created as a Battelle spin-off. Aligned with, and supported by leading life sciences-focused investors, we partner with our clients to provide preclinical CRO services from single study and through full IND enabling studies. We have a strong focus and commitment to helping accelerate the commercialization of advanced therapies such as cell and gene therapies and vaccines.
Moving forward we will combine continuous improvement and innovation to become the preferred preclinical CRO in the industry, by working in partnership with our clients, and leveraging state of the art technologies and platforms we will enable our customers to accelerate and improve the product development cycle, from
concept to commercial. When you join our team , you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians and specialists across a variety of disciplines.
Our chemists, biologists, veterinarians, data scientists, engineers, pathologists, and other experts collaborate to deliver new and exciting breakthroughs. The future for Amplify Bio is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees. Amplify Bio is seeking to hire a SR. /GLP Quality Assurance
Auditor to join our growing team! The Sr. /GLP QA Auditor Conducts audits and performs inspections to assure compliance to federal regulations, Amplify Bio standards, client specifications, internal policies, and any other applicable guidelines.
What You'll Do Here: Audits protocols, raw data, documents, records, reports, and inspects work being performed to assure compliance to regulatory requirements, standards, specifications, internal policies, and any other applicable guidelines. Performs inspections of Amplify Bio facilities and corresponding documentation to assure compliance to requirements. Issues recommended actions and backsses corrective actions based on observation(s).
Reports audit findings to project leadership and management. Advises operations regarding issues observed during inspections to mitigate risk. May review project planning documents (technical protocols, project plans, test plans, etc. ) for compliance with stated requirements. Utilizes knowledge of specific instrumentation and equipment, laboratory techniques, and current FDA industry guidance to advise on compliant operations. Interprets and applies existing and new regulatory requirements and industry standards to operations methods and practices. Develops and executes Quality Assurance Audit Plans per project.
Proven leadership with mentoring responsibilities. Demonstrates initiative and accountability, with ownership of complex projects. Demonstrates ownership of assignments with accountability and instills trust in project team. Proven risk management skills including mitigation strategies. Established internally as a regulatory subject matter expert and amongst peers as a leader in the organization. Identifies compliance gaps and actively drives process/continuous improvement efforts to minimize risk to the organization. Drives change management through use of effective strategies and own skills in order to facilitate organizational change initiatives.
We Would Love to Hear from You If: Bachelor's Degree in a related field; 10 years of experience in a quality assurance program and proven communication skills; or an equivalent combination of education and/or experience in a related field. Experience in a Gx P environment. Desired But Not Required: Experience with System Validation and Method Qualification. Experience with electronic Quality Management Systems, Laboratory Information Management Systems and 21 CFR Part 11 compliance. Experience interacting with external audits and regulatory agencies.
At Amplify Bio , we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization. Research shows that oftentimes women and minority groups only apply to open roles if they meet 100% of the listed criteria. Amplify Bio encourages everyone - including women, people of color, individuals with disabilities and those in the LGBTQIA+ community - to apply for our available positions, even if they don't necessarily check every box on the job description.
Hire for attitude and train for aptitude creates unique opportunities to build strong teams of smart, motivated individuals who love what they do. Amplify Bio is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), interactionual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law.
Amplify Bio will not tolerate discrimination or harassment based on any of these characteristics. If you have a disability or special need that requires accommodation, please let us know during the recruiting process. We are committed to the safety and wellness of our employees and customers. Therefore, COVID vaccination is required. Why You Will Love Working Here: We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work.
From a wellness program (did we mention we have an onsite gym and ping pong table? ), to financial planning and legal assistance, we make sure to take care of our own. Health, Dental, and Vision insurance that starts on your first day at Amplify Bio Competitive Compensation Package We take work-life balance seriously and we back it up with a FLEXIBLE PTO policy! Life and AD&D insurance Supplemental insurance Live Health Online Smart Shopper (helps you shop for better medical care and earn cash rewards while you save) 4 weeks paid Parental Leave Wellness Program 401(k) match Tuition Reimbursement EAP/work-life support system A fun work environment where everyone's voice matters!
