428 Qms Implementation Jobs - Page 2

Vacancy for QMS Engineer in Sheet Metal Industry Exp - 3 to 5 years IATF 16949:2016, Internal Auditing, QMS, MR Responsibilities IATF/EHS Qualification - BE / Diploma Mechanical Location - Chakan Pune. On Roll Job Call on - 8408824722/ 9518340393

Job Responsibilities Operations Build successful relationships with Life Sciences (LS) client stakeholders to promote confidence in quality and compliance, as well as forward planning. Provide management and leadership direction for the development and implementation of quality and compliance programs. Collaborate with other Life Sciences accounts to proactively accumulate, share and reapply all learnings, successes as well as best practices. Collaborate with Global Life Sciences Quality Vertical for development, revision and implementation of QMS and quality documents. Responsible for ensuring Lide Sciences facilities teams adhere to the required training and ensuring in compliance to clients QMS and quality training requirements. Responsible for ensuring that the work conducted by the Facilities team, and its subcontractors is in full compliance with contractual requirements, clients SOPs, GxP, FDA and other regulations. Able to perform/support internal JLL compliance audits and prepare SOPs, and training materials for use by the Life Sciences facilities team in the performance of their work. Guide Life Sciences facilities team in closing recommendations from clients audit. Expected to interface with the clients quality personnel to ensure that all of the clients SOPs are followed, work performed by the LS facilities team is properly documented for traceability in the framework of GDP. Sustain quality assurance support and develop a Quality Engineering Maintenance program for a controlled-environment manufacturing and laboratory facility as it relates to the facilities maintenance of this plant. Conduct investigations and drive accountability for all quality events. Lead programs to create value for client to ensure program deliveries meet or exceed expectations. Facilitate quality-relevance investigation via structured Root Cause Analysis. As part of career development, lead Life Sciences accounts as an IFM leader.Reporting Manage and report on critical & key performance measurements. Develop and submit periodic site status reports related to the Quality Program. People Management Effectively lead and guide a Life Sciences Quality team by clearly communicating expectations, accountabilities and providing performance feedback for continuous improvement. Ensure Life Sciences Operations team members complete relevant quality and compliance training. Coach new Life Sciences team members on quality and compliance for their adaptation into specific Life Sciences accounts. Mentor, develop and train peer and direct report team members. Provides direction/information to vendors, facilities staff and service providers as required to ensure that quality assurance expectations are communicated and followed.Others Any other quality-relevant duties and tasks assigned. Knowledge, Skills & Abilities. MINIMUM REQUIRED / PREFERRED - Education/training Bachelor degree preferred Degree in science, technical or relevant discipline Sound fundamental knowledge in process utilities. 6+ Years of relevant experience preferred with minimum 4+ years in Quality and Compliance discipline in GxP manufacturing or laboratory environment. Six-Sigma and Root Cause Analysis training is essential. Skills and knowledge Background in technical documentation Work independently and within a team. Strong mindset of compliance and client-focus. Communicate effectively with technical, quality assurance and other personnel. Proficient in Word, Excel and other Microsoft Office Suite programs Ability to investigate, recognize and diagnose trends and patterns. Solid understanding of cGMPs as they relate to the performance of maintenance and repairs to facilities, utilities and equipment utilized for the manufacturing plants and laboratories for drug products. Experience working at an FDA regulated manufacturing facility in a quality assurance or quality control capacity. Support investigations and corrective action plans for appropriate discrepancies. Investigation of compliance issues as required, collaborating with relevant Compliance Partner(s) Understanding of FDA regulations including 210 CFR part 210 and 211. Strong commitment to quality assurance, and a willingness to help develop a quality first culture on the site. Knowledge of Quality Engineering techniques, CMMS systems, and Quality Management Systems English communication is essential Other abilities Good oral and written communication skills including the ability to communicate to all levels of management and willing to interface with a diverse customer base including technical and non-technical personnel.Physical work requirements and work conditions Familiar with process utilities and GxP environment.

Set & maintain quality policy. Integrate QMS into processes. Provide necessary QMS resources. Lead support participation QMS. Meet customer legal requirements. Identify address risks and opportunities. Assign QMS roles, reporting, change management.

Oversee the development, implementation, and continuous improvement of the organizations QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS), as well as other statutory or regulatory bodies. Required Candidate profile DO NOT CONTACT RECRUITERS DIRECTLY ,APPLY ON NAUKRI AND RECRUITERS WILL GET BACK TO YOU

Assist in maintaining & updating QMS documentation. Help coordinate &Perform basicQC checks & inspections maintain supplier documentation & support risk management files. Ensure proper document control & record retention in compliance with ISO 13485.

Focus on ISO COORDINATION, QMS IMPLEMENTATION, QUALITY MANUALS, PLANT INTERNAL AUDIT SYSTEM, conduct QUALITY SYSTEM AUDITS, QMS TRAINING, INTERNAL QMS AUDIT, DOCUMENT CONTROL, EXTERNAL AUDIT COORDINATION, MR ACTIVITY, Plan SOPs, QA CERTIFICATIONS etc Required Candidate profile BE 2+yrs exp with AUTO / ENGG Unit into QA with strong exp in SYSTEM QUALITY / QMS Must have proven exposure in ISO, TS, AITF etc Exposure in INTERNAL & EXTERNAL AUDIT, ISO COORDINATION etc must Perks and benefits Excellent Perks. Call Mr. Prabhu @ 7010863499 now

QMS Documentation: Handling change control, deviation, CAPA (Corrective & Preventive Actions), complaints, OOS (Out of Specification), OOT (Out of Trend), etc. Audits & Compliance: Risk Assessment: Product Quality Review (PQR)

Role & responsibilities The ability to manage tasks, delegate responsibilities, and lead a team effectively. Strong communication to provide feedback, resolve disputes, and interact with staff and customers. The capacity to identify issues, develop solutions, and make decisions, especially in the manager's absence. Preferred candidate profile

Role & responsibilities Work closely with the Head of InfoSec & Process Quality to define, implement, and institutionalize process quality frameworks in line with industry best practices. Assist in setting up and maintaining a Quality Management System (QMS). Conduct compliance checks, internal audits, and process reviews to ensure adherence. Facilitate the collection and analysis of metrics, trends, and benchmarks to drive improvements. Identify process gaps and propose pragmatic, value-driven improvements. Support change management by engaging with cross-functional teams, addressing concerns, and building buy-in for process initiatives. Contribute to the creation of process documentation, SOPs, and training materials. Provide feedback to improve efficiency, productivity, and quality across service lines. Qualifications, Experience & Skills A bachelor's degree in computer science, information technology, or a related field. Strong problem-solving skills with the ability to challenge the status quo. Excellent communication (verbal and written) and stakeholder management skills. Ability to work independently and collaboratively with cross-functional teams. Change management mindset ability to influence and gain acceptance in environments resistant to process adoption. Detail-oriented with a passion for driving quality and continuous improvement.

Quality Manager for Wiring Harness & Cable Assembl QMS Work with the Cross functional team to put together a Quality Management System encompassing the lifecycle of NPD projects comprising of initiation, planning, execution, control and close-out. Required Candidate profile 14+ years of experience in implementing ISO 9001,14001,IATF ISO 13485 in Manufacturing sector implementing Quality tools like Process capability MSA SPC FMEA PPAP APQP review quality performance KPIs

Responsibilities: * Lead ISO audits and document findings * Ensure compliance with IATF standards * Conduct internal process audits * Collaborate on lean manufacturing initiatives * Develop QMS policies and procedures Food allowance Provident fund Health insurance Annual bonus

Ensures incoming inspection of components Checks and/or fills in control documents (PVRI) Maintains product traceability. Knowledge of Quality management system ISO 9001 (ISO 45001, 14001.Knowledge of measuring instruments. Required Candidate profile 3 to 7 years in plant quality operation, Incoming inspection ,supplier quality management. Experience in Aerospace, Electrical ,Manufacturing. Well experienced in ISO/TS , inspection tools & processes

Key Responsibilities : Consulting & Implementation Lead client engagements for QMS implementation and certification readiness for IATF, ISO standards. Develop and implement QMS frameworks, policies, processes, and documentation tailored to client needs. Conduct gap analyses and recommend corrective actions. Guide clients on compliance with statutory and customer-specific requirements. Facilitate Lean Manufacturing projects including Kaizen, 5S, VSM, TPM, SMED, and waste elimination. Support clients in root cause analysis, problem-solving (8D, FMEA, PDCA), and error-proofing techniques. Conduct internal audits, pre-certification audits, and supplier audits. Provide guidance for successful external audits and certification renewals. Prepare progress reports, presentations, and project documentation. Build long-term client relationships through value-added consulting. Qualifications & Experience: Bachelors degree / Diploma in Engineering (Mechanical/Automobile/Production/Industrial preferred). Lead Auditor / Internal Auditor certification in IATF 16949, ISO 9001 (ISO 14001 / ISO 45001 preferred). Minimum 510 years of experience in QMS implementation, audits, and Lean Manufacturing, with at least 12 years in consulting/training. Strong knowledge of Automotive Core Tools (APQP, PPAP, MSA, SPC, FMEA, Control Plans). Experience in leading Lean/Kaizen projects and change management. Exposure to Tier-1/Tier-2 automotive manufacturing preferred. Key Skills: Strong understanding of IATF 16949 and ISO standards. Hands-on expertise in Lean Manufacturing tools & techniques. Strong analytical, problem-solving, and project management skills. Effective communication and stakeholder management abilities.

Role & responsibilities Develop, implement, and monitor the Quality Management System (QMS) in compliance with ISO, AS9100, or other relevant industry standards. Ensure product quality and reliability in thermal systems/components (e.g., heat exchangers, combustors, thermal assemblies, etc.). Lead quality assurance and quality control activities across manufacturing operations. Establish and monitor key quality performance indicators (KPIs) for production processes. Conduct root cause analysis, corrective action, and preventive action (CAPA) for internal and external quality issues. Work closely with R&D, production, and supply chain teams to ensure design for quality and manufacturability. Supervise and train QA/QC engineers, inspectors, and technicians. Liaise with customers, auditors, and regulatory authorities regarding quality audits and inspections. Drive continuous improvement initiatives such as Lean, Six Sigma, Kaizen for process optimization and waste reduction. Ensure supplier quality management through audits, approvals, and performance monitoring. Maintain documentation, certifications, and compliance with relevant safety, environmental, and quality standards. Preferred candidate profile Minimum 7 -10years experience

- Conduct inspections & review batch production, analytical records as per defined procedures for release. - Maintain comprehensive records & documentation; manage physical records storage & Location mapping. - Coordinate Supplier Questionnaires Required Candidate profile - Master`s degree in a life science or related fields with 2+ years of relevant industrial experience (Pharmaceutical or cGMP preferred) - Familiarity with compliance & regulatory standards

Looking for a QMS Quality Engineer to drive ISO/IPC compliance, audits, CAPA, and process improvements. Ensure documentation, customer satisfaction, and continual quality enhancement in EMS operations

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Oversee the development, implementation, and continuous improvement of the organization’s QMS. Ensure compliance with relevant ISO standards (e.g., ISO 9001,14001) and Bureau of Indian Standards (BIS), as well as other statutory or regulatory bodies. Required Candidate profile Lead root cause analysis, corrective actions, and process improvement initiatives to reduce defects and enhance quality. Design and implement KPIs. Calibration, Supplier Quality, Testing & Validation

