דרושים Quality Auditor ב-Honeywell ב-ארהב

• JOB ID: HRD9085821
• Category: Information Technology
• Location: 115 Tabor Road,Morris Plains,New Jersey,07950,United States
• Exempt

As a Quality Engineer here at Honeywell, you will play a crucial role in ensuring the delivery of high-quality products and solutions. You will be responsible for driving quality control processes and implementing strategies to meet customer requirements and drive business growth. Your expertise and leadership will be instrumental in maintaining our position as a global technology leader and delivering innovative solutions that improve the quality of life for people around the world. You will report directly to our Quality Manager, and you'll work out of our Spokane, WA location on a hybrid work schedule.

In this role, you will impact on the success and growth of the company by ensuring the highest standards of quality in our products and solutions. You will collaborate with cross-functional teams to develop and execute quality control processes, identify and resolve quality issues, and drive continuous improvement initiatives.
• Develop and implement quality control processes to ensure product quality and reliability
• Collaborate with cross-functional teams to identify and resolve quality issues
• Conduct quality audits and inspections to ensure compliance with industry standards
• Analyze data and implement corrective actions to improve product quality
• Drive continuous improvement initiatives to enhance quality control processes

• 0-3 years of experience in quality engineering or a similar role
• Strong knowledge of data analysis
• Strong knowledge of quality control principles, methodologies, and tools

• Bachelor’s degree from an accredited institution in a technical discipline such as science, technology, engineering, mathematics
• Advanced Engineering degrees like Material Engineering, Mechanical Engineering are desired
• Experience with quality management systems and processes,
• Six Sigma Green belt is preferred; Six Sigma Black Belt is an advantage.
• Experience with SQL is preferred,
• Strong analytical and problem-solving skills

• JOB ID: HRD264173
• Category: Integrated Supply Chain
• Location: 15128 E Euclid Ave,Spokane,Washington,99216,United States
• Nonexempt

• JOB ID: HRD249396
• Category: Engineering
• Location: One-HON-UTC-2+4F ,UTC, 2F 4F, Sushant Lok Phase I,,Sector 43,Sushant Lok Phase I,,Gurgaon,HARYANA,122022,India
• Exempt

Essential Duties and Responsibilities:

Following is a summary of the essential functions for this job. Other duties may be added and performed, which are not mentioned below. Specific activities may change from time to time. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Ensures cGMP analytical activities, such as analytical methods, test results and Certificates of Analysis (CoA), Batch Records comply with internal SOPs, company policies and procedures, safety and environmental and regulatory requirements
• Reviews cGMP batch manufacturing and packaging records and provides recommendations for approval/rejection and disposition
• Manages and approves cGMP investigations, quality incidents, deviations, CAPAs, change control and out-of-specifications/out-of-trends (OOS/OOTs); follows up to verify effectiveness
• Assists with development and implementation of cGMP compliant systems, including internal SOPs, forms, and work instructions
• Performs Independent audits for compliance to policies and procedures: on paper vs. practice
• Assists corporate quality group in preparation of internal quality audit programs and conducts internal audits per approved schedules in accordance with pertinent quality documents; prepares all corresponding documents and reports
• Leads all external cGMP audits of vendors, including US and International cGMP, GLP, GDP vendor audits, as needed
• Coordinates annual and ongoing cGMP training
• Acts as a primary contact for cGMP regulatory inspections
• Oversees release of commercial product
• Maintains the quality function for drug products, including but not limited to:
• Manages and reviews Product Complaints and Recall program for EU and US products
• Releases or rejects intermediates for use outside of the control of the manufacturing company
• Establishes a system to release or reject raw materials, intermediates, packaging and labeling materials; Well versed with IPEC, ICH Q7, 21 CFR 210/211 and Eudralex volume 4 Good Manufacturing Practice (GMP) guidelines
• Reviews unexecuted and completed batch production and laboratory control records of critical process steps before release of drug products
• Reviews and monitors release and stability data
• Reviews and approves changes that potentially impact quality of intermediates, drug products
• Reviews and approves validation protocols and reports, Specifications, certificates of analysis (CoAs), release of raw materials, and product disposition
• Approves selection of contract manufacturers for intermediates, drug products
• Approves all specifications and master production instructions
• Approves all procedures impacting the quality of intermediates, drug products
• Ensures effective systems are used for maintaining and calibrating critical equipment
• Ensures materials are appropriately tested and the results are reported
• Ensures there is stability data to support retest or expiry dates and storage conditions on drug products, and intermediates where appropriate; performs product quality reviews
• Manages and maintain mock recall procedures and policies
• Develops with the CMC team and CMOs: drug substances (DSs), drug products (DPs), key raw material and intermediates specifications and stability requirements, master batch records, validated manufacturing processes and analytical methods, and CTM and commercial packaging and labeling
• Work closely with internal and external departments to assure compliance with cGMP quality systems and regulations issued by the FDA, and other applicable regulatory bodies

Must Have

• Auditing experience in a GMP and GCP environment
• Excipient cGMP production and quality assurance experience
• Knowledge of US, EMA, NMPA, PMDA, HC, and ICH regulations, guidance and industry standards for CMC, GMP and GCP
• 10 + years in pharmaceutical Quality Assurance

