1332 Quality Jobs - Page 28

Monitor and ensure final inspection process (OQC) adherence for all outgoing shipments. Ensure compliance with customer specifications and product quality standards. Maintain PDI records and support customer audits as required. Maintain inspection records, quality reports, and ensure traceability. Drive improvement in OQC yield and reduce outgoing defects.

Role & responsibilities Ensure customer / Internal issues are timely resolved and minimized. Ensuring customer market complaints, issues and rejections are analyzed and minimized. Ensuring the Quality of product at development stage. Ensuring section objectives are fulfilled and necessary reporting is done. Ensure adherence to IATF 16949 systems. On time mass production daily lot clearance related activities. Analyse defect with CFT members of rejected parts if received or the phenomena. Communicate customer concerns to all concerned and follow-up for necessary actions. Conduct meetings with CFT members for discussing the present situation and countermeasures for the problem. Confirming analysis done at customers end for warranty parts. Discussing and documenting actions for fulfilling customers requirement. Discussing and receiving approval from section head. Discussing the factors with lower rating with CFT members. Ensure customer issues, complaint and rejections are intimated to all concern in company through customer flash reports and UQI. Ensuring all concern system documents are revised regarding the action taken. Ensuring customer complaint register is updated. Ensuring that problem analysis and countermeasures are documented in prescribed formats. Ensuring UQI verification is done as planned. Follow-up and monitoring with concerned persons for implementation of corrective action. Intimating Section head regarding actions decided and getting approval of analysis. Maintaining updated customer complaint register for all raised issues. Monitoring of customer quality rating and analysing points with lower rating requiring improvement. Monitoring the countermeasures effectiveness. Monitoring the customer quality rating. Understand issues reported by customer during visit. Conducting CFT meeting for customer issues. Discussing corrective actions for issues. Getting approval for actions form section head. Ensure customer returns are updated in SAP system. Analysis the customer returned material along with concerned department. Confirming rework procedure for returned material and ensuring abnormal process form is raised. Doing necessary follow-up for getting customer returned material reworked from production. Calculating rework cost manpower and part cost used for rework, after receiving list of parts replaced from production. Ensuring the product meets all quality specification as mentioned in drawings while different trials. Ensuring that past trouble data are taken into consideration while developing new models. Ensuring all requirements like masters, and specifications are made available to concerned production for trials. Ensure new product development meetings like DCN, G Document and Prototype are attended is represented in meeting. Tracking the development through time line chart and ensuring that issues are raised in PDI meetings and analysis is done for raised issues. Confirming layout inspection of new product, ensuring all dimensions are within specification. Ensuring history of all Initial product tag customer end and internal are maintained. Monitoring the status of objectives defined by section head. Doing necessary analysis for identifying improvement potentials. Prepare necessary slides of departmental business plan. Updating preliminary Japan MOR. Prepare and circulate quality news to members of organization. Identifying training needs of colleges and providing on job training to colleges while working. Strive to achieve departmental objectives & initiate necessary actions as required. Ensure necessary revisions and updating are done in manual. Ensure environment management programs are decided and executed, monitoring of the status of program. Initiating actions for closing of NCR and points for improvement if any highlighted in internal quality audit. Ensure lots checking on performance machine as per procedure and clearing lots as per decided target and frequency. Ensure daily monitoring of Model wise internal & customer graphical trends, Problem discussion take necessary actions for solving the same. Ensuring all required jets are checked inspected for master events. Ensure new die results are thoroughly inspected and prior to implementation of die. Preferred candidate profile Education - B.Tech/Diploma ( Mechanical Stream ) Excel, Power Point, Customer Quality experience, Good Analysis skill, Good Communication Skill. Personal Attributes: Potential, Team Work

Minimum 4+ years experience in SAP BI Vendor management Handle contract negotiations with vendors and suppliers Researches and evaluates vendors to compare pricing call @ 8447732667 Required Candidate profile Qualifications for Purchasing In charge Graduate degree Prior experience working in the purchasing department in manufacturing setup. Good Knowledge of SAP and MS Office will be preferred.

