Location: Duluth, GA
Company: S & Me
on our communities. Our people are the heartbeat of our company, which is a place where you control your future, and the possibilities are far-reaching. As individuals we are great, and together we are even better so come help us make a difference as we are currently seeking a full-time Asphalt Laboratory Supervisor/QA Manager to join our Construction Services team in Duluth, Georgia.
This individual will be responsible for the following. Typical assignments and responsibilities for this position include (but are not limited to): Laboratory testing of construction related materials with an emphasis in asphalt, aggregate, and rock; Review of project specific plans and specifications in
preparation of laboratory testing; Performance of laboratory testing for compliance with ASTM, AASHTO, GDT, and/or project specifications; Assist in pricing of testing for proposals and establishing agreements/contracts with clients; Maintain relationships/frequent communication with existing clients and prospecting for new clients.
Contacts will be made via phone, email, in-person visits and attendance of trade associations; Ability to work safely and effectively around ovens, drop hammers, and other lab equipment required to perform laboratory testing; Maintain an organized and safe laboratory space; Communication of laboratory testing results with Project Management staff, contractors,
and clients; Calibration of laboratory equipment to industry codes and standards.
Qualifications: High school diploma or GED, required; Experience with asphalt testing and mix designs, required; Experience with ASTM, AASHTO, and GDOT standards, required; Effective communication skills (speaking, reading, and writing), using the English language, required; Math skills and experience with Microsoft Word and Excel, required; Ability to routinely lift 40 to 50 lbs. (field/laboratory samples and equipment), required; An understanding of professionalism and tact, relative to interaction with co-workers, clients and other industry professionals; One or More Active Certification(s) Required: Georgia Department of Transportation (GDOT) QCT Level I and/or II Superpave Mix Design American Concrete Institute (ACI) Field Testing Grade I; Laboratory Technician; Aggregate Testing.
Why work at S&ME? We are an industry leading, 1,100 employee-owned engineering firm, which means the hard work and dedication you provide every day directly contributes to the health and performance of a company you partly own. With employee ownership at our foundation, we are all vested in the success of each other and S&ME as a whole. We know that creating an environment where employees can grow and flourish, both professionally and personally, leads to our collective drive for success.
We offer professional development, leadership and employee engagement programs and tasks forces to exemplify our purpose of " helping you prosper" and our commitment to culture. Learn more about us in this video: We Are S&ME and our website: / S&ME Benefits to Help You Thrive: Competitive Compensation Medical/ Dental/ Vision Plans Health Savings Account with company contributions Flexible Spending Account 401 (K) with Matching Employee Stock Ownership Program (ESOP) PTO / Holidays with the ability to carryover Credential Incentive Program and Tuition Reimbursement Company vehicle with gas card (if applicable) This is a full-time position with competitive pay based on experience.
Successful candidate must meet requirements of the company's Fleet Management Program, Substance Policy and Reference check program. Submit resume, cover letter, and salary expectations for consideration. Only qualified candidates with acceptable employment eligibility verification (I-9) will be considered. Visa assistance not provided. S&ME reserves the right to fill this position with an internal or external candidate at any time during the search.
S&ME is not responsible for unauthorized job postings or submissions of resumes using external links/websites. No candidate/recruiter calls, personal calls or walk-ins accepted. EOE including disability/vets VEVRAA Federal Contractor Job Posted by Applicant Pro
by giving back in the communities around the world where we live and work. Nordson Adhesive Dispensing Systems (ADS) sets the global standard in hot melt machines and dispensing, coating, and laminating systems. Manufacturers rely on our equipment for packaging, product assembly and surface treatment applications.
With a leading services and support network, we help our customers worldwide increase manufacturing efficiencies and produce the highest quality products. JOB SUMMARYThe Supplier Quality Engineer is responsible for driving exceptional supplier performance thus creating a world-class supply base that exceeds expectations for the business group and the global Supply Chain team.
Specific focus will be supplier analysis, development activities, technical support, part qualifications, improvement activities, corrective actions, and new product introductions to ensure component parts and assemblies are consistently manufactured in total compliance to specified requirements.
