Quality manager jobs in Glendale, WI - 201 jobs

Salary: $125,000-$135,000 Benefits: Medical, Dental, Vision, Life, 401k, Holidays, Vacation Job Type: Full-Time Typical Hours: M-F; 8 AM - 6 PM Quality Assurance Manager (pharmaceutical and/or biotechnology quality exp. req.) Description Our client, a growing pharmaceutical manufacturing company, is seeking a Quality Assurance Manager to join their team in the Greater Milwaukee Area. Reporting to the Director of Quality, this hands-on role is responsible for ensuring that quality standards, regulatory requirements, and customer expectations are consistently met through strong systems, precise documentation, and proactive compliance oversight. The company's US site is backed by a global parent company that's investing heavily in its American operations, so there's a lot of excitement and growth ahead. You'd be joining a close-knit team of 40 in Wisconsin, which means your days will have plenty of variety. They're seeking someone who can adapt as processes and systems evolve, and who can translate complex, technical information into clear, understandable insights for the entire team. If you have a well-rounded background in QA with experience overseeing GMP requirements, and bring an approachable, patient demeanor, this role could be an excellent fit. Your contributions will be visible and valued across an organization with a strong international footprint. Quality Assurance Manager (pharmaceutical and/or biotechnology quality exp. req.) Responsibilities • Establish, uphold, and enhance quality and compliance standards • Monitor internal systems to ensure alignment with regulatory and customer requirements • Oversee supplier and partner quality programs, including audits, qualifications, etc. • Manage compliance processes such as deviations, investigations, and product release activities • Support regulatory submissions and interactions with external agencies and certification bodies • Lead audit programs, ensuring timely reporting, follow-up, and corrective actions • Author, evaluate, and approve, equipment IQ/OQ protocols • Supervise QA documentation, including SOPs, batch record reviews, and material approvals • Promote adherence to cGMP or nutraceutical quality systems • Respond to customer quality concerns, complaint investigations, and product inquiries • Collaborate across departments to maintain a culture of continuous improvement Quality Assurance Manager (pharmaceutical and/or biotechnology quality exp. req.) Qualifications • Bachelor's degree in life sciences required • Current experience within pharmaceutical or biotech required • Minimum 5 years of quality assurance experience required • Supplier management experience required

We are seeking an experienced and highly motivated Quality Manager to join our team. In this role, you will be responsible for ensuring that our products and processes meet the highest quality standards. You will also be responsible for developing and implementing quality management systems, as well as leading and mentoring a team of quality professionals. Responsibilities: Exhibit superior safety practices every day. Treat all associates with courtesy and dignity. Exceed customer quality and service expectations. Protect the environment by fostering and supporting responsible operating procedures. Manage quality practices and deliver operational performance. Ensure the organization's Quality Management System conforms to ISO 9001, IATF16949, VDA, and other requirements. Manage the monitoring, measurement, and review of internal and external processes. Engage with customers, employees, contractors, and outsourcing firms. Develop and lead a cross -functional team on the integration of Process Flows, FMEA's, Control Plans, and FTP. Support advanced product quality planning (APQP). Make recommendations that promote continuous improvement. Manage the problem resolution process. Act as an organization representative. Develop and upgrade the talent of the operational quality team. Maintain the Cost of Quality process and drive improvement. Requirements Qualifications: Bachelor's degree preferred. 5+ years of experience in a quality management role. Experience in the automotive industry is required. Strong knowledge of ISO 9001, IATF16949, and VDA standards. Excellent leadership and communication skills. Benefits Benefits: Competitive wages 401(k) with company match Medical and Dental Insurance Paid holidays and vacation Company -paid Short Term Disability #qualitymanager #automotive #manufacturing #ISO9001 #IATF16949 #VDA #qualitymanagement #continuousimprovement #hiring #jobopportunity

The Food Safety and Quality Manager is responsible for owning, leading, and continuously improving the Food Safety, Quality Assurance, and Sanitation programs at SafetyFresh Foods. This position functions as a strategic leader and decision-maker, partnering Operations, Sales, and Senior Leadership to drive a strong food safety culture, continuous improvement, and readiness for internal, customer, and third-party audits while supporting company growth. ESSENTIAL JOB RESPONSIBILITIES/FUNCTIONS: * Own and manage the site Food Safety and Quality Management System, including HACCP, GMPs, SOPS, SSOPs, and employee training programs. * Serve as audit lead for all third-party, customers, and regulatory audits, including BRC, and Organic certifications. * Coordinate audit preparation, execution, corrective actions, root cause analysis, and verification of effectiveness. * Act as primary liaison with regulatory agencies (FSA, USDA, state and local authorities) and customers on food safety and quality matters. * Maintain traceability, mock recalls, crisis management procedures, and food defense programs. * Develop, maintain, and continuously improve quality and food safety documentation and polices. * Conduct internal audits and trend analysis to identify risks and improvement opportunities. * Lead investigations into quality deviations, complaints, and non-conformances using CAPA and root cause methodologies. Analyzes process control charts, develops quality cost analysis and inspects system design annually. * Analyze product and environmental testing data and process control metrics to drive corrective and preventative actions. Completes product and environmental sample collection. * Evaluate and implement food safety and quality software solutions to support system effectiveness and scalability. * Implements necessary internal quality assurance systems and infrastructure to support company growth. * Maintains current knowledge of trends and changes affecting food safety and develops and recommends appropriate program changes to ensure food safety and governmental compliance. * Promote a strong food safety culture through engagement, visibility on the floor, and cross-functional collaboration. * Partner with Operations to ensure Safety, Quality, Cost, and Delivery objectives are aligned. Advises Senior Management staff of any quality control and food safety issues in addition to presenting plausible solutions. * Provide concise, executive-level summaries of food safety and quality risks, trends and recommendations. * Support customer quality requirements, specifications and inspections. * Actively support company values, culture, and continuous improvement initiatives. * Support and assist with Occupational Health and Safety programs in coordination with Operations leadership. * Promote compliance with OSHA and workplace safety requirements. * Other duties as assigned. Requirements QUALIFICATIONS: * Bachelor's Degree in Quality Assurance, Food Science, Biology, Microbiology, Engineering, Operations Management, or a related field, or an equivalent combination of education and experience. * Technical knowledge of food safety and quality. * Knowledge of GFSI audit schemes and the GFSI audit process. * Experience dealing with regulatory agencies (i.e. USDA, FDA, and BRC) and working knowledge of local, state, and federal regulations. * Hands on Experience supporting or managing Organic certification programs. * Experience with BRC issue 9. * 5-7 years experience in Quality Assurance or Food Safety Leadership. * 3-5 years experience in management handling: hire, termination, discipline, training/development, employee relations, mediation, and retention. * Previous experience in produce preferred. * Previous HACCP and PCQI certification preferred. * Bilingual (English & Spanish) preferred. COMPETENCIES: * Strong leadership skills. * Strong verbal and written English communication skills. * Strong implementation and execution skills. * Strong analytical skills. * Good organizational and planning skills. * Ability to be relatable, personable, and productive within a team environment. REASONING AND COGNITIVE ABILITY: The person assigned to this role must be able to think independently. Must be able to define problems, collect data, establish facts, and draw valid conclusions. Must be able to interpret and analyze a variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. WORK ENVIRONMENT: While performing duties of this job, the employee is regularly exposed to moving mechanical parts. The employee is frequently exposed to extreme cold, extreme heat, risk of electrical shock, and vibration. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; and outside weather conditions. