2371 Qms Jobs - Page 33

Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving customer identification, customer due diligence & enhanced due diligence. What are we looking for Communication SkillsIn this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shifts Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shiftsStrong coping, emotional resilience, and stress-management skillsExcellent comprehension and communication Ability to perform duties objectively, devoid of inherent biases or personal beliefs, in the best interest of client policies Strong attention to detail Comfort synthesizing and analyzing information from multiple streams Strong critical thinking and decision-making skills Qualification Any Graduation

Key Responsibilities: Quality Assurance Leadership Process Improvement Inspection and Testing Supplier Quality Management Customer Quality Management Training and Development Required Candidate profile Bachelor's degree in quality management, Engineering, or a related field. Advanced degree or certifications (CQE, CQM, Six Sigma) Min15 yrs exp in engineering and Min 5 yrs exp in quality management

Role & responsibilities: Develop and implement quality plans, procedures, and standards for E-Compressor, IPM Motors, and Inverter projects . Conduct regular audits and inspections to ensure compliance with quality standards and regulatory requirements. Collaborate with design, manufacturing, and testing teams to identify and mitigate quality risks. Analyze and resolve quality issues, implementing corrective actions and preventive measures. Develop and maintain quality documentation, including test reports, inspection records, and certification documents. Ensure compliance with industry standards, regulatory requirements, and company quality policies. Collaborate with suppliers to ensure quality of incoming materials and components. Provide quality training and support to production and testing teams. Alignment with the customer technical department on special customer requirements and standards for validation of MAHLE products. Preferred candidate profile: B.E in Electrical and Electronics / Mechatronics / Mechanical with 5 to 10 years of experience in handling Quality functions. IATF 16949 implementation knowledge is mandatory. Experience with E-Compressor, IPM Motors, or Inverter products. VDA 6.3 certified person. Strong knowledge of quality management systems (ISO 9001, IATF 16949). Experience with quality tools and methodologies (APQP, FMEA, SPC, MSA). Excellent analytical and problem-solving skills. Implementing Process Failure mode analysis concept on assembly process. Ability to work in a fast-paced environment and prioritize tasks effectively. Person with right leadership Quality and capabilities to manage the function through people. Ability to influence, convince with assertive communication to the stakeholders like customers, suppliers and internal key stakeholders. Strong communication and collaboration skills.

We are looking for a highly skilled and experienced Field Risk Officer to join our team at Equitas Small Finance Bank. The ideal candidate will have 2-3 years of experience in the BFSI industry. Roles and Responsibility Conduct risk assessments and evaluations to identify potential threats to the organization. Develop and implement effective risk management strategies to mitigate identified risks. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze market trends and competitor activity to inform business decisions. Identify and report on key performance indicators (KPIs) to senior management. Provide expert guidance on risk management best practices to stakeholders. Job Requirements Strong understanding of risk management principles and practices. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a fast-paced environment with multiple priorities. Strong communication and interpersonal skills, with the ability to build relationships with stakeholders. Experience working with financial data and systems, including risk management software. Strong knowledge of regulatory requirements and industry standards related to risk management.

We are looking for a skilled Branch Receivable Manager to join our team at Equitas Small Finance Bank. The ideal candidate will have 5 years of experience in the BFSI industry, with a strong background in managing receivables and collections. Roles and Responsibility Manage and oversee the branch's receivable portfolio, ensuring timely payments and minimizing bad debts. Develop and implement effective strategies to improve collection efficiency and reduce delinquencies. Collaborate with internal stakeholders to resolve customer complaints and disputes related to loan recoveries. Analyze and report on key performance indicators (KPIs) such as delinquency rates and recovery metrics. Ensure compliance with regulatory requirements and company policies regarding debt management. Lead and motivate a team of collection professionals to achieve their targets and goals. Job Requirements Strong knowledge of accounting principles, financial regulations, and banking practices. Excellent communication, negotiation, and problem-solving skills. Ability to work in a fast-paced environment and meet deadlines. Proficiency in MS Office and other relevant software applications. Strong analytical and reporting skills, with attention to detail and accuracy. Experience working in a similar role within the BFSI industry, preferably in a bank or NBFC setting.