Simultaneously and in conjunction with the Strategic Purchasing Group this position will support the balanced improvement of quality, cost, and service, all while operating within Nordson's Lean manufacturing principals. ESSENTIAL JOB DUTIES & RESPONSIBILITIES Track the supplier's performance indicators, based on their scorecards and rankings, to facilitate and develop the supply base's ability
to consistently meet or exceed our defined expectations. Improve Supplier Quality metrics Routinely provide performance communication to the supply base and internal personnel to ensure the proper use of suppliers based on performance.
Develop the supplier's ability to support Nordson's Lean manufacturing principles and problem avoidance processes through the use of best-in-class quality, delivery, and lead-time performance processes. Drive a systematic problem solving and process improvement approach utilizing Lean Six Sigma principles. Function as a technical liaison between suppliers, engineering, SCM group, business group, and manufacturing sites, to resolve supplier related issues.
Assure supplier's corrective and preventive action plans are developed and executed in compliance with Nordson expectations. Report on the status of corrective actions, as required, to manufacturing, business group and executive management. Perform supplier on-site backssments and assistance visits for supplier selection, to improve supplier performance, and achieve Nordson's balanced improvement objectives. Develop and implement (APQP) Advanced Product Quality Planning for new and existing purchase parts. Review supplier processes, collaborate with suppliers on process improvement, and value enhancement opportunities.
Support and utilize the Strategic Group's activities and direction on supplier development, risk management, reduction, and consolidation. Promote early supplier involvement at project development stages. Support and coordinate with the Business Unit's new product activities and direction to better ensure component manufacturability, more than satisfactory and sustainable quality performance for every component, particularly critical components, during the transition from new product development to production. Perform Supplier Visits & Audits.
NPD and resourcing activities: supplier selection, Create technical drawing review - 1. ) CTQ w/engineering 2. ) discuss expectations w/ supplier 3. ) review supplier capability. Create SAP inspection plans, support part qualification process, resolve QN & obtain supplier CAR Manage Mfg (Internal ZV & ZA) QNs and Customer & Field (External ZF & ZW), CAR's support Manage Supplier Development Watch List; coordinate and run monthly meetings with the suppliers on the watch list Conduct Supplier backssments/Audits Participate in a Development of new suppliers Provide support in Supplier Reduction process Provide support to global purchasing team members on supplier related issues/questions.
Act as a Quality point of contact Other duties as assigned EDUCATION & EXPERIENCE REQUIREMENTEducation: Bachelor's degree in Engineering is required, or related field Experience: 2 -5 years experience in direct supplier relationship management or industrial engineering with supplier interaction required; experience in supplier quality or manufacturing quality role. Experience in Lean Six Sigma techniques and tools strongly preferred; Six Sigma Green Belt strongly preferred PREFERRED SKILLS & ABILITIES Strong communication skills with the ability to communicate effectively at any level Fundamentally sound in all aspects of the function, including: Inspection techniques FAI PPAP Control Plans PFMEA 8D Corrective Action A balanced professional capable of seeing the big picture while managing the details Motivated by results Ability to manage supplier quality related projects and drive to completion with improvement Thrive in a team environment and work well with others as well as independently Ability to understand and communicate engineered drawings and specifications.
Detail-oriented, self-starter with strong organizational skills. Demonstrated ability to develop effective processes and drive results. Ability to work under pressure and to tight deadlines Ability to organize and priorities workloads. Ability to act on own initiative, dealing with unexpected problems that arise Problem solve and handle multiple tasks effectively Proficiency with MS Office applications: Word, Power Point, Excel WORKING CONDITIONS & PHYSICAL DEMANDSOffice environment. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed above are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. TRAVEL REQUIREDEstimated 15-30%#LI-KS1#-LI-Onsite Nordson Corporation provides equal employment opportunity to all applicants and employees. No person is to be discriminated against in any aspect of the employment relationship due to race, religion, color, interaction, age, national origin, ancestry, disability, interactionual orientation, gender identity, genetic information, citizenship status, marital status, pregnancy, veteran status or any other status protected by applicable federal, state, or local law.
