Quality manager jobs in Athens, GA - 68 jobs

At ABB, we help industries outrun - leaner and cleaner. Here, progress is an expectation - for you, your team, and the world. As a global market leader, we'll give you what you need to make it happen. It won't always be easy, growing takes grit. But at ABB, you'll never run alone. Run what runs the world. This Position reports to: Manufacturing Unit Manager In this role, you will take the lead in shaping and executing the quality strategy for a local organizational unit. You'll build a strong quality culture, implement effective systems and tools, and develop capable teams-all with the goal of exceeding customer expectations while driving sustainable operations. Every day, you'll champion the local quality system by balancing prevention, continuous improvement, thorough root cause analysis, rapid response, and lasting solutions. Your expertise will shine as you coordinate across all functions that influence quality outcomes, ensuring targets are met and performance reaches world-class standards. You will also play a key role in maintaining essential certifications and compliance requirements across the organization. The work model for the role is: Onsite, Athens, TN #LI- Onsite Your role and responsibilities: Deploy and lead strategy and objectives for quality and C/I management in line with the ABB management system Fosters awareness and commitment regarding continuous improvement at local management level. Identifies and works to remove roadblocks that prevent the successful implementation and adoption of continuous improvement initiatives and oversees cases of conflicting priorities. Ensures appropriate internal and external communication relevant to quality management system. Promotes and leads improvement programs and projects within their own area of responsibility, with a hands-on (Gemba) and lean mfg. mindset. Leads a systematic fact-based approach to identify and evaluate opportunities for future improvement within the local organization. Provides guidance and support towards disseminating a continuous improvement mindset and culture at all levels, activities, and functions to promote behavioral change for continuous performance improvement at local level. Identifies the appropriate methods and tools to develop and conduct training programs and knowledge management mechanisms that align with the local organization's needs. Enables performance management at local unit with target setting and follow-up processes based on clear Key Performance Indicators (KPIs) and quantified facts. Drives resolution of customer cases to completion, following robust root cause analysis and implementing preventive and corrective actions. Ensures benchmarking within the industry, inside and outside ABB, to continuously challenge the status quo and further develop the organizational self-perception Ensures the use of appropriate Continuous Improvement tools, templates, and applications in collaboration and alignment with Quality and IS locally. Collaborate with production, engineering and leadership teams to resolve quality issues and enhance quality performance Lead both internal and external quality audit activities. Qualifications for the role: Bachelor's degree in engineering or other relevant discipline is required 5+ experience in implementing Lean manufacturing processes The ability to train others and lead Kaizen activities Lean Six Sigma Green Belt or greater certification preferred Experience with Six Sigma and ISO Standards Appropriate interpersonal styles and communication methods to work effectively with business partners to meet mutual goals required, motivate employees and elicit work output Knowledge of and ability to effectively use computer software as it pertains to business Metal stamping and plating knowledge preferred Ability to foster growth of personnel through coaching and developmental planning for internal bench talent Strong Analytical Skills Candidate must already have work authorization to work in the United States Why ABB? You will join a dynamic, talented, high performing team where you will be able to thrive What's in it for you We want you to bring your full self to work-your ideas, your energy, your ambition. You'll have the tools and freedom to grow your skills, shape your path, and take on challenges that matter. Here, your work creates impact you can see and feel, every day. ABB is an Equal Employment Opportunity and Affirmative Action employer for protected Veterans and Individuals with Disabilities at ABB. All qualified applicants will receive consideration for employment without regard to their- sex (gender identity, gender expression, sexual orientation), marital status, citizenship, age, race and ethnicity, inclusive of traits historically associated with race or ethnicity, including but not limited to hair texture and protective hairstyles, color, religious creed, national origin, pregnancy, physical or mental disability, genetic information, protected Veteran status, or any other characteristic protected by federal and state law. For more information regarding your (EEO) rights as an applicant, please visit the following websites: ******************************************************************************************** As an Equal Employment Opportunity and Affirmative Action Employer for Protected Veterans and Individuals with Disabilities, applicants may request to review the plan of a particular ABB facility between the hours of 9:00 A.M. - 5:00 P.M. EST Monday through Friday by contacting an ABB HR Representative at **************. Protected Veterans and Individuals with Disabilities may request a reasonable accommodation if you are unable or limited in your ability to use or access ABB's career site as a result of your disability. You may request reasonable accommodations by calling an ABB HR Representative at ************** or by sending an email to ****************. Resumes and applications will not be accepted in this manner. While hourly pay rate is determined by things such as the successful applicant's qualifications and experience, this position is expected to pay between $93,800 and $174,200 and is eligible for bonus. ABB Benefit Summary for eligible US employees [excludes ABB E-mobility, Athens union, Puerto Rico] Go to MyBenefitsABB.com and click on “Candidate/Guest” to learn more Health, Life & Disability Choice between two medical plan options: A PPO plan called the Copay Plan OR a High Deductible Health Plan (with a Health Savings Account) called the High Deductible Plan. Choice between two dental plan options: Core and Core Plus Vision benefit Company paid life insurance (2X base pay) Company paid AD&D (1X base pay) Voluntary life and AD&D - 100% employee paid up to maximums Short Term Disability - up to 26 weeks - Company paid Long Term Disability - 60% of pay - Company paid. Ability to “buy-up” to 66 2/3% of pay. Supplemental benefits - 100% employee paid (Accident insurance, hospital indemnity, critical illness, pet insurance Parental Leave - up to 6 weeks Employee Assistance Program Health Advocate support resources for mental/behavioral health, general health navigation and virtual health, and infertility/adoption Employee discount program Retirement 401k Savings Plan with Company Contributions Employee Stock Acquisition Plan (ESAP) We value people from different backgrounds. Could this be your story? Apply today or visit *********** to read more about us and learn about the impact of our solutions across the globe.

Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect, protect, and purify our world. Summary of Responsibilities: The Quality Manager is a key member of the Operations Leadership Team responsible for ensuring the effective implementation of the Quality Management System and delivery of Customer satisfaction. Primary Responsibilities: * Act as a member of the site leadership teams, promoting a culture of safety, quality and fostering the Mativ leadership behaviors in support of delivery of site KPIs. * Ensure the effective implementation of the site Quality Management Systems and compliance with external system and product certifications, including ISO 9001, overseeing the Internal Audit program, and conducting routine reviews with Management to manage risks, gaps and drive continuous improvement. * Support the evaluation and onboarding of new business and product changes with respect to meeting all quality and regulatory requirements, such as quality agreements, product specifications, validations, and supplier and supplied material qualification. * Provide oversite for manufacturing product quality, including risk assessments, raw material quality, product specification process, laboratory and test equipment oversite, qualification and execution of product testing/verification, and nonconforming product management. * Oversee the site supplier quality program, including ongoing monitoring of suppliers, Supplier Corrective Action Requests, post market change control, and continual improvement of the supply chain quality. * Responsible for the execution of the customer complaints and CAPA processes, ensuring thorough investigations, corrective and preventative actions, and communication to internal and external stakeholders. * Oversee the operations post market change control process to ensure all changes are managed based on risk and in a compliant manner. * Lead a team of 3-10 team members, in the Quality Assurance and Quality Control areas, providing development and performance feedback - establishing the quality resource plan, defining work scope, setting annual objectives, and supporting individual development priorities. * Participate as a team member of a global quality organization to share, develop and implement best practices in a systematic and scalable manner. Essential Skills / Experience / Qualifications: * BS in the Sciences, e.g., Chemical Engineering, Mechanical Engineering, Natural Sciences, Biomedical Engineering, or equivalent. * 10 years of manufacturing experience, with at least 3 years experience in Manufacturing Quality Assurance Management role * Experienced Auditor * Proficient with business and technical software such as ERPs, Minitab, electronic Quality Management Systems Preferred Skills / Experience / Qualifications Strong problem solving, quantitative, and analytical skills. Six Sigma or ASQ Certification a plus Highly motivated and self-directed to enable success in working in a matrix reporting environment. * Experience with standards and regulations related to ISO 13485, ISO/TS 16949 * Certified Auditor * LSS Black Belt WHAT WE OFFER At Mativ, our benefits reflect how much we value and care for each other. We know that employees and their families have unique needs, so our comprehensive benefits offer flexibility, quality, and affordability. Here are just a few of the ways we support your well-being and that of your loved ones: * Medical, dental and vision insurance * Consumer-Driven Health Plan (CDHP) * Preferred Provider Organization (PPO) * Exclusive Provider Organization (EPO) * Company-paid basic life insurance and Additional voluntary life coverage * Paid vacation and competitive personal time off * 401(k) savings plan with company match * Employee assistance programs - available 24/7 to you and your family * Wellness and Work Life Support - career development and educational assistance ABOUT MATIV Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible. Mativ and its subsidiaries are Equal Opportunity Employers. Qualified applicants will be considered without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

The Quality Control Manager is responsible for establishing and overseeing quality control processes to ensure the safe and consistent production of bakery products, including bread and cake. This role includes managing inspections from raw material intake to production and finished product shipping, while addressing any quality or food safety issues. The role also encompasses supplier management, food regulatory compliance, labeling, and the inspection of materials and products. ESSENTIAL JOB FUNCTIONS: The Quality Control Manager will be responsible for, but not limited to, the following: · Respond to food safety and quality issues related to the production of 50100 types of bakery products (bread and cake). · Manage and oversee process controls to ensure that quality inspectors can record and analyze inspection results in the SAP system. · Develop and maintain food safety programs such as SQF and HACCP to proactively prevent food safety incidents. · Establish and maintain infrastructure for microbiological analysis and baking test labs for bakery items. · Lead internal, customer, and government responses in the event of a food safety issue. QUALIFICATIONS: · BA/BS degree in Food Science, Food Engineering, or a related field; equivalent experience may be considered. · Minimum of 8 years of hands-on experience in quality control within the food or bakery industry. · Strong communication and reporting skills, both verbal and written. · Demonstrated passion for quality control and bakery product excellence. · Bilingual in English and Korean strongly preferred. · Experience with SAP or similar ERP systems is a plus. · Familiarity with food safety regulations and global standards (e.g., HACCP, GMP, FSMA) EMPLOYEE BENEFITS: · Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date. · Life Insurance (Company 100% paid) · Flexible Time (starting time can vary everyday) · Short Term and Long-Term Disability Leave (short term 100% covered) · Lifestyle Allowance (up to net $70 per Month) · Cellphone reimbursement eligible · Employee Discounts (40% off Company products & services) · 401(k) 5% Match (no vesting period!) from Day 1 · Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier. · Wellness Day: 40 Hours (Use it or Lose it System) · Paid Maternity Leave (paid 100% for 12 weeks) · Paid Secondary Caregiver Leave (up to 2 weeks) · Paid Creative Leave · Paid Holidays (11 days) · Educational Benefit · Employee Club Activities · & Much More!

The name Astemo stands for Advanced Sustainable Technologies for Mobility , reflecting our mission to deliver safe, sustainable, and comfortable mobility through innovative technologies that support a more advanced and sustainable society. Our people are central to that mission, and we're proud to be an equal opportunity employer. We believe in the value of diverse experiences and backgrounds. We hire people who bring fresh perspectives and a commitment to excellence. If you're looking to shape the future of mobility, we invite you to be part of our journey. We're currently hiring for the role of Quality Manager at our Georgia facility. Key Responsibilities Lead and manage the Astemo Georgia Quality Assurance System, ensuring alignment with corporate standards and customer expectations. Oversee the corrective action process and analyze customer and regulatory requirements to evaluate their impact on internal quality systems. Represent customer interests internally and ensure quality standards are understood and met across the plant. Define and monitor plant-level quality objectives, driving continuous improvement. Develop and implement quality control programs to ensure incoming materials and finished products meet specifications. Coordinate internal, customer, and third-party audits, ensuring prompt and effective resolution of non-conformities. Serve as the primary contact for customer and supplier quality representatives, ensuring concerns are addressed with proper corrective action. Lead and manage the Quality Assurance department, including setting direction for staffing, budgeting, and process improvement. Develop training materials and qualify personnel involved in specialized quality processes. Oversee the calibration and testing programs that support production operations. Maintain inspection records and prepare reports on trends, issues, and improvements for executive management. Continuously evaluate and improve procedures, tools, and standards to maintain high product quality. Required Qualifications Bachelor's degree in Engineering or a related field. Minimum 5 years of experience in Quality Assurance within the automotive industry. In-depth knowledge of IATF/ISO standards and internal quality systems. Strong familiarity with GD&T and various measuring instruments. Experience with statistical process control and documentation methods. Proven ability to lead and manage quality teams. Strong written and verbal communication skills. Excellent attention to detail and ability to prioritize multiple tasks. Proficient in Microsoft Word, Excel, and PowerPoint; knowledge of Microsoft Access is a plus. Supervisory Responsibilities Directly manage a team including quality technicians, supervisors, and engineers. Working Conditions Primarily an office-based role with routine access to manufacturing areas. Must be able to sit for extended periods; occasional lifting of up to 35 pounds. Some work will be in production zones where personal protective equipment, including steel-toe shoes, is required. Additional Information We only consider complete applications. Final candidates must successfully complete a background check and drug screening. Astemo is an Equal Opportunity Employer. We welcome candidates of all genders, backgrounds, and abilities. Equal Opportunity Employer (EOE) - Qualified applicants will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender, identity, disability, protected veteran status and national origin. At Astemo, we're challenging the status quo with the power of diversity, inclusion, and collaboration. Our goal is to build an inclusive work environment that celebrates the differences of our employees. We want to ensure that every employee feels valued, respected and empowered. We don't just accept difference-we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. Astemo is proud to be an equal opportunity employer. If you need a reasonable accommodation to apply for a job at Astemo, please send the nature of the request and contact information to ************************* when applying for the position.