We are looking for a highly skilled and experienced professional to join our team as a Regional Asset Disposal specialist at Equitas Small Finance Bank. The ideal candidate will have 14 years of experience in the BFSI industry, with expertise in asset disposal and management. Roles and Responsibility Manage and oversee the disposal of assets across multiple locations. Develop and implement strategies to optimize asset utilization and minimize losses. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze market trends and competitor activity to identify opportunities for growth. Build and maintain relationships with key stakeholders, including customers and partners. Monitor and report on asset disposal performance metrics to senior management. Job Requirements Strong understanding of asset disposal principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment and meet deadlines. Effective communication and interpersonal skills. Experience working with financial institutions or similar industries. Strong knowledge of regulatory requirements and industry standards.

We are looking for a highly skilled and experienced Receivable Officer to join our team at Equitas Small Finance Bank. The ideal candidate will have 1-7 years of experience in the BFSI industry, with expertise in receivables management. Roles and Responsibility Manage and oversee the collection process to ensure timely recovery of outstanding amounts. Develop and implement effective strategies to minimize bad debt and improve cash flow. Collaborate with internal teams to resolve customer complaints and disputes. Analyze and report on delinquency trends and provide insights for improvement. Ensure compliance with regulatory requirements and company policies. Maintain accurate records and reports of all transactions and interactions. Job Requirements Strong knowledge of accounting principles and practices. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and meet deadlines. Proficient in MS Office and other relevant software applications. Strong analytical and problem-solving skills. Ability to maintain confidentiality and handle sensitive information. Experience working in a similar role within the BFSI industry is preferred. For more information, please contact us at 1403780.

Job Description Summary Develop and maintain systems, rules, and processes to ensure fulfillment of internal and external requirements. Ensures that projects and products are capable and will meet specified standards (Preventive). Impacts quality of own work and the work of others on the team. Focused on execution of standard enabling activities/provision of advice subject to policy and work routines within an enabling discipline. There may be some latitude to rearrange the sequence to complete task/duties based on changing situations. tex Job Description Roles and Responsibilities Creates a Quality culture by driving compliance activities around a specific product, site or region. This includes being responsible for the total quality management system for the business and driving Quality metrics. Ensures quality and regulatory compliance while driving process effectiveness and efficiency. Represents GE Healthcare to external agencies and champions the evolution of the quality culture which includes executing and driving quality objectives, metrics, reporting and operating mechanisms. Broadening knowledge of theories, practices and procedures in own discipline to execute functional policy/strategy; still developing functional knowledge and skills. Basic understanding of key business drivers; uses this understanding to accomplish own work. Good understanding of how work of own team integrates with other teams and contributes to the area. May have some autonomy to make decisions within a defined framework. Resolves issues in situations that require good knowledge and judgment within established procedures. Consults more senior team members for issues outside of defined policy/parameters. A job at this level requires good interpersonal skills. For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. Explains technical information to others. Management of Internal Quality Audit Leading Quality Management review for Multi site Lead QMS change implementation Required Qualifications This role requires basic experience in the Quality & Healthcare Quality. Knowledge level is comparable to a Bachelors degree from an accredited university or college ( or a high school diploma with relevant experience). Desired Characteristics Strong oral and written communication skills. Ability to document, plan, market, and execute programs. Note: Inclusion and Diversity . Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you d expect from an organization with global strength and scale, and you ll be surrounded by career opportunities in a culture that fosters care, collaboration and support. Disclaimer: GE HealthCare will never ask for payment to process documents, refer you to a third party to process applications or visas, or ask you to pay costs. Never send money to anyone suggesting they can provide employment with GE HealthCare. If you suspect you have received a fraudulent call , please fill out the form below: https: / / www.ge.com / careers / fraud #LI-MC1 #LI-Onsite