We are just getting started! More benefits on the way! An Opportunity to Change the World! PI61d PDN-9ad9dcfd-13c6-44a6-83ea-b285da3690b2
judgment, discretion, and have or obtain the necessary experience and certifications required to perform their duties. ESSENTIAL DUTIES: 1. ) Responsible for performing all quality control tests required by specifications, including density, and gradations.2.
) Take samples of incoming aggregates and monitor the storage of the aggregates in the stockpiles.3. ) Be prepared to assist in adjusting plant feed systems to produce a blended aggregate gradation that is in compliance with specifications.4. ) Assist in preparing mix designs and job mix formulas.5. ) Prepare a checklist to ensure that the required mix designs are approved and are being properly dispatched according to the contract
or customer request.6. ) Perform those tests necessary to evaluate, adjust and otherwise control the quality of the mix.7. ) Make recommendations to production personnel of corrective actions necessary to ensure a quality product is being produced.8.
) Work together with customers and/or Department of Transportation personnel to solve problems that may occur in testing or with mix that is out of the specification limits.9. ) Maintain good relations with general public, engineers, architects, inspectors and customers to facilitate job progress and to promote a positive company image.10. ) Perform necessary work while complying with all company policies and procedures.11. ) Perform additional
duties as required, or as directed by the supervisor. MINIMUM REQUIREMENTS: Education: Must be a minimum of 21 years old.
Work Experience: Experience in asphalt testing preferred but not required. Other: Valid Driver's License Required. Work may require night or weekend work. Some overnight travel maybe required. Must have a good MVR. NCDOT QMS Level I or II Plant Technician Certification preferred but not required. Heavy Physical Demands : Heavy physical effort required including pulling and lifting or moving heavy weight material with frequent lifting or moving materials or equipment (over 80 pounds). If a position specific Physical Demands sheet is attached, it will describe in more detail the physical demands that are required.
Physical Activity: Position requires the ability to continuously work around any or all of the following: noise, dust, heat, cold, oil and heavy equipment. Personal protective equipment is normally required of the position. Position requires ability to exchange ideas quickly and clearly and the ability to receive and evaluate detailed information and instructions. The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required of the position.
All employees may have other duties assigned at any time. EOE. Minorities/Women/Protected Veterans/Individuals with Disabilities.
and helps establish root cause. Strives to reduce scrap & rework, and eliminate customer returns, by developing and supporting in-house processes. Communicates with customers, as well as vendors, regarding quality issues before, during and after parts are produced and shipped.
Management Representative for ISO 9001 conformance, internal auditing and oversees annual audit. quality, QA, QC, ISO, production, inspection, inspector
the web, process them, and fulfill them at any manufacturing facility within the company. Shutterfly IT Operations is responsible for supporting any Manufacturing floor equipment that produces customer orders; including testing out software changes planned for the equipment.
Shutterfly IT Operations is looking for a stellar Software Quality Assurance Engineer to join the team in Plano, TX. As a Software Quality Assurance Engineer, you will be a key player across development, scrum and product teams - which have complete ownership from inception to end-of-life, for various application suites. What You'll Do Here: Perform on-site software testing in the Plano, TX manufacturing facility
Establish and implement QA/QE standards and best practices Assist Technology Manager with Technical Requirements Definition process Assist Technology Manager with creating a QA testing process Work with development/scrum/product teams to ensure quality code and deliverables Assist with UAT, production support, and production releases Assist development team with performance and scalability analysis and load testing Provide defect analysis and reporting Provide documentation of test plans, which can be used across multiple product categories Responsible for monitoring the test coverage and reporting per software release Develop, debug, and maintain test cases, test plans, test scripts and automation
frameworks (as needed) for our web applications The Skills You'll Bring: 3+ years overall Quality Assurance experience 3+ years of experience writing test cases Experience with Cloud platforms such as AWS Ability to adhere to timelines and execute in a fast-paced environment Experience working with remote software development/scrum/product teams It is helpful, but not required to have: Experience with Agile and Waterfall methodologies Experience with JIRA, GIT and Bitbucket or similar tools Experience with Test Rail, REST-assured, Maven, Sure Fire or similar technologies Supporting a diverse and inclusive workforce is important to Shutterfly not only because it directly reflects our value of Embracing our Differences, but also because it's the right thing to do for our business and for our people.