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL DEMANDS: While performing the duties of this job, the employee is regularly required to use hands to finger, handle or feel; talk or hear; and taste or smell. The employee frequently is required to stand, walk, sit, and reach with hands and arms. The employee is occasionally required to dump or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The Food Safety and Quality Manager is responsible for owning, leading, and continuously improving the Food Safety, Quality Assurance, and Sanitation programs at SafetyFresh Foods. This position functions as a strategic leader and decision-maker, partnering Operations, Sales, and Senior Leadership to drive a strong food safety culture, continuous improvement, and readiness for internal, customer, and third-party audits while supporting company growth. ESSENTIAL JOB RESPONSIBILITIES/FUNCTIONS: Own and manage the site Food Safety and Quality Management System, including HACCP, GMPs, SOPS, SSOPs, and employee training programs. Serve as audit lead for all third-party, customers, and regulatory audits, including BRC, and Organic certifications. Coordinate audit preparation, execution, corrective actions, root cause analysis, and verification of effectiveness. Act as primary liaison with regulatory agencies (FSA, USDA, state and local authorities) and customers on food safety and quality matters. Maintain traceability, mock recalls, crisis management procedures, and food defense programs. Develop, maintain, and continuously improve quality and food safety documentation and polices. Conduct internal audits and trend analysis to identify risks and improvement opportunities. Lead investigations into quality deviations, complaints, and non-conformances using CAPA and root cause methodologies. Analyzes process control charts, develops quality cost analysis and inspects system design annually. Analyze product and environmental testing data and process control metrics to drive corrective and preventative actions. Completes product and environmental sample collection. Evaluate and implement food safety and quality software solutions to support system effectiveness and scalability. Implements necessary internal quality assurance systems and infrastructure to support company growth. Maintains current knowledge of trends and changes affecting food safety and develops and recommends appropriate program changes to ensure food safety and governmental compliance. Promote a strong food safety culture through engagement, visibility on the floor, and cross-functional collaboration. Partner with Operations to ensure Safety, Quality, Cost, and Delivery objectives are aligned. Advises Senior Management staff of any quality control and food safety issues in addition to presenting plausible solutions. Provide concise, executive-level summaries of food safety and quality risks, trends and recommendations. Support customer quality requirements, specifications and inspections. Actively support company values, culture, and continuous improvement initiatives. Support and assist with Occupational Health and Safety programs in coordination with Operations leadership. Promote compliance with OSHA and workplace safety requirements. Other duties as assigned. Requirements QUALIFICATIONS: Bachelor's Degree in Quality Assurance, Food Science, Biology, Microbiology, Engineering, Operations Management, or a related field, or an equivalent combination of education and experience. Technical knowledge of food safety and quality. Knowledge of GFSI audit schemes and the GFSI audit process. Experience dealing with regulatory agencies (i.e. USDA, FDA, and BRC) and working knowledge of local, state, and federal regulations. Hands on Experience supporting or managing Organic certification programs. Experience with BRC issue 9. 5-7 years experience in Quality Assurance or Food Safety Leadership. 3-5 years experience in management handling: hire, termination, discipline, training/development, employee relations, mediation, and retention. Previous experience in produce preferred. Previous HACCP and PCQI certification preferred. Bilingual (English & Spanish) preferred. COMPETENCIES: Strong leadership skills. Strong verbal and written English communication skills. Strong implementation and execution skills. Strong analytical skills. Good organizational and planning skills. Ability to be relatable, personable, and productive within a team environment. REASONING AND COGNITIVE ABILITY: The person assigned to this role must be able to think independently. Must be able to define problems, collect data, establish facts, and draw valid conclusions. Must be able to interpret and analyze a variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. WORK ENVIRONMENT: While performing duties of this job, the employee is regularly exposed to moving mechanical parts. The employee is frequently exposed to extreme cold, extreme heat, risk of electrical shock, and vibration. The employee is occasionally exposed to high, precarious places; fumes or airborne particles; toxic or caustic chemicals; and outside weather conditions. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. PHYSICAL DEMANDS: While performing the duties of this job, the employee is regularly required to use hands to finger, handle or feel; talk or hear; and taste or smell. The employee frequently is required to stand, walk, sit, and reach with hands and arms. The employee is occasionally required to dump or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Quality Manager is responsible for coordinating and performing activities for the proper application of inspection methods, ensuring compliance with all quality standards and responsible for driving corrective action and non-conformance reduction related to manufactured and supplied product. This customer facing role will have a keen opportunity to drive improvements within the plant and work with customers and internal stakeholders to solve problems. This individual, be key to maintaining ISO9001-2015 certification by supporting all corporate policies, procedures, work instructions and required documentation. This role will also supervise hourly Quality Technicians. Essential Functions: Establish and implement quality systems to include guidelines, processes and standards for raw materials, in-process, and finish products. Ensure proper documentation of quality systems, processes, and standards. Review quality non-conformance rejections and quality problems, supporting engineering and manufacturing with considerations as to cost, customer acceptance, scrap, and deciding on allowable deviations. Lead systematic problem-solving and risk-based methodologies in identifying, prioritizing, communicating, and resolving internal and external complaints, such as RCCA. Investigates customer complaints, develops corrective action plans and verifies effectiveness Updates critical quality documents including FMEA, PFD, and Control Plans Work cross functionally with Tooling, Engineering, Manufacturing, and purchasing to identify and develop improvements to the processes Understand inspection techniques, record systems, and process control procedures to ensure production of finished products meet quality specifications and standards. Conduct research and recommend where improvements can be made to Quality and/ or Plant manager. Customer service mindset, working closely with customers to understand their issue, provide quick resolution, while developing win-win solutions for both the business and external customers. Lead the processing of customer complaints and returns to determine root cause and corrective action. Assist with 3rd party certifications, such as ISO9001-2015. Conduct internal quality system audits to determine compliance to ISO 9001 standards. Maintain charts and graphic illustrations of quality control metrics, scorecards, customer complaints, etc Understanding of part prints and be able to connect to the severity of customer complaints Participate in various company programs such as training, safety, communications, etc. Key Competencies Ability to coordinate FMEA, PFD, and Control Plans Knowledge of and ability to implement statistical techniques / inspection plans Clear understanding of corrective action processes (8-D, 5-why, etc.) Knowledge of 3rd party Audit specifications Ability to build relationships with customers Qualifications Bachelors or Associates degree (preferably Quality or Engineering related) or equivalent experience/training Excellent written and verbal communication skills 3+ years of prior Quality Assurance experience 1+ year of prior Management Experience preferred Experience or knowledge of in First Article Inspection (FAI) and Production Part Approval Process (PPAP) Six Sigma certification preferred Experience in Problem Solving techniques Benefits Medical, Dental, Vision and Prescription Drug Coverage Spending accounts (HSA, Health Care FSA and Dependent Care FSA) Paid Time Off and Holidays 401k Retirement Plan with Matching Employer Contributions Life and Accidental Death & Dismemberment (AD&D) Insurance Paid Leaves Tuition Assistance About Regal Rexnord Regal Rexnord is a publicly held global industrial manufacturer with 30,000 associates around the world who help create a better tomorrow by providing sustainable solutions that power, transmit and control motion. The Company's