Followings will be the responsibilities of the position holder: 1. Act as a receiving team for new and reformulated product from I&D to AHPL Baddi. 2. Scale up/scale down for new and existing products for review the occupancy in RMG and Blender. 3. Preparation of MMD of new and existing products. 4. Review of sampling plan for engineering & process validation. 5. Technical inputs for product improvisation w.r.t equipment and process, formulation, or shelf life changes through appropriate QMS. 6. Handling of reprocessing, reworking of existing formulation. 7. To support for failure investigation or exceptions (as per applicability) 8. All documentation & process steps for trial/non-commercial batches manufactured in production facilities. 9. New/ Old material approval (API/Excipient) - technical input if required, revision of TD & BD limits 10. Products externalization/ internalization from AHPL, Baddi to LL/ TP and vice versa. 11. Preparation of Standard operating procedure (SOPs) pertaining to department. 12. Analytical/Formulation support (troubleshooting) for existing products (including method development). 13. Compete projects identification and execution. 14.Floor execution/Documentation of proposal or technical write up. In absence of the position holder, the sub-ordinate Executive / Manager working in the section or the authorized designee (as applicable) shall be responsible for day to day working. JOB FAMILY: Supply Chain t SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Kindly share your resume on sv14@svmanagement.com Key Responsibilities: Carry out supplier Initial assessment audit in case of new suppliers to ensure manufacturing/ Technology capability to meet product and process requirement. Supplier Quality Improvement audits for existing suppliers to ensure effective implementation of Quality Management System & process controls. Support suppliers for advanced product quality planning (APQP) Perform on-site supplier visits for process and product audits, root cause analysis and verification of corrective actions of supplier quality issues Collate and evaluate supplier quality data, manufacturing process to identify process improvement and value enhancement opportunities within the supply chain. Promote the use of preferred techniques for continuous improvement such as Lean manufacturing, Six-Sigma, Poka-Yoke (Error Proofing), Measurement System Analysis, SPC and Process Failure Mode and Effects Analysis (PFMEA). Report on Key Performance Indicators (KPIs) in order to adhere to process and prevent occurrence of any non-conformity relating to product, process or system Qualifications and Skills: Degree in Mechanical, Automobile and Production with 8-10 years experience in automotive OEM, Tier I auto components manufacturing companies. Experience of working in Quality Assurance Department, preferably in Supplier Quality & New Product Development. Additional preference to certified VDA 6.3 & IATF 16949 lead auditor. Strong knowledge of Advanced Product Quality Planning (APQP), Production Part Approval Process (PPAP), Failure Mode and Effect Analysis (FMEA). Knowledge of Quality Management System, IATF16949 and VDA 6.3, Measurement techniques, metrology and equipments. Understanding and interpretation of engineering drawings Knowledge of manufacturing processes such as Casting, Forging, machining & Heat Treatment.

1. Job Responsibility To handle the day-to-day activities of Process equipment and its related Works. To attend to the breakdown of equipment and resolve it in minimum time to ensure fewer losses. Coordination with external agencies if required to rectify the breakdowns. To attend breakdowns related to automation, instrumentation, electrical and mechanical works. Prepare work order reports and ensure completion of the activity as per the requirements and specified timelines. To ensure the execution of activity as per regulatory standards with the current Good Manufacturing Practices. Preparation, execution, and monitoring of the Preventive maintenance of plant Equipment. To check and daily update the Preventive Maintenance status. To Support Plant operations for Engineering & production. To ensure smooth operation of Plant machinery. To support the team for validations & revalidations of all areas and equipment available at the site. To ensure compliance with the Quality management system. Initiation and closure of the Change controls, CAPAs, Deviations, and Breakdowns. Preparation of Monthly trends. To prepare, review, verify, and follow SOPs. Direct installation and alterations of machinery, and equipment as per sop and change control or CAPA. To submit daily reports of daily activities to Process Maintenance in charge. To monitor the safety in the execution of projects and maintenance activities in smooth condition. Maintaining equipment critical spares and availability on site. To perform any job allocated by the head of engineering/superior. To keep track of the consumption of materials procured and their reconciliation on a monthly basis. Day-to-day activity job allocation to Technicians. To follow and ensure the safety rules and regulations in the plant.

