Location: Jackson, GA
Company: Axiom Engineered Systems Of Georgia
for making sure that engineering and manufacturing processes are performed correctly using the right tools, materials and processes. An important part of the job involves designing the company's quality standards and testing processes against those criteria.
You will be also responsible for coordinating and administering the company quality program in relationship with designated customers. It is required to work with all departments to develop and maintain effective systems to achieve quality objectives, in addition to identifying continuous improvement opportunities. What you can expect as our next Quality Engineer: Design, implement, and maintain testing & reliable quality systems
within the manufacturing guidelines Contribute to the launch and transfer of new products to production through APQP process and prepares Production Part Approvals (PPAPs) on new and existing products Develop, update, and maintain control plans, PFMEAs, process flow diagrams and other quality/manufacturing documentation Supervise Quality Control Inspectors, including making decisions on quality problems found during production, allocating work, reviewing performance, and maintaining records created by the Q.
C. Inspectors Address internal and external quality issues, including containment & disposition of suspect and nonconforming products and communicates these issues to the customer
and internal functions Conduct root cause analysis and implements corrective & preventive actions for nonconforming products and processes (8D) Verify the effectiveness of corrective & preventive actions Communicate directly with customers on APQP, PPAP, and quality issues Conduct process capability and performance studies Develop gauge/fixture requirements and assists in gauge/fixture design, calibration and maintenance Assist in preparing, implementing, and reviewing quality policies and procedures Evaluate parts and processes for continuous improvement of production operations Perform dimensional layouts as required Ensure compliance to IATF 16949 systems and procedures Perform other quality related activities as required Do you have what is takes to be our next Quality Engineer?
Minimum 3 years of experience working as a Quality Engineer or equivalent in the automotive industry, preferably in Plastic Injection Molding and/or assembly process University degree within the engineering field and/or related experience Ability to speak proficiently in Korean is an asset ASQ CQE Certification is preferred Experience in launching new programs for various OEMs (FCA, Tesla, VW) Good understanding of IATF 16949:2016 and Quality Management System Hands-on experience in AIAG Core Tools (APQP, FMEA, MSA, SPC, PPAP) along with continuous improvement (customer support) and systemic/product quality Strong knowledge of Geometric Dimensioning and Tolerancing (GD&T) Knowledge of use, calibration, and measurement analysis of various inspection and testing instruments Strong knowledge of statistical process control and statistical methods Strong written and oral communication skills Tech savvy & Strong computer skills Able to work flexible hours and overtime Able to travel to customer/supplier destinations within North America with short notice Perks?
To name a few, we offer a cool air-conditioned plant, a very clean facility, an amazing work environment/culture, ability to participate in multiple fun-filled company events and so much more! Don't forget to ask us about our competitive total compensation package! We, at Axiom are an equal opportunity employer. We are always looking for talented individuals who are motivated to meet and exceed their goals. We are proud of what we've been able to accomplish, and searching for new and talented additions to our team has always remained a priority. Axiom is committed to providing reasonable accommodation for people with disabilities.
If you require an accommodation, we will work with you to meet your needs in all stages of the hiring process. Axiom 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.
to create a vertically integrated business that is uniquely positioned to address the world’s evolving vision needs and the global demand of a growing eyewear industry. With over 180,000 dedicated employees in 150 countries driving our iconic brands, our people are creative, entrepreneurial and celebrated for their unique perspectives and individuality.
Committed to vision, we enable people to “see more and be more” thanks to our innovative designs and lens technologies, exceptional quality and cutting-edge processing methods. Every day we impact the lives of millions by changing the way people see the world. Our unique business model and relentless pursuit of operational excellence ensures
that consumers everywhere have access to products. Balancing speed, efficiency and proximity, the Company manages a global supply chain with cutting-edge technology, based on centralization for frames and on a capillary network for lens finishing and prescription laboratories.
Greasing the wheels behind the scenes, our people in Operations are the backbone of our Company. GENERAL FUNCTION The Quality Assurance Supervisor is responsible for planning, organizing, leading, and controlling the Quality System function within the Manufacturing Operations facility. The Supervisor is accountable for the supervision and development of assigned QS associates. MAJOR DUTIES & RESPONSIBILITIES Sets
work schedules, provides training and coaching, conducts performance evaluations and sets departmental goals and expectations in accordance with the goals of the facility.
Leads in the identification of quality, process, workflow and personnel concerns and works to resolve these quickly according to company policy, practice, and guidelines. Facilitates team workflow management, workforce scheduling, and team member placement to ensure the department, facility, and organizational goals are met or exceeded. Utilizing the Quality Managements System and ISO9001 standards - conducts, leads and implements the appropriate process audits; the audits will identify the need for the appropriate containment, corrective, and preventive actions, which minimize or eliminate process deviations and non-conforming product results.
Facilitates data collection, summary and analysis to support problem solving activities that will lead to root cause problem solving, team building strategies, process control methods, and continuous improvement actions in order to meet or exceed the facility key internal and external operating metrics. Leads personnel and activities associated with Inbound Inspection to ensure timely and accurate receipt, review, and disposition of identified purchased products.
Interviews, hires and plans appropriate training for new team members Interacts with associates to establish rapport with team members, takes an interest in the individual and their work and obtains knowledge of workplace issues. Supervise team members’ performance and discipline issues in a timely manner. Evaluates performance expectation plans (30/60/90 days, mid-year, and year-end) with team lead and team members to meet individual goals and facility objectives. Communicates business needs, schedule changes, process problems, success stories, etc. Maintains adherence to company policies, safety standards and good housekeeping practices.
Assumes additional responsibilities and performs special projects as needed or directed. BASIC QUALIFICATIONS Bachelor’s degree 2+ years supervisory or management experience 5+ years’ experience in Quality Control Proficiency in MS Office Knowledge and understanding of Statistical Process Control including trend analysis Knowledge and understanding of Lean Manufacturing principles and concepts ISO9001 Lead Auditor Certified Advanced problem solving skills Good knowledge of optical theory and hands-on application Good technical knowledge of lab process Excellent Supervisory and leadership skills Excellent verbal and written communication skills Competent in PC skills and the use of statistical information Ability to work with peers and upper level management PREFERRED QUALIFICATIONS Six Sigma Green Belt or Black Belt Certified Quality Engineer Optical Training/Certification 3+ years optical manufacturing lab experience
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