Learn more about our commitment to Diversity, Equity and Inclusion at Shutterfly DE&I. #SFLYTechnology PDN-9ad9c568-11b9-43fc-8730-8784bfcc014c
We work hard day in and day out to make the highest quality products so our customers are getting exactly what they need to stay healthy and keep doing what they love. We are currently looking for a Quality Assurance Inspector to join our Team! Job Summary: This position is responsible for assisting the Quality Team Leader.
This person will be working closely with other departments to maintain Quality and GMP policies, including product investigations, internal audits, maintaining the QA database, and working with customers on product specifications. This position will also aid in QC Inspection needs as required to assure manufacturing results meet all required specifications. Pay Range:
$18.75/hr. - $22.00/hr. - Depending on Experience Benefits: Medical, Dental & Vision Life AD&D & LTD 401k match 100 hours PTO Monthly Luncheons provided Monthly Events such as Nacho Day, Ice Cream Sundae Bar Special Events such as Hot Ones, 3 on 3 Basketball Games, Pickle Ball, Etc.
Plus, many more fun activities! Hours: Monday-Thursday 4pm-2:30am Primary Responsibilities: In-process QA checks for Manufacturing. Standard Operating Procedures. Maintenance of the Master Manufacturing Batch Record. Plant-wide compliance for CGMP's. Internal Monthly QA GMP walk through audits. Surprise internal audits. Sample collection for all raw material/in process/finished goods. Manage appropriate samples
for products. Manage batch record history/archives for audits.
Training as needed/annually. Responsible for QA holds, rejects, and returns. Internal investigations if product is non-compliant. All micro testing. All QA analysis by third party labs. Other duties as assigned. Knowledge and Skill Requirements: Demonstrates organizational skills. Good skills in working with people and as part of a team. Capable of partnering and working with other departments. Basic Math skills of addition, subtraction, multiplication, division. Ability to understand, remember, and apply oral and/or written instructions or other information in English. Ability to lift, push, and pull 25 pounds unassisted.
Education and Experience: High School Diploma required. 1 year of experience in a Quality Assurance capacity in a related industry required. Working Conditions: Working conditions are normal for an office environment. Work may require flexible hours with occasional evening and weekend work.
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 meet the compliance of ISO 9001 business needs. - Ensure activities and processes comply with ISO 9001 QMS standards, company QA standards and applicable contractual standards. - Perform analysis and identify trends in the review of performance standards, work instructions, and policies and procedures; and recommend Opportunities for Improvement and Corrective and Preventative Action plans when necessary.
- Ensure that established performance standards, sampling and statistical process control procedures are followed. - Train staff for the purpose of achieving and maintaining Quality Assurance goals. - Coordinate and perform ISO based internal audits. - Develop and maintain reports
based on audit findings. - Develop and implement corrective and preventive action plans based on audit findings. - Develop other routine and ad-hoc reports when necessary.
- Develop updates and maintain quality manuals, and policies and procedures manuals. Minimum Requirements: - Bachelor's degree with 3+ years of experience. - May have additional training or education in area of specialization. - Develop solutions to a variety of problems of moderate scope & complexity. - General application of concepts & principles. - Contribute to the completion of organizational projects & goals. - Frequent use and general knowledge of industry practices, techniques, and standards. - Apply knowledge
and skills to complete a wide range of tasks. - Communicate on complex or sensitive issues or drafts such responses for supervisor or manager.