Energy, it defines LanceSoft. Consider our unique ‘keep apace' operational culture, the spirited lot of hand-picked professionals, our ‘up-to-the-minute' knowledge base, together they form a dynamic mix of value-generating characteristics that help us delve into the heart of a problem to deliver precise services and solutions - repeatedly. In business since 2000, LanceSoft is a reputed and credible Contingent Workforce Management Services firm that has established itself as a pioneer in providing highly scalable workforce solutions and exceptionally competent global Pharmaceutical & IT services to a diverse set of customers across various industries around the globe. LanceSoft is headquartered out of the Washington DC Metropolitan (Herndon, VA) and operates out of various locations in the US, Canada and India. LanceSoft specializes in recruiting and retaining top clinical research & scientific talent for leading pharmaceutical and biotech companies. Our staff maintains a commitment to excellence by developing lasting and professional relationships with both hiring managers and job seekers throughout the industry. Our dedicated & professional Account Management and experienced delivery team is well versed in industry specific requirements and market trends. We provide staffing solutions specializing in all areas of the clinical development process for the Pharmaceutical, Biotechnology, and Medical Device industries. We understand the clinical trial process from Phase I through Phase IV. We provide the most experienced, highly screened candidates on a contract, contract to hire, or permanent hire basis. Our Clientele: Johnson & Johnson, Merck, Pfizer, Novartis, Purdue, Eisai, Aetna, Becton & Dickinson, Actavis Pharmaceutical, Shire Pharmaceutical. Follow up on LinkedIn and keep up to date with our newest and hottest openings. Job Title: Supplier Quality Manager Detailed Job Description: • Coordinate completion of Specification Agreements with suppliers. • Coordinate completion of Quality Agreements with suppliers. • Perform actions associated with Change Control documents and Corrective/Preventive Acton's (CAPA); including ownership of these records. • Provide updates to Supplier Records on behalf of account owners. • Complete Supplier data for metrics and risk management documents. • Manage low risk (low criticality) supplier accounts as needed. • Support Supplier Quality projects as needed. • Establish information for supplier updates in SAP. • Perform supplier risk assessments (paper-based). • Support documentation activities for delisting of suppliers. • Perform assessments for leveraging of existing audits. • Assist in audit preparation to enable a Third Party Auditor to perform supplier audits. Qualifications Requirements: • cGMP (Current Good Manufacturing Practices) knowledge and experience. • Supplier Quality experience preferred. • Computer skills - database entry, MS Office applications (Word/Excel), general electronic application use. • Self-motivated. • Works both individually and in a team. • Effective communication; capable to coordinate with suppliers and internal departments. Additional Information • Full-time: 40 hours per week/(5 days/8 hours) • Periodically accessible to either Athens, GA, Horsham, PA, or Raritan, NJ office locations. All your information will be kept confidential according to EEO guidelines.

The QA/QC Manager will oversee the quality assurance and quality control functions to ensure that all products meet the specified standards and customer requirements. Develop and implement quality management systems in compliance with IATF 16949/ISO 9001 and ISO 14001 standards. Provide leadership and guidance to the QC team, manage quality audits, and drive continuous improvement initiatives. Ensure that the testing area is maintained efficiently, and that all data is accurately recorded. Job Status This is an exempt position with the company. You will be responsible for supervising the QC team and all QA functions reporting directly to the Engineering Director. General Accountabilities Manage and oversee all quality assurance and quality control activities. Develop and implement quality management policies and procedures. Lead and mentor QC staff, providing training and development opportunities. Conduct regular audits to ensure compliance with ISO standards and other regulatory requirements. Analyze quality data to identify trends, issues, and opportunities for improvement. Collaborate with other departments to resolve quality issues and improve processes. Ensure that the testing area is maintained efficiently and remains compliant with safety and environmental regulations. Maintain accurate records of quality assurance activities, including inspections, tests, and corrective actions. Coordinate and oversee the calibration and maintenance of monitoring and measuring devices. Ensure adherence to OSHA safety regulations and environmental regulations (ISO 14001). Prepare and present quality reports and metrics to senior management. Participate in management meetings and provide input on quality-related topics. Drive continuous improvement initiatives to enhance product quality and operational efficiency. Ensure that all QC procedures and documentation are up-to-date and accurately reflect current practices. Assist in the development of new product quality standards and testing methods. The company reserves the right to add or change duties at any time. Work Environment This job operates in a manufacturing environment subject to OSHA and Environmental regulations. This company is ISO 9001 and 14001 certified. You must be able to comply with all regulations. Physical Requirements You are required to lift heavy items between 25 to 50 pounds in accordance with OSHA requirements. You are required to be able to bend, stoop, walk, and stand throughout your shift. You are required to work independently or as a member of a team as required. Job Qualifications Education: Bachelors degree in a relevant field or equivalent experience. Certification: Relevant quality management certifications (e.g., Six Sigma, Internal Auditor) preferred. Experience: 5 years of related experience, including supervisory experience in a QA/QC role. Demonstrated ability to interpret quality documentation and understand compliance requirements. Proven track record of managing quality processes and driving continuous improvement. Skills Computer: Proficiency in Microsoft Office (Word, Excel, PowerPoint). Excellent verbal and written communication skills. Strong leadership and team management abilities. Ability to analyze complex data and make informed decisions. Strong attention to detail and problem-solving skills. Punctuality and adherence to deadlines are essential. Demonstrated commitment to high professional ethical standards. This job description is not intended to be an all-inclusive of every duty and responsibility that will be required of an employee in this position. Additional duties can be assigned at any time deemed necessary by Management.

