in addressing quality systemrequirements. Participate in internal quality audits to determine theeffectiveness of the quality system. Ensure that production identification, traceability, process control, packaging instructions, first off/ last offprocedures are all being adhered to.
Utilize skills such as FMEA, APQP, MSA, SPC, Kaizen, 5s, 8D and PPAP. Travel (up to 20%) to variousunanticipated US locations depending upon the project/assignmentrequirements for customer concerns and supplier issues. Requirements: Bachelor's degree or equivalent in Industrial Engineering, Mechanical Engineering or related plus 5 years of post-bachelor progressive workexperience in Quality engineering field.
Name : Martinrea Heavy Stampings Inc. Description : Martinrea is located at 1000 Old Brunerstown Road, Shelbyville, Kentucky40065 USA. It is a wholly owned and controlled subsidiary of Martinrea International Inc.
(TSX : MRE), a leader in the development and productionof quality metal parts, assemblies and modules, fluid managementsystems, and complex aluminum products focused primarily on theautomotive sector and industrial. Martinrea operates in 57 locations in Canada, the United States, Mexico, Brazil, Germany, Slovakia, Spain, Japan, South Africa, and China. Martinrea's vision is to make lives betterby being the best supplier we can be in the products we make and theservices we provide.
For more information on Martinrea, please visit . Type : Direct Employer Address : 1000 Old Brunerstown Road Shelbyville, KY 40065Apply by mail : Attn: Human Resources - Martinrea Heavy Stamping Send resumes to: Martinrea Heavy Stampings Inc.
Human Resources manager, 1000 Old Brunerstown Road, Shelbyville, Kentucky, 40065. Ref Job #: SQE4423. Martinrea International Inc. is proud to provide employment accommodations during the recruitment process. Should you require any accommodations, please notify us if you are contacted for a job interview.
exceptional skills with those of people from all over the globe. Join Astra Zeneca and help us deliver life-changing medicines! Be among our employees who continue to make us an innovation-driven company that stands firmly among the leaders in Biomedicals. Why Join Quality?
In Quality, our work is important and valued. An unrivalled forward-looking mindset, there's no better place to work at the forefront and learn how to add real value to a business throughout the lifecycle of our products - discovery, development and commercialization. As the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trailing
the latest models and technologies to improve reliability and excellence in our processes. A place to take Quality seriously - we draw learnings from others, to develop and understand what it takes to drive our modern mindset forward.
Here you'll feel empowered to step up, follow the science and evidence to make decisions that put patients first. If you have the passion and the drive to accelerate growth and make people's lives better - then this is the place for you. What you'll do: The Senior Quality Assurance Specialist is a highly-visible, multi-functional, proactive site leader who is instrumental in maintaining AZ's Quality System and completing QA activities critical to delivering
safe and timely supply of life-saving products to the market. The role also achieves AZ's continuous improvement targets by lifting site compliance capabilities, simplifying Quality System business processes, representing the site on regional and global forums, continuous professional development, and driving GMP/Good Distribution Practice compliance performance forward.
This individual will execute routine QA responsibilities to support daily Operations / business targets by releasing products and resolving quality issues to ensure product quality, patient safety, site safety and site compliance. The individual will actively develop and improve quality system processes, and quality performance at the local, regional, and global level.
Responsibilities: Serving as local business process owner (BPO) for several AZ quality system elements (e. g. change control, document control, investigations, complaints, self-inspection, supplier quality management, etc. ) to ensure their compliant and timely execution and continuous improvement. Ensuring site operations, equipment, processes and product comply with local, regional, and corporate procedures Maintaining controlled material status and distribution authorizations to ensure timely supply availability for distribution operations Collecting, analyzing and reporting site Quality System metrics for the site leadership team to ensure effective Quality System monitoring.
Confirming technical quality and compliance for Validation, Facilities, Change Control, Investigations, Operations to ensure technically- and scientifically-sound, and GMP-compliant technical decisions and documentation. Ensuring robust risk management, problem solving, and root cause analyses at the site for investigations, change controls, risk backssments that subsequently ensures effective problem / risk management and reduction, and prevents problem recurrence.
Continuously building up the site quality culture, driving continuous improvement, and building site cohesiveness / relationships. May also be responsible for or involved in: Oversight of local GMP suppliers to ensure compliant supplier operations and change management. Local, corporate and external audits to ensure sufficient support and successful outcomes. Conducting product complaint investigations to backss distribution / distribution center factors contributing to reported complaints. Compiling, analyzing and reporting product-specific quality metrics data for annual product review / periodic quality review.
Experience: Essential BS Degree in Chemistry-, Microbiology-, or Engineering- or Science/medical field. 5-7 years' experience in medical GMP commercial operations 3+ years direct experience in implementing or managing medical / biologics GMP commercial quality management systems and processes Solid and broad understanding of key medical GMP Quality Systems (e. g. deviation, CAPA, change control, document control) Strong technical / operations experience and aptitude Knowledge and practical experience of risk management, problem solving, root cause analysis, concepts and methodologies Practical knowledge of federal and international medical regulations Data analysis, data verification, and problem-solving abilities.
