Chemistry/Pharmaceutical Sciences) Job Responsibilities 1.Responsible for preparation and review of Stability Study Protocols, Stability Study Reports, and Stability Summary Sheets for all products (General Injectables and OSD). 2 Responsible for initiation, monitoring, and timely execution of stability studies for registration batches, validation batches, and commercial batches as per ICH guidelines. 3 Responsible for managing stability chambers, their qualification, calibration, and monitoring as per regulatory and internal guidelines. 4 Responsible for monitoring pull-out schedules, analysis of stability samples, and ensuring timely reporting. 5 Responsible for statistical analysis, trending, and evaluation of stability data, including identification and investigation of Out of Trend (OOT) and Out of Specification (OOS) results. 6 Responsible for preparation, review, and approval of analytical reports for Finished Products, In-process materials, Raw Materials, Packaging Materials, Water and Steam (Condensate) samples, including stability samples. 7 Responsible for preparation, review, and execution of Analytical Method Transfers and Method Validations related to stability and routine testing. 8 Responsible for preparation and review of Standard Operating Procedures (SOPs), Analytical Test Data Sheets, General Test Procedures, Specifications, and Calibration Data Sheets. 9 Responsible for review and handling of laboratory incidents, Out of Calibration (OOC) reports, deviations, OOS, OOE, OOT events, Change Controls, and Corrective and Preventive Actions (CAPA). 10 Responsible for Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) implementation and compliance across the team. 11 Responsible for preparation/review of Qualification Reports/Protocols for instruments and equipment used in the QC Laboratory. 12 Responsible for preventive maintenance schedules, calibration schedules, and management of instruments, including handling of breakdowns. 13 Responsible for management of Working Standards, Reference Standards, and Impurity Standards, including procurement, qualification, issuance, and maintenance. 14 Responsible for allocation of work, supervision, and review of activities performed by the QC team members and ensuring section-wise coordination. 15 Responsible for providing GMP/SOP/Analytical training to QC personnel and ensuring compliance to safety practices within the QC department. 16 Responsible for acting as Section Head and taking charge in the absence of the QC Head to ensure continuity and compliance. 17 Responsible for executing and monitoring QC activities related to the General block and Oncology block (ADL, R&D) at BDR Pharmaceuticals International Pvt Ltd, Baska Site. 18 Responsible for self-training and tracking of training status for self and team members on all applicable SOPs and protocols. 19 Responsible for cross-functional communication with R&D, QA, Production, and Regulatory Affairs teams for new product stability requirements, troubleshooting, and regulatory submissions. 20 Additional responsibilities shall be assigned as per organizational requirements based on operational needs.

Work Type : Contract role Contract duration : 6 months (extension or permanent based on performance) Key Responsibilities Production Monitoring: Track daily production across teams and update internal logs. Monitor floor-level activities to ensure adherence to schedules. Identify and escalate production delays or resource shortages. Help arrange jigs, fixtures, and tools to improve manufacturing speed. Quality Control: Inspect fabrication quality by checking frame size, diagonal, twist, and weld quality. Perform critical dimension checks on machined parts using Vernier caliper and micrometer. Maintain alignment and quality checklists for each assembly. Document inspection results and assist in preparing QC reports. Skills & Qualifications Diploma in Mechanical Engineering. Minimum 2 years of experience in production or quality inspection. Proficiency in Excel for production and inspection reporting. Strong knowledge of measuring tools: Vernier caliper, micrometer, measuring tape. Comfortable with hands-on inspection and floor-level coordination. Note: This is a 6-month contract role , with the possibility of extension based on performance and project continuity.

