24 Qa Systems Jobs

As a Principal Piping Designer at our company, you will play a crucial role in the success of your team and related projects. You will be responsible for effectively exchanging ideas and information related to Piping Design, working autonomously while following established procedures, and acting as a lead to coordinate the work of others. Your contributions will include proposing improvements to processes and methods within the Piping Design discipline. Key Responsibilities: - Perform Design and Engineering process facilities within specified timelines while maintaining safety, quality, and constructability standards. - Develop 3D Models and ensure clash-free models in coordination with all other disciplines" requirements. - Approve drawings including plot plans as per project specifications and McDermott Procedures. - Set priorities, organize work, and forecast resource requirements when acting as a Lead Designer. - Lead the design team to complete tasks within the planned schedule and budget, in accordance with standards and project-specific procedures. - Act as the project-based discipline point of contact in communications with Project Team, Client, vendors, and subcontractors. - Coordinate all activities within your discipline and interface with other disciplines effectively. - Identify issues promptly, raise change notifications, and support less-experienced team members. - Ensure work is carried out in accordance with McDermott requirements, Client, and Statutory Design Codes, focusing on Health and Safety Policies. Qualifications: - Minimum 10 years of experience in oil and gas performing Pre-FEED, FEED, and Detailed Design. - High School graduate with a diploma in Mechanical Design or equivalent experience. - Detailed knowledge of 3D CAD systems including E3D or SP3D. - Familiarity with AutoCAD and associated industry standards and specifications. - Capable of Leading projects and understanding process equipment maintenance and operation. - Flexibility for business traveling/assignments and knowledge of QA Systems. If you are a proactive and detail-oriented professional with a strong background in Piping Design, this role offers an exciting opportunity to contribute to cutting-edge projects in the energy sector. Join us in driving the energy transition and making the impossible possible. Your work matters here.,

Role & responsibilities Responsible for overall refrigerators production in REF plant as per plan. Responsible for yearly budget preparation, Cost Control & monthly production as per plan. Effective utilization of all machinery in the plant. Ensure 100% Daily, weekly production order closure & ensure delivery on time as per model mix. Reduction of SFRN cost in the plant and improve FTR, RTY of the processes. Improve UPH, Productivity and manpower optimization of production dept. Set Product quality standards and Effective implementation of quality systems in the plant. Ensure employees safety and safety working conditions in the production departments. Coordination with other functional departments for smooth functioning of production. Preferred candidate profile Knowledge of Production and Mfg. Systems and Techniques. Knowledge of refrigerator product and all mfg. related departments. Knowledge of various raw Materials. Knowledge Knowledge of QA systems and standards Knowledge of Process improvements

Lead PPAP, & FMEA activities for new product launches & engineering changes, Conduct root cause analysis & implement corrective/preventive action, Lead internal audits & support second-/third-party audits, Monitor process capability. Required Candidate profile Qualification : - B. E. Electrical Experience :- 5-7 yrs. exp. in plant maintenance Maintain & improve the Quality Management System in line with IATF 16949, ISO 9001.

DME/BE - Mech with at least 10-15 years of experience in automotive industries, Knowledge of IATF 16949,VDA 6.3, Pokayoke, Kaizen. Having ERP Knowledge shall be preferred.

Role & responsibilities: Primary (60% KPIs QA/NPD & Audit Management): 1. Develop and implement Quality Management Programs for NPDs aligned with protocols (supplier selection, FMEA, quality risk audits, validations, tech-transfer, FG release). 2. Collaborate with QC teams to ensure AQL, sampling, and analytical protocols are followed for RM/PM/Bulk/FG across all units. 3. Manage quality audits for plants, warehouses, and vendors to sustain QA across the value chain. 4. Ensure timely closure of audit CAPA through coordination with internal teams and external partners. Secondary (40% KPIs Systems, SOPs, MIS, and Voice of Customers): 5. Review/create SOPs, processes, and specifications to maintain QA standards. 6. Manage Customer Complaint Program; ensure timely processing and closure of investigations. 7. Oversee On-Shelf-Quality Program; analyse trends for improvement. 8. Generate and analyse monthly Quality MIS and KPI reports for decision-making Preferred candidate profile: Qualifications & Experience Education: M.Sc. Chemistry / B-Pharma Strong knowledge of NPD, QMS, 2P/3P operations, FMCG quality, and warehouse audits. Certifications: Lead Auditor for ISO, Six Sigma. Relevant Experience: 510 years of experience with 2–4 years in managing 2P/3P quality systems. Experience in audits, ISO certifications, validations, and incoming quality control. Familiarity with SAP (QM module) preferred. Expertise in FG/warehouse/supplier audits and complaint resolution (CAPA). Proficiency in SOPs, process improvements, risk audits, and FMEA Soft Skills: Ability to align customer needs with manufacturing processes. Strong analytical and structured problem-solving skills. Excellent communication and teamwork abilities. Strategic thinking for reducing product failures and enhancing satisfaction.