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.

Job Description The Quality Control Manager is responsible for establishing and overseeing quality control processes to ensure the safe and consistent production of bakery products, including bread and cake. This role includes managing inspections from raw material intake to production and finished product shipping, while addressing any quality or food safety issues. The role also encompasses supplier management, food regulatory compliance, labeling, and the inspection of materials and products. ESSENTIAL JOB FUNCTIONS: The Quality Control Manager will be responsible for, but not limited to, the following: Respond to food safety and quality issues related to the production of 50-100 types of bakery products (bread and cake). Manage and oversee process controls to ensure that quality inspectors can record and analyze inspection results in the SAP system. Develop and maintain food safety programs such as SQF and HACCP to proactively prevent food safety incidents. Establish and maintain infrastructure for microbiological analysis and baking test labs for bakery items. Lead internal, customer, and government responses in the event of a food safety issue. QUALIFICATIONS: BA/BS degree in Food Science, Food Engineering, or a related field; equivalent experience may be considered. Minimum of 7 years of hands-on experience in quality control within the food or bakery industry. Strong communication and reporting skills, both verbal and written. Demonstrated passion for quality control and bakery product excellence. Bilingual in English and Korean strongly preferred. Experience with SAP or similar ERP systems is a plus. Familiarity with food safety regulations and global standards (e.g., HACCP, GMP, FSMA) EMPLOYEE BENEFITS: Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date. Life Insurance (Company 100% paid) Short Term and Long-Term Disability Leave (short term 100% covered) Lifestyle Allowance (up to net $70 per Month) Cellphone reimbursement eligible Employee Discounts (40% off CJ products & services) 401(k) 5% Match (no vesting period!) from Day 1 Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier. Wellness Day: 40 Hours (Use it or Lose it System) Paid Maternity Leave (paid 100% for 12 weeks) Paid Secondary Caregiver Leave (up to 2 weeks) Paid Creative Leave Paid Holidays (11 days) Educational Benefit Employee Club Activities & Much More!

As a Warehouse Quality Assurance Administrator, you'll monitor and evaluate inventory control processes and procedures. You'll lend your talents to verifying inventory accuracy in Best Buy distribution centers, delivery pads and service depots. Using established procedures, you'll also audit receiving, shipping and warehousing operational processes. To help us improve our practices, you'll report your audit results to the relevant supply chain leaders. What you'll do * Assist in monitoring inventory discrepancies, diagnosing problems, developing recommendations and requesting inventory adjustments * Advise warehouse staff and managers regarding concerns, potential issues, opportunities and operational recommendations * Communicate with corporate teams regarding inventory discrepancies and progress towards resolution * Provide training assistance related to procedural processes, systems knowledge and inventory management to warehouse employees * Help maintain clean work areas by removing empty pallets, sweeping and cleaning up boxes and other debris Preferred qualifications * Able to lift up to 75 pounds with or without reasonable accommodation * Able to stand, sit and walk for long periods of time * Proper training and certification on necessary equipment * Experience with inventory, warehousing or general office responsibilities What's in it for you We're committed to helping our people thrive at work and at home. We offer generous benefits that address your total well-being and provide support as you need it, especially key moments in your life. Our benefits include: * Competitive pay * Generous employee discount * Financial savings and retirement resources * Support for your physical and mental well-being About us As part of the Best Buy team, you'll help us fulfill our purpose to enrich lives through technology. We bring that to life every day by humanizing and personalizing tech solutions for every stage of life - in our stores, online and in customers' homes. Our culture is built on deeply supporting and valuing our amazing employees who make it all possible. We're committed to being a great place to work, where you can unlock unique career possibilities. Above all, we aim to provide a place where you can bring your full, authentic self to work now and into the future. Tomorrow works here. Best Buy is an equal opportunity employer. Application deadline: Minimum of 5 days from the posting date. You can find that date above the job title at the top of the page. Auto Req. ID1012386BR Location Number 000618 ATLANTA - SVC Address 1605 BROADMOOR BLVD STE 905$17.16 - $26.3 /hr Pay Range $17.16 - $26.3 /hr

medmix is a global leader in high-precision delivery devices. We occupy leading positions in the healthcare, consumer, and industrial end-markets. Our customers benefit from our dedication to innovation and technological advancement that has resulted in over 900 active patents. Our 14 production sites worldwide, together with our highly motivated and experienced team of nearly 2'600 employees provide our customers with uncompromising quality, proximity, and agility. medmix is headquartered in Baar, Switzerland. Our shares are traded on the SIX Swiss Exchange (SIX: MEDX). **************** As Quality Control Manager, you will be responsible for managing incoming, in-process and final inspections for the manufactured product(s) for the Quality Control laboratory. Job Description Main Accountabilities and tasks Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office The Manager, Quality Control Bioanalytical & Analytical Transfer provides leadership and scientific and technical expertise for QC and transfer activities These activities include the timely qualification of in-process and release testing of drug delivery systems, qualification/validation of analytical methods for support of cGMP manufacturing, and the transfer and validation of assay methods from clients and/or Assay Development & Analytics to the cGMP QC testing laboratory The manager ensures cGMP compliance, operates within budgets, and supervises bioanalytical lab staff directly and QC scientists and technicians indirectly Review and approval of customer manufacturing batch record Responsibilities include hiring, training, goal setting, and performance evaluation The manager collaborates with departments and project teams for planning and timelines, improves QC services, and maintains safe working conditions Additionally, the manager serves as the primary technical liaison with clients and Regulatory Bodies Lead all aspects of and drive the Bioanalytical lab operational readiness plan to ensure on-time approval of analytical equipment and test methods needed for GMP testing Build a trained, competent team of QC analysts to support GMP testing Coordinate any required daily Quality Control activities Ensure compliance, accuracy, and timeliness of testing processes Lead the introduction of new technology, equipment, methodologies, and validations Provide QC leadership and support across the organization Hire and develop employees within the department Assign work, coach staff, and take vital disciplinary actions Serve as primary QC Bioanalytical contact for regulatory inspections and client audits Provide support for method qualification and validation from Assay Development and Analytics and/or clients Provide frequent overall departmental feedback to senior management Ensure adequate staffing is hired and trained Qualifications Work Experience: 5-7 years of experience manufacturing in a highly regulated quality control lab environment. Education: Bachelor's degree Other: Experience with writing Deviations, Lab investigations, and OOS required; experience with Root Cause Analysis required Experience with regulatory inspections from the FDA, EMA, Notified Body, or other regulatory authorities required Capable of writing reports, business correspondence, and procedure manuals Strong organizational skills with the ability to prioritize and lead through complex processes/projects Ability to read, analyze, and interpret business periodicals, common scientific, professional, and technical journals, financial reports, governmental regulations, and legal documents Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community Ability to effectively present information to employees, top management, public groups, and/or boards of directors Ability to interpret and carry out an extensive variety of technical instructions in written, oral, schedule, mathematical, or diagram form Ability to define problems, collect data, establish facts, and draw valid conclusions Ability to apply principles of logic or scientific thinking to a wide range of intellectual and practical problems Able to lead abstract and concrete variables in situations where only limited standardization exists Communication skills, both oral and written, as required to communicate effectively with others at all levels in the organization and to provide clear and concise reports and policies as needed. Ability to effectively present information publicly. Ability to work well with subordinates, peers, and superiors in all departments. Additional Information Benefits we offer: An innovative, vibrant and agile culture Growth opportunities in a globally successful and dynamic business on a growth trajectory Excellent employee benefits including: Medical, dental, vision, Life/AD&D, Short- and Long-Term Disability Employee Savings Plan / 401k with 100% employer match