Knowledge of fitup Report,LHS,weld Visual Report,testing Reports,Loop file, blasting NDT level 2 degree must RT /UT/DPT Knowledge is Must

Role & responsibilities Will be responsible for in-process quality control at the supplier end at the site, with good communication with the manufacturing and quality control team. Will do incoming inspection, after receiving parts and units from the vendor, do incoming inspection, subject items are purchase parts, machining parts, assembled units and etc. Make statistics of incoming inspection items, make statistics of the number of inspection items and defect ratio based on each vendor. Instruct the vendor based on the statistical results of the incoming inspection, and instruct the vendor as necessary. Ensure no product is delivered with an open non-conformance. To perform in-process Quality checks as derived in the Quality checklists for vendors. Raise nonconformance observed during in-process stages. Coordinate with the responsible department for Root cause & CAPA. Arrange periodic NCR review meetings with the Operations team, along with the vendor & Supplier. Responsible for defining Manufacturing Quality Plans (MQP) based on contracts & relevant standards. Coordinate the stage inspections of the Core assembly and prepare the relevant report for the clearance. Follow up on NCRS & Coordinate Root Cause Analysis (8D, etc.) and define the action-related team that comes from internal audits, customer audits, and during manufacturing inspections. Preferred candidate profile Machinery Manufacture, Blow Moulding Machine, Injection Moulding Machine, In-process Quality in the Transformer Industry

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC data and generate reports to identify trends and areas for improvement. Compliance & Audits Ensure compliance with ISO, GMP, or other industry-specific standards. Coordinate and support internal and external audits. Problem Solving Investigate product quality issues and customer complaints. Implement corrective and preventive actions (CAPA).

2 to 6 years experience in the respective field. Knowledge of physical analysis methods.Knowledge of QMS. observation and organizational skills.In-depth knowledge of quality control procedures.Good technical and IT skills.

Position Summary: We are seeking an experienced and proactive Quality Control Manager with a strong background in In Vitro Diagnostics (IVD) to lead and oversee all QC activities within our manufacturing and development operations. The QC Manager will be responsible for ensuring that IVD products meet internal quality standards and comply with international regulatory requirements. This role plays a key part in managing a QC team, improving processes, and supporting product development and commercial release. Role & responsibilities Lead and manage the Quality Control team, ensuring daily testing activities are conducted efficiently and in compliance with regulatory requirements (ISO 13485, FDA 21 CFR Part 820, and CE-IVD). Develop, implement, and maintain QC procedures for raw materials, in-process controls, and final product testing for IVD devices, including immunoassays, molecular diagnostics, and rapid tests. Oversee method validation, equipment qualification (IQ/OQ/PQ), and routine calibration and maintenance of laboratory instruments. Review and approve QC test results, reports, and batch records, ensuring timely product release. Manage investigations of non-conformances, deviations, out-of-specification (OOS) results, and implement corrective and preventive actions (CAPAs). Participate in cross-functional teams for new product development, transfer-to-manufacturing activities, and continuous improvement initiatives. Ensure compliance with GLP/GMP requirements and prepare for internal and external audits (e.g., ISO, FDA, notified bodies). Provide leadership, training, and mentorship to QC staff, fostering a culture of quality and accountability. Monitor QC metrics and KPIs, and report regularly to senior management. Maintain and improve the Quality Control Laboratory environment, including documentation, data integrity, and safety practices. Education: Bachelors or Masters degree in Biotechnology, Biochemistry, Microbiology, Life Sciences, or a related field. Experience: Minimum 610 years of experience in Quality Control, with at least 3 years in a managerial or supervisory role within the IVD or medical device industry. Skills: In-depth knowledge of IVD regulations and quality standards (ISO 13485, FDA QSR, CE-IVD). Strong leadership, team-building, and project management skills. Proven experience in implementing and improving QC systems and processes. Excellent problem-solving skills and experience with RCA and CAPA tools. Proficiency in LIMS, statistical analysis, and data management tools. Preferred candidate profile Experience with regulatory submissions, audits, and inspections (FDA, ISO, EU MDR). Familiarity with risk management (ISO 14971), design controls, and product lifecycle management. Quality certifications (e.g., ASQ CQM/OE, Six Sigma Green/Black Belt) are a plus

Conduct random inspections of goods to ensure continuous quality monitoring. timely elevation to the factory owners Monitor & manage timelines for interim & final inspections to ensure timely delivery.production Planning & Execution, Required Candidate profile Oversee and manage the workload of the Quality Control (QC) team. Ensure quality standards are met for a variety of products, including bathmats, area rugs, pillows, throws, table linen, and storage

Handling of ISO, IATF and other required certifications and all QMS systems. Handling customer audits and QMS queries. Responsible for heading a team of chemists Required Candidate profile Proper knowledge of QC SOP, MOA, Specification, BIS, ASTM, physicochemical Analysis and ISO documentation. Operating equipments like AAS, Surface Area Analyser, pH Meter etc.

