Indoor Air Quality Specialist | Alexandria, KY

pride ourselves on the multitude of services we can offer our customers. Privately owned and operated until 2006, the Mountain Companies later joined CRH. By being a part of the CRH family, we are a proud reflection of the hundreds of family businesses, local and regional companies and mid to large sized enterprises that come together to form CRH.

CRH is the number one asphalt producer and paver, the largest aggregates producer and the second largest ready-mix producer in North America. We are also the number four cement producer in North America and a leader in Canada. CRH operates with a decentralized, diversified structure, letting you work in a small company environment while having

the career opportunities of a large enterprise. Job Summary Intern is responsible for working with the Quality Control department for sampling concrete product to ensure the product meets required specification and tests.

This position will provide work exposure to the following duties and responsibilities of a QC Technician. Essential Duties and Responsibilities Partners and coordinates daily/weekly scheduling with QC Manager, other Management, Plant personnel and crewmembers, as well as, Department of Transportation inspectors to obtain necessary samples and mix designs. Clear understanding of concrete procedures/production. Must be self-motivated with a desire to learn, obtain certifications

as needed. Must partner with other members of staff reporting to Quality Control Manager to ensure quality control specifications are met, as well as daily production schedules/estimates.

Knowledge to ensure ethical behavior and safety standards as required by the company and OSHA guidelines. Ability to prepare and submit proper documentation to the appropriate Quality Control personnel on a timely basis. Must understand how to evaluate test results and address problems when they arise. Attitude/Cooperation: Must always maintain a courteous and professional manner with co-workers, customers, and the general public. Ability to be flexible with last minute schedule changes, location changes, time of shift changes.

Overtime work required. Some night work may be required. Initiative to perform/assist with other positions for job completion. Ability to adhere to personal protective equipment (PPE) policy and maintain individual PPE in functional condition. Maintain a clean and safe work environment. Must be able to lift and carry 50 lbs. Must pass drug test and criminal background check. Qualifications To perform this job successfully, an individual must be willing to learn to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required.

Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties of the job. Requirements / Education / Experience Previous experience in the concrete industry preferred. High school diploma or equivalent is preferred Obtain State certifications as required. Must have valid driver’s license. Knowledge of Microsoft Office applications. Ability to work independently and with group What CRH Offers You Highly competitive base pay Comprehensive medical, dental and disability benefits programs Group retirement savings program Health and wellness programs A culture that values opportunity for growth, development, and internal promotion About CRH CRH has a long and proud heritage.

We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of large international organization. If you’re up for a rewarding challenge, we invite you to take the first step and apply today!

Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day. Thank you for your interest! What CRH Offers You Highly competitive base pay Comprehensive medical, dental and disability benefits programs Group retirement savings program Health and wellness programs A diverse and inclusive culture that values opportunity for growth, development, and internal promotion About CRH CRH has a long and proud heritage.

We are a collection of hundreds of family businesses, regional companies and large enterprises that together form the CRH family. CRH operates in a decentralized, diversified structure that allows you to work in a small company environment while having the career opportunities of large international organization. If you’re up for a rewarding challenge, we invite you to take the first step and apply today! Once you click apply now, you will be brought to our official employment application. Please complete your online profile and it will be sent to the hiring manager. Our system allows you to view and track your status 24 hours a day.

Thank you for your interest! Mountain Enterprises, Inc. a CRH Company, is an Affirmative Action and Equal Opportunity Employer. EOE/Vet/Disability--If you want to know more, please click on this link.

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.

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.

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? Own all aspects of supplier & sourcing relationships production and service only parts suppliers, which impact the Cost of Quality (COQ) to GEA and the Parts Distribution Microenterprise (ME). Measure, prevent, react, and enforce processes, policies, and procedures with the suppliers and their assigned SQEs, providing near real time data around supplier receiving defects

and the corresponding corrective actions. Provide clear data and direction for all service parts suppliers relative to quality and processing aspects of their delivery, using data and metrics to track and improve top problematic suppliers.

From the customer facing side of the operation, you are responsible for improving the customer experience by ensuring timely and accurate resolution of field quality issues, packaging issues, NPI and product line Service Execution Leader (SEL) escalated issues. Engage with and support the 3PL teams at multiple sites. Position Senior Supplier Quality Engineer Location USA, Louisville, KY How You'll Create Possibilities Essential Duties & Responsibilities:

Responsible for all commodities, product lines, and suppliers for JEF and RVR service parts warehouses Protect running production by identifying good vs.

bad and driving immediate containment of nonconforming or suspect material Reduce recurrences by auditing incoming shipments and use of the SCAR system. Engage in and manage projects to drive improvement within the supplier's processes Decrease supplier's PPM Track supplier's processes to reduce control plan violations Implement standardized project management for sort/rework with Stratosphere Quality at warehouses Work with SQE, Technology, and Buyers to help contain obsolete product when superseded Measure parts and compare to drawings to determine specifications and whether the parts meet the spec Pull CAD files for scan lab measurements and empis specs for AP35 lab testing Create billback communications to retrieve money lost due to supplier issues Standardize quality process flow to maintain systematic organization and separate quality issues caused by the supplier vs quality issues caused by the warehouse Improve response timing and resolution of reported incidents quickly and efficiently Work with suppliers and materials to improve pack plans and supplier shipping processes to reduce receiving discrepancies Establish quality nonconformance area at RVR and train quality personnel to help increase their knowledge of basic quality Respond to customer service inquiries and resolve issues quickly to avoid concessions What You'll Bring to Our Team Minimum Qualifications: Engineering or Technical degree (Physics, Chemistry, Mathematics) or equivalent technical experience Five (5) years of Supply Chain, Quality, and/or Technical experience in a manufacturing environment Strong background in applying statistical tools for process and product development and control (i.

e. Gage R&R, Process Capability, Control Plans, SPC, Process Failure Mode Effects Analysis (PFMEA), and Design of Experiments (DOEs)).

Skilled and experienced with reading and understanding prints, dimensions, and tolerances. Basic understanding of GD&T. Experienced with problem-solving tools and techniques (i. e. 8-D, 5 Whys, 7 Ways, DOE, e CAR, Fishbone, Pareto, Six Sigma, First Piece, PPAP). Ability and willingness to travel domestically and internationally Excellent communication skills, both verbal and written Demonstrated leadership to influence and drive change within a highly matrixed organization.

Preferred Qualifications: Master's Degree Experience with assigned commodity manufacturing processes Demonstrated ability to independently develop, manage and implement aggressive project plans both globally and domestically Demonstrated ability to simplify complex information and prepare concise executive summaries Prior international work experience & multi-lingual (Chinese, Spanish, etc. ) Demonstrated ability to simplify complex information and prepare concise executive summaries Demonstrated ability to independently develop, manage and implement aggressive project plans both globally and domestically Working Conditions: Primary work location will be the Jeffersonville, IN parts warehouse.

Ability and willingness to travel domestically and internationally (20%) 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-9ac9b3f1-f7ca-4d53-9e0b-edba7949c228