Desirable 10+ years medical / GMP commercial operations Professional Certifications in Compliance, Quality Management, Quality Engineering, or Lean Six Sigma. Knowledge of medical distribution Proficient in Veeva Vault and SAP Proficient in MS Word, Excel, Power Point, Teams, Share Point Effective project management skills and/or substantial exposure to project-based work structures. Why Astra Zeneca?
At Astra Zeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-medical company can be. This means we're opening new ways to work, groundbreaking cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey. NOTE: This position will require you to be on site for 5 days a week Date Posted 27-Nov-2023 Closing Date Astra Zeneca embraces diversity and equality of opportunity.
We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics (e. g. race, color, religion, interaction, interactionual orientation, gender identity, national origin, disability or protected veteran status).
We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements. Astra Zeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.
and services while on-site. Johnson Heating is offering you a chance to become part of our positive team culture. Our great reputation is built around our loyal customer base. If you have a strong passion for our industry and are willing to go above and beyond to achieve client satisfaction, then this is the right opportunity for you!
If you are a driven individual, we can help you to achieve your career goals. Pay Scale: $19.00 - $25.00 per hour, dependent upon experience Schedule: Monday through Friday (overtime as needed) / Flexible schedule options may be available Why work for us? IRA with a 3% company match Opportunities for spiffs and commissions on top of hourly pay 7 Paid holidays
Paid Vacation Medical insurance Company vehicle with gas card Tool program Growth and advancement opportunities Professional Development Paid training and continuing education Christmas Holiday Party Year-round work with full-time hours - No layoffs!
Required Qualifications: 1+ years of Duct Cleaning Valid license and insurable driving record Mechanically inclined and understand how to utilize basic hand and power tools safely Impeccable Customer Service skills Ability to lift and carry 75 lbs Experience in construction or trade would be a plus! hvac jobs, install jobs, entry level jobs, labor jobs, ducts, hvac install, manual work
learns, and lives. Our sustained investment in research, development, and invention means we’re always ready to solve the toughest challenges alongside our customers. Corning’s businesses are ever evolving to best serve our customers, industries, and consumers.
Today, we accelerate and transform life sciences, mobile consumer electronics, optical communications, display, and automotive markets. We are changing the world with: • Trusted products that accelerate drug discovery, development, and delivery to save lives • Damage-resistant cover glass to enhance the devices that keep us connected • Optical fiber, wireless technologies, and connectivity solutions to carry information and ideas
at the speed of life • Precision glass for advanced displays to deliver richer experiences • Auto glass and ceramics to drive cleaner, safer, and smarter transportation Scope of Position: Strengthen the Product Quality Systems and Architecture within the organization by driving fundamental understanding and continual improvements that positively influence the Quality Management System.
Will act as Performance Excellence (PEx) champion for both Harrodsburg plant and MCE (Mobile Consumer Electronics) Division. Required Education/Experience/Skills: • Bachelors in a Technical field (Engineering preferred) • Six Sigma Green Belt Certified (Black Belt preferred) • 4 years in manufacturing/process
experience; quality experience preferred • Ability to articulate risks and influence decisions on product quality • Ability to make decisions independently based upon sound engineering and scientific methods • Experience with data collection and data analysis software and techniques, including Excel, SPC XL, Pi, Access, etc.
Desired Skills: • Product Quality Architecture training • Familiarity with product specifications and measurements • Experience coaching/mentoring • Statistical Process Control understanding • Experience with ISO 9001 or similar certification process Key Responsibilities: • Facilitates root cause analysis on products and processes not meeting specified requirements.
Works with manufacturing and engineering on completing sustainable solutions which are compliant with our quality system and customer agreements. • PEx champion is a leader of process improvements by assuring the effective use of the different improvement methodologies (DMAIX, LEAN, DESGN, MEE, PQA, etc. ) towards the achievement of plant/division strategic goals. Assist and coach belts and managers in the project nomination, selection, implementation, and documentation processes. Actively engage in advising plant management and leaders on the use of Quality tools, methods, and processes.
• Understand internal and external customers stated and implied needs as well as ensuring their expectations are met every time by monitoring, maintaining, supporting, and continuously improving plant quality systems. • Facilitates efforts in understanding processes capability and product quality architecture. Designs new and improves existing quality architecture systems and for new products. • Participates in or leads quality system improvements including those focused on product disposition tools and inventory management. Hours of work/work schedule: Typically, 8 AM – 5 PM Monday – Friday, some flex including off shift and weekend coverage is possible to support production.
Some after-hour phone conferences will be required. This position does not support immigration sponsorship. The range for this position is $69,156.00 - $95,090.00. Starting pay for the successful applicant is dependent on a variety of job-related factors, including but not limited to geographic location, market demands, experience, training, and education. The benefits available for this position include medical, dental, vision, 401(k) plan, pension plan, life insurance coverage, disability benefits, and PTO.