Lead QMS / SYSTEM QUALITY handling QA INTERNAL AUDITS, TIMELY NON-CONFIRMANCE CLOSURE, SUPPORT CUSTOMER AUDITS, TL9000, ISO 14001, ISO 45001, ISO 10002, 5S AUDITS, QA TRAINING, MONTHLY QA MIS, CPR SURVEILLANCE AUDIT, EIL CERTIFICATION, RoHS REGULATIN Required Candidate profile BE 8+yrs exp into QA handling QMS & strong exp QA AUDITS, QA CERTIFICATION, TL9000, ISO 14001, ISO 45001, ISO 10002, 5S AUDITS, QA TRAINING, RoHS, OCP OPRICAL FIBER CABLE exp must Relocate to CHENNAI Perks and benefits Excellent Perks. Call Singaraj @ 97897 94540 now

QMS Specialist, Management Review Meetings with Directors and Review with Customer like Maruti, HONDA and Many OEMs. Implement quality assurance procedures/documentations & quality system in accordance with current ISO 9001 / IATF 16949 requiremnt. Required Candidate profile Should have excellent interpersonal skills, Taking accountability for the effectiveness of the quality management system & Product audits, Customer Audits, Quality systems audits,

Flex is the diversified manufacturing partner of choice that helps market-leading brands design, build and deliver innovative products that improve the world. A career at Flex offers the opportunity to make a difference and invest in your growth in a respectful, inclusive, and collaborative environment. If you are excited about a role but dont meet every bullet point, we encourage you to apply and join us to create the extraordinary. Job Summary To support our extraordinary teams who build great products and contribute to our growth, we re looking to add a Technician - Manufacturing Engineering in Chennai, India. What a typical day looks like: Knowledge on Electronics components and PCBA Support Engineering team for Manufacturing process. Knowledge on Work instruction, process flow. Knowledge in SMT process. Knowledge in Quality Management System. Knowledge in Engineering Change Management process. Creative and innovative thought on PCBA Document creations for NPI products. Liaise with Process and manufacturing team to come up with detailed manufacturing information (When needed) Adhere to process and look for possible process improvements. Knowledge in PLM/ERP Tools. The experience we re looking to add to our team: Diploma / B. Sc. - Electronics / Physics graduate with (0-2) years of experience as PCBA Process / Manufacturing / Assembly , Preferably in EMS Industry. Experienced in technical document preparation. Knowledge in SMT process. Good English Communication skill Should have good Microsoft Office Good analytical skills and logical thinking. Should be open for shifts. What you ll receive for the great work you provide: Health Insurance PTO PM15 Job Category Production Engineering Required Skills: Optional Skills: Flex pays for all costs associated with the application, interview or offer process, a candidate will not be asked for any payment related to these costs. Flex is an Equal Opportunity Employer and employment selection decisions are based on merit, qualifications, and abilities. We do not discriminate based on: age, race, religion, color, sex, national origin, marital status, sexual orientation, gender identity, veteran status, disability, pregnancy status, or any other status protected by law. Were happy to provide reasonable accommodations to those with a disability for assistance in the application process. Please email accessibility@flex. com and well discuss your specific situation and next steps (NOTE: this email does not accept or consider resumes or applications. This is only for disability assistance. To be considered for a position at Flex, you must complete the application process first).

QC/QA Executive, QC/QA Manager, QC/QA chemist Industry: Ayurvedic Pharmaceutical Qualification: M.sc/M.pharm/B.bharm/B.sc Experience: 7-8/Y in Pharma comp. Salary: best in the industry Skills Required QUALITY CONTROL CHEMIST RESPONSIBILITIES:- Assist in QC stability testing, prepare and maintain stability records and summaries. Involve in training and transfer of methods to and from QC and contract manufacturers as assigned. Modify and validate analytical procedures to meet QCs needs. Support design and development of experimental protocols, SOP’s, etc., consistent with cGMP/GLP. Participate in special projects and department meetings via input, feed Contact :- 9099507270 Ms. Anila Patel [HR Manager]

Approval, issue, control and updating of QMS documents, Decide schedule of internal quality Audit.(IATF+EHS), Verification implementation of IATF-16949:2016 EHS in the organization Knowledge of TPM, IATF, OSHAS, 6 sigma, manufacturing process, SAP, Required Candidate profile Must have experience in BE/B. Tech from Rubber Compounding. with Management Representative (MR),Improvement in integrated management system, ISO, TS16949 system, manage APQP projects PPAP preparation

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.