All employment offers are contingent upon successful completion of our pre-employment drug screening and background/criminal check, consistent with applicable laws. Third party recruiters and agencies should not contact employees of Nordson or its subsidiaries directly. Any resumes sent to a hiring manager or submitted to Nordson employees are considered unsolicited and property of Nordson. Nordson will not pay a placement fee unless the agency or recruiter has a signed contract with Nordson's Human Resources department in advance of submitting a candidate for consideration.
Verbal and written approvals will not be considered a valid contract for service.
nurturing our nimble culture of innovation; Having an impact on the healthcare challenges we all face, and the lives of people and communities around the world.
At Avanos you will find an environment that strives to be independent and different, one that supports and inspires you to excel and to help change what medical devices can deliver, now and in the future.
The Avanos COVID-19 Vaccine Policy: This Policy applies to U. S. customer-facing / field-based employees & Avanos leadership: All U. S. customer-facing / field-based employees hires must be fully vaccinated against COVID-19. Proof of being fully vaccinated does not need to be disclosed until a job offer has been made
but must be submitted within 48 hours after the acceptance of the job offer. If you have a qualifying medical condition or sincerely held religious belief or practice that precludes you from receiving a COVID-19 vaccine, you may apply for an exemption or deferral after you accept the job offer and before your scheduled start date.
The reasonable accommodation provided to the employee, if any, will depend on the employee's job and the applicable facts, but it may include weekly COVID-19 testing and masking requirements. New hires who do not submit, before their scheduled start date, proof of being fully vaccinated or a request for a reasonable accommodation will have their job offer revoked.
Avanos is a medical device company focused on delivering clinically superior breakthrough solutions that will help patients get back to the things that matter.
We are committed to creating the next generation of innovative healthcare solutions which will address our most important healthcare needs, such as reducing the use of opioids while helping patients move from surgery to recovery. Headquartered in Alpharetta, Georgia, we develop, manufacture and market recognized brands in more than 90 countries. Avanos Medical is traded on the New York Stock Exchange under the ticker symbol AVNS. For more information, visit . The purpose of this position is to lead the Risk Management and Design Control activities related to the New Product Development as a key member of the medical device development team.
General Expectations and Accountabilities: Independently develop the Risk Management files; includes Product Hazards Analysis, Design FMEA, Use FMEA & Process FMEA for new products. Software FMEA as needed. Development of Manufacturing Control Plan Realization documentation. Provide technical leadership in solving challenging technical problems related to quality issues and technologies and consults on complex issues and projects. Position Specific Accountabilities: Quality Leadership for Medical Device New Product Development (90% of time) Facilitate and actively participate in the development of deliverables required for medical device product development ensuring adherence to the Avanos design control process.
Lead and ensure compliance to all risk management requirements. Actively participate in the development of statistical plans and rationale for design control activities/requirements. Actively partner with the project teams to facilitate the incorporation of all quality system elements, root cause analysis, corrective action and continuous improvement principles throughout the entire product redesign.
Systems Compliance and Audit Support (10% of time): Implement the Root Cause Analysis concepts to investigate issues requiring Corrective and Preventative Actions. Support notified body and internal audits. Qualifications Required: B. S. in Engineering (prefer Biomedical/Mechanical/Electrical) 5-7 years of experience in product development & design control Medical Device quality experience required, Medical Electrical preferred Statistical software experience, such as Minitab, JMP Microsoft Office suite, specifically Excel The ability to lead and influence others The ability to travel to support project needs Ability to collaborate on-site in Alpharetta HQ at least 5 days per month Avanos Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, disability status, protected veteran status, interactionual orientation, gender identity or any other characteristic protected by law.
If you are a current employee of Avanos, please apply here. Join us at Avanos Join us and you can make a difference in our products, solutions and our culture.
Most of all, you can make a difference in the lives, people, and communities around the world. Make your career count Our commitment to improving the health and wellbeing of others begins with our employees - through a comprehensive and competitive range of benefits. We provide more than just a salary - our Total Rewards package encompasses everything you receive as an employee; your pay, health care benefits, retirement plans and work/life benefits. Avanos offers a generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting.
free onsite gym benefits on day 1 HQ region voted 'best place to live' by USA Today Requisition ID: 5595 Job Title: Senior Design Quality Engineer Job Country: United States (US) Here at Avanos Medical, we passionately believe in three things: Making a difference in our products, services and offers, never ceasing to fight for groundbreaking solutions in everything we do; Making a difference in how we work and collaborate, constantly nurturing our nimble culture of innovation; Having an impact on the healthcare challenges we all face, and the lives of people and communities around the world.