Education and Experience Requirements Must have a call center customer service experience. Strong analytical and statistical skills Active listening, attention to detail and strong verbal/written communication skills. Proficient in MS Office: Word, Excel, Power Point and typing proficiency. Ability to be a self-starter and work independently with minimal supervision. #Quality Assurance Analyst Jobs #Quality Assurance Jobs #QAJobs #Quality Analyst Jobs #QAVacancy #Job For QA #Job Of QA #Job Of Quality Assurance #Job Quality Analyst #QAQuality Assurance Jobs #QAJobs #Quality And Assurance Jobs #Quality Assurance Associate Jobs #Quality Assurer Jobs #Quality Analyst Testing #Remote QAJobs #Remote Quality Assurance Jobs #Remote QAPositions #Remote Quality Assurance Analyst Jobs #QAAnalyst #Quality Control Jobs #Quality Assurance Analyst #Quality Inspector #Quality Assurance Tester Jobs #Quality Control Positions #Job Of Quality Control #Job Vacancy Quality Control #QAQuality Analyst #max Priority MAXIMUS Introduction Since 1975, Maximus has operated under its founding mission of Helping Government Serve the People, enabling citizens around the globe to successfully engage with their governments at all levels and across a variety of health and human services programs.
Maximus delivers innovative business process management and technology solutions that contribute to improved outcomes for citizens and higher levels of productivity, accuracy, accountability and efficiency of government-sponsored programs. With more than 30,000 employees worldwide, Maximus is a proud partner to government agencies in the United States, Australia, Canada, Saudi Arabia, Singapore and the United Kingdom. For more information, visit.
EEO Statement EEO Statement: Active military service members, their spouses, and veteran candidates often embody the core competencies Maximus deems essential, and bring a resiliency and dependability that greatly enhances our workforce. We recognize your unique skills and experiences, and want to provide you with a career path that allows you to continue making a difference for our country. We're proud of our connections to organizations dedicated to serving veterans and their families. If you are transitioning from military to civilian life, have prior service, are a retired veteran or a member of the National Guard or Reserves, or a spouse of an active military service member, we have challenging and rewarding career opportunities available for you.
A committed and diverse workforce is our most important resource. Maximus is an Affirmative Action/Equal Opportunity Employer. Maximus provides equal employment opportunities to all qualified applicants without regard to race, color, religion, interaction, interactionual orientation, gender identity, national origin, protected veteran status or disabled status. Pay Transparency Maximus compensation is based on various factors including but not limited to job location, a candidate's education, training, experience, expected quality and quantity of work, required travel (if any), external market and internal value analysis including seniority and merit systems, as well as internal pay alignment.
Annual salary is just one component of Maximus's total compensation package. Other rewards may include short- and long-term incentives as well as program-specific awards. Additionally, Maximus provides a variety of benefits to employees, including health insurance coverage, life and disability insurance, a retirement savings plan, paid holidays and paid time off.
Compensation ranges may differ based on contract value but will be commensurate with job duties and relevant work experience. An applicant's salary history will not be used in determining compensation. Maximus will comply with regulatory minimum wage rates and exempt salary thresholds in all instances. Posted Max USD $45,000.00/Yr. Posted Min USD $42,400.00/Yr.
and safety standards. Implement employment policies and procedures. Implement and manage training programs to enhance the skills of the shop floor operators. Be involved in planning, budgeting, and problem solving to ensure production and quality goals are met.
Required Skills/Abilities Leadership - Dependability - Attention to Detail - Goal Oriented Excellent interpersonal and communication skills. Spanish speaking is a plus. Strong reasoning and decision-making ability. 5+ years' experience in manufacturing or production 2+ years in supervisory role Associate degree or higher-level education Experience with ISO9001/ AS9100 QMS systems Working knowledge of OSHA regulations Physical Requirements:
Must be able to lift up to 50 pounds at times. Ability to move around the production area. Benefits: Medical, Dental, and Vision Insurance. 401(k) Plan.
Paid Time Off - 3 weeks first year accrued monthly. Paid Holidays. Company Paid Life Insurance. Company Paid Short-Term Disability. Company Paid Long-Term Disability. Professional Development. About Us: Surface Prep founded in 1956 is the largest national network of regional distributors of high-quality abrasive blasting media, specialty ceramics, and abrasive finishing equipment. We have 50 facilities across the U. S. A, Canada, and the U. K. all of which are focused on improving product quality, consistency, productivity, and profitability
for our customers. These facilities and job shops are run by skilled experts who work closely with local manufacturers to develop the best possible solution for every process.