Transdev in Norcross, GA is hiring a Quality Assurance Manager. The Quality Assurance Manager is responsible for collecting, researching, and documenting all compliments, grievances, and feedback from callers regarding transportation services. We are seeking customer service-oriented professionals who are dedicated to safety. Transdev is proud to offer: Competitive compensation package of minimum $56,000 - maximum $70,000 Benefits include: + Vacation: minimum of two (2) weeks + Sick days: 5 days + Holidays: 12 days; 8 standard and 4 floating + Other standard benefits: 401(k) retirement plan, medical, dental and vision, life insurance, short-term disability, voluntary long-term disability. Benefits may vary depending on location policy. The above represents the standard Corporate Policy. Key Responsibilities: + Ensure overall quality in bus conditions, operator attendance, missed service and service interruptions + Monitor Bus Operator safety & security compliance, service delivery at sites and pre-determined passenger boarding and alighting points. + Other duties as required. Qualifications: + High School Diploma or GED required. + Computer literate with working knowledge of Word, Excel, and PowerPoint. + Excellent customer service & communication skills. + Subject to DOT drug testing and physical if applicable. DOT Regulation 49 CFR Part 40 does not authorize the use of Schedule I drugs, including cannabis, for any reason. Physical Requirements: + Must be able to work shifts or flexible work schedules as needed. + The employee is generally subjected to long periods spent sitting, typing, or looking at a computer screen. + Work environment will be a combination of both indoors and outdoors. About Transdev: Cities, counties, airports, companies, and universities across the U.S. contract with Transdev to operate their transportation systems, maintain their vehicle and fleets, and deliver on mobility solutions. Transdev U.S. employs a team of 32,000 across 400 locations while maintaining more than 17,000 vehicles. Part of a global company, Transdev is a leader in mobility with operations in 19 countries, proudly operated by 110,000 team members from around the world. As an operator and global integrator of mobility, we are driven by our purpose. Transdev - the mobility company - empowers the freedom to move every day thanks to safe, reliable, and innovative solutions that serve the common good. Find out more at ****************** or watch an overview video at ******************* O5cv0G4mQ The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. 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 upon request. Transdev is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, gender identity, sexual orientation, religion or other legally protected status. 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 upon request. California applicants:Please Click Here for CA Employee Privacy Policy. Job Category: Maintenance Management & Supervisory Job Type: Full Time Req ID: 6672 Pay Group: ZTT Cost Center: 450 The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. 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 upon request. Transdev is an Equal Employment Opportunity (EEO) employer and welcomes all qualified applicants. Applicants will receive fair and impartial consideration without regard to race, sex, color, national origin, age, disability, veteran status, genetic data, gender identity, sexual orientation, religion or other legally protected status, or any other classification protected by federal, state, or local law. Drug-free workplace If based in the United States, applicants must be eligible to work in U.S. without restrictions for any employer at any time; be able to pass a drug screen and background check. California applicants: Please Click Here for CA Employee Privacy Policy. About Transdev Cities, counties, airports, companies, and universities across the U.S. contract with Transdev to operate their transportation systems, maintain their vehicle and fleets, and deliver on mobility solutions. Transdev U.S. employs a team of 32,000 across 400 locations while maintaining more than 17,000 vehicles. Part of a global company, Transdev is a leader in mobility with operations in 19 countries, proudly operated by 110,000 team members from around the world. As an operator and global integrator of mobility, we are driven by our purpose. Transdev - the mobility company - empowers the freedom to move every day thank to safe, reliable, and innovative solutions that serve the common good. Find out more at http://****************** or watch an overview video.