electric motors and air moving subsystems provide the power to create motion. A portfolio of highly engineered power transmission components and subsystems efficiently transmits motion to power industrial applications. The Company's automation offering, comprised of controls, actuators, drives, and precision motors, controls motion in applications ranging from factory automation to precision control in surgical tools. The Company's end markets benefit from meaningful secular demand tailwinds, and include factory automation, food & beverage, aerospace, medical, data center, warehouse, alternative energy, residential and commercial buildings, general industrial, construction, metals and mining, and agriculture. Regal Rexnord is comprised of three operating segments: Industrial Powertrain Solutions, Power Efficiency Solutions, and Automation & Motion Control. Regal Rexnord has offices and manufacturing, sales and service facilities worldwide. For more information, including a copy of our Sustainability Report, visit RegalRexnord.com. Equal Employment Opportunity Statement Regal Rexnord is an Equal Opportunity and Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex/gender, sexual orientation, gender identity, pregnancy, age, ancestry, national origin, genetic information, marital status, citizenship status (unless required by the applicable law or government contract), disability or protected veteran status or any other status or characteristic protected by law. Regal Rexnord is committed to a diverse and inclusive workforce. We are committed to building a team that represents diverse and inclusive backgrounds, perspectives, and skills. If you'd like to view a copy of the company's affirmative action plan for protected veterans/individuals with disabilities or policy statement, please email ***************************. If you have a disability and you believe you need a reasonable accommodation in order to search for a job opening or to submit an online application, please e-mail ***************************. Equal Employment Opportunity Posters Notification to Agencies: Please note that Regal Rexnord Corporation and its affiliates and subsidiaries ("Regal Rexnord") do not accept unsolicited resumes or calls from third-party recruiters or employment agencies. In the absence of a signed Master Service Agreement or similar contract and approval from HR to submit resumes for a specific requisition, Regal Rexnord will not consider or approve payment to any third-parties for hires made.

We Are: Are you ready to step into the heart of digital transformation in one of the world's most critical - and most dynamic - industries? The Chemicals Industry is evolving at lightspeed: demand for sustainability-driven products is on the rise. At the same time, digital platforms, real-time analytics, AI, and SAP-enabled processes are no longer "nice to have" - they are foundational. As part of Accenture's SAP Chemical's Practice, you'll be delivering major SAP engagements (for example, Business Transformation Strategy & Roadmaps, migrations to SAP S/4HANA, process standardization, cloud-enablement) that help clients win in this new environment and guide major Chemical clients through the journey of business-model reinvention, process excellence and enterprise technology enablement You Are: Do you have a passion for storytelling and for originating, selling and delivering SAP-based Supply Chain Transformation projects that make a positive impact in your clients' business? Are you inspired by working with the best companies in their industries? Want a role that provides you with a sense of purpose and satisfaction? Then join Accenture and build a rewarding career improving the way the world works and lives, as you help clients innovate with leading-edge SAP and Accenture Supply Chain solutions and technologies on some of the most innovative projects in the world You will thrive in our highly collaborative, digitally-driven and innovation-led environment while nurturing your talent for thoughtful and game changing solutions in our inclusive culture that values diversity of ideas, experiences and backgrounds. Ultimately, you are a confident manager who spots and stays ahead of the SAP platform, industry and Supply Chain trends and knows how to translate client goals into clear and actionable outcomes that everyone can get behind. You know how to fully utilize the capabilities of various SAP platforms to drive business value, transform end-to-end functions and drive leading practices for your clients in markets all over the globe. The more complex their challenges, the more excited you are about leading the charge to solve them. The Work: Team with clients on their SAP functional transformation programs through your combined SAP application and functional process expertise which includes your ability to: + Engage with client executives on the business challenges/trends and the potential value of SAP solutions (current & future) + Lead customers in defining their SAP journey through the development of business cases & roadmaps including during sales origination, proposal development and client presentations + Architect E2E solutions that leverage SAP technologies, custom apps, & add on partner solutions + Advise, design and deliver solutions based on the latest industry and technology best practices leveraging a SAP solutions and embedded innovation. + Lead small teams - helping them achieve transformational roadmaps - onsite with clients or within Accenture + Become a trusted expert and advisor to your clients, team, and Accenture Leadership by staying current on regulations, trends, and innovations across your area of expertise + Be a thought leader, build assets and best practices and develop the next level of transformation experts Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements Here's what you need: + Minimum of 5 years of SAP functional and technical experience/expertise in Quality Management and/or Manufacturing. + Minimum 3 years of experience in SAP projects supporting Chemicals clients. (SAP support / managed services experience will not be considered for this requirement) + Minimum 2 end-to-end SAP S/4 implementations, including project planning, estimation and solution architecture for Chemicals clients + Experience managing SAP delivery teams, in a Global Delivery Model, including but not limited to the following responsibilities: driving complex workshops and leading design decisions, as well as leading the design and execution of system build, configuration, testing, cutover, and go-live in the SAP Transportation Management or Quality Management area + Prior experience in a Consulting and/or Advisory role + Bachelor's degree or equivalent (minimum 12 years' work experience). If Associate's Degree, must have equivalent minimum 6-year work experience Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. (************************************************************ Role Location Annual Salary Range California $94,400 to $293,800 Cleveland $87,400 to $235,000 Colorado $94,400 to $253,800 District of Columbia $100,500 to $270,300 Illinois $87,400 to $253,800 Maryland $94,400 to $253,800 Massachusetts $94,400 to $270,300 Minnesota $94,400 to $253,800 New York/New Jersey $87,400 to $293,800 Washington $100,500 to $270,300 Requesting an Accommodation Accenture is committed to providing equal employment opportunities for persons with disabilities or religious observances, including reasonable accommodation when needed. If you are hired by Accenture and require accommodation to perform the essential functions of your role, you will be asked to participate in our reasonable accommodation process. Accommodations made to facilitate the recruiting process are not a guarantee of future or continued accommodations once hired. If you would like to be considered for employment opportunities with Accenture and have accommodation needs such as for a disability or religious observance, please call us toll free at **************** or send us an email or speak with your recruiter. Equal Employment Opportunity Statement We believe that no one should be discriminated against because of their differences. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. For details, view a copy of the Accenture Equal Opportunity Statement (******************************************************************************************************************************************** Accenture is an EEO and Affirmative Action Employer of Veterans/Individuals with Disabilities. Accenture is committed to providing veteran employment opportunities to our service men and women. Other Employment Statements Applicants for employment in the US must have work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States. Candidates who are currently employed by a client of Accenture or an affiliated Accenture business may not be eligible for consideration. Job candidates will not be obligated to disclose sealed or expunged records of conviction or arrest as part of the hiring process. Further, at Accenture a criminal conviction history is not an absolute bar to employment. The Company will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. Additionally, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the Company's legal duty to furnish information. California requires additional notifications for applicants and employees. If you are a California resident, live in or plan to work from Los Angeles County upon being hired for this position, please click here for additional important information. Please read Accenture's Recruiting and Hiring Statement for more information on how we process your data during the Recruiting and Hiring process.