4 Scar Jobs nearby Navi Mumbai

As a member of the Electronics Supplier Industrialization Engineering team at Tesla, you will play a crucial role in developing and qualifying critical component and electronic part top-level assembly processes with suppliers. Your responsibilities will include providing regional support for New Product Introduction (NPI) and legacy product management within the supply chain. This will involve collaborating with Tesla sourcing and design teams to conduct early supplier sourcing assessments, make-sourcing decisions, industrialization, and quality control activities. Communication skills, supplier management expertise, and the ability to make critical decisions in time-sensitive situations are essential for this role. You will support a diverse product portfolio including low/high voltage products, controllers, audio and sensing projects, and optical lens and camera projects. - Supporting Design for Manufacturing (DFM) principles during early product development and providing valuable feedback to NPI SIE and design teams. - Conducting onsite supplier audits to assess sourcing decisions and develop new suppliers meeting Tesla's requirements. - Driving continuous improvement in supplier scalability, cost, and quality performance while managing and optimizing supplier On-Time Delivery (OTD) performance. - Overseeing supplier production capacity and operations management, ensuring clear communication of technical requirements between suppliers and Tesla's GSM, SIE, and Design teams. - Collaborating with Tesla supply chain teams to establish optimal performance specifications and supplier metrics. - Leading, tracking, and improving supplier manufacturing process development and launch readiness for new products and design changes. - Managing and enhancing production and product quality by guiding suppliers in developing robust processes and procedures for efficient, high-quality product manufacturing. - Following up and driving SCAR (supplier corrective actions review) with suppliers, validating corrective actions to prevent recurrence. To be successful in this role, you should have: - A minimum of 5 years of experience in supply chain or mechanical engineering, with expertise in PCBAs, PCBs, and PCBA top-level assemblies (TLAs) preferred. - A BS degree in Electrical, Mechanical, Industrial, or Manufacturing Engineering or equivalent experience with exceptional abilities. - Demonstrated experience with Design for Manufacturing (DFM), Design for Assembly (DFA), and Six Sigma methodologies. - Proficiency in GD&T, 3D CAD software, and hands-on experience with quality statistical analysis tools. You should possess a strong mechanical background, including statistical tolerance analysis, design quality assessment, and improvement techniques. Skills in supplier development and management, self-motivation, and the ability to work independently are crucial. Being hands-on and adaptable to a fast-paced environment, as well as a willingness to travel up to 50% domestically and internationally to engage with Contract Manufacturers (CMs), are important for this role.,

Job Description: As an Airlines Ticketing Executive, your primary role will involve handling airlines ticket booking mails from both internal and external customers. You will be responsible for ensuring the safety and security of passengers during flights. Additionally, you will need to serve meals on board to customers with a hospitality attitude. Key Responsibilities: - Handle airlines ticket booking mails from both internal and external customers - Ensure the safety and security of passengers on flights - Serve meals on board to customers with a hospitality attitude Qualifications Required: - Excellent verbal and written communication skills in both Hindi and English - Unblemished complexion and good body language - Height will not be an issue for Ground Staff & Air Ticketing Executive - Should not be overweight or underweight, and should not have any visible marks, scars, or tattoos - Freshers with a minimum qualification of +2 are eligible to apply - Age between 18 to 25 years If you meet the eligibility criteria and are interested in this opportunity, please contact us at 9128526927.,