4-8 years experience in food processing companies. 3-4 years in food quality Food Quality compliances, Audits, certifications, regulatory matters, Overall quality measures in the company

Job Summary We are looking for an individual for the Quality Assurance team to review and revise SOPs, oversee document control in product development, and conduct risk assessments. Responsibilities include reviewing specifications and STPs, ensuring data integrity, proposing QbD (Quality by Design) process changes, and participating in phase gate reviews. Roles & Responsibilities • You will be responsible for reviewing and revising SOPs (Standard Operating Procedures), obtaining supervisor approval for system-related revisions, and communicating SOP changes to all High-Performance Teams (HPTs). • Your role involves the preparation, review, approval, and control of documents generated during product development. • You will conduct, review, and approve risk assessments throughout the product development process. • You will review and approve specifications and Standard Testing Protocols (STPs) for various materials at different development stages, ensuring compliance with guidelines and SOPs during all stages of development and technology transfer. • Your responsibilities include exercising control over data integrity, checking documentation and product development reports related to filings, and participating in proposing Quality by Design (QbD) process changes. • You will also conduct, review, and approve phase gates for drug products in coordination with development, and conduct self-inspections at the Integrated Product Development Organization (IPDO) according to the schedule. • You will be responsible for ensuring compliance in development laboratories, reviewing and approving facility/equipment qualifications at IPDO, and managing Quality notifications such as incidents and change controls through the Quality management system. Qualification Educational qualification: A Bachelor's degree in Pharmacy, Pharmaceutical Sciences, or a related field; advanced degree in Pharmaceutical Sciences or Regulatory Affairs is advantageous Minimum work experience : 5-7 years of experience in the pharmaceutical industry, with a focus on product development and quality management Skills & attributes: Technical Skills • Thorough understanding and practical application of regulatory requirements in pharmaceutical development. • Proficient in implementing Quality by Design (QbD) principles in the product development process. • Experience in reviewing, revising, and managing SOPs in alignment with industry standards. • Expertise in conducting, reviewing, and approving risk assessments throughout the product development lifecycle. • Strong focus on ensuring data integrity and compliance with documentation standards. Behavioural skills • Effective communication skills to relay SOP changes and ensure understanding across cross-functional teams. • Meticulous attention to detail for reviewing specifications, STPs, and development reports to maintain data integrity. • Ability to adapt to changes in the development process and propose improvements in the QbD approach. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Education : Diploma/B.E./B.Tech. (Mechanical/Automotive/Production) or ITI Experience : Min 1 year & Max 3 years Industry :Related to Machined Components Manufacturing Industry Responsibilities : 1. Experience in Product inspection (Visual & Dimensional). 2. Hands of experience on Layout Inspection (Mandatory) 3. Hands-on experience in measuring instruments handling like (Vernier , Micrometre, Height Gauge, Attribute gauges, Air gauges, Surface roughness etc.) 4. Good knowledge of inspection, measurement techniques, GD&T. 5. Depth understanding of Quality standards; inspection reports; Quality Plan. 6. Ability to read Blueprints/Drawings. 7. Good written & verbal communication skills Other Requirement : 1. Aggressive Attitude. 2. Willing to stay near the plant location. 3. Medically fitness mandatory. 4. Work Discipline (Safety, Quality). 5. Communication on daily work management to Client SPOC person/ Project Leader

Assistant Manager-OMQ: Job Description Performance Indicators Key Tasks: 1) Implements the weekly beat plan and works with technicians to support OMQ in his/her allocated area. 2) Coordinates with AM, SM and State Head in resolving the issues 3) Coordinates the execution of OMQ activities such as machinery installation, plumbing work, electrical work, water sample collection and testing, filter replacement, distribution of consumables regarding O&M in his/her area of operations 4) Monitors and guides technicians and interact with technicians only daily basis. 5) Collects and analyzes OMQ data of his/her allocated area and assists OMQ manager in report generation of OMQ. Profile (Attributes): 1) A Proactive person. 2) A person who can handle the team 3) A person that demonstrates willingness to learn and ready to get his hands dirty. 4) A person with commitment, integrity and responsibility. 5) A person with problem solving ,trouble shooting skills and eye for detail 6) A person who can consolidate the plant level MIS and report the same to his/her reporting officer. 7) A person with positive mindset 8) A person motivated to do something good for his community 9) A person with qualification of BE/ B.Tech with 3-4 years of experience. Should be able to Analayse 1) OMQ issues identified VS Issues rectified in past 3 months 2) Preparation and updating of MIS of the plants Availability of data regarding OMQ issues / Shut down trackers , Visit reports Speed and accuracy of data collected and updating it to the reporting officer 3) Commissioning of new plants as per the OMQ manual 4) Turnaround time for resolving issues 5) Cost Reduction - Overall in Project Execution Handling team of technical experts , Knowledge of R.O machinery complete maintenance