1. Looking for Graduate Engineer with 6-8 years of experience in QA department of an engineering or FMCG company. 2. Shall be well versed with ISO 9001, ISO45001 and willing to take responsibility for setting up the QMS. 3.Person possessing knowledge about TQM with experience in implementing POKA-YOKE is preferred. 4. Should have experience of documentation of audit process.

Responsibilities: * Conduct internal audits & customer audits. * Prepare audit documentation & system audit reports. * Ensure compliance with ISO standards & customer *Maintain Auditing of Documentation under Q.M.S ISO 14000 and 45000. Onsite creche facility Shift allowance Travel allowance House rent allowance Health insurance Provident fund Annual bonus

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 10-12 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge -ISO 9001, GMP & other quality standards

Efficiently monitor all operations which affect the quality. Devise procedures for inspecting and reporting all the persisting quality issues. Assure the consistency and reliability of production with thorough checking procedures and final output. Supervise and guide inspectors, technicians, and all other staff. Report all malfunctions to production executives only to ensure immediate action. Appraise all the requirements of customers and ensuring they are quite satisfied. Facilitate proactive solutions by collecting and analyzing quality data. Keep permanent records of quality reports, statistical reviews, and relevant documentation. Review the current standards and policies. Communicate with external quality assurance officers during on-site inspections. Efficiently ensure that all the legal standards are met with great care. Provide assistance during the recruiting process. Efficiently create reports for tracking progress.Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications. Perks and benefits: Mention available facilities and benefits the company is offering with this job.

Responsibilities * Head the Quality Department *Customer Complaints Handling * Carry out Process & Product audits * Carry out MR Related activities such EMS, IATF and other relevant certifications Annual bonus Provident fund

Roles and Responsibilities Ensure compliance with ISO standards through implementation, documentation, and auditing processes. Conduct internal process audits to identify areas for improvement and implement corrective actions (CAPAs). Manage vendor audits, MRM systems, PPAP documentation, IATF certification requirements. Develop and maintain quality management systems (QMS) policies, procedures, and guidelines. Collaborate with cross-functional teams to ensure effective communication and coordination.

Good knowledge SMT, Wave soldering, Robotic soldering quality. knowledge presentation skill on well versed with MS office tools. knowledge of ISO standard (IATF 16949). PCB CP dalect analysis & implementating countermeaure and prepare 8D report.

Req.Mgr QC for precision components manufacturer near Chandigarh.B Tech Mech. with exp of 8 to 10 years in QC Can apply .He should have knowledge of ISO System,Inspection & Testing. He should have knowledge of Auto cad and MS Office.

Manage the Quality Assurance function at manufacturing site Ensure compliance with ISO, GMP & REACH standard Develop, implement & monitor Quality Management Systems including SOPs, documentation & CAPA systems Handle customer complaints, conduct RCA Required Candidate profile 8–12 years of experience in QA, preferably in specialty chemicals Knowledge of analytical instruments, QC processes & technical documentation Strong knowledge - ISO 9001, GMP & other quality standards

Develop and implement quality assurance protocols and procedures Conduct inspections and tests to ensure product quality Maintain documentation and records as per industry standards Ensure compliance with IATF 16949:2016 and other relevant standards Required Candidate profile Bachelor's degree in Engineering or related field. 5–6 years of experience in QA . Strong understanding of quality control standards and methodologies