As a PCBA Supplier Industrialization Engineer, your role involves planning, organizing, directing, and conducting industrialization related activities within the supply chain team. You will be responsible for developing, managing, auditing, improving, and correcting supplier planning and execution of component manufacturing and assembly techniques, as well as quality control processes from the advanced development phase to mass production qualification. **Key Responsibilities:** - Perform Design for Manufacturing (DfM) on PCBAs using DFM software such as Valor and Vayo and provide design guidance to Engineering Teams. - Drive Contract Manufacturers (CM) on quality, responsiveness, and process efficiency. - Own and be responsible for field quality failures through Supplier Corrective Action Requests (SCARs). - Participate in supplier quotations by acting as the technical expert and providing expert knowledge on PCBA line layout and setup. - Determine and manage production line layout capacity by balancing cycle time and driving process flow changes. - Audit and improve suppliers onsite to meet Tesla requirements. - Act as the critical-to-quality (CTQ) leadership during New Product Introductions (NPIs) for suppliers. **Qualifications Required:** - Bachelor's degree in Electrical Engineering, Industrial Engineering, or Mechanical Engineering. - Experience with Problem Solving tools, including RCCA, Fishbone, Process Mapping, and/or 5 Ss. - Solid experience with launching NPIs and project management. - Strong knowledge of Production Part Approval Process (PPAP). - Good working knowledge and understanding of design rules regarding THT, Reflow, Conformal Coating, Underfill, Washing, Press Fit, Pin Insertion, and depanelization. - International travel is required to engage with manufacturing partners, sometimes on short notice. - Excellent spoken and written English.,

As a member of Tesla's Electronics Supplier Industrialization Engineering team, you play a crucial role in developing and qualifying critical component and electronic part top-level assembly processes with suppliers. Your responsibilities include: - Supporting Design for Manufacturing (DFM) principles during early product development, providing valuable feedback to NPI SIE (Supplier Industrialization Engineer) and design teams. - Conducting onsite supplier audits and providing assessments for sourcing decisions, as well as developing new suppliers to meet Tesla sourcing requirements. - Driving continuous improvement in supplier scalability, cost, and quality performance. - Managing and optimizing supplier On-Time Delivery (OTD) performance. - Overseeing supplier production capacity and operations management. - Facilitating clear communication of technical requirements between suppliers and Tesla's GSM, SIE, and Design teams. - Conducting supplier audits to ensure compliance with part performance, delivery, and reliability expectations. - Collaborating with Tesla supply chain teams to establish optimal performance specifications and supplier metrics. - Leading, tracking, and improving supplier manufacturing process development and launch readiness for new products and design changes. - Managing and enhancing production and product quality, guiding suppliers in developing robust processes and procedures for efficient, high-quality product manufacturing. - Following up and driving SCAR (supplier corrective actions review) with suppliers, validating corrective actions for design and/or process changes to prevent recurrence. - Contributing to the evaluation of new or alternative materials for improved design, manufacturability, or cost reduction. In order to be successful in this role, you are required to have: - Minimum 5 years of experience in supply chain or mechanical engineering, preferably with experience in Printed Circuit Board Assemblies (PCBAs), Printed Circuit Boards (PCBs), and PCBA top-level assemblies (TLAs). - A BS degree in Electrical, Mechanical, Industrial, or Manufacturing Engineering, or equivalent experience and exceptional ability. - Proven experience with Design for Manufacturing (DFM) and Design for Assembly (DFA). - Practical experience with Six Sigma methodologies; DAMIC experience is a plus. - Solid hands-on experience with quality statistical analysis tools and applications (e.g., JMP, Minitab). - Strong mechanical background, including statistical tolerance analysis, design quality assessment, and improvement techniques. - Proficiency in GD&T and 3D CAD software. - Demonstrated supplier development and management skills. - Self-motivation and the ability to work independently. - Ability to work in a fast-paced environment and willingness to travel domestically and internationally up to 50% of the time, often with short notice, to engage with Contract Manufacturers (CMs).,