Lead professionals and Plan and implement processes to improve efficiency and cost-effectiveness, Product analysis, New product Development Quality, close successfuly various audits like Customer quality, Supplier audits, ESD audits, etc. Required Candidate profile candidate must be from Electronics background and having experience in Automotive Switches mandatory

Develop and implement business development strategies. Identify and engage potential clients. Collaborate with internal and external stakeholders. Monitor business development performance and suggest improvements. Prepare reports and documentation. Provide training and support to staff.

Responsibilities: * Develop analytical methods using HPLC, ELISA , colorimetry & spectrophotometry. * Validate methods according to GLP & GDP guidelines. * Conduct quality control testing on biologics products.

Oral solid dosage manufacturing area arrangement, operation and technical knowledge in the area of Granulation/Compression/ Coating /Packing or any two areas online documentation, Daily calibrations, QMS activity involvement.

Executive-CQA Long Description 1. To perform and track the Vendor Qualification Compliance and review for all vendors & AVDs. 2. To review, approve, and extend the Q info for new alternate vendors. 3.To execute vendor Audits, CAPA tracking, and qualification documentation 4.To schedule and monitor the Vendor Audits 5.To work on VQ special projects in coordination with Project IT team 6.To track the project till its implementation and Go Live across all sites Competencies 1. Strategic Agility 2. Innovation & Creativity 3. Customer Centricity 4. Developing Talent 5. Result Orientation Work Experience 5 - 8 years

Executive-CQA-VQG 1. To perform and track the Vendor Qualification Compliance and review for all vendors & AVDs. 2. To review, approve, and extend the Q info for new alternate vendors. 3.To execute vendor Audits, CAPA tracking, and qualification documentation 4.To schedule and monitor the Vendor Audits 5.To work on VQ special projects in coordination with Project IT team 6.To track the project till its implementation and Go Live across all sites Competencies 1. Strategic Agility 2. Innovation & Creativity 4. Developing Talent 3. Customer Centricity 5. Result Orientation Education Masters in Chemistry Post Graduation in Pharmacy 5-8 YearsWork Experience

Work Experience 12 to 15 years of experience in Pharma Vendor Audit Management 1. To perform and track the Vendor Qualification Compliance and review for all vendors & AVDs. 2. To review, approve, and extend the Q info for new alternate vendors. 3. To execute vendor Audits, CAPA tracking, and qualification documentation 4. To schedule and monitor the Vendor Audits 5. To work on VQ special projects in coordination with Project IT team 6. To track the project till its implementation and Go Live across all sites Technical , behavioral & managerial 1. Strategic Agility 2. Innovation & Creativity 4. Developing Talent 5. Result Orientation 3. Customer Centricity Education Masters in Pharmacy Post Graduation in Science or Chemistry

Long Description 1 Responsible for lifecycle management of DSRM procedural documents in EDMS and non-procedural documents within due date which includes document creation, document revision, making document obsolete, making document effective, releasing document, sharepoint update and communication to relevant stakeholders 2 Responsible as SOP coordinator to perform roles as Author in edit step and QA authorisation in Release approval step 3 Responsible to perform role of Training Coordinator in Training step within EDMS as required 4 Oversight and management of compliance of DSRM training requirements and activities in LMS 4 Support and oversight of subsidiary Global PV training status as applicable 5 Oversight and management of Annual Basic PV compliance for India 6 Oversight on team's task completion, annexures, sharepoint updates and people management. 9 Creation of status presentations and other adhoc presentations as required 7 People Management Competencies Strategic Agility Innovation & Creativity Process Excellence Customer Centricity Collaboration Stakeholder Management Developing Talent Result Orientation Education- Life Science Post Graduate, MPharm, BPharm, Work Experience Experience in Pharmacovigilance operations, Quality Management System, Training, Use of Systems for SOPs and Training Management