Education : Diploma/B.E./B.Tech. (Mechanical/Automotive/Production) only Experience : Min 1 years & Max 3 years Industry : Machine Shop / Gear Manufacturing Industry Responsibilities : 1. Experience in Product inspection (Visual & Dimensional). 2.Hands-on experience in measuring instruments handling like (Vernier , Micrometre, Height Gauge, Attribute gauges, Aig guages,TPG etc.) 3. Good knowledge of inspection, measurement techniques, GD&T. 4. Depth understanding of Quality standards; inspection reports; Quality Plan. 5. Ability to read Blueprints/Drawings. 6. Good written & verbal communication skills Other Requirement : 1. Aggressive Attitude. 2. Willing to stay near the plant location. 3. Medically fitness mandatory. 4. Work Discipline (Safety, Quality). 5. Communication on daily work management to Client SPOC person/ Project Leader

We are Hiring Assistant Manager - Quality Assurance for our client. If you have skill and experience in the same industry and profile, Kindly send updated resume. Designation : Assistant Manager Job Location: Haridwar, Surat & Ahmedabad Gender: Male Department: Quality department Nutraceuticals & Personal care Job Function: Quality Assurance and Control Role & responsibilities 1. Assisting Quality Manger for on going Quality Control check activities 2. Knowledge about Quality Control & Quality Assurance tools 3. Knowledge about testing of Nutraceutical and Personal care products 4. Sensory Evaluation 5. Sound knowledge of Google sheets and Good computer proficiency 6. Able to manage the trackers related to ongoing Quality Control task 7. Coordination with cross functional team and Third-Party Manufacturers 8. GMP 9. Knowledge about Regulatory requirements of FSSAI Preferred candidate profile Knowledge about Regulatory requirements of FSSAI and Personal Care industry Regards, Shivika Sharma 9220541221

SUMMARY Job Description : Quality Control - Executive / Senior Executive Responsibilities: Managing customer complaints and providing solutions in coordination with the team. Scheduling appointments and resolving complaints received from end users. Investigating root causes and conducting further analysis. Coordinating with the head office and factory for complaint closure within specified timelines. Preparing weekly and monthly reports for management, including observations and the number of resolved cases. Ensuring clear communication on complaint closure with key stakeholders. Requirements IPIRITI pass out or candidate should have Quality Control experience within Plywood Industry. Excellent knowledge of plywood. Strong communication and interpersonal skills. Proficiency in MS Excel and PowerPoint. Willingness to travel.

Process Trainer /Soft skills Trainer BPO TNA TNI TTT Refresher NHT PKT IMMEDIATE JOINER Call/Whtapp cv to Amit 8178259405 Neha 8287267407

QA & R Manager is responsible for functions under QA from R.M. Inspection to Customer complaints systems compliance, audits leading all the QA operations in the company initiating & implementing continuous improvements to enhance product reliability Required Candidate profile Production Manager is responsible for heading the manufacturing operations. Monitor production output adjust workflow to meet customer demands & deliveries. Utilization manpower, material, machines

Job Role : Quality Inspector (Quality Associate)Work Location : Sipcot Industrial Complex, Phase II, Moranapalli Village, Hosur 635109Education : Diploma/B.E./B.Tech. (Mechanical/Automotive/Production)onlyExperience : Min 1 year & Max 3 yearsIndustry :Related to Machined Components Manufacturing Industry Responsibilities : 1. Experience in Product inspection (Visual & Dimensional).2. Hands of experience on Layout Inspection (Mandatory)3. Hands-on experience in measuring instruments handling like (Vernier , Micrometre, Height Gauge, Attribute gauges, Air gauges, Surface roughness etc.)4. Good knowledge of inspection, measurement techniques, GD&T.5. Depth understanding of Quality standards; inspection reports; Quality Plan.6. Basic understanding of CMM Inspection / report. 7. Ability to read Blueprints/Drawings.8. Good written & verbal communication skills Other Requirement : 1. Aggressive Attitude. 2. Willing to stay near the plant location.3. Medically fitness mandatory.4. Work Discipline (Safety, Quality).5. Communication on daily work management to Client SPOC person/ Project Leader Food Facility: Available. Transport Facility: Not Available.Working Days : 6. Working Hours : 8 Hrs (Excluding Breaks)Shift : Rotational ShiftWeekly Off : SundayAttendance bonus: For 100% attendance you will get 500/- Rs attendance bonus every month. Location - Sipcot Industrial Complex, Phase II, Moranapalli Village, Hosur 635109

Quality Control- Development - Iron & steel Industry

Quality Control- Development - MFR -Iron & steel Industry

Eligibility Criteria. 1 years of experience in Manufacturing Environment Any Arts & Science Graduate Candidate Need to work in Rotational Shift Timings Job Type Duration: 12 Months Fixed Term Contract Salary – INR 18200 – Per Month Job Description. Fresh Arts & Science Graduate Ability to learn new tasks quickly & perform efficiently Willingness to work in cross functions Preferred knowledge of electronic assembly process' Roles and responsibilities. Operation and maintenance of SMT machines and equipment and perform Assemble the electromechanical parts as per the work instruction without any defects Perform the given task effectively and follow shop floor best practices Follow 5S & safety practices in shopfloor and maintain the area neat, clean & tidy Handle electronic modules carefully and preserve appropriately Learn and perform new stage operations to become more competent and multiskilled Follow I Own Quality concept to produce quality products Benefits. Transportation – Available as per Shift timing – Both Pick and drop, additionally for Women employees, House Pick up and drop if shift timing is on 6.00PM to 6.00AM along with escorts Food – Yes Available As per Shift timing Other benefits: Group Medical Insurance, Group Personal Accident Insurance and Group Term Life Insurance are as per applicable Company Policy. Pre-engagement medical test: Will be organized by Nokia, and all apprentices are required to undergo the same.

1. Strategic Manage the shifts during season and shift operations to achieve factory business goals and performance standards Work towards control of sugar losses in case of molasses, press cake Control and minimize in steam consumption and power consumption in Boiling House Reduce the consumption towards Lime, Sulphur and other chemicals for removal of impurities to ensure that the manufactured product is as refined as possible Generate inputs for MIS, efficiencies report etc. and ensure proper quality of the job done Responsible for physical testing of process samples in shift (setting time, blain, residue etc.) Work towards minimization of cost of inventory spare parts 2. Liaising Responsible for institutionalizing company values among the employees in the section Ensure safe working condition in plant area and other machine areas during maintenance and repair of machinery 3. Operations Oversee operation of equipment /machines in an efficient way during shifts to keep a check on the quantity and the quality of produced sugar Follow up to check the availability of material during off-season Undertake Preventive maintenance of boiling house equipment during season in shifts & coordination with Section In charge Engineering to reduce the equipment downtime Ensure implementation of SOP during shift operation, and responsible for product changeover Analyze collected data, implement corrective actions and validate test equipment during shift 4. Self/ Team Development Review and monitor performance of team members and provide requisite developmental support/ inputs Recommend training as required for teams development Develop the team and update their knowledge base to cater the organization need Strategize avenues for enhancing employee satisfaction in the function, resulting in high engagement levels of employees

Eligibility Criteria. Freshers Diploma graduate from 2025,2024 and 2023 pass out students. Any Diploma Graduate Other than Civil Stream Min 65% of percentage in Diploma Candidate Need to work in Rotational Shift Timings Job Type Duration: 12 Months Fixed term Contract Job Description. Fresh Diploma in Electrical & Electronics Engineering, Computer Science, Mechanical Engineering Ability to learn new tasks quickly & perform efficiently Willingness to work in cross functions Preferred knowledge of electronic assembly process Roles and responsibilities. Operation and maintenance of SMT machines and equipment and perform Assemble the electromechanical parts as per the work instruction without any defects Perform the given task effectively and follow shop floor best practices Follow 5S & safety practices in shopfloor and maintain the area neat, clean & tidy Handle electronic modules carefully and preserve appropriately Learn and perform new stage operations to become more competent and multiskilled Follow I Own Quality concept to produce quality products Benefits. Transportation Available as per Shift timing Both Pick and drop, additionally for Women employees, House Pick up and drop if shift timing is on 6.00PM to 6.00AM along with escorts Food Yes Available As per Shift timing Other benefits: Group Medical Insurance, Group Personal Accident Insurance and Group Term Life Insurance are as per applicable Company Policy. Pre-engagement medical test: Will be organized by Nokia, and all apprentices are required to undergo the same.

Quality Manager- Indira IVF- Matcare Wellness-, Gurugram Indira IVF is looking for an experienced and detail-oriented Quality Manager to join our Gurugram team. If you have a passion for ensuring top-level quality in healthcare and compliance with regulatory standards, youll thrive in this role! Location- Gurugram, (Sector-14), Haryana (on-site) Employment Type- Full-time About the Role: As Quality Manager, you’ll lead our quality assurance initiatives across IVF operations. You will develop, implement, and oversee quality systems to maintain the highest patient care standards and comply with national and international regulations. Key Responsibilities 1. Establish and maintain robust quality management and total quality assurance systems. 2. Lead internal and external audits, including NABH, NABL, ISO, and regulatory bodies, and manage corrective action plans. 3. Develop, implement, and review SOPs, work instructions, and forms. 4. Collect and analyze quality metrics (KPIs), oversee trend analysis, and enforce continuous improvement. 5. Drive CAPA processes—investigation, root-cause analysis, corrective/preventive actions. 6. Facilitate staff training on quality policies, procedures, and regulatory compliance. 7. Manage document control and records systems to maintain data integrity. 8. Act as liaison for quality inspections and coordinate with regulatory authorities. 9. Conduct risk management and quality impact assessments and participate in product/process validation. 10. Promote a quality-focused culture through awareness campaigns and process engagement. Key Requirements: 1.More than 8 years of quality assurance/quality control experience in a healthcare or clinical lab environment. 2. Strong knowledge of applicable quality systems. 3. Hands-on experience with internal & external audits and CAPA management. 4. Excellent documentation, analytical, and data interpretation skills. 5. Clear leadership ability, strong communication, and team-building skills. 6. Proficiency in MS Office; familiarity with LIMS or QMS software is a plus. What We Offer: 1. Competitive salary commensurate with experience. 2. Opportunity to impact patient care quality across a leading IVF network. 3. Dynamic and supportive work environment. 4. Career development and continuous training. #Quality #Quality_manager #NABH #NABL #Hospital_operations #Healthcare_jobs #Hospital_jobs #Indira_IVF

Role Purpose: This position will be responsible for Electrical commodity and will be based at New Delhi Plant. This position will be responsible for ensuring quality and compliance of supplier-produced parts by reviewing and approving Global PPAP submissions in the PPAP module. Major Accountabilities: PPAP Review & Approval: Evaluate submitted Global PPAP documentation and samples from suppliers against the organization's quality requirements and customer specifications. Verify the completeness and accuracy of PPAP package elements, including Design Records, Engineering Change Documents, Process Flow Diagrams, PFMEA, Control Plans, MSA, Dimensional Results, Material Certifications, and Test Results. Utilize the PPAP module/system to review, track, and document the approval status of each suppliers PPAP submission. Approve or reject PPAP submissions based on compliance with quality standards, documenting reasons and feedback for rejections. Supplier Collaboration & Communication: Work closely with suppliers to resolve PPAP discrepancies, non-conformances, or incomplete submissions. Facilitate corrective actions and re-submissions as necessary to ensure all PPAP requirements are met. Coordinate cross-functional communication between engineering, manufacturing, and quality teams regarding PPAP statuses and concerns. Process Improvement: Identify trends in PPAP submissions and common non-compliance issues. Recommend improvements to supplier quality processes and PPAP requirements to mitigate risks. Documentation & Reporting: Maintain accurate records of PPAP reviews, approvals, and correspondence within the PPAP module/system. Generate reports on PPAP submission status, supplier quality performance, and approval cycle times. Ensure compliance with CNH and industry quality standards (e.g., ISO/TS 16949, IATF 16949). Leadership/Team Management Responsibility: Self-driven personality Speedy & aggressive in achieving organizational objectives on time. Minimum Qualifications, Skills, Experience and Language(s): Education/Qualifications (Min): Diploma / Graduate Electrical Engineer Essential experience and skills: 3~10 years of experience in OEM or Auto ancillary in Supplier Quality function. Preferably Female Detail-oriented with strong organizational skills and the ability to manage multiple PPAP submissions simultaneously. Experience with global supplier base and managing multi-location PPAP reviews. Knowledge of other quality tools such as APQP, SPC, and Root Cause Analysis. Proficient in PPAP module/system software and MS Office tools. Excellent communication skills for effective supplier interaction. Should be well versed with Electrical commodity parts & review. New Part development process exposure in Electrical commodity. Key Internal and External Relationships: Internal: Interactions with Peers of Purchasing commodity, Product Development, Testing & Validation, Manufacturing & Quality & Product Behavior. External: Suppliers Desired Behavior Traits: Attention to Detail : Meticulous in reviewing drawings, defining processes, conducting Technical review performance metrics to ensure accuracy and compliance with requirements. Proactive Problem-Solving : Anticipates potential risks and issues in the supplier process and takes initiative to resolve them before they impact project timelines or budgets. Effective Communication : Clearly conveys information and expectations to suppliers, stakeholders, and team members, ensuring alignment and understanding across all parties. Collaboration and Teamwork : Works well with cross-functional teams, sharing knowledge and resources to achieve common goals and support successful project outcomes. Adaptability and Flexibility : Adapts to changing project requirements, market conditions, and organizational needs, demonstrating resilience in a dynamic environment. Integrity and Ethical Conduct : Upholds high ethical standards in all part development activities, ensuring transparency, fairness, and compliance with company policies and regulations. Results-Oriented : Focused on delivering high-quality outcomes within specified timelines and budgets, consistently meeting or exceeding expectations. Continuous Improvement Mindset : Committed to learning and improving processes, staying updated on industry trends, and implementing best pr