As a motivated individual, you will play a crucial role in supporting cGMP compliance within procurement operations at Regeneron. Your responsibilities will include investigating deviations, supporting CAPAs, coordinating supplier audits, handling change controls, and contributing to the development and implementation of the Supplier Corrective Action Report (SCAR) process. **Role Overview:** You will be essential in ensuring successful audit closures by proactively addressing issues with suppliers and maintaining clear communication to achieve satisfactory outcomes. Additionally, you will manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of all actions. Your partnership with team members will facilitate discussions on Quality and Compliance, align category priorities with Procurement management, and achieve interpersonal goals. You will implement strategies to enhance process efficiency, drive value across procurement operations, and utilize your knowledge of global procurement processes within the biopharmaceutical industry to support the growth of the Global Procurement organization. **Key Responsibilities:** - Ensuring successful audit closures and maintaining clear communication with suppliers - Managing SCARs, following up with suppliers and internal team members, and ensuring timely reporting and closure of all actions - Partnering with team members to facilitate discussions on Quality and Compliance and aligning category priorities with Procurement management goals - Implementing strategies to improve process efficiency and drive value across end-to-end procurement operations - Applying in-depth knowledge of global procurement processes within the biopharmaceutical industry - Contributing to quality and compliance initiatives to maintain adherence to GxP standards and relevant regulatory requirements - Demonstrating data insights to guide decisions and deliver successful quality and compliance outcomes **Qualifications Required:** - Bachelor's degree in a relevant field and at least 8 years of experience in a cGMP environment focusing on quality, compliance, and/or procurement, with specific experience in the Pharma/BioPharma sector - Proven record in supporting global quality or category teams, processes, and suppliers across diverse categories - Strong relationships with customers and suppliers to achieve impactful results - Success in supporting cross-functional teams in areas such as SCARs, ASLs, CAPAs, Change Notifications, and other Quality and Compliance processes - Valuable insights and expertise in handling Quality and Compliance processes successfully - Ability to apply external data, market trends, and supplier engagement to enhance understanding of supply market dynamics - Experience operating with integrity, focus, and transparency in ambiguous environments to drive relevant change and improvement - Familiarity with quality and compliance electronic tools/systems is beneficial - Proficiency in standard business applications such as Word, Excel, and PowerPoint for communication, presentations, and analysis - Continuous improvement approach and collaboration with leadership to implement solutions If you meet the above qualifications and are eager to contribute to the future of healthcare at Regeneron, we encourage you to apply and take the first step towards living the Regeneron Way!,

As a Senior Quality Engineer at SFO Technologies located in Kochi, your primary responsibility will be to oversee and manage quality engineering tasks. You will ensure that quality control processes are followed and implement quality assurance protocols. Your role will involve independently managing all QA related functions of a Relay Manufacturing Plant. Your focus will be on understanding and communicating customer expectations throughout the organization, implementing a Continuous Improvement culture, and effectively implementing Quality Management Systems (QMS). Key Responsibilities: - Assist HOQ in all Total Quality related activities - Implement SPC Practices - Initiate SCAR/Process and Final NCs and monitor effective closure - Maintain all QA Related Documents - Plan and implement Calibration system - Train team members in all QC Tools - Ensure final inspection of finished products as per the WI for Final Inspection - Implement corrective actions for reported Non-conformances - Utilize Quality techniques like 7QC, 8D, SPC, MSA, Process Capability studies to reduce rejection in the manufacturing process - Manage QRQC process and report status to HOD - Monitor and Improve Department KPIs - Implement Supplier Quality Management - Preparation of Quality records such as Incoming, In-process, Final Inspection Reports - Participate in Internal Quality Audit Programme - Support NPI programs and their effective implementation in the manufacturing process - Participate in internal audits as a qualified internal auditor - Ensure First Article and PPAP Approval - Timely closure of all Customer complaints Qualifications Required: - BE/B Tech in Electronics/Electrical Engineering - 5 to 6 years of experience in EMS or a similar industry, with Relays Exposure preferred - Exposure to ISO 9001:2015 Implementation - Knowledge of Quality tools like 7QC, 8D, MSA, SPC, FMEA, etc. SFO Technologies, a leading ODM Plus Service Provider under NeST Group, specializes in offering innovative solutions across industries such as Healthcare, Communications, Industrial & Energy, Transportation, Semiconductors, and Space. With state-of-the-art manufacturing facilities in Kochi, Trivandrum, Bangalore, Mysore, and the USA, the company focuses on Industry 4.0 to empower leading OEMs worldwide. SFO Technologies" expertise lies in digital electronics, RF/wireless technologies, fiber optics, optronics, and more. Their commitment to sustainability is evident through eco-friendly product designs and responsible manufacturing practices.,