Quality Assurance Inspection and Testing: Documentation Compliance Collaboration & Support **Min 2 yrs Experience in Elevator **Job Location Maldives Call or WA +919073304030 / 9674678007 www.crosborder.co.in Free Food Accommodation by Company

Must be a local candidate from Tirupur.Strong knowledge of knits and kids apparel production, including quality control processes.Conduct various quality audits, including: PPM (Pre-Production Meeting).Inline inspections.Mid-production audits Required Candidate profile Final inspections as per AQL (Acceptable Quality Level) system and buyer requirements. Strong computer skills for documentation, reporting, and communication.Good communication skills to coordinate

Role & responsibilities A Quality Assurance/Quality Control (QA/QC) civil engineer's role is to ensure that construction projects meet specified standards and quality requirements. This involves inspecting materials, workmanship, and construction activities to ensure compliance with project specifications, codes, and industry standards. They also document findings, analyse performance, and communicate with stakeholders regarding quality issues. Key Responsibilities: Inspections: Conducting regular inspections of materials, workmanship, and construction activities to identify any deviations from project plans and specifications. Testing: Performing tests on materials and structures to ensure they meet quality requirements, such as concrete slump tests, material density tests, and core sampling. Documentation: Maintaining detailed records of inspections, tests, and any non-compliance issues, ensuring compliance with industry standards and contractual obligations. Compliance: Ensuring that all construction activities adhere to project specifications, codes, and industry standards. Reporting: Generating reports on quality performance, including any non-compliance issues and corrective actions taken. Communication: Communicating with project managers, clients, and other stakeholders regarding quality-related issues and solutions. Problem Solving: Identifying and resolving quality issues, recommending corrective actions to prevent future problems. Training: Ensuring that construction workers are aware of and adhere to QA/QC procedures. Process Improvement: Continuously seeking ways to improve quality management practices and processes. Preferred candidate profile Reviewing and verifying construction documents, including plans, specifications, and submittals. Overseeing the implementation of QA/QC plans and procedures. Conducting audits of quality management systems to ensure effectiveness. Collaborating with other professionals, such as engineers, contractors, and clients, to ensure project quality. Developing and implementing inspection procedures to verify compliance. Monitoring the disposition of non-conformance reports and ensuring corrective actions are taken. Providing technical guidance and support to construction teams. In essence, QA/QC civil engineers play a crucial role in ensuring the quality and reliability of civil engineering projects, contributing to the safety, durability, and longevity of infrastructure and buildings.

Manage & Supervise of the metal casting department, recruit new workers, Fill out order status sheets, Responsible for QC of cast metal components and furniture pieces, Tracking material requirements, Keeping track of machinery in the department . Required Candidate profile Excellent Written and Spoken English. Strong knowledge of various Metal Casting Processes. 4-6 years’ experience (in export of luxury furniture). Must be a resident of the Noida or nearby area.

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.

S&S Properties Job Description: A Quality Control Engineer in the construction industry ensures that projects meet required standards and specifications. Their responsibilities typically include: Roles and Responsibilities: • Inspection & Testing: Conducting site inspections and material testing to ensure compliance with quality standards. • Process Improvement: Identifying defects and recommending corrective actions to enhance construction quality. • Documentation & Reporting: Maintaining records of inspections, test results, and quality assessments. • Compliance Assurance: Ensuring adherence to industry regulations, safety protocols, and contractual requirements. • Collaboration: Working closely with project managers, contractors, and suppliers to maintain quality control. • Training & Guidance: Educating teams on quality standards and best practices Interested candidates kindly share your resume on 9686137747/hr@sspgroup.org.in

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces