106 Qms Implementation Jobs - Page 5

Role & responsibilities - To Monitor Working of Quality Department Incoming, In process, Outgoing. - To ensure timely completion of new projects for customers - To control process sheets and process changes - To audit working of quality department - To monitor statistical process control - Raw material / product development sample management Verification - Carry out and monitor quality and cost improvement initiatives - Responsible for conformity to product requirements have the authority to stop shipment and stop production to correct quality problems - To ensure the customer requirements are met - Conduct Internal Quality Non- Conformance Review - IATF -16949 audit certification renewal - Secondary supplier status analysis - FMEA, APQP, Incoming Inspection, Internal& External Failure Verification - New product and New development report with management approval - Evaluating NC point & Countermeasure submission to the customer - Maintain the mixing ration history for tracking - Verification. - Existing and new raw material MSDS report – Validation - New raw material supplier 4M changes report reviewed Preferred candidate profile - Customer specification test standard – Validation - DQC will be checked on weekly & monthly - Improve the product quality analysis report verification and implementation. - Zero Rejection - verification of daily production product. - Quality tracking system verification. - Basic Lot Test & Long-term Test Result - Validation. - Incoming RM /Product Improvement status analysis - Inward Inspection report - Validation. - Daily production test - Result validation. - Product Revalidation report – Review - Lot Test report for each product – Review - Existing product improvement result Review - Line problem and customer improvement analysis - Customer Quality audit support. Perks and benefits Yearly Bonus: Twice in a Year (120% on Gross) Travel Facility: Gummidipoondi to Madhavaram Food Allowance: Free of cost twice per day Special Allowances: Benefits for marriage, new born babies & other scenarios. Accommodation: Provide free Accommodation for Bachelors Other Benefits: PF, ESI & Group Medical Insurance.

Role Summary: OSD Production QMS is responsible for ensuring adherence to quality standards within the production process. The role involves monitoring production activities, implementing quality control measures, maintaining compliance with regulatory requirements, and driving continuous improvement initiatives. Roles And Responsibilities Quality Compliance: Implement and monitor compliance with QMS standards Industry-specific standards. Conduct periodic audits of production processes to identify deviations and enforce corrective actions. Ensure all production processes align with regulatory and company quality standards. Documentation & Reporting: Maintain and update standard operating procedures (SOPs), work instructions, and quality records. Prepare detailed reports on quality performance, including non-conformance incidents and corrective actions taken. Process Improvement: Analyze production workflows and recommend improvements to enhance efficiency and quality. Participate in root cause analysis for production issues and implement preventive measures. Key Skills and Competencies: In-depth knowledge of Quality Management Systems and standards. Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Proficiency in using quality management tools and techniques. Familiarity with relevant USFD, EU, TGA regulatory requirements and industry best practices.

Job Description: QMS Executive Qualifications: Bachelor's degree in Computer Science, Information Technology, or related field. 1-3 years of relevant experience in Quality Management Systems (QMS). Preferred certifications: ISO 9001 Internal/Lead Auditor, ISO 27001 Internal/Lead Auditor. Skill Set: Knowledge of Quality Management Systems (QMS). Familiarity with ISO standards 9001 and 27001. Proficiency in reviewing/auditing internal projects and documentation. Exposure to Configuration Management Systems (e.g., SVN). Understanding of RCA (Root Cause Analysis) and CAPA (Corrective and Preventive Action). Knowledge of software development methodologies. Excellent communication and documentation skills. Proficiency with MS Office tools. Responsibilities: Maintain and update document repositories related to QMS and ISMS. Ensure the master list of QMS documents is up-to-date. Support the QMO team in tasks assigned by the QMS Manager. Collect and analyze QMS-related data from project teams (e.g., best practices, metrics). Plan, execute, and report internal quality audits and track findings to closure. Review and suggest improvements for QMS/ISMS documentation. Assist in training coordination for Quality Management and ISMS. Support teams in implementing QMS processes during project lifecycle stages. Maintain records for customer feedback, CAPA management, and internal audits. Participate in Management Review Meetings (MRM) and monitor action item status. Coordinate with teams / departments during third-party audits and ensure compliance.

Implement the IMS procedure, Formats & Supporting Document and ensure at the point of use/Conduct regular audits to improve the IMS processes/Manage the audit non conformity data base and detailed analysis of Non conformities/Conduct DRM & MRM Required Candidate profile The candidate should have the VDA certified auditor and should have minimum 6 Years experience in QMS.

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

Manage QMS Act as managment representative for IATF and EHS Requirements exp in QA Roles ideally in the seals or mechanical components industry strong understanding of IATF 16949 ISO STANDERDS EXP IN RUBBER STEEL INDUSTRY REQUIRED 9812001068