Role Overview: As a Satellite Imagery Analyst, you will be responsible for acquiring, preprocessing, and analyzing satellite imagery utilizing open-source datasets such as Sentinel, Landsat, MODIS, DEM, among others. Your role will involve efficiently processing and managing large-scale geospatial catalogs. You will conduct vegetation, water stress, and land cover analysis by employing various indices like NDVI, NDWI, EVI, SAVI, and thermal bands. Key Responsibilities: - Utilize AI/ML algorithms to perform classification, segmentation, anomaly detection, and time-series pattern recognition on both raster and vector data. - Apply spatial analysis techniques to estimate biomass, carbon storage, forest loss, and environmental footprints. - Detect and map tree cover, land use change, water bodies, and burn scars using multispectral and temporal satellite imagery. - Implement pest/disease detection frameworks through image analysis and pattern matching techniques. - Translate raw satellite data into decision-support insights using GIS tools and visual dashboards. Qualifications Required: - Bachelor's degree in Geography, Remote Sensing, Geoinformatics, or a related field. - Proficiency in utilizing open-source satellite imagery datasets like Sentinel, Landsat, and MODIS. - Experience with indices such as NDVI, NDWI, EVI, SAVI, and thermal bands for geospatial analysis. - Strong knowledge of AI/ML algorithms for image analysis and pattern recognition. - Familiarity with GIS tools for translating satellite data into actionable insights. (Note: No additional details of the company were provided in the job description.),

Role Overview: As an Image Editor for E-commerce at our company, you will be a vital part of ensuring that our product images meet the visual standards and reflect our brand identity. Your skills in image editing and meticulous attention to detail will greatly contribute to enhancing the overall customer experience. We are seeking individuals with a passion for image editing specifically within the E-commerce industry. Key Responsibilities: - Perform clipping, wrinkle removal, skin color correction, and shadow creation - Execute garment ghost creation and garment color correction - Conduct basic retouching such as removing tattoos, scars, and moles - Handle advanced retouching tasks including lightning adjustment and pattern color correction Qualifications Required: - Proficiency in clipping, wrinkle removal, skin color correction, and shadow creation - Experience in garment ghost creation and garment color correction - Ability to perform basic retouching tasks like removing tattoos, scars, and moles - Familiarity with advanced retouching techniques including lightning adjustment and pattern color correction Join Flixstock Today! Let us guide you towards your ideal career and discover the difference by being a part of our team! Role Overview: As an Image Editor for E-commerce at our company, you will be a vital part of ensuring that our product images meet the visual standards and reflect our brand identity. Your skills in image editing and meticulous attention to detail will greatly contribute to enhancing the overall customer experience. We are seeking individuals with a passion for image editing specifically within the E-commerce industry. Key Responsibilities: - Perform clipping, wrinkle removal, skin color correction, and shadow creation - Execute garment ghost creation and garment color correction - Conduct basic retouching such as removing tattoos, scars, and moles - Handle advanced retouching tasks including lightning adjustment and pattern color correction Qualifications Required: - Proficiency in clipping, wrinkle removal, skin color correction, and shadow creation - Experience in garment ghost creation and garment color correction - Ability to perform basic retouching tasks like removing tattoos, scars, and moles - Familiarity with advanced retouching techniques including lightning adjustment and pattern color correction Join Flixstock Today! Let us guide you towards your ideal career and discover the difference by being a part of our team!