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Lilly is entering an exciting period of growth, and we are committed to delivering innovative medicines to patients around the world. Lilly is working to build a stronger Sterility Assurance function and capability to provide increased technical capacity across the network. The purpose of this position is to provide oversight and drive / maintain harmonization of technical programs that govern implementation and execution of Sterility Assurance control strategies across the Lilly Parenteral Network. This position also influences peers within Lilly globally and at the site level, as well as external to Lilly, to ensure strategies are in-line with technical, quality and regulatory guidance, current expectations and business needs. This role also aids and enables building technical capability at Lilly sites to ensure the vital capabilities are developed and in place to meet business objectives. Finally, this role provides ad-hoc technical support to Lilly PR&D, external contract manufacturing, and non-sterile drug substance (API) manufacturing. Responsibilities: * Assess differences in current sterility assurance programs across the sites and drive harmonization * Work closely with site and multi-functional SMEs to drive cohesion. Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. * Ensure control strategies are robust, consistent with regulatory and compliance expectations, and are continuously improved. * Assume SME leadership role for a specific topic area within Sterility Assurance across the network, including harmonization of aspects of the topic area and facilitation of the knowledge across the network. * Represent TS/MS on network Science Lead Team and other appropriate governance forums. Ensure that Sterility Assurance programs and similar topics are frequently presented to network team in order to align across sites. Ensure that learnings and best practices are shared across sites: set-up appropriate forums in order to achieve this and present case studies to site SMEs. * Provide mentoring leadership to site SMEs to help build continue to build capability, particularly at the newer sites or where deep technical expertise is lacking. * Building, maintaining, and growing capability across the organization in the sterility assurance space * Provide technical support to new sites/ filling lines during design and start-up activities to ensure sterility assurance programs and process/ product requirements are supported at these sites, particularly while the sites are in early stages of building capability. * Provide technical support for significant sterility assurance investigations to help identify root cause and implement appropriate corrective actions. Share best practices / learnings / CAPAs across the other sites. * Benchmark industry trends and emerging regulatory guidance / requirements in the field through building an extensive peer network and attendance at relevant industry and regulatory meetings and advocacy groups. Advance Lilly agenda in the field. Represent Lilly on relevant external bodies related to Sterility Assurance; be influential in terms of representing Lilly's position on technical/ regulatory positions papers and guidance. Assess new technologies to ensure Lilly stays current with new trends and technologies and share with the network with the goal of staying current with industry best practice. * Work with PR&D on new technology / platform development and implementation for pipeline products. Influence the agenda within PR&D to ensure the needs of Manufacturing are met, and the control strategies are fit for-purpose for robust and compliant commercial manufacturing. * Provide ad-hoc technical support to Lilly organizations outside of the PPN including PR&D, external contract manufacturing, and non-sterile drug substance (API) manufacturing. * Engage in providing support during regulatory interactions such as RtQ of submissions, and on-site inspections * Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate Goals Basic Qualifications: * BS Degree required. * MS/PhD in a biological science preferred. * 10+ years' experience working in Parenteral Sterility Assurance / Environmental Monitoring or equivalent roles preferred. * 10+ years' experience in parenteral manufacturing sterility assurance control systems - development of systems, execution and operation of systems and continuous improvement of systems in a highly regulated environment preferred. * Deep technical understanding of sterility assurance, from a science and compliance perspective. Current in technological and compliance developments across the parenteral manufacturing industry (e.g. filling technology, Annex 1 interpretation) * Proficiency in data analysis, ability to prioritize, attention to detail, critical decision-making skills, complex problem-solving abilities * Strong written and oral communication skills * Ability to mentor and develop scientists in the fields of sterility assurance and applied pharmaceutical microbiology * Understanding of cGMP's, policies, procedures, and guidelines relating to sterility assurance * Demonstrated experience influencing site and network leaders to advance technical agenda projects Additional Preferences: * Work closely with senior technical staff in the parenteral network TSMS group to provide full oversight to new and existing facilities. Be available to help with inspection readiness and inspection preparation at each site, particularly the new sites. Provide guidance to investigations and ensure root cause, CAPA are quickly developed. * Support the establishment of a sterility assurance network or hub in global TSMS * Support inspection preparation and execution during health authority on-site or remote inspection as an expert in Sterility Assurance * Experience in leading external committees or conferences to ensure Lilly remains a leader in the sterility assurance space * Work with engineering SME's to support Lilly platforms to maximize the performance and minimize the risk of sterility assurance * Strength in scientific and practical thinking to ensure the best options are selected following a thorough evaluation of applicable options. * Strong capability to influence personnel and management across the organization * Close interaction with quality to enable internal audits that identify risks * Past experience in creating effective working relationships with all levels across internal and external stakeholders impacting the success of sterility assurance. Additional Information: * Approximately 25% travel Lilly currently anticipates that the base salary for this position could range from between $133,500 to $220,000 and will depend, in part, on the successful candidate's qualifications for the role, including education and experience. Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Of course, the compensation described above is subject to change and could be higher or lower than the range described above. Further, Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $133,500 - $246,400 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Job Title: Quality ManagerJob Description Manage and coordinate quality and regulatory functions to ensure compliance with processes and procedures. Provide leadership and direction across the plant to enhance the overall effectiveness and efficiency of the quality system. Responsibilities + Manage audits (internal and external), annual regulatory reporting, recall program, regulatory product registrations, and facility registrations. + Oversee medical device document management, internal investigations (including Deviations and CAPAs), artwork review, training program, sanitation program, and customer complaint program. + Lead the validation program, change control program, quality system administration, product specification management, and support new product development. + Serve as the regulatory expert to ensure product compliance with regulatory and customer requirements. + Advise senior leadership on compliance issues and recommend corrective actions. + Stay informed about regulatory updates and changes impacting the business. + Participate in the development and approval of standard operating procedures and validations to support production processes. + Ensure all procedures comply with FDA cGMPs and other regulatory requirements. + Maintain compliance programs for FDA and other regulatory requirements. + Act as an unofficial liaison between federal, state, and local regulatory agencies. + Notify executive management of regulatory compliance requirements and deficiencies. Essential Skills + Expertise in regulatory and quality assurance. + Experience in OTC, pharmaceuticals, and medical devices. + Knowledge of GMP, FDA, and OTC regulations. Additional Skills & Qualifications + Bachelor's Degree in Sciences. + 5 years of experience in OTC, Drug, Medical Device, or Cosmetics. + Experience with FDA and cGMP regulations. + 5-10 years of management experience. + Understanding of labeling in an OTC/Medical Device environment is a plus. Work Environment The role requires work within the manufacturing area, office, and laboratory as needed. The company is rapidly growing, focusing on streamlining processes and enhancing efficiency. The work culture emphasizes maintaining a healthy work-life balance, encouraging hard work during office hours without making work the entirety of one's life. Job Type & Location This is a Permanent position based out of Jackson, WI. Pay and Benefits The pay range for this position is $105000.00 - $115000.00/yr. Working at Wisconsin Pharmacal offers employees a close‑knit, collaborative environment where individual contributions are genuinely valued. Team members benefit from cross‑department exposure that helps them grow their skills and understand the full lifecycle of the company's products. The organization encourages continuous improvement, giving employees opportunities to innovate and influence internal processes. With a culture that prioritizes stability, respect, and long‑term development, Wisconsin Pharmacal fosters a workplace where people can build meaningful careers. Workplace Type This is a fully onsite position in Jackson,WI. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Highly competitive compensation at one of Plastics News Best Places to Work. Hands-on leadership of the Quality Team at a state-of-the-art custom plastic injection molding plant with a global reach. As Quality Manager, you're responsible for leading all aspects of the Quality Management Systems supplying precise plastic parts to both automotive and medical customers. Ensuring products meet all customer, regulatory, and internal quality requirements through robust systems, disciplined process control, and an engaged quality culture. About this Job Lead, coach, and develop a high-performing team of Quality Engineers and QA Technicians. Maintain and continuously improve the Quality Management System (QMS) in accordance with IATF 16949, ISO 13485, and ISO 9001 standards. Lead quality planning activities for new products from design phase through production launch. Partner with Production and Engineering to monitor and improve process capability and reduce internal defects. Serve as primary contact for customer quality issues, audits, and quality performance reporting. Manage and maintain the plant's Environmental Management System (EMS) to comply with ISO 14001 or corporate environmental standards. About this Company Successful plastic injection molding company with global reach and state-of-the-art facilities. Recognized as one of the best places to work (Plastics News) for the past eight years. Multi-national plant locations. Minimum Job Qualifications Bachelor's degree in Engineering, Quality, or a related technical discipline. Minimum 7-10 years of experience in Quality Management within plastics molding or precision manufacturing environments. Demonstrated experience in both automotive (IATF 16949) and medical (ISO 13485 / FDA) regulated sectors. Proven leadership experience managing technical quality teams. Quality Manager/ Quality Assurance Quality Engineering / Engineer Plastic Injection Molding IND123

**This role is not open for submissions from outside staffing agencies** Quality Manager pay range: $75,000-$85,000 Trulite is GROWING! We are looking for a Quality Manager to be based at our New Berlin, WI plant. The Quality Manager is accountable for monitoring and support of the manufacturing activities to produce a quality product that meets or exceeds our customer's expectations through continued review and analysis of quality and production process. Who You Are: The successful candidate will be a hands-on, “on the plant floor” person who has proven experience leading effective behavioral change in the process, procedures, implementations with a functional area to ensure performance and productivity in a manufacturing environment. What You Will Be Doing: Develop and implement quality standards, quality control systems and quality measures. Inspect and test materials, equipment, processes, and products to ensure quality specifications are met. Develop and implement quality improvement parameters by finding statistical methods relevant to manufacturing processes. Develop statistical confidence by finding sample size and acceptable error and setting up confidence levels. Prepares reports by collecting, analyzing, and summarizing data; and making recommendations. Develops sampling and experimental plans by applying attributes and variable sampling methods. Collaborate with operations to develop and implement controls and improvements. Ensuring that workflows, processes, and products follow industry and safety regulations/standards. Excellent troubleshooting skills and to be able to ensure that processes and products consistently meet established quality standards. Investigates operational errors to find the cause and effect, making recommendations for corrective action. Required to work in a team environment with customers, co-workers, production supervisors, shipping and receiving, customer service, sales, and company management. Assist COD and sales in resolving customer quality complaints. Process all returned RGA's (Return Goods Authorization) evaluating reason for return and decide and recommendation to the plant manager for resolution. Use accepted methods to inspect, sample and test materials for quality control and quality control tolerance. Monitor, Inspect, and test process functions, product, and materials daily at all stages to ensure our products meet or exceed industry standards. Record and log all test data per production process and report weekly to the plant manager. Oversee all aspects of Quality Control including overall implementation of the quality program and supply support as needed to the key personnel who manage the processes. Daily reviews of key metrics to ensure budgeted goals are being met. Interpret information and coordinate any required changes or new directives with employees. Review daily production statistics and ensure implementation of measures for continuous improvement in safety, quality, efficiency, and preventive loss. Work with Supply chain (Purchasing) team on supplier quality related issues. Daily inspections - Look for any unsafe objects, check equipment, etc. Maintains safe operations by adhering to safety procedures and regulations. Performs other duties as assigned. Skills You Bring: Education- Associate Degree or five years industry experience Minimum of five years of experience managing Quality Control/ Operational Standards in a manufacturing needed. The successful candidate will be a hands-on, “on the plant floor” person who has proven experience leading effective behavioral change in the process, procedures, implementations with a functional area to ensure performance and productivity in a manufacturing environment. Excellent project management skills. Strong analytical, statistical, and problem-solving skills. Persuasive communication and interpersonal skills. Must work well in a cross-functional, dynamic, collaborative environment. Works directly with all departments in quality issues and in preventative and corrective actions. Actively pursue learning goals for added opportunities in growth and development in production and quality. Contribute to continued process improvement updating and writing new process procedures. Create understanding of workflow, employee relations and processes through hands-on experience with production equipment and working with production supervisor. Aid production supervisors in training, motivating, and instructing employees engaged in process improvement, documenting, and recording activities. Why Trulite: Trulite offers the most comprehensive benefit coverage in the industry. Including immediate access to all health, dental, vision and life insurance for you and your family. Our commitment to you as a member of our team also includes both Long Term and Short-Term Disability coverage to help protect you financially. Because we value your financial health, we provide not only a comprehensive wellness initiative, but we also provide financial literacy, providing all employees with a comprehensive financial wellness program. Stay with us for a year and your 401k employer match is 100% vested and immediately becomes part of your ever improving financial plan. This is also true for those who select and contribute to their Health Savings Account. We match on both employee and family coverage to help cover out-of-pocket expenses and if unused continues to grow until need. Employer match is also vested immediately at 100% improving your financial health. Trulite bears most of the cost of your benefits. We structured these benefits because we care not only about your physical wellbeing but your financial health and welfare too. Let us show you a way to financial independence while being a valuable member of our team. We are an Equal Opportunity Employer. We embrace and encourage our employees' differences in age, color, disability, ethnicity, gender identity or expression, language, national origin, physical and mental ability, political affiliation, race, religion, sexual orientation, socioeconomic status, veteran status, and other characteristics that make our employees unique.