The Company Zurn Elkay Water Solutions Corporation is a thriving, values-driven company focused on doing the right things. We're a fast growing, publicly traded company (NYSE: ZWS), with an enduring reputation for integrity, giving back, and providing an engaging, inclusive environment where careers flourish and grow. Named by Newsweek as One of America's Most Responsible Companies and an Energage USA Top Workplace, at Zurn Elkay Water Solutions Corporation, we never forget that our people are at the center of what makes us successful. They are the driving force behind our superior quality, product ingenuity, and exceptional customer experience. Our commitment to our people and their professional development is a recipe for success that has fueled our growth for over 100 years, as one of today's leading international suppliers of plumbing and water delivery solutions. Headquartered in Milwaukee, WI, Zurn Elkay Water Solutions Corporation employs over 2800 employees worldwide, working from 24 locations across the U.S., China, Canada, Dubai, and Mexico, with sales offices available around the globe. We hope you'll visit our website and learn more about Zurn Elkay at zurnelkay.com. If you're ready to join a company where what you do makes a difference and you have pride in the work you are doing, talk to us about joining the Zurn Elkay Water Solutions Corporation family! If you are a current employee, please navigate here to apply internally. Quality Supervisor is responsible for overseeing the inspection and testing of products to ensure they meet specified standards. This role involves managing a team of quality control inspectors, documenting inspection outcomes, and implementing process improvements to enhance product quality. The Quality Supervisor must have a keen eye for detail, excellent problem-solving skills, and the ability to train and develop team members. They play an essential role in maintaining the company's reputation for high-quality products and services. Quality Supervisor Responsibilities & Duties Supervise and lead the quality control team. Develop and implement quality control procedures and policies. Inspect and test products to ensure they meet quality standards. Document inspection outcomes and maintain accurate records. Identify and address recurring quality issues. Collaborate with production teams to resolve quality concerns. Analyze data to identify trends and areas for improvement. Ensure compliance with industry regulations and company standards. Train and mentor quality control inspectors. Conduct regular audits and reviews of quality control processes. Quality Supervisor Qualifications & Skills Bachelor's degree in Quality Management, Engineering, or a related field. Certification in Quality Control (e.g., Six Sigma, ISO 9001). 5+ years of experience in a quality control or assurance role. Proficiency in quality control software and data analysis tools. Strong Gd&T Training Strong leadership and team management skills. Excellent written and verbal communication skills. Experience with process improvement methodologies. Knowledge of industry-specific quality standards. High school diploma or equivalent; degree in a related field preferred. Previous experience in quality control or a related role. Strong attention to detail and problem-solving skills. Ability to interpret technical documents and specifications. Proficient in Microsoft Office Suite and quality control software. Excellent organizational and time management skills. Strong communication and interpersonal skills. Ability to work independently and as part of a team. Familiarity with industry-specific standards and regulations. People Management Skills Total Rewards and Benefits Competitive Salary Medical, Dental, Vision, STD, LTD, AD&D, and Life Insurance Matching 401(k) Contribution Health Savings Account Up to 3 weeks starting Vacation (may increase with tenure) 12 Paid Holidays Annual Bonus Eligibility Educational Reimbursement Matching Gift Program Employee Stock Purchase Plan - purchase company stock at a discount! **THIRD PARTY AGENCY: Any unsolicited submissions received from recruitment agencies will be considered property of Zurn Elkay, and we will not be liable for any fees or obligations related to those submissions.** Equal Opportunity Employer - Minority/Female/Disability/Veteran

Job Description Position Description: The Quality Control Manager is an essential part of CSPC Solution's team at the Federal Law Enforcement Training Center in Glynco, GA. Our team assists with the vital training of federal law enforcement officers and as a member, you'll reap the satisfaction of knowing you contribute to the safety of the Nation on a daily basis. Duties will include supervising the safety and performance quality of role players participating in realistic law enforcement training scenarios. The Quality Control Manager is responsible for observing role player activities and formulating reports and recommendations to address performance shortfalls or safety hazards. The Quality Control Manager is a detail-oriented individual with the professionalism and maturity to execute the mission to a high standard without direct supervision. Typical work hours will be 7:30 to 5:30, Monday through Friday, but may adjust on occasion in response to customer demands. This is a fulltime position and includes benefits plan enrollment, including the option to participate in CSPC's 401K contribution matching plan. Required Qualifications: -18 years of age or older and legally authorized to work in the U.S. -Capable of passing a criminal history background screening -Minimum of five years' experience in a Quality Control or related position -Experience at FLETC or performing Quality Control and Assurance in a similar training environment is highly preferred -Law Enforcement or Military experience is highly preferred

About the role: WEG Electric Corp. has an excellent opportunity for a Quality Technician. The position will be responsible for acting in the internal quality and service investigation processes, performing technical analysis of products that failed in the field or at the customer's line and other related non-conforming product evaluations. These investigations might include the use of measurement systems, mechanical and/or electrical devices. Also responsible for training new quality and service employees to help them developing skills to understand better the types of failures they might see within our products. Primary Responsibilities: Coordinate field failure analysis, and report the results to the Engineers in an organized and summarized way containing all key points. Maintain all records of these analysis updated on SAP for the correct assessment of our internal KPIs. Support repairs, inspections and containments whenever necessary and make sure they use adequate quality records. Establish a good network with all the supporting areas (Sales, After Sales, Warehouse, Mod Shop etc.) to help on any problem-solving process. Collaborate with the Service Team on data collection for any problem-solving initiative. Participate on cross-functional teams to evaluate quality issues. Monitor their respective KPIs and report issues to the management team whenever necessary. Education: (minimum education or equivalent in relevant experience) Field of Study if required: Bachelor of Science in Electrical, Mechanical Engineering Knowledge / training: Strong analytical and problem-solving skills required. Demonstrated 5S skills required. Proficiency with Microsoft Office suite (Word, Excel, PowerPoint, Outlook). Experience and knowledge of electric motors strongly desired. Familiarity with shop tools and equipment desired. Must be eager to learn new technologies and techniques. Must be able to frequently sit and/or stand for long periods of time. Experience: 1-4 years of relevant work experience with LV and/or MV motors About WEG Electric Corp. WEG is the largest industrial electric motor manufacturer in the Americas and one of the largest manufacturers of electric motors in the world producing more than 21 million units annually. Founded in 1961, WEG operates mainly in the sector of capital goods, having five main businesses: Motors, Energy, Automation, Coatings Transmission & Distribution, providing global solutions for electric motors, variable frequency drives, soft starters, controls, panels, transformers, and generators. The US corporate office is located in Duluth, GA with manufacturing units in Minnesota, Indiana and Missouri with over 30 thousand employees worldwide. Visit our website to learn more: *********** We offer a pleasant work environment, competitive compensation and full benefits package. To Apply: All candidates must submit an updated resume and complete our application in order to be considered for this position. You must be authorized to work in the United States without sponsorship. WEG does not offer visa sponsorship for this role. We are proud to be an Equal Opportunity/Affirmative Action employer. Qualified applicants will receive consideration for employment without regard to race, sex, disability, veteran, or other protected status.