Role Overview: As the QC Head, you will be responsible for leading the Quality Control function in medical device manufacturing to ensure that products meet global regulatory, safety, and performance standards. Your role will involve overseeing raw material testing, in-process quality checks, stability studies, validation protocols, and final product release in compliance with applicable regulatory guidelines. Key Responsibilities: - Establish, implement, and maintain QC protocols, SOPs, testing procedures, and specifications. - Ensure batch-wise testing, documentation, and release of raw materials, intermediates, and finished products. - Oversee microbiological and biochemical testing for sterile and non-sterile medical devices. - Conduct periodic trending of QC results and take corrective actions. - Ensure compliance with ISO 13485:2016, ISO 14971 (Risk Management), EU CE, and CDSCO norms. - Prepare documentation for audits, regulatory submissions, CAPA, NCR investigations, SCAR, change control, and traceability. - Manage QC laboratory infrastructure, calibration, and validation of analytical instruments. - Lead sterility assurance, endotoxin testing, and environmental monitoring in cleanroom and production areas. - Design and monitor stability studies for product shelf-life determination. - Train and guide QC managers, executives, analysts, and technicians. - Coordinate with R&D, QA, Production, Validation, and Regulatory Affairs. - Implement quality improvement initiatives using Lean / Six Sigma methodologies. - Support and lead investigations for deviations, OOS (Out-of-Specification) results, and customer complaints. Qualification Required: - Strong knowledge in microbiology, biocompatibility, plasma/chemical additives, or IVD reagent chemistry. - Hands-on experience with laboratory QC instrumentation (HPLC, UV-Vis, autoclave validation, endotoxin analyzers, etc.). - Sound understanding of sterile manufacturing, cleanroom classifications, and aseptic techniques. - Ability to interpret regulatory and audit requirements. - Strong leadership, communication, and documentation skills. Additional Details: No additional details of the company are mentioned in the job description.,

As a Quality Data and Improvement Analyst, you will play a crucial role in providing administrative and operational support for Quality Management. Your focus will be on data analysis, quality assessment, process improvement, and performance reporting. You will be responsible for structuring, collecting, compiling, and analyzing data from complaints, customer feedback, CAPAs, supplier audits, and SCARs reporting to uphold Quality Management operational standards and metrics. Key Responsibilities: - Establish and maintain good working relationships throughout the organization to support department, division, and organizational goals and objectives. - Organize and prioritize multiple tasks and deadlines among concurrent projects, project teams, and/or management staff. - Partner with internal customers to define business needs and issues and translate ideas into effective strategies and action plans for various types of stakeholders. - Develop metrics, research designs, and reports using business rules and requirements. - Collect and summarize performance data, identify opportunities for improvement, and present findings. - Analyze current workflows and standards against performance data to assess process adherence and make recommendations for improvement. - Improve quality and operational effectiveness by developing strategies and recommendations from findings associated with record reviews, audits, spreadsheets, and surveys. - Utilize different statistical techniques and tests (i.e., Chi-square test or Fishers exact) to interpret and report on the statistical significance of various quality projects. - Assist with data collection, analysis, and reporting of quality improvement activities and projects. - Present results, findings, interpretations, and recommendations regarding quality management to both internal and external stakeholders. - Implement quality management principles, theories, and tools to facilitate process improvements. - Develop or adapt process and outcome measures in support of quality improvement goals. - Conduct regular data audits and quality assessments. - Ensure compliance with data governance and industry standards. Qualifications & Education Requirements: - Bachelors degree in Data Science, Statistics, Engineering, Quality, Business Administration, or related field(s). - At least two years of experience as a business, quality, or performance analyst required. - Experience in the medical device industry is strongly preferred.,

As a Dermatologist at DR.PATKI - Remedial Multicare Hospital & Institute in Surat, your role will involve daily patient consultations, administering Botox and filler injections, performing thread lifts, and providing acne and scar therapies. You will also engage in cosmetic dermatology treatments and collaborate with other medical professionals to ensure comprehensive patient care. Key Responsibilities: - Conduct daily patient consultations - Administer Botox and filler injections - Perform thread lifts - Provide acne and scar therapies - Engage in cosmetic dermatology treatments - Collaborate with other medical professionals Qualifications: - Expertise in Dermatology and Cosmetic Dermatology - Experience in administering Botox, fillers, and performing thread lifts - Skilled in treating acne and providing scar therapies - Strong background in Medicine and Cosmetology - Excellent patient communication and interpersonal skills - Ability to work collaboratively in a clinical setting - MD or DO degree in Dermatology - Valid medical license to practice in India,