We offer a complete selection of abrasive blast media, ranging from various types of aluminum oxide to steel shot and grit. We also provide parts, accessories, and tools to meet customer needs.
controls, tests, and verifications. Must be able to work independently and with a team and knows how to create or improve systems that meet our quality assurance goals. Duties and Tasks: Reviews design plans, process procedures, test procedures, and quality manuals to understand the scope, requirements, and function of products.
Ensures products meet the organization's and customers' quality and product integrity requirements. Participates in the development and maintenance of the company Quality Plan/ISO 9001 Certification. Collaborate with departments and teams to identify and implement process improvements. Supports product development and operations team by providing analysis and
expertise throughout the inspection and QA process. Identifies root causes of problems in the production process; recommends and/or implements corrective measures. Analyzes data to identify trends in product quality or defects with the goal of mitigating and preventing recurrence and future defects.
Provides timely recommendations to management and others based on analysis and facts. May inspect raw materials, metals, components, mechanical systems and/or incoming and outgoing final products. Track and review corrective and preventative actions. Create and maintain Maintenance and Calibration Policies, Procedures and Schedules companywide. Performs other duties as assigned. Required Skills:
Excellent verbal and written communication skills. Excellent organizational skills and attention to detail.
Extensive knowledge of or the ability to quickly learn the organization's production processes. Excellent interpersonal skills with ability to serve as a liaison with developers, project managers, and customer support. Strong analytical and problem-solving skills. Proficient with Microsoft Office Suite or related software. Must be transparent, provide detailed frequent updates to management and be accountable. Well organized Physical Requirements: Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 25 pounds at times.
Education/Experience: Bachelor's degree in Engineering or related discipline required. Three years of related experience required. Join an exceptional and energized team that shares a common belief in the value of creativity, operating with integrity, and leading through innovation. Parabit Systems is focused on growth and growing leaders. Parabit Systems is an equal opportunity employer, offering a great work environment, and challenging career opportunities. Please email your resume to xyz X@ , or fax resume to 516-253-xyz X.
direction to Quality team(s) to ensure quality and compliance for the applicable products and processes for assigned department(s). Develop strategy, translate into functional plans and guide execution of long-term goals. This position follows a hybrid model of work (Tues/Thurs in office).
Based out of Northfield, IL corporate campus. MAJOR RESPONSIBILITIES Direct the development of product specifications for Medline branded products; such as the testing requirements, procedures and methods for testing, inspecting or qualifying new products and suppliers. Partner with Supplier Audit department and Division to determine optimal Supplier relationship. Develop and implement strategy for
the Quality department(s) based upon Quarterly Management Review. Prepare and deliver Customer presentations. Act as liaison with Senior Leadership of Divisions, Suppliers, Manufacturing, and/or Operations to ensure quality products, on time delivery, and customer satisfaction.
Collaborate with Suppliers, manufacturing partners and product managers in developing and implementing QA programs. Oversee QSR for assigned department(s) and ensure compliance as measured by FDA/ISO/internal audits. Management responsibilities include: --Typically, manages through multiple Managers. Provides leadership and management to one or more major departments of an operating unit or to a department that
has system-wide accountability. --Strategic, tactical and operational planning (12 + months) for the function or department; --Direct budgetary responsibility for one or more departments, functions or major projects/programs; --Interpret and execute policies for departments/projects and develops; --Recommend and implement new policies or modifications to existing policies; --Hiring staff, recommending pay increases, performing performance reviews, training and development of staff, estimating personnel needs, assigning work, meeting completion dates, interpreting and ensuring consistent application of organizational policies.
MINIMUM JOB REQUIREMENTS Education Typically requires a Bachelor's degree in Engineering, Science, or Technical Field.
Work Experience At least 7 years of experience related to the design/operation of medical device or drug combination product platforms, design controls, risk management, including working in compliance with QSR/GMP/ISO requirements or other regulated industries (21CFR 820, ISO 13485, ISO 14971, MDSAP, and MDR). At least 4 years of management experience. Knowledge / Skills / Abilities Depth of technical knowledge of relevant standards and regulations (21CFR 820, ISO 13485, ISO 14971, MDSAP, and MDR etc. )Proficiency in analyzing and reporting data in order to identify issues, trends, or exceptions to drive improvement of results and find solutions.