Quality Manager - Assurance Location: SVA Offices (On-site preferred; regular travel required) - includes Madison, WI; Brookfield, WI; Colorado Springs, CO Reports To: Director of Quality Management At SVA, we believe in Serving People Better-our clients, our communities, and each other. The Quality Manager - Assurance plays a key role in advancing the firm's assurance practice by supporting audit quality, consistency, and compliance across the firm. This position supports the Director of Quality Management by performing Engagement Quality Reviews (EQRs)-with a strong emphasis on Government Auditing Standards (HUD, USDA-RD, and Single Audits)-and by contributing to firm-wide initiatives that strengthen assurance quality, efficiency, and technical excellence. Essential Functions Perform Engagement Quality Reviews for assurance engagements, focusing on audits under GAGAS / Yellow Book standards. Assist with the implementation and ongoing maintenance of the firm's Quality Management Policies and Procedures (QMPP). Monitor new accounting and auditing standards and support firm-wide implementation efforts. Maintain and enhance the firm's Assurance Resources, including practice aids, technical guidance, and intranet/Teams sites. Provide technical research and guidance on complex accounting and auditing matters. Support assurance quality initiatives and efficiency-improvement projects. Participate in internal training efforts, including CPE programs and the annual A&A Update. Assist with maintaining compliance with GAGAS / Yellow Book requirements. Serve as a Qualified Reviewer or Assurance Manager on engagements, as needed. Qualifications Bachelor's degree in Accounting or related field required; Master's preferred 7+ years of public accounting audit experience Experience with Government Auditing Standards and Single Audits preferred Active CPA license required Skills & Attributes Strong expertise in audit documentation review and quality standards Excellent written, verbal, and interpersonal communication skills Ability to research and clearly communicate complex technical issues Highly motivated, detail-oriented, and capable of working independently Strong ethical standards and professional judgment Ability to manage deadlines and perform well under pressure Located near and willing to travel regularly to SVA offices (on-site work preferred) Demonstrates SVA's core value of Serve People Better and aligns with the SVA DNA Fundamentals

Quality Manager1st shift Monday-Friday Position OverviewThe Quality Manager will play a critical leadership role in establishing and maintaining the Quality Management System (QMS) for a new state-of-the-art clear aligner manufacturing facility in Oak Creek, Wisconsin. This position is responsible for building the quality function from the ground up-ensuring all processes, systems, and personnel are aligned with FDA, ISO 13485, MDSAP, and MDR regulatory standards.The ideal candidate is a hands-on, strategic quality leader with a strong background in medical device manufacturing and 3D printing technologies, capable of fostering a culture of quality and continuous improvement within a growing organization. This is a full-time, on-site role with no travel required.Key ResponsibilitiesQuality Management System (QMS) Development & Oversight Establish, implement, and maintain a comprehensive Quality Management System in alignment with ISO 13485, FDA 21 CFR Part 820, MDSAP, and MDR requirements. Ensure compliance with all applicable medical device regulatory standards and customer requirements. Develop and document quality processes, policies, and standard operating procedures (SOPs) to support production startup and scale-up. Lead the site's efforts to obtain and maintain relevant quality certifications and regulatory approvals. Product Quality & Compliance Oversee all product quality control and quality assurance activities from incoming inspection through final release of finished products. Review and approve product releases to ensure full compliance with specifications and regulatory requirements. Partner with production, R&D, and engineering teams to implement robust in-process controls and drive defect prevention strategies. Lead root cause investigations, CAPA development, and risk management activities to ensure effective and sustainable corrective actions. Leadership & Team Management Build, mentor, and lead a growing team of 6-7 quality professionals. Provide training and guidance to ensure adherence to QMS requirements and promote a strong culture of quality and accountability. Collaborate closely with cross-functional leaders (Operations, Engineering, Supply Chain, and Regulatory Affairs) to drive quality alignment across the organization. Customer Feedback & Continuous Improvement Establish and maintain a customer feedback and complaint-handling system in accordance with regulatory requirements. Collect, analyze, and report post-market surveillance data to identify trends and guide continuous improvement initiatives. Conduct regular quality review meetings to assess product performance, customer complaints, and audit findings-developing actionable improvement plans. Audits & Management Reviews Lead internal quality audits and prepare for external audits from regulatory agencies and notified bodies. Drive management reviews by providing data-driven insights, key performance indicators (KPIs), and recommendations for system enhancements. Qualifications Bachelor's degree or higher. 5+ years of progressive quality management experience in the medical device industry, preferably with Class II or III devices. Deep understanding of ISO 13485, FDA 21 CFR 820 (QSR), MDSAP, and MDR quality system requirements. Proven success in establishing or scaling quality systems in a new or expanding facility is highly preferred. Strong leadership, team-building, and organizational skills with the ability to thrive in a fast-paced start-up environment. Excellent communication, analytical, and problem-solving skills with a continuous improvement mindset. Work Environment & Schedule In-person, on-site role at the Oak Creek, WI facility. Standard business hours, Monday-Friday. No travel required.

Job Description HiFyve is hiring a Quality Manager in Plymouth, WI! Salary: $106,000/year Shift: 1st Shift Benefits: Full benefits package The Quality Manager oversees all aspects of plant quality systems, ensuring products meet customer and regulatory standards. This role manages the Quality team, leads audits, and drives continuous improvement across the operation. Reports to the Plant Manager with a matrix reporting line to the Quality Director. Key Responsibilities Lead, coach, and develop the quality team of inspectors and technicians Manage the site Quality Management System (QMS) and document control processes Develop and implement quality assurance policies and procedures Conduct internal audits and manage external customer or regulatory audits Track and report key quality metrics, including DPPM for internal and external issues Analyze data and trends to identify root causes and drive corrective/preventive actions Partner with production and engineering teams to resolve quality issues Maintain compliance with ISO 9001 and other applicable standards Provide training to employees on quality standards and procedures Prepare and present regular quality performance reports to leadership Qualifications Bachelor's degree in Engineering, Business, or related field preferred (or equivalent experience) 5-7 years of experience in Quality Management within manufacturing Strong understanding of quality systems and methodologies (ISO 9001 or equivalent) Proven ability to lead and develop high-performing teams Excellent analytical, communication, and problem-solving skills Proficient with Microsoft Office and QMS software Additional Details Travel up to 25% as needed Manufacturing environment with moderate to high noise; PPE required If you're interested, please apply!