Job description ISO Consultant Job Type: Full-time, Permanent, Freelance Remuneration :- 6,00,000 to 12,00,000 per year for ISO , 6,00,000 to 12,00,000 per year for ZED , 18,00,000 for each MCLS cluster of 10 clients for Intermediate and Advance level, which is done in 18 to 24 months. Total Remuneration 12,00,000 to 24,00,000 per year. Hybrid Working – Visit to the client’s factory is required at your & client’s mutual convenience. Schedule : Flexible shift Education: ( Any of the following) 1. Any Gradutate with knowledge of ISO consultancy/ISO Auditing/ Quality Related fields 2. Any Graduate with minimum 8 years industrial experience in manufacturing. 3. Diploma with 10 years industrial experience in manufacturing 4. BE/BTech with 8 years industrial experience in manufacturing 5. Knowledge of ISO &/or Lean tools implementation/Documentation/Consultancy/Systems/Quality related fields shall get additional weightage Place of Posting:- Shall be required to cover industries near your residence to provide onsite/ Offsite consultancy in factories. Roles and Responsibilities :- 1. To provide onsite and offsite consultancy to the MSME manufacturing clients for doing ISO 9001/14001/45001 consultancy at client’s site and offsite. 2. Same Consultants shall be trained to provide ZED consultancy of the Central government scheme of Zero Defect Zero Effect (ZED) promoted by Ministry of MSME. 3. Same consultants shall also be trained to provide consultancy for lean tools under MCLS MSME Competitive (Lean) Scheme promoted by government of India. Training :- 1. The candidate shall be trained by our company so that he can pass an online examination of Quality Council of India (QCI) to become a national level approved ZED certified consultant and subsequently trained to become national level approved MCLS certified consultant. 2. After clearing the online exam, the consultant shall be allotted MSME manufacturing clients by our company for implementation of ZED scheme. 3. ZED consultant shall be required to implement the ZED &/or lean techniques / modules to help the client obtain ZED/MCLS certification as per the guidance of our company. 4. Consultant shall be provided regular training, support and guidance from the head office so that the ZED/MCLS modules can be implemented properly at client’s factory and ZED &/or lean certificate is delivered in time. Perks and Benefits: 1. Performance incentives Like New Laptop, New Mobile, New Inverter for your residence after starting at least 3 projects as per company norms. 2. No outstation travel required 3. Cell phone reimbursement 4. Flexible schedule 5. Internet reimbursement ABOUT THE COMPANY – BMCPL Boon Management Consultants Pvt. Ltd. (BMCPL) is a consultancy organization (Incorporated in 2005) that specializes in providing services for improvement of systems including capacity building, implementation of lean tools, ZED Consultancy etc. BMCPL is providing consultancy and training services to it’s clients all over India through our consultants located pan India. Besides many private and services sector clients , we are providing services to government/semi-government organizations. Some of our government clients are 33 ZILLA PARISHADS, RURAL DEVELOPMENT DEPARTMENT- GOVERNMENT OF MAHARASHTRA, OFFICE OF GOVERNOR OF MAHARASHTRA, etc. For the ZILLA parishad project done by us, RURAL DEVELOPMENT DEPARTMENT (RDD) has won National Award. MoMSME has selected Quality Council of India (QCI) which is an autonomous body under Govt. of India for implementing and Monitoring ZED scheme across India. QCI has selected BMCPL as a ZED consulting organization and also for MCLS consulting organization for pan India operations. About the ZED Scheme: The Ministry of MSME has selected the Quality Council of India (QCI), an autonomous body under Govt. of India to implement and Monitor the ZED (Zero Defect Zero Effect ) scheme across India. QCI has selected BMCPL as a ZED consulting organization for pan-India operations. The majority of the fees for this project shall be paid by govt. (Ministry of MSME/QCI) and negligible cost shall be borne by the client.The details of the scheme can be seen on govt. website zed.msme.gov.in Till date Boon has trained 150+ ZED consultants and 40+ MCLS consultants from different parts of India Like Maharashtra, West Bengal , Gujrat, Telangana, Tamil Nadu, AP, Karnataka, etc. The consultants have passed the Quality Council of India Examination and have received ZED Consultant certificate. BMCPL has 700+ MSME clients who have taken Pledge to become a ZED certified organisation. Out of this 500+ MSME clients have already received ZED Bronze certification, 200+ clients have received ZED Silver certification and others are in process to get ZED Silver/Gold certification. BMCPL has 100+ MSME clients who have taken pledge to do MCLS and out of this more than 50 MSME clients have received MCLS BASIC level certificate.

Drafting and adherence to Quality Assurance Procedures including: Standard Operating Procedures & Work Instructions Change Control Process Validation Document Control. cGMP Compliance Planning and Co-ordination for External and Internal Audits Ensure that CAPA and adhered for Nonconformances Investigate and Review Customer Complaints Training to stakeholders w.r.t. updated procedures and compliances IMS, TQM and 5S Procedures and compliances Desired Candidate Profile Ideal candidate must be a Full Time M.Sc. (First Class) in Chemistry/Industrial Chemistry with 8-11 years of experience in QA Function in a Chemical/API manufacturing plant

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.

Role & responsibilities Graduate engineer + having 5 to 7 years Exp. Of training documentation and implementation Capable to organise training related to management system Standard .prepare quality manual and system procedures, co-ordinate with department for completing & implementing the work related to audit. To conduct MRM & internal audit as per requirement of API, ISO 9001-14001 standard. To prepare record of internal audit ,data analyses .To review the quality environment and health and safety policy periodically and endure safety management system is effectively implemented and maintain to the requirement of customer standards. The work related to audit.