As a candidate for this role, your key responsibilities will include: - Issue Documentation & Resolution: - Create and maintain documentation when an issue is raised. - Work directly with suppliers to ensure effective Corrective Actions and Preventive Actions (CAPA) are implemented. - Track these actions to prevent recurring issues in quality, delivery, or production. - SCAR Management: - Manage Supplier Corrective Action Requests (SCARs) with over 100 open SCARs. - Collaborate with various internal teams and suppliers to close SCARs within agreed timelines. - Root Cause Analysis & Prevention: - Determine the cause of quality issues, prevent them, and ensure supplier commitments are followed. - Investigate why corrective actions failed in case of repeat issues and escalate as needed. - Cross-Functional Coordination: - Communicate resolutions and preventive measures with internal teams. - Share supplier commitments and ensure adherence across different functions. You should preferably have a background in Biopharma or Pharma Manufacturing, but candidates from any manufacturing sector are welcome. Experience in Quality Control (QC) or Quality Assurance (QA) is relevant. Familiarity with CAPA processes, SCARs, PPM (Parts Per Million), supplier management, documentation, and company quality policies is required. In addition to the responsibilities, you should possess the following desired skills and attributes: - Global exposure is essential, with experience working with international stakeholders. - Ability to coordinate and drive resolutions across different global manufacturing sites. - Strong governance, dashboard reporting, escalation management, and process improvement skills.,

You are expected to have 2-5 years of experience with a background in Mechanical Engineering, showcasing strong knowledge of Mechanical components along with an interest in inspection and documentation. Key Responsibilities: - Conduct dimensional, visual, and functional inspections of mechanical components, assemblies, and products based on drawings, specifications, and standards. - Utilize measuring instruments such as Vernier calipers, micrometers, height gauges, dial indicators, etc. - Carry out incoming inspection procedures. - Verify welding, machining, fabrication, and surface finish requirements. - Prepare and manage inspection reports, test records, and quality documentation. - Identify and report non-conformities (NCR) while ensuring proper documentation of deviations. - Keep calibration records of measuring instruments used in inspections. Qualifications Required: - Hands-on experience in inspection. - Basic knowledge of ERP. - Knowledge of SCAR (Supplier Corrective Action Request), defects identification, RCCA (Root Cause Corrective Action), and MRB (Material Review Board) process. - Proficiency in handling basic instruments like Vernier, micrometer, height gauge, bevel protractor, bore gauge, etc. Company Additional Details: No additional details provided in the job description.,

You will join Regeneron, a company dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. Your role will involve supporting cGMP compliance within procurement operations by assisting with various key activities. **Role Overview:** As part of the team, you will be responsible for ensuring successful audit closures, managing Supplier Corrective Action Reports (SCARs), partnering with team members for Quality and Compliance discussions, implementing process efficiency strategies, and contributing to maintaining adherence to regulatory requirements. **Key Responsibilities:** - Proactively address issues to achieve successful audit closures and maintain clear communication with suppliers - Manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of actions - Partner closely with team members to align category priorities with Procurement management goals - Implement strategies to improve process efficiency and drive value across end-to-end procurement operations - Support quality and compliance initiatives to maintain adherence to relevant regulatory requirements - Demonstrate data insights to guide decisions and deliver successful quality and compliance outcomes **Qualifications Required:** - Bachelor's degree in a relevant field and at least 8 years of experience in a cGMP environment - Experience in supporting global quality or category teams, processes, and suppliers - Strong relationship-building skills with customers and suppliers - Success in supporting cross-functional teams in areas such as SCARs, ASLs, CAPAs, and Change Notifications - Proficiency in standard business applications such as Word, Excel, and PowerPoint - Continuous improvement approach with the ability to find opportunities for enhancement If you have the required qualifications and experience, apply now to be a part of Regeneron's inclusive culture and take the first step towards living the Regeneron Way. Visit the Regeneron careers website for more information on benefits and rewards.,