Job Summary: The Quality Manager is a hands-on leadership role responsible for ensuring all component drawings comply with GD&T standards, defining appropriate inspection methods, managing both physical and transactional material disposition, and overseeing equipment calibration. This position directly supervises the Quality Team, organizing workloads and setting clear priorities to ensure efficient, accurate, and timely completion of all inspection requirements. This leader will effectively hire, train, and lead people, communicate clearly, set expectations, provide feedback, and resolve conflicts when they arise. They also need to be able to lead by example-their own performance needs to be consistent with the standards they're setting for their team members and be consistent with DeltaHawk's Corporate Culture statement and values. Essential Duties & Responsibilities: An individual in this position must be able to successfully perform the duties and responsibilities listed below. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position. Other duties may be assigned. Support the Quality Team by providing clear direction, resources, and guidance. Ensure product compliance through dimensional, incoming, and outgoing inspections Build, mentor, evaluate and lead Quality and inspection team members. Establish training programs to continually upgrade employees technical capabilities and knowledge of governing procedures. regulations, and requirements. Collaborate cross-functionally to achieve quality goals. Respond to customer complaints with urgency and confidence. Facilitate customer-facing activities, including visits, responses, and audit preparation Review engineering drawings to ensure compliance with GD&T standards. Define efficient and accurate inspection methods. Allocate quality resources in alignment with workload priorities. Manage and maintain the calibration program. Develop and support training programs to enhance technical skills and knowledge of applicable procedures, regulations, and requirements. Create accurate, efficient, and timely quality work instructions and procedures consistent with the DeltaHawk Quality Manual. Participate in design and development projects to represent quality and customer interests. Support internal quality audits. Oversee and manage Internal Corrective Action Requests (CARs), ensuring timely and effective root cause analysis and resolution. Establish systems for collecting and analyzing statistical data to identify trends and drive product quality improvements. Report on quality issues, trends, concerns, and improvement initiatives. Qualifications Required: Bachelor's degree or 10-years of relevant quality experience. Proficient in GD&T. Proficient in inspection methods and equipment. 3-years of experience as a Quality Engineer and/or Quality Manager. 3-years of experience with tight tolerance machine part inspection. Strong Leadership and communication skills. Preferred: Experience working in a regulated industry. ASQ Certified Quality Manager, Engineer, or Auditor (CQM, CQE, CQA). Lean, Six Sigma or other Continuous Improvement process background. Experience with Infor Syteline/CSI or similar ERP system. Experience with Solidworks or similar CAD software. Passion for aviation. Working Conditions Work will be performed in an office environment. Periodically assignments may require work be performed in a production area or at a supplier, requiring the use of PPEs determined appropriate for the environment by the resident authority. Some travel will be required. DeltaHawk Engines, Inc. is an equal employment opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, status as a qualified individual with a disability, marital status, pregnancy, sexual orientation, ancestry, genetic information, or any other characteristic protected by law.

STV is currently looking for a QA/QC Construction Manager to join our Construction Management team. STV is seeking a QA Manager will be part of the team responsible for the development of Power Harvesting Projects. The QA Manager will manage overall project objectives including design and construction within approved budgets. Responsible for overseeing and coordinating the day-to-day activities in the field, managing and coordinating the flow of information, controlling costs, managing and controlling the schedule, monitoring the safety programs, as well as verifying that the completed work is constructed to a quality level consistent with the requirements of the construction documents. Roles and responsibilities include: Demonstrate commitment to an Injury-Free Environment through own actions and mentoring others, ensuring Safety program is followed Provide QA construction and design management, and project leadership Provide QA project single point of contact for project development and delivery Facilitate decision-making to drive solutions, schedules, and manage change as required Attend and participate in project meetings for design and construction including the OAC, discipline work groups, progress, pre-construction and pre-award Apply influence, strategies, and negotiation skills to identify options and recommend solutions Oversee and report project progress on scope, schedule, budget and contractor performance weekly or as required Review trade contracts and bid packages, as well as coordinate the receiving process Maintain relationships with internal partners, designers, consultants and GC team Set-up QA/QC procedures, review inspection and test data for compliance with specifications and standards and conduct quality field inspections Review and maintain site logistics plan, in coordination with GC, Operations team and Consultant team Qualifications include: Bachelor's Degree in Mechanical Engineering, Electrical Engineering, Civil Engineering, Architecture, Construction Project Management, or Construction Management or equivalent experience Possess excellent communication, organization, and leadership skills Proficiency in commercial and industrial architecture and engineering with a primary focus on datacenter design and construction Able to work with other technical and non-technical groups in a fast-paced environment and do so with an even temperament. Experience required: Minimum of 10 years of relevant experience in construction management Compensation Range: $112,253.66 - $149,671.54 Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At STV, we are fully committed to expanding our culture of diversity and inclusion, one that will reflect the clients we serve and the communities we work in, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description we encourage you to apply anyways. You may be just the right candidate for this or other roles. STV offers the following benefits • Health insurance, including an option with a Health Savings Account • Dental insurance • Vision insurance • Flexible Spending Accounts (Healthcare, Dependent Care and Transit and Parking where applicable) • Disability insurance • Life Insurance and Accidental Death & Dismemberment • 401(k) Plan • Retirement Counseling • Employee Assistance Program • Paid Time Off (16 days) • Paid Holidays (8 days) • Back-Up Dependent Care (up to 10 days per year) • Parental Leave (up to 80 hours) • Continuing Education Program • Professional Licensure and Society Memberships STV is committed to paying all of its employees in a fair, equitable, and transparent manner. The listed pay range is STV's good-faith salary estimate for this position. Please note that the final salary offered for this position may be outside of this published range based on many factors, including but not limited to geography, education, experience, and/or certifications.

Skill (QA) efforts for IT Project Services Total Experience 8 yrs. Max Salary $ DOE Per Hour Employment Type Contract Jobs (Temp/Consulting) Job Duration 12+ Months Domain Any Description • Drive quality assurance (QA) efforts for IT Project Services team. • Collaborate with IT leadership to define and execute QA roadmaps and strategies. • Develop, implement and improve innovative QA capabilities, strategies, approaches and services. • Build and maintain a stable and reliable automation infrastructure. • Oversee test automation usage to optimize project quality and delivery. • Develop, implement and maintain QA methods, processes and deliverables. • Develop best practices, document processes, and operational and procedural improvements. • Identify, define and track QA metrics and KPIs. • Teach teams to develop applicable testing procedures and expectations. • Analyze and assess current QA processes and assist with strategic QA planning. • Initiate, plan, execute, manage and complete QA activities related to complex application and system implementation projects. • Create and maintain test strategies, plans, scenarios and cases. • Coordinate and manage holistic testing efforts for multiple projects and software releases, including integration, system, regression, performance and user acceptance testing. • Document test results, track and manage defects, and troubleshoot issues. • Monitor and communicate QA activity status. • Lead and manage test schedules, environments and configuration requirements for testing activities. • Provide testing estimates for resourcing, levels of effort and timelines. • Establish and manage traceability of requirements through test plans and cases. • Partner with Business Analysts to ensure requirements are met and accurately tested. • Provide input on go / no-go decisions for production releases. • Create, execute and manage manual and automated test cases. • Develop and maintain automated test scripts. • Bachelor's degree in computer science or related technical discipline. • Development background a must. • 10+ years of QA experience in an IT environment. • years experience in automation testing and tools. • Experience with software development life cycle and agile methodology. • Knowledge of QA processes, procedures and systems. • Extensive experience planning, executing and managing integration, system, regression and user acceptance testing. • Ability to manage concurrent projects, activities and tasks under time constraints. • Experience with a variety of technologies, platforms and development languages (AS400, Java, .NET, etc.). • Experience with performance and load testing. • Knowledge of supply chain and logistics preferred. Experience with IBM Rational Team Concert, TFS and JIRA a plus Additional Information Multiple Openings for OPT/CPT/H4/L2/EAD/Citizen's.