Hiring: Assistant Manager Nominated Quality Assurance (QA) | Bangalore Industry: Appare l Experience: 5–10 Years CTC: 8–10 LPA We are looking for a skilled QA professional with strong experience in the apparel industry. The ideal candidate should be well-versed in buyer manuals, quality audits, inspection protocols, and production processes from sampling to shipment. Key Skills: Strong knowledge of garment construction & fabric properties Quality inspection, AQL standards, defect analysis Root cause analysis & corrective action Effective communication & team collaboration Location: Bangalore Qualification: Degree/Diploma in Textile or Apparel Engineering Reporting to: Head QA & Technical If this sounds like your next move, drop your CV or DM for more details! Send Your Resume To anjuman.aara@Unisoninternational.Net Whatsapp: 9319975460

Required: B.Tech (Electronics/Electrical/Mechanical) with 2-5 years of experience in Supplier quality. Knowledge of ISO 13485, FDA, EUMDR and regional medical device regulatory requirements. Ability to effectively communicate information to team members, leaders, management, and suppliers. Experience supporting third-party inspection (FDA, Notified Body etc.) within the medical device industry. Proficient in MS Office Suite (including Word, Excel, Power Point etc). Strong interpersonal skills to work with cross-functional teams (engineering, R&D, manufacturing, regulatory affairs). Preferred: Understanding of Medical Device Regulatory Compliance (ISO 13485, CFR 820, or comparable standard / regulation) and EU's Medical Device Directive. Excellent communication and influencing skills, with the ability to manage multiple tasks and represent the Quality function across teams Preferred German Language exposure . ISO 13485 Lead Auditor certification or equivalent

Job Profile :- Traine / QHSE Location:- hapur, Noida, Bijnor Call/ whatsapp :- Lucky B - 8130991006 • Conduct the technician induction training as per defined training curriculum. • Responsible for training in 3 divisions. • Verifying the training participants details & candidature. • Verifying the PPEs, Tools & Tackles of participants. • Capture the training participants attendance in defined format & online tool. • Sharing the training attendance to respective circle QHSE officer. • Close coordinate with divisional officer & circle QHSE officer for training infra setup & other requirements.

Focus on NPD, IPQC & CUSTOMER QA handling 8D, PPAP, APQP Methodology, Customer Handling, EMS Product knowledge, PCBA, IPC 610 & 620 Standards , Expertise in Soldering, ISO 9001:2015, IATF Knowledge, DFMEA, PFMEA, R&D, Product & Process Specification Required Candidate profile Only BE EEE Only FEMALE 8+yrs exp into NPD, In-Process QA & Customer Quality with EMS industry Good understanding of EMS Products & PCBA Willing to work @ ORAGADAM Send CV to cv.ch2@adonisstaff.in Perks and benefits Excellent Perk. Send CV to cv.ch2@adonisstaff.in

Lead SUPPLIER QUALITY, SUPPLIER AUDIT & DEVELOPMENT, SUPPLIER TECHNICAL ANALYSIS, SPE, PART DEVELOPMENT, SUPPLIER HANDLING, SUPPLIER ASSESSMENT, SUPPLIER EVALUATION, RATING SQE, MATERIAL INSPECTION etc Strong exp in AUTOMOTIVE INJECTION MOLDING must Required Candidate profile Diploma/BE 6-14yrs exp into VD/STA/SQA with AUTO/ENGG/EMS Unit Supplier Development, Supplier Audit, STA, SPE, SQE Process, ISO Standards, Rating SQE exp must Automotive Injection Molding exp must Perks and benefits Excellent Perks. Send CV to cv.ch2@adonisstaff.in