Position Objective : Support to manages all company Food Safety Management through implementation and maintenance of Quality Assurance system of Group and procedures that ensure product compliance to FSSAI and customer specifications Roles & Responsibilities Implement defined QA systems and process in Plant and at suppliers location. Manage the customer complaint redressal process which includes but not limits to follow up activities and verification of correction action. Partner with operation to train on QA systems and processes. Monitor and liaison with product owners to resolve product quality or operational issues. Manage and Summarize suppliers audit reports with solutions to the problems and prioritizing the most important opportunities for Quality, safety and cleanliness improvements at all level. Develop a strong professional relationship and communication with the industry associations & market to keep updated on the development related to food. Follow up with suppliers on validation of their lab testing methods which correlate with testing methods and procedures of local regulatory labs to ensure total compliance. Coordinate with training and operations management to provide training on food safety systems and technical advice to prevent food safety problems. Work closely with Operations and Training management to establish quality and safety measurement systems so opportunities for improvement are identified and acted on. Leverage technical resources of key raw material suppliers to provide training and product information at shop level. Support introduction of new suppliers as per the OYI Supplier guidelines. Skills Strong knowledge of Food Safety Systems and practices to Food Hygiene, Sanitation, SSOPs, GMPs Experience and knowledge of ISO 22000, ISO 9000 and certifications in auditing principles Please go the JD and If you are interested, kindly share your updated resume along with the following details : Few bullet points on Current CTC (fixed plus variable) Offer in hand (fixed plus variable) Expected CTC Notice period Experience on Food Manufacturing Plant Contact us Email:sp@intellisearchonline.net Mobile: 9590270707

AI Solutions Engineer at Edwisely | Jobs at Edwisely Experience: 0-3 Years Role Overview We re seeking an AI Solutions Engineer to lead the integration of GenAI tools such as ChatGPT or Claude into our core platform. You ll design, prototype, and deploy features that elevate student outcomes, make teaching exciting, and enrich dashboards with intelligent insights, all while upholding privacy and governance standards. Key Responsibilities Design and build GenAI-powered features like guided study assistants, automated remediation engine, and intelligent feedback tools. Develop end-to-end pipelines (prompt design model integration CI/CD deployment) that align with Edwisely s Intelligent Learning Infrastructure. Collaborate with product teams, faculty, and UX designers to deploy AI features in classrooms and dashboards. Ensure all AI implementations meet ISO 27001 security and CERT-In data protection guidelines. Measure adoption and impact via analytics dashboards support evidence-based learning outcomes. What You ll Bring Strong in prompt engineering, RAG, embeddings, or QA systems using frameworks like OpenAI API, LangChain, Hugging Face Transformers. Familiarity with ML deployment FastAPI, Docker, AWS/GCP within production-grade applications. Experience with education data, knowledge graphs, student modeling, or assessment systems is a big plus. Results-driven: ability to turn prototypes into scalable features. Passionate about improving higher education with impactful, AI-driven solutions. Why Edwisely? Be part of a high-impact EdTech startup, transforming learning journeys of engineering students nationwide. Work with a product that uses AI + analytics to personalize learning, support faculty, and guide institutional decisions . Career growth: define your ownership architecture, implementation, or research-led product development. Competitive package, fast-paced work culture, and freedom to drive real-world impact. Application Process Submit your CV + GitHub or project links (especially showcasing GenAI integrations or NLP projects). for Edwisely

We are hiring Q.A Officer for our pharma intermediate organization. Requirements:- Qualification :- Pharm/M. Pharm/M.Sc. Location :- Panoli (Gujarat) Experience :- 0 TO 3 year Benefits:- PF/Bonus Salary :- 15000-20000

Role & responsibilities Quality Assurance (QA): Assist in implementing and maintaining quality control processes. Conduct routine quality inspections and audits to ensure compliance with company policies and regulatory requirements. Support the investigation of non-conformities and customer complaints, recommending corrective and preventive actions. Assist in preparing QA reports and documentation. Ensure adherence to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs). System Management: Support the implementation and maintenance of Quality Management Systems (ISO 9001, ISO 14001, etc.). Assist in documentation control and management of standard procedures. Monitor and update system records for audits and compliance checks. Coordinate with different departments to ensure system improvements align with organizational goals. Process Improvement: Identify gaps in existing processes and suggest improvements. Support the development and implementation of continuous improvement initiatives. Assist in training employees on QA & system protocols Preferred candidate profile Education: BE - Mechanical Experience: 0-2 years of experience in Quality Assurance or System Management. Knowledge of quality standards such as ISO 9001, ISO 14001 Strong analytical and problem-solving skills. Good communication and documentation skills.

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