Demonstrated ability to control and coordinate concurrent projects, competing priorities and critical deadlines. Advanced level skill in Microsoft Excel (for example: using AVERAGE function, merging and centering cells, printing centered page and/or creating a pivot table). Position requires travel up to 30% of the time for business purposes (within state, out of state and/or internationally). PREFERRED JOB REQUIREMENTS Work Experience At least 6 years of managerial experience preferred.
At least 8 years of related experience in Medical Device, medical, Food, Cosmetic, or Personal Products industries preferred.
Quality Engineer position for you. The Associate Advanced Quality Engineer is responsible for the overall customer quality requirements for new products through the design and development stage of the project, leading all the relative quality-based activities from corporate level and support of continuous improvement of existing product at Con Met.
The Associate AQE will work within cross functional teams to drive upstream quality metrics to develop products and manufacturing processes. This role requires working in an office environment (not hybrid or remote) at Con Met's corporate headquarters in Vancouver, Washington. Non-local candidates must be open to relocation (relocation assistance
available. Key Duties Responsible for achieving our customer’s quality requirements. Support quality engineering requirements within APQP process and lead customer APQP activity.
Facilitate prototype and pre-production dimensional layouts. Lead cross functional meetings to review all quality documents and status updates. Report items with highest risk to management, develop plan to reduce/eliminate risks whenever possible. Lead problem solving activities. Qualifications Bachelor’s degree in a technical field required. Will consider an associate degree or technical certification with 4 years’ experience in lieu of a bachelor’s degree. One to Two (1-2) years’ experience in plastics
injection molding preferred and commercial vehicle knowledge or commercial vehicle component knowledge desired.
Greenbelt or Blackbelt Six Sigma training preferred. About Con Met Con Met, a division of Amsted Industries, is a leading global supplier of wheel hubs, aluminum castings, and structural plastics to original equipment manufacturers and aftermarket channels in the commercial vehicle industry. Founded in 1964, Con Met innovation has been critical in designing, engineering, and manufacturing revolutionary technologies for trucks and trailers. Today, Con Met products are standard equipment on most heavy-duty vehicles in North America and have a growing footprint worldwide.
Con Met is committed to creating products and services that align with critical customer needs. The development of more efficient products, processes, and technology that transform the way customers run and maintain their vehicles is central to Con Met’s vision. Diversity & Inclusion Pledge At Con Met, differences are not ignored, but celebrated. Our goal is to encourage a deeper knowing of our people, pulling out knowledge and experiences to ignite creativity. We are committed to achieving workplace equity by intentionally creating a work environment where all people are respected, accepted and have a sense of belonging.
Because people are what drive our success, Con Met’s Diversity and Inclusion program empowers all employees to embrace their individuality and share their abilities to further our innovations, thus improving the lives of our employees and customers, and strengthening our position as a leader in our market. Compensation & Benefits New hires generally start between $62,549 - $89,356. The full salary range for the position, across all geographies is, $62,549 - $107,277 per year. The upper portion of the salary range is typically reserved for existing employees who demonstrate strong performance over time.
Starting salary will vary by location, qualifications, and prior experience. Targeted annual bonus is based on company performance to objectives during the fiscal plan year which runs from October 1 – September 30. Comprehensive employee benefits package, including medical/dental/vision coverage, life and disability protection. Vacation plan – Con Met offers exempt employees a paid vacation benefit that provides the flexibility to take time off from work based on factors including good discretion, sound performance, and consideration of overall team and business needs.
Paid sick leave up to 10 days (80 hours) per calendar year Con Met offers an extremely strong retirement package: + ESOP - Participation (100% company paid) in the Con Met/Amsted Employee Stock Ownership Program (ESOP). The Company contributes 10% of considered compensation into this plan each fiscal year. + 401k - The Company provides a 401(k) Plan with a 4% employer contribution match. Ten paid holidays per year. Con Met provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, interaction, national origin, disability status, genetics, protected veteran status, interactionual orientation, gender identity or expression or any other characteristics protected by federal, state, or local laws (“Protected Characteristics”).