We Value

• BA or BS degree in a scientific discipline preferred, or comparable experience
• Previous experience of manufacturing and/or analytical testing is a plus
• Proficiency using Office 365, LIMS, SCICORD, SAP, Adobe Acrobat (standard), DYMO labeler, Adobe Acrobat (standard), and various internet browsers
• Ability to travel, including overnight

• JOB ID: HRD258156
• Category: Integrated Supply Chain
• Location: Ontario & Lupine Streets,Baton Rouge,Louisiana,70821-2830,United States
• Exempt

RESPONSIBILITIES:
Execute transformation of legacy services to contemporary solutions using software defined networks, virtualization, automation, orchestration, segmentation, and edge intelligence.
Design, develop and deploy network solutions that meet or exceed cyber security, compliance and regulatory requirements of the business and our customers.
Architect & implement solutions that are highly available and cost efficient.Provide expert advice during all important ‘Go-Live’ activities of new deployments.

• JOB ID: req480976
• Category: Procurement
• Location: 111 S 34th St.,Phoenix,Arizona,85034,United States
• Exempt

As ahere at Honeywell, you will play acritical role in ensuring the quality and reliability of our products. You willbe responsible for developing and implementing quality control processes,conducting inspections and audits, and driving continuous improvementinitiatives. Your expertise in quality engineering will contribute to thesuccess and reputation of Honeywell as a global technology leader.You will report directly to ourand you'll work out of ourIn this role, you will impact the quality and reliability of our products,ensuring that they meet customer requirements and comply with industrystandards. You will collaborate with cross-functional teams to identify andresolve quality issues, implement corrective actions, and drive processimprovements.
KEY RESPONSIBILITIES

• Develop and implement quality control processes and procedures
• Conduct inspections and audits to ensure compliance with quality standards
• Analyze data and trends to identify areas for improvement
• Collaborate with cross-functional teams to resolve quality issues
• Drive continuous improvement initiatives to enhance product quality and reliability

YOU MUST HAVE

• 5+ years of experience in quality engineering
• Strong knowledge of quality control processes and methodologies
• Excellent problem-solving and analytical skills
• Must be a U.S. Citizen only

WE VALUE

• Bachelor’s degree in engineering or related field
• ASQ Certified Quality Engineer (CQE) certification
• Experience in the aerospace or defense industry
• Six Sigma Green Belt or Black Belt certification
• Provide clear and concise communications
• Proficient computer skills
• Ability to partner with others on projects
• Understanding of quality processes
• Proficient in Quality Management Systems

• JOB ID: HRD263507
• Category: Integrated Supply Chain
• Location: 13350 US Hwy 19 N,Clearwater,Florida,33764,United States
• Exempt
• Due to US export control laws, must be a US citizen, permanent resident or have protected status.

The future is what you make it.

That means changing the way we fly, fueling jets in aneco-friendly way, keeping buildings smart and safe and even making it possibleto breathe on Mars.

THE POSITION

As afor North America here at Honeywell, you willlead a team of quality engineers to ensure that our suppliers meet Honeywell'squality standards and strategy in the manufacture of components for PersonalProtective Equipment (PPE). You will be responsible for driving supplierperformance improvement, managing supplier relationships, and ensuring thehighest level of quality in our supply chain. You will report directly to our Director of Supplier Management and BTS Quality andyou'll work out of our Charlotte, NC location on a hybrid work schedule.

KEY RESPONSIBILITIES

• Manage the day-to-day activities of direct reports, providing initiative and guidance on Quality Tools and Processes and Problem Solving
• Drive Supplier Performance improvement initiatives to achieve world-class levels of quality
• Develop and implement supplier quality strategies to ensure compliance with quality standards and regulatory requirements
• Conduct supplier audits to assess supplier capabilities and identify areas for improvement
• Drive root cause analysis and corrective actions to address quality issues and prevent recurrence
• Collaborate with cross-functional teams to drive NPI and continuous improvement projects and resolve quality issues
• Monitor supplier quality metrics to identify trends and opportunities for improvement
• Provide technical support and guidance to suppliers to help them meet Honeywell's quality requirements

YOU MUST HAVE

• Bachelor’s degree from an accredited institution in a technical discipline such as science, technology, engineering, mathematics
• 6+ years of experience in supplier quality engineering or a related role
• Strong knowledge of quality engineering practices (PPAP, FAI, RCCA) and methodologies
• Excellent problem-solving and analytical skills
• Strong communication and interpersonal skills
• Ability to work effectively in a cross-functional team environment
• Willingness to travel as required

WE VALUE

• Six Sigma Black Belt Certification
• Automotive background including experience TS 16949
• Experience in Medical Devices and Drugs industry
• Experience in conducting supplier audits and performing root cause analysis
• Strong project management skills
• Ability to influence and negotiate with suppliers

• JOB ID: HRD261315
• Category: Procurement
• Location: 855 S Mint St,Charlotte,North Carolina,28202,United States
• Exempt
• Must be a US Person or able to obtain export Authorization.