The Quality Control Manager is responsible for establishing and overseeing quality control processes to ensure the safe and consistent production of bakery products, including bread and cake. This role includes managing inspections from raw material intake to production and finished product shipping, while addressing any quality or food safety issues. The role also encompasses supplier management, food regulatory compliance, labeling, and the inspection of materials and products. ESSENTIAL JOB FUNCTIONS: The Quality Control Manager will be responsible for, but not limited to, the following: Respond to food safety and quality issues related to the production of 50100 types of bakery products (bread and cake). Manage and oversee process controls to ensure that quality inspectors can record and analyze inspection results in the SAP system. Develop and maintain food safety programs such as SQF and HACCP to proactively prevent food safety incidents. Establish and maintain infrastructure for microbiological analysis and baking test labs for bakery items. Lead internal, customer, and government responses in the event of a food safety issue. QUALIFICATIONS: BA/BS degree in Food Science, Food Engineering, or a related field; equivalent experience may be considered. Minimum of 7 years of hands-on experience in quality control within the food or bakery industry. Strong communication and reporting skills, both verbal and written. Demonstrated passion for quality control and bakery product excellence. Bilingual in English and Korean strongly preferred. Experience with SAP or similar ERP systems is a plus. Familiarity with food safety regulations and global standards (e.g., HACCP, GMP, FSMA) EMPLOYEE BENEFITS: Health Insurance options: PPO Medical, Dental, Vision covered (Company 100% paid) *insurance starts on the very 1st date. Life Insurance (Company 100% paid) Flexible Time (starting time can vary everyday) Short Term and Long-Term Disability Leave (short term 100% covered) Lifestyle Allowance (up to net $70 per Month) Cellphone reimbursement eligible Employee Discounts (40% off company's products & services) 401(k) 5% Match (no vesting period!) from Day 1 Paid Time Off (generous and increases by tier!): Max ceiling of 180 hours PTO (15 days) the 1st year and increases by tier. Wellness Day: 40 Hours (Use it or Lose it System) Paid Maternity Leave (paid 100% for 12 weeks) Paid Secondary Caregiver Leave (up to 2 weeks) Paid Creative Leave Paid Holidays (11 days) Educational Benefit Employee Club Activities & Much More!

Energy, it defines LanceSoft. Consider our unique ‘keep apace' operational culture, the spirited lot of hand-picked professionals, our ‘up-to-the-minute' knowledge base, together they form a dynamic mix of value-generating characteristics that help us delve into the heart of a problem to deliver precise services and solutions - repeatedly. In business since 2000, LanceSoft is a reputed and credible Contingent Workforce Management Services firm that has established itself as a pioneer in providing highly scalable workforce solutions and exceptionally competent global Pharmaceutical & IT services to a diverse set of customers across various industries around the globe. LanceSoft is headquartered out of the Washington DC Metropolitan (Herndon, VA) and operates out of various locations in the US, Canada and India. LanceSoft specializes in recruiting and retaining top clinical research & scientific talent for leading pharmaceutical and biotech companies. Our staff maintains a commitment to excellence by developing lasting and professional relationships with both hiring managers and job seekers throughout the industry. Our dedicated & professional Account Management and experienced delivery team is well versed in industry specific requirements and market trends. We provide staffing solutions specializing in all areas of the clinical development process for the Pharmaceutical, Biotechnology, and Medical Device industries. We understand the clinical trial process from Phase I through Phase IV. We provide the most experienced, highly screened candidates on a contract, contract to hire, or permanent hire basis. Our Clientele: Johnson & Johnson, Merck, Pfizer, Novartis, Purdue, Eisai, Aetna, Becton & Dickinson, Actavis Pharmaceutical, Shire Pharmaceutical. Follow up on LinkedIn and keep up to date with our newest and hottest openings. Job Title: Supplier Quality Manager Detailed Job Description: • Coordinate completion of Specification Agreements with suppliers. • Coordinate completion of Quality Agreements with suppliers. • Perform actions associated with Change Control documents and Corrective/Preventive Acton's (CAPA); including ownership of these records. • Provide updates to Supplier Records on behalf of account owners. • Complete Supplier data for metrics and risk management documents. • Manage low risk (low criticality) supplier accounts as needed. • Support Supplier Quality projects as needed. • Establish information for supplier updates in SAP. • Perform supplier risk assessments (paper-based). • Support documentation activities for delisting of suppliers. • Perform assessments for leveraging of existing audits. • Assist in audit preparation to enable a Third Party Auditor to perform supplier audits. Qualifications Requirements: • cGMP (Current Good Manufacturing Practices) knowledge and experience. • Supplier Quality experience preferred. • Computer skills - database entry, MS Office applications (Word/Excel), general electronic application use. • Self-motivated. • Works both individually and in a team. • Effective communication; capable to coordinate with suppliers and internal departments. Additional Information • Full-time: 40 hours per week/(5 days/8 hours) • Periodically accessible to either Athens, GA, Horsham, PA, or Raritan, NJ office locations. All your information will be kept confidential according to EEO guidelines.

The QA/QC Manager will oversee the quality assurance and quality control functions to ensure that all products meet the specified standards and customer requirements. Develop and implement quality management systems in compliance with IATF 16949/ISO 9001 and ISO 14001 standards. Provide leadership and guidance to the QC team, manage quality audits, and drive continuous improvement initiatives. Ensure that the testing area is maintained efficiently, and that all data is accurately recorded. Job Status This is an exempt position with the company. You will be responsible for supervising the QC team and all QA functions reporting directly to the Engineering Director. General Accountabilities Manage and oversee all quality assurance and quality control activities. Develop and implement quality management policies and procedures. Lead and mentor QC staff, providing training and development opportunities. Conduct regular audits to ensure compliance with ISO standards and other regulatory requirements. Analyze quality data to identify trends, issues, and opportunities for improvement. Collaborate with other departments to resolve quality issues and improve processes. Ensure that the testing area is maintained efficiently and remains compliant with safety and environmental regulations. Maintain accurate records of quality assurance activities, including inspections, tests, and corrective actions. Coordinate and oversee the calibration and maintenance of monitoring and measuring devices. Ensure adherence to OSHA safety regulations and environmental regulations (ISO 14001). Prepare and present quality reports and metrics to senior management. Participate in management meetings and provide input on quality-related topics. Drive continuous improvement initiatives to enhance product quality and operational efficiency. Ensure that all QC procedures and documentation are up-to-date and accurately reflect current practices. Assist in the development of new product quality standards and testing methods. The company reserves the right to add or change duties at any time. Work Environment This job operates in a manufacturing environment subject to OSHA and Environmental regulations. This company is ISO 9001 and 14001 certified. You must be able to comply with all regulations. Physical Requirements You are required to lift heavy items between 25 to 50 pounds in accordance with OSHA requirements. You are required to be able to bend, stoop, walk, and stand throughout your shift. You are required to work independently or as a member of a team as required. Job Qualifications Education: Bachelors degree in a relevant field or equivalent experience. Certification: Relevant quality management certifications (e.g., Six Sigma, Internal Auditor) preferred. Experience: 5 years of related experience, including supervisory experience in a QA/QC role. Demonstrated ability to interpret quality documentation and understand compliance requirements. Proven track record of managing quality processes and driving continuous improvement. Skills Computer: Proficiency in Microsoft Office (Word, Excel, PowerPoint). Excellent verbal and written communication skills. Strong leadership and team management abilities. Ability to analyze complex data and make informed decisions. Strong attention to detail and problem-solving skills. Punctuality and adherence to deadlines are essential. Demonstrated commitment to high professional ethical standards. This job description is not intended to be an all-inclusive of every duty and responsibility that will be required of an employee in this position. Additional duties can be assigned at any time deemed necessary by Management.