Greetings from Compliance Quest, ComplianceQuest was founded in 2013 and is based in Tampa, Florida.ComplianceQuest is a highly flexible 100% cloud based EQMS built using the Salesforce platform.ComplianceQuest is a next generation modern cloud platform with AI powered solutions for Clinical,Quality, Health and Safety and Environment natively built and run on Salesforce technologies.We help our customers of all sizes deliver quality products and services in the safest,most sustainable way by mitigating risk, problems, and inefficiencies while protecting customers,employees, suppliers and brand. Roles and Responsibilites: Provide consulting services to assigned projects as required, including product functional consulting, business process re-engineering, customization requirements, product validation and custom report analysis. Provide Product training to customers as required on the modules that the Sr. Consultant is certified in. Continue to improve knowledge of CQs solution, quality standards, industry, and technology to better serve the internal and external customers. Proactively improve one’s productivity and quality. Participate in refresher training classes to renew certification and new training classes for new products, quality standards, industry, and technology. Provide product and industry training to company employees as assigned. Timely and quality delivery of project deliverables in accordance with the project’s schedule and timeline under the direction of the project manager. Escalate any issues that cannot be immediately resolved to the project manager in charge of the team. Ensure that appropriate reports are written for all the appropriate deliverables.

Manage and oversee project quality to ensure compliance to codes, standards, regulations, equipment specific specifications, and QMS requirements. Development and implementation of the QMS for fabrication, inspection and operations activities. Health insurance Provident fund

Responsibilities: * Lead quality initiatives * Conduct regular audits * Develop & implement QMS * Ensure ISO compliance * Manage PPAP process Annual bonus Leave encashment

Oversee the entire Quality Control department, ensuring compliance with all regulatory requirements and company standards.Provide leadership,strategic direction for the QC department, aligning QC activities with organizational goals and objectives. Required Candidate profile Manage huma, material resources within the QC department, including staffing, budgeting, resource allocation.Plan,Conduct routine and non-routine analyses of in-process ,packaging raw materials,

Responsibilities: * Ensure compliance with ISO standards through regular audits * Develop & maintain QMS procedures & documentation * Collaborate with cross-functional teams on quality initiatives Health insurance Annual bonus Office cab/shuttle Provident fund

Position: Senior Quality Engineer Experience: 8 - 12 years Industry: Electronics Manufacturing Services (EMS) Work Location: Mysore Job Summary: The Senior Quality Engineer is responsible for supporting the organization in achieving customer satisfaction by ensuring compliance with customer requirements, regulatory standards (such as ISO 13485, AS9100, and NADCAP ), and the continual improvement of quality systems. This role plays a key part in root cause investigations, development of inspection documentation, and implementation of APQP processes. Primary Responsibilities: Quality Management System (QMS): Maintain and update controlled documents within the QMS. Ensure QMS updates are compliant with ISO 13485, AS9100, NADCAP, and any future applicable standards. Root Cause & Corrective Action (RCCA): Participate in internal and external corrective action activities. Support leaders and teams in the use of RCCA tools (e.g., fishbone diagrams, 5-Whys, Pareto analysis, FMEA, process maps). Guide teams to identify true root causes and develop corrective actions that address systemic and human factors. Review completed corrective action plans for effectiveness and return inadequate plans to the owner for improvement. Ensure RCCA documentation is objective and complete. Advanced Product Quality Planning (APQP): Assist in the creation of Control Plans, FMEA, Process Maps, and Process Validation Plans. Develop and implement APQP processes and procedures. Supplier Quality Management: Collaborate with Supply Chain to ensure Purchase Orders include appropriate quality and regulatory requirements. Review supplier documents (e.g., Certificates of Conformance, FAI packages) for compliance with PO, drawings, and applicable standards. Create supplier PPAP/FAI/FMEA expectations based on customer drawings and specifications. Verify supplier compliance with regulatory standards such as REACh, RoHS, Conflict Minerals, and UL. Inspection & Training Documentation: Prepare inspection checklists and training materials based on customer specifications and engineering drawings. Assist in developing Final Inspection and In-Process Inspection Forms for finished goods. Support the creation of training materials to reduce or eliminate repeat defects. Knowledge & Skill Requirements: Strong verbal and written communication skills. Ability to read and interpret engineering drawings and assembly prints. Proficient in working both independently and within cross-functional teams. Familiarity with quality tools such as FMEA, Control Plans, Process Mapping, and RCCA methodologies. Knowledge of ISO 13485, AS9100, NADCAP, and related quality and regulatory standards. Experience with supplier quality management and documentation review. Education: Bachelors /Masters degree in Engineering, or a related field.

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review