Ensuring fair wages is an important Company value. Accordingly, the Company will not pay wages to any employee at a rate less than the Company pays to other employees for work that is substantially equivalent and requires comparable skills unless a bona fide factor justifies a pay differential.
The Company prohibits pay disparity based on Protected Characteristics or prior salary history. The Company prohibits retaliation against employees for discussing compensation.
preferred partner. The Facility Quality Manager (FQM) provides oversight at the facility for incoming raw materials, intermediates, and finished products manufactured in operations and finished goods in packaging and warehousing. Quality oversight includes assisting with development and commercialization trials, and ensuring acceptance criteria are met, managing, measuring, and monitoring quality metrics for daily operations per the facility Quality Control Plan and meeting or exceeding our customers' expectations.
This position assures that site operations meet regulatory and compliance requirements for Safe Quality Food (SQF), Good Manufacturing Practices (GMP) and internal processes
(procedures and policies). Our Team The individual will report into the Mill Manager (VP - Manufacturing) and guide a small team of quality and lab professionals at the site.
This role leads quality efforts across this fully integrated production operation and its over 400 total associates. What You Will Do Foster a culture of transformation and continuous improvement, building a quality culture and capability in the organization. Drive sustainable quality processes and systems through application of management systems and a cadence of verification through self and with operations leaders. Provide leadership and coaching to employees through a shared Quality vision for the operation.
Apply Operational Excellence Strategy and Principled Based Management® (PBM®) Principles for managing continuous improvement of Quality Systems and Processes.
Work with Operations and corporate capabilities to better align the Voice of the Customer (VOC) with the Voice of the Process (VOP). Be a Champion for Product Safety and Quality certification programs. Oversee and implement Production and Commercialization trials within the facility, ensure acceptance criteria is established and approved. Conduct quality reviews with product systems and track performance against key action plans. Build collaborative relationships with strategic customers. Lead and facilitate the root cause and corrective action process, with a mindset of eliminating future defects, and providing timely resolution to customer inquiries.
Assure supplier quality is meeting our needs to produce quality products. Use statistical methods to track, monitor, and report quality performance in a way that informs leadership of the critical few opportunities to work on, with recommended actions. Collaborate with other GP quality leaders to leverage knowledge and build a transformational quality system that achieves our vision. Who You Are (Basic Qualifications) Experience driving measurable improvement in product and/or process quality in a manufacturing environment Experience leading a team.
Knowledge and use of statistical tools for data analysis to monitor quality performance. Experience with executing quality processes including change management, CAPA/RCA, and continuous improvement. What Will Put You Ahead Bachelor of Science Degree in Engineering or Technical Discipline Paper manufacturing or related industry experience Six Sigma, Lean Manufacturing, or similar experience or certification Demonstrated capability to lead sustainable change. HACCP Experience Quality certifications from a recognized industry organization Demonstrated experience with Global Food Safety Initiative (GFSI), SQF preferred certifications and proven track record for related program management and implementation.
At Koch companies, we are entrepreneurs. This means we openly challenge the status quo, find new ways to create value and get rewarded for our individual contributions. Any compensation range provided for a role is an estimate determined by available market data. The actual amount may be higher or lower than the range provided considering each candidate's knowledge, skills, abilities, and geographic location.
If you have questions, please speak to your recruiter about the flexibility and detail of our compensation philosophy. Hiring Philosophy All Koch companies value diversity of thought, perspectives, aptitudes, experiences, and backgrounds. We are Military Ready and Second Chance employers. Learn more about our hiring philosophy here. Who We Are As a Koch company and a leading manufacturer of bath tissue, paper towels, paper-based packaging, cellulose, specialty fibers, building products and much more, Georgia-Pacific works to meet evolving needs of customers worldwide with quality products.
In addition to the products we make, we operate one of the largest recycling businesses. Our more than 30,000 employees in over 150 locations are empowered to innovate every day -to make everyday products even better. At Koch, employees are empowered to do what they do best to make life better. Learn how our business philosophy helps employees unleash their potential while creating value for themselves and the company. Our Benefits Our goal is for each employee, and their families, to live fulfilling and healthy lives. We provide essential resources and support to build and maintain physical, financial, and emotional strength - focusing on overall wellbeing so you can focus on what matters most.