medmix is a global leader in high-precision delivery devices. We occupy leading positions in the healthcare, consumer, and industrial end-markets. Our customers benefit from our dedication to innovation and technological advancement that has resulted in over 900 active patents. Our 14 production sites worldwide, together with our highly motivated and experienced team of nearly 2'600 employees provide our customers with uncompromising quality, proximity, and agility. medmix is headquartered in Baar, Switzerland. Our shares are traded on the SIX Swiss Exchange (SIX: MEDX). **************** As Quality Control Manager, you will be responsible for managing incoming, in-process and final inspections for the manufactured product(s) for the Quality Control laboratory. Job Description Main Accountabilities and tasks Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office The Manager, Quality Control Bioanalytical & Analytical Transfer provides leadership and scientific and technical expertise for QC and transfer activities These activities include the timely qualification of in-process and release testing of drug delivery systems, qualification/validation of analytical methods for support of cGMP manufacturing, and the transfer and validation of assay methods from clients and/or Assay Development & Analytics to the cGMP QC testing laboratory The manager ensures cGMP compliance, operates within budgets, and supervises bioanalytical lab staff directly and QC scientists and technicians indirectly Review and approval of customer manufacturing batch record Responsibilities include hiring, training, goal setting, and performance evaluation The manager collaborates with departments and project teams for planning and timelines, improves QC services, and maintains safe working conditions Additionally, the manager serves as the primary technical liaison with clients and Regulatory Bodies Lead all aspects of and drive the Bioanalytical lab operational readiness plan to ensure on-time approval of analytical equipment and test methods needed for GMP testing Build a trained, competent team of QC analysts to support GMP testing Coordinate any required daily Quality Control activities Ensure compliance, accuracy, and timeliness of testing processes Lead the introduction of new technology, equipment, methodologies, and validations Provide QC leadership and support across the organization Hire and develop employees within the department Assign work, coach staff, and take vital disciplinary actions Serve as primary QC Bioanalytical contact for regulatory inspections and client audits Provide support for method qualification and validation from Assay Development and Analytics and/or clients Provide frequent overall departmental feedback to senior management Ensure adequate staffing is hired and trained Qualifications Work Experience: 5-7 years of experience manufacturing in a highly regulated quality control lab environment. Education: Bachelor's degree Other: Experience with writing Deviations, Lab investigations, and OOS required; experience with Root Cause Analysis required Experience with regulatory inspections from the FDA, EMA, Notified Body, or other regulatory authorities required Capable of writing reports, business correspondence, and procedure manuals Strong organizational skills with the ability to prioritize and lead through complex processes/projects Ability to read, analyze, and interpret business periodicals, common scientific, professional, and technical journals, financial reports, governmental regulations, and legal documents Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community Ability to effectively present information to employees, top management, public groups, and/or boards of directors Ability to interpret and carry out an extensive variety of technical instructions in written, oral, schedule, mathematical, or diagram form Ability to define problems, collect data, establish facts, and draw valid conclusions Ability to apply principles of logic or scientific thinking to a wide range of intellectual and practical problems Able to lead abstract and concrete variables in situations where only limited standardization exists Communication skills, both oral and written, as required to communicate effectively with others at all levels in the organization and to provide clear and concise reports and policies as needed. Ability to effectively present information publicly. Ability to work well with subordinates, peers, and superiors in all departments. Additional Information Benefits we offer: An innovative, vibrant and agile culture Growth opportunities in a globally successful and dynamic business on a growth trajectory Excellent employee benefits including: Medical, dental, vision, Life/AD&D, Short- and Long-Term Disability Employee Savings Plan / 401k with 100% employer match

As a Warehouse Quality Assurance Administrator, you'll monitor and evaluate inventory control processes and procedures. You'll lend your talents to verifying inventory accuracy in Best Buy distribution centers, delivery pads and service depots. Using established procedures, you'll also audit receiving, shipping and warehousing operational processes. To help us improve our practices, you'll report your audit results to the relevant supply chain leaders. What you'll do Assist in monitoring inventory discrepancies, diagnosing problems, developing recommendations and requesting inventory adjustments Advise warehouse staff and managers regarding concerns, potential issues, opportunities and operational recommendations Communicate with corporate teams regarding inventory discrepancies and progress towards resolution Provide training assistance related to procedural processes, systems knowledge and inventory management to warehouse employees Help maintain clean work areas by removing empty pallets, sweeping and cleaning up boxes and other debris Preferred qualifications Able to lift up to 75 pounds with or without reasonable accommodation Able to stand, sit and walk for long periods of time Proper training and certification on necessary equipment Experience with inventory, warehousing or general office responsibilities What's in it for you We're committed to helping our people thrive at work and at home. We offer generous benefits that address your total well-being and provide support as you need it, especially key moments in your life. Our benefits include: Competitive pay Generous employee discount Financial savings and retirement resources Support for your physical and mental well-being About us As part of the Best Buy team, you'll help us fulfill our purpose to enrich lives through technology. We bring that to life every day by humanizing and personalizing tech solutions for every stage of life - in our stores, online and in customers' homes. Our culture is built on deeply supporting and valuing our amazing employees who make it all possible. We're committed to being a great place to work, where you can unlock unique career possibilities. Above all, we aim to provide a place where you can bring your full, authentic self to work now and into the future. Tomorrow works here.™ Best Buy is an equal opportunity employer. Application deadline: Minimum of 5 days from the posting date. You can find that date above the job title at the top of the page.