Corning Puts YOU First! We are committed to supporting your health, financial, career development, and life goals as you grow professionally and personally to achieve your highest potential. All benefits begin as soon as you start your career at Corning. Our monetary peer-to-peer recognition program is tied to our Values and celebrates you and your colleagues’ contributions. Health and well-being benefits include medical, dental, vision, paid parental leave, mental health/substance use, fitness, and disease management programs. Financial benefits include a 401(k) savings plan with company matching contributions and a 100% company-paid pension benefit that grows steadily throughout your career.
Companywide bonus and attractive short- and long-term compensation programs are available based on your role and responsibilities. Professional development programs help you grow and achieve your career goals. We prohibit discrimination on the basis of race, color, gender, age, religion, national origin, interactionual orientation, gender identity or expression, disability, veteran status or any other legally protected status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.
To request an accommodation, please contact us at xyz X@.
to explore, discover and build good things, together. The GE Appliances philosophy, backed by three simple commitments defines the way we work, invent, create, do business, and serve our communities: we come together , we always look for a better way , and we create possibilities.
Interested in joining us on our journey? As a Senior Manufacturing Quality Engineer, you will play a pivotal role in ensuring the highest standards of product quality and cost efficiency in Refrigeration Production. You will be responsible for overseeing the Manufacturing Control Plan (MCP) in an assigned manufacturing area, driving continuous improvement, and fostering a culture of excellence. The role involves
collaboration with various stakeholders to implement and maintain quality systems, improve manufacturing processes, and achieve financial targets. Position Senior Manufacturing Quality Engineer Location USA, Louisville, KY How You'll Create Possibilities Partner with Business Operations and Manufacturing Engineering Leaders to cultivate a culture that upholds and sustains product quality through disciplined systems (Training and Certification, QMS, TPM, PM, Calibration, ESD, Risk Management).
Identify and execute projects to enhance operational costs. Act as the area owner for Corrective and Preventative Actions (CAPA), employing the Corrective Action Request (SCAR / CAR) approach to
problem-solving. Drive continuous improvement in quality and related areas.
Coach team members to follow escalation processes for quality-related issues. Develop performance metrics linked to the overall factory financial plan (AY, Scrap), and establish systems to track and adjust as necessary. Identify and execute projects to enhance operational costs. Act as the area owner for Corrective and Preventative Actions (CAPA), employing the Corrective Action Request (SCAR / CAR) approach to problem-solving. Take ownership of all attributes of the Manufacturing Control Plan for the assigned area, including technical knowledge of the supporting supply chain. Lead the training, execution, auditing, and improvement of the Manufacturing Quality Control Plan.
Provide technical leadership for the development, sustainment, and continuous improvement of factory quality measurement systems, including gaging and testing equipment. Collect and analyze data as part of SPC. Implement escalation plans as required by MCI/MCP. Monitor and respond to data trends, identifying root causes and leading corrective actions. Lead and support 1x1 problem-solving for the assigned area, collaborating with various teams to improve product quality by identifying and eliminating root causes of issues.
Provide guidance to the NPI team on manufacturing process capabilities. Evaluate and implement new testing technologies to support new product innovations and improve outgoing quality. What You'll Bring to Our Team Bachelor of Science Degree in Engineering or related discipline preferred.3+ years of experience interpreting data to solve problems associated with high-volume, short-cycle manufacturing of consumer products.3+ years of experience in manufacturing quality/quality improvement projects or process improvement in a fast-paced, high-volume manufacturing environment, or equivalent military experience.
Ability to work within large cross-functional teams at multiple organizational levels. Experience in the development or sustaining of data collection and measurement systems. Demonstrated ability to drive continuous improvement in a manufacturing environment. Moderate experience in Excel, Word, Power Point, Auto CAD, Minitab, and Outlook. Travel (up to 10%) to suppliers and other manufacturing locations as needed. Flexibility to work off-shifts and weekends as required. Our Culture At GE Appliances, creativity meets passion and conversations lead to exceptional outcomes and experiences.
We respect and value the unique backgrounds and experiences that everyone brings to GE Appliances. We believe a diverse workplace, where everyone is included and people can be their true and authentic selves, fosters creativity and innovation. We know our differences are our greatest strength. The very best innovations across every function of a company come from diverse teams. Our commitment to ensuring a safe and inclusive workplace where everyone is valued allows employees to perform at their best, every day. Diversity at GE Appliances helps us achieve zero distance to our owners, innovate smartly and connect to the communities and customers we serve.
We encourage and support the ideas, aspirations, and the wellbeing of everyone - our employees and our communities GE Appliances is a trust-based organization. It is important we offer our employees the flexibility they need to do their best work while balancing the needs of the business and individuals. When you join GE Appliances, you will have the opportunity to work with your leader to create a flexible work arrangement that balances the needs of the individual, team, and organization. GE Appliances is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, religion, national or ethnic origin, interaction, interactionual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Appliances participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U. S If you are an individual with a disability and need assistance or an accommodation to use our website or to apply, please send an e-mail to xyz X@ PDN-9ad5c42d-4bbb-48fb-8043-cbd623bfbb3f