Our benefits plan includes - medical, dental, vision, flexible spending and health savings accounts, life insurance, ADD, disability, retirement, paid vacation/time off, educational assistance, and may also include infertility assistance, paid parental leave and adoption assistance. Specific eligibility criteria is set by the applicable Summary Plan Description, policy or guideline and benefits may vary by geographic region. If you have questions on what benefits apply to you, please speak to your recruiter.
Equal Opportunities Equal Opportunity Employer, including disability and protected veteran status. Except where prohibited by state law, all offers of employment are conditioned upon successfully passing a drug test. This employer uses E-Verify. Please visit the following website for additional information: http: ///doc/Everify. pdf #LI-BR1
Inspectors the following benefits: Medical Dental Vision So, now that you've learned the who, what, where, and why, you may be wondering HOW? It's easy! Just fill out our initial mobile-friendly online application. We hope to meet you soon! DAY-TO-DAY As a Quality Control Inspector, you enjoy getting out of the office and out in the field.
You provide daily site inspections to ensure compliance with approved plans, specifications, and codes. Once you arrive at job sites, you backss general progress, quality of workmanship, and conformity of the work with the contract documents. You feel good about the part you play in our success and know that you are always valued at our company. ABOUT
WALLACE MONTGOMERY Since 1975, our multi-disciplined engineering organization has grown to become a recognized leader in planning, engineering, and construction management.
As an Engineering News-Record (ENR) Top 500 design firm, our staff of professional engineers, planners, surveyors, technicians, construction inspectors, and support personnel work on a diverse portfolio of projects involving highways, bridges, mass transit facilities, water resources, utilities, as well as water and wastewater facilities. Our mission is to provide quality professional engineering and technical services to develop innovative solutions that meet the needs of our clients and help build sustainable, resilient
projects within our communities. We strive to be the best public infrastructure firm in the Mid-Atlantic region.
Our growth and reputation are a result of our incredible team of highly respected and well-trained professionals. We value integrity, quality, teamwork , and respect. Those values are integral to our positive culture. Join our innovative team and enjoy competitive pay , an excellent benefits package , and the chance to make a difference. OUR IDEAL QUALITY CONTROL INSPECTOR Career-minded - Looking for more than just a job Dependable - Reliable, shows up on time and prepared Takes pride in your work - Pays close attention to detail and goes above and beyond Team player - Works well with others Respectful - Treats others with kindness and dignity If this sounds like you, keep reading about this inspection position!
REQUIREMENTS FOR A QUALITY CONTROL INSPECTOR High school diploma or equivalent Valid driver's license Reliable transportation If you meet the above requirements, we need you. Apply today to join our team as a Quality Control Inspector! Location: 23503 Job Posted by Applicant Pro
to laboratory safety protocols. Ability to operate various lab equipment Organize and maintain flavor library Skills Strong Math Skills Knowledge of Excel and Word SAP Knowledge Strong Verbal & Communication skills Experience High School Diploma At least 1 year Lab experience 2 years Compounding Experience PDN-9ad9c417-949c-45cf-9552-5201446035a7
on industry leading whey and milk protein isolates, concentrates, and hydrolysates - backed by the speed, execution, and passion it takes to exceed the expectation of our customers. We are currently seeking a Quality Assurance Technician to join the Hutchinson, MN team.
The shift for the position is Nights. Starting wage for this position is $20.00 per hour and up based on experience. The Quality Technician has the responsibility for performing departmental analytical and clerical work in support of the plant Quality function which includes conducting lab tests, preparing samples for shipment, and responding to internal calls. Ideal candidates will have 1 – 2 years of prior laboratory
experience, preferably in a food grade manufacturing facility. We are committed to identifying and recruiting dedicated and reliable candidates to join the team of passionate employees.
Milk Specialties Global prides itself on advancement opportunities for our current workforce to promote from within. We offer a comprehensive benefits package which includes medical, dental, vision and life insurance as well as a healthy 401(k) company match program.