You will be supporting cGMP compliance within procurement operations at Regeneron. Your responsibilities will include investigating deviations, supporting CAPAs, coordinating supplier audits, handling change controls, and contributing to the development and implementation of the Supplier Corrective Action Report (SCAR) process. You will need to ensure successful audit closures, manage SCARs, partner with team members on Quality and Compliance discussions, implement strategies to improve process efficiency, provide insights for decision-making, and contribute to maintaining adherence to GxP standards and other regulatory requirements. **Key Responsibilities:** - Ensure successful audit closures by proactively addressing issues and maintaining clear communication with suppliers. - Manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of all actions. - Partner with team members to facilitate discussions on Quality and Compliance and align category priorities with Procurement management goals. - Implement strategies to improve process efficiency and drive value across end-to-end procurement operations. - Apply knowledge of global procurement processes within the biopharmaceutical industry to support the growth of the Global Procurement organization. - Contribute to quality and compliance initiatives to maintain adherence to GxP standards and other regulatory requirements. - Demonstrate data insights to guide decisions and deliver successful quality and compliance outcomes. **Qualifications Required:** - Bachelor's degree in a relevant field and at least 5 years of experience in a cGMP environment, focusing on quality, compliance, and/or procurement in the Pharma/BioPharma sector. - Proven record in supporting global quality or category teams, processes, and suppliers. - Strong relationship-building skills with customers and suppliers. - Experience in supporting cross-functional teams in areas such as SCARs, CAPAs, and other Quality and Compliance processes. - Proficiency in quality and compliance electronic tools/systems is helpful. - Proficient in standard business applications such as Word, Excel, and PowerPoint. - Continuous improvement approach and ability to collaborate with leadership to implement solutions. If this role aligns with your experience and interests, apply now to take the first step towards working at Regeneron and crafting the future of healthcare. You will be supporting cGMP compliance within procurement operations at Regeneron. Your responsibilities will include investigating deviations, supporting CAPAs, coordinating supplier audits, handling change controls, and contributing to the development and implementation of the Supplier Corrective Action Report (SCAR) process. You will need to ensure successful audit closures, manage SCARs, partner with team members on Quality and Compliance discussions, implement strategies to improve process efficiency, provide insights for decision-making, and contribute to maintaining adherence to GxP standards and other regulatory requirements. **Key Responsibilities:** - Ensure successful audit closures by proactively addressing issues and maintaining clear communication with suppliers. - Manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of all actions. - Partner with team members to facilitate discussions on Quality and Compliance and align category priorities with Procurement management goals. - Implement strategies to improve process efficiency and drive value across end-to-end procurement operations. - Apply knowledge of global procurement processes within the biopharmaceutical industry to support the growth of the Global Procurement organization. - Contribute to quality and compliance initiatives to maintain adherence to GxP standards and other regulatory requirements. - Demonstrate data insights to guide decisions and deliver successful quality and compliance outcomes. **Qualifications Required:** - Bachelor's degree in a relevant field and at least 5 years of experience in a cGMP environment, focusing on quality, compliance, and/or procurement in the Pharma/BioPharma sector. - Proven record in supporting global quality or category teams, processes, and suppliers. - Strong relationship-building skills with customers and suppliers. - Experience in supporting cross-functional teams in areas such as SCARs, CAPAs, and other Quality and Compliance processes. - Proficiency in quality and compliance electronic tools/systems is helpful. - Proficient in standard business applications such as Word, Excel, and PowerPoint. - Continuous improvement approach and ability to collaborate with leadership to implement solutions. If this role aligns with your experience and interests, apply now to take the first step towards working at Regeneron and crafting the future of healthcare.