QUALITY ASSURANCE MANAGER A successful ground beef further processing facility located in Norcross, Ga has an immediate need for a QA Manager. Environment: Departments: Fresh and Frozen Departmental QA and the HACCP / Food Safety policies and processes Techs: Oversee 1 Manager, 2 Supervisors, and 20 QA technicians Development and aptitude. Reports to: Director of Operations and a dotted line to Corp. Director of QA / Food Safety Co-Chairs the HACCP team with the Director of Operations. Monthly meetings BRC & Silliker auditing requirements Challenge and evaluate all quality processes in the production areas for consistency. Lead the production departments in answering to customer complaints Has HACCP certification and can audit the plants plan. Handles USDA Food Safety Audits when they arrive. Heads USDA and Weekly meeting Primary duties will include: Overseeing the operation and function of the QA Technicians and Supervisors Maintaining and enforcing programs, procedures, policies and manuals Ensuring the safety and quality of incoming raw materials and outgoing finished products Meet personnel objectives by planning, monitoring, appraising, and reviewing job contributions; providing awareness education, enforcing policies and procedures. Meet operational objectives by providing analysis and insight to strategic planning; creating action plans; implementing quality and food safety standards, identifying and resolving problems; analyzing the results of audits and processing data to identify strengths and weaknesses and identify the path to continuous improvement process. Design and develop SOP's using the principles of HACCP to assure uniformity of purpose. Validate quality processes by reviewing and fine tuning product specifications and quality attributes; measuring production; documenting evidence; determining operational and performance qualification; reviewing and critiquing quality assurance procedures. Maintain and improve product quality by analyzing and trending the results of product, plant, regulatory compliance, and third-party audits collaborating with other members of management to study and improve process control. The ideal candidate will have previous quality assurance experience at the managerial level in the meat industry, solid knowledge of USDA regulations and policies, ability to handle customer and global standard audits, verifiable experience in addressing quality and food safety issues from both a corrective and a preventive posture. SPC skills are a plus.

We Are: Are you ready to step into the heart of digital transformation in one of the world's most critical - and most dynamic - industries? The Chemicals Industry is evolving at lightspeed: demand for sustainability-driven products is on the rise. At the same time, digital platforms, real-time analytics, AI, and SAP-enabled processes are no longer "nice to have" - they are foundational. As part of Accenture's SAP Chemical's Practice, you'll be delivering major SAP engagements (for example, Business Transformation Strategy & Roadmaps, migrations to SAP S/4HANA, process standardization, cloud-enablement) that help clients win in this new environment and guide major Chemical clients through the journey of business-model reinvention, process excellence and enterprise technology enablement You Are: Do you have a passion for storytelling and for originating, selling and delivering SAP-based Supply Chain Transformation projects that make a positive impact in your clients' business? Are you inspired by working with the best companies in their industries? Want a role that provides you with a sense of purpose and satisfaction? Then join Accenture and build a rewarding career improving the way the world works and lives, as you help clients innovate with leading-edge SAP and Accenture Supply Chain solutions and technologies on some of the most innovative projects in the world You will thrive in our highly collaborative, digitally-driven and innovation-led environment while nurturing your talent for thoughtful and game changing solutions in our inclusive culture that values diversity of ideas, experiences and backgrounds. Ultimately, you are a confident manager who spots and stays ahead of the SAP platform, industry and Supply Chain trends and knows how to translate client goals into clear and actionable outcomes that everyone can get behind. You know how to fully utilize the capabilities of various SAP platforms to drive business value, transform end-to-end functions and drive leading practices for your clients in markets all over the globe. The more complex their challenges, the more excited you are about leading the charge to solve them. The Work: Team with clients on their SAP functional transformation programs through your combined SAP application and functional process expertise which includes your ability to: * Engage with client executives on the business challenges/trends and the potential value of SAP solutions (current & future) * Lead customers in defining their SAP journey through the development of business cases & roadmaps including during sales origination, proposal development and client presentations * Architect E2E solutions that leverage SAP technologies, custom apps, & add on partner solutions * Advise, design and deliver solutions based on the latest industry and technology best practices leveraging a SAP solutions and embedded innovation. * Lead small teams - helping them achieve transformational roadmaps - onsite with clients or within Accenture * Become a trusted expert and advisor to your clients, team, and Accenture Leadership by staying current on regulations, trends, and innovations across your area of expertise * Be a thought leader, build assets and best practices and develop the next level of transformation experts Travel may be required for this role. The amount of travel will vary from 0 to 100% depending on business need and client requirements Qualification Here's what you need: * Minimum of 5 years of SAP functional and technical experience/expertise in Quality Management and/or Manufacturing. * Minimum 3 years of experience in SAP projects supporting Chemicals clients. (SAP support / managed services experience will not be considered for this requirement) * Minimum 2 end-to-end SAP S/4 implementations, including project planning, estimation and solution architecture for Chemicals clients * Experience managing SAP delivery teams, in a Global Delivery Model, including but not limited to the following responsibilities: driving complex workshops and leading design decisions, as well as leading the design and execution of system build, configuration, testing, cutover, and go-live in the SAP Transportation Management or Quality Management area * Prior experience in a Consulting and/or Advisory role * Bachelor's degree or equivalent (minimum 12 years' work experience). If Associate's Degree, must have equivalent minimum 6-year work experience Compensation at Accenture varies depending on a wide array of factors, which may include but are not limited to the specific office location, role, skill set, and level of experience. As required by local law, Accenture provides a reasonable range of compensation for roles that may be hired as set forth below. We accept applications on an on-going basis and there is no fixed deadline to apply. Information on benefits is here. Role Location Annual Salary Range California $94,400 to $293,800 Cleveland $87,400 to $235,000 Colorado $94,400 to $253,800 District of Columbia $100,500 to $270,300 Illinois $87,400 to $253,800 Maryland $94,400 to $253,800 Massachusetts $94,400 to $270,300 Minnesota $94,400 to $253,800 New York/New Jersey $87,400 to $293,800 Washington $100,500 to $270,300 Locations

QC Manager Shift: 1st, (7am-3:30pm) Pay: $90-$110k/yr (Based on experience) Are you a proven quality leader with a passion for process improvement, team development, and precision manufacturing? Our client, a well-established machining organization, is seeking an experienced Quality Control Manager to oversee all quality operations on 1st shift. Job Description: Lead, mentor, and develop a high-performing quality team while fostering growth and accountability. Develop and execute departmental goals, budgets, and cost controls aligned with corporate objectives. Ensure compliance with ISO 9001:2015 and other relevant standards; maintain all documentation and audit readiness. Oversee PPAP, SPC, PFMEA, and APQP processes. Analyze data, establish quality metrics, and implement corrective and preventive actions. Collaborate with production management to maximize product reliability and reduce cost of quality. Manage supplier quality performance and conduct vendor evaluations. Investigate customer complaints, lead root cause analysis, and implement sustainable corrective actions. Drive continuous improvement initiatives and quality training across all departments. Qualifications: Bachelor's degree in engineering, Business, or a related technical field preferred; equivalent experience considered. 20+ years in machining environments, including CNC (3-, 4-, and 5-axis) or multi-spindle operations. Minimum 5 years of leadership experience managing a Quality department with direct reports. Strong knowledge of raw material processing (steel bar, tube stock, castings, forgings).