At Avanos you will find an environment that strives to be independent and different, one that supports and inspires you to excel and to help change what medical devices can deliver, now and in the future. The Avanos COVID-19 Vaccine Policy: This Policy applies to U. S. customer-facing / field-based employees & Avanos leadership: All U. S. customer-facing / field-based employees hires must be fully vaccinated against COVID-19. Proof of being fully vaccinated does not need to be disclosed until a job offer has been made but must be submitted within 48 hours after the acceptance of the job offer.
If you have a qualifying medical condition or sincerely held religious belief or practice that precludes you from receiving a COVID-19 vaccine, you may apply for an exemption or deferral after you accept the job offer and before your scheduled start date. The reasonable accommodation provided to the employee, if any, will depend on the employee's job and the applicable facts, but it may include weekly COVID-19 testing and masking requirements. New hires who do not submit, before their scheduled start date, proof of being fully vaccinated or a request for a reasonable accommodation will have their job offer revoked.
Avanos is a medical device company focused on delivering clinically superior breakthrough solutions that will help patients get back to the things that matter. We are committed to creating the next generation of innovative healthcare solutions which will address our most important healthcare needs, such as reducing the use of opioids while helping patients move from surgery to recovery. Headquartered in Alpharetta, Georgia, we develop, manufacture and market recognized brands in more than 90 countries.
Avanos Medical is traded on the New York Stock Exchange under the ticker symbol AVNS. For more information, visit . The purpose of this position is to lead the Risk Management and Design Control activities related to the New Product Development as a key member of the medical device development team. General Expectations and Accountabilities: Independently develop the Risk Management files; includes Product Hazards Analysis, Design FMEA, Use FMEA & Process FMEA for new products. Software FMEA as needed. Development of Manufacturing Control Plan Realization documentation. Provide technical leadership in solving challenging technical problems related to quality issues and technologies and consults on complex issues and projects.
Position Specific Accountabilities: Quality Leadership for Medical Device New Product Development (90% of time) Facilitate and actively participate in the development of deliverables required for medical device product development ensuring adherence to the Avanos design control process. Lead and ensure compliance to all risk management requirements. Actively participate in the development of statistical plans and rationale for design control activities/requirements.
Actively partner with the project teams to facilitate the incorporation of all quality system elements, root cause analysis, corrective action and continuous improvement principles throughout the entire product redesign. Systems Compliance and Audit Support (10% of time): Implement the Root Cause Analysis concepts to investigate issues requiring Corrective and Preventative Actions. Support notified body and internal audits. Qualifications Required: B. S. in Engineering (prefer Biomedical/Mechanical/Electrical) 5-7 years of experience in product development & design control Medical Device quality experience required, Medical Electrical preferred Statistical software experience, such as Minitab, JMP Microsoft Office suite, specifically Excel The ability to lead and influence others The ability to travel to support project needs Ability to collaborate on-site in Alpharetta HQ at least 5 days per month Avanos Medical is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, interaction, national origin, disability status, protected veteran status, interactionual orientation, gender identity or any other characteristic protected by law.
If you are a current employee of Avanos, please apply here. Join us at Avanos Join us and you can make a difference in our products, solutions and our culture. Most of all, you can make a difference in the lives, people, and communities around the world. Make your career count Our commitment to improving the health and wellbeing of others begins with our employees - through a comprehensive and competitive range of benefits. We provide more than just a salary - our Total Rewards package encompasses everything you receive as an employee; your pay, health care benefits, retirement plans and work/life benefits.
Avanos offers a generous 401(k) employer match of 100% of each pretax dollar you contribute on the first 4% and 50% of the next 2% of pay contributed with immediate vesting. free onsite gym benefits on day 1 HQ region voted 'best place to live' by USA Today PDN-9addcba3-8db8-48e9-9c29-1a66c6d9518e
