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Support manager in identifying business opportunities to grow the business while maintaining leadership, recognition and credibility in relevant technologies. Project management (personnel, tasks, budget, schedule), including familiarity with computerized tools.
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The company hiring for the Project Manager - Multifamily position is a well-established organization within the business services industry, known for its commitment to delivering quality construction projects. A successful Project Manager - Multifamily should have: A strong understanding of construction management principles and multifamily project execution.
The ideal candidate will have a proven track record in managing commercial construction projects within New England and ideally this person will have some level of exposure to healthcare projects as well. This highly reputable and award-winning firm serves both Rhode Island and the Greater Boston area, known for its versatile approach to construction projects.
p>We are seeking a highly motivated and experienced Business Development Manager focused on electronics repair services for the U.S. Navy and NAVSUP (Naval Supply System). We have undersea operations experience, combined with engineering and specific subject matter expertise, that provides an in-depth understanding of the problem and a novel, innovative and cost-effective solution.
The position partners closely with Operations, Quality, Supply Chain, and other cross-functional teams to ensure consistent product quality, regulatory compliance, and operational excellence. These products enable the production of microchips that power technologies such as artificial intelligence, electric vehicles, consumer electronics, and data infrastructure.
The organization plays a critical role in enabling technologies across AI, electronics, automotive, and digital infrastructure through high-performance, high-purity chemical manufacturing. The role blends technical depth, team leadership, and cross-functional collaboration to enhance site performance.
The role will serve as the primary commercial interface between the customer and the organization's global business units, coordinating strategy, growth initiatives, product expansion efforts, and executive-level relationships across multiple regions. Backed by substantial investment and long-term growth initiatives, the organization continues to expand its presence within the semiconductor materials market and is seeking a strategic commercial leader to support one of its most important global customer relationships.
Explore Uline.jobs to learn more!
Oversee the Inventory Control team, directing daily cycle counts to ensure warehouse inventory accuracy and strong performance.
div> Uline, a name millions of businesses across North America know and trust, is looking for an experienced Territory Sales Manager to build our growing Braintree, Massachusetts market. Explore Uline.jobs to learn more!
div> Uline, a name millions of businesses across North America know and trust, is looking for an experienced Sales Account Manager to build our growing Braintree, Massachusetts market. Explore Uline.jobs to learn more!
Placement in the range depends on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, relevant experience, skills, seniority, performance, shift, travel requirements, and business or organizational needs and may change over time. Reporting to the Quality Director, this person will be responsible for identifying opportunities for continuous improvement, formulating corrective and preventive actions, and working to implement those actions to improve quality levels and regulatory compliance.
Placement in the range depends on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, relevant experience, skills, seniority, performance, shift, travel requirements, and business or organizational needs and may change over time. Reporting to the Quality Director, this person will be responsible for identifying opportunities for continuous improvement, formulating corrective and preventive actions, and working to implement those actions to improve quality levels and regulatory compliance.
p>The ideal candidate must be able to lead through ambiguity, stabilize quality performance during supplier/process changes, support customer escalations, and develop a high-performing Quality Engineering team capable of sustaining IATF 16949 expectations, automotive core tools, product validation, traceability, and continuous improvement. The Quality Manager will ensure that quality processes are not only documented but effectively implemented on the manufacturing floor including control plans, quality gates, incoming inspection, process controls, layered audits, nonconformance management, APQP, PPAP, supplier qualification, and customer-specific requirements.
p>The Surgical Services Quality Manager, in collaboration with the Chief and Nursing Leadership for the Operating Room, is the third member of the surgical Triad team and works closely with members of the Surgical and Anesthesia departments to support the Chief in maintaining quality care within the acute care setting; the Surgical Services Quality Manager assists to integrate quality care across service lines through the tenets of the organizations Culture of Safety and care delivery model. This individual works with Service Chiefs to establish key metrics that will enhance surgical management and drive continuous improvements in patient outcomes, including reducing unexpected outcomes.
Maintains and improves product quality by completing product, system, compliance and surveillance audits; investigates customer complaints; collaborates with other departments (production, sales and purchasing) as needed. Prepares quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, corrective actions and re-validations.
p class="cs2654AE3A"/> This global manufacturing organisation offer the opportunity to join their established, friendly and successful team working at their Bristol facility.
p>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/.
The position supervises a QA staff and ensures that documentation and design controls are appropriate for regulatory agencies and customer requirements. Ensure that all products and related documents are properly handled within applicable QA, Engineering and other databases.
Your leadership will directly influence site performance, team development, customer satisfaction, and long-term business success, and it will be critical to supporting operational excellence, developing talent, and enabling continued growth at the site.
li>Ability to read English (to review and comprehend quality assurance reports, schematics/blueprints, quality procedures and policy manuals).
p>Quality Manager (Heavy Civil Construction) Providence RI, US US6680 Early career Construction Permanent.
Pay Transparency: The salary range for this role is $114,700 - $134,800 USD. If you have the courage to take on a wide variety of complex challenges, then you will experience a unique working environment where innovative teams blend different perspectives, disciplines, and technologies to discover new ways of solving complex problems.
li>Documentation and Reporting: Maintain detailed documentation of inspection findings, including photographs, data sheets, and non-conformance reports, and generate regular quality reports for project management.
p>Experience in children's residential or educational programs, adult residential or day habilitation services, or similar regulated human services with licensing, accreditation, and external oversight is preferred. Employees will be expected and required to perform all essential functions with or without accommodation.
p>• Bachelor's Degree (engineering or technical preferred) from an ABET accredited program • 6-10 years quality assurance-related experience • Proficient in Microsoft Office: Excel, Word, and PowerPoint • Experience working in an ISO 90000 manufacturing environment or equivalent • Demonstrated intermediate problem-solving skills - Root Cause Analysis/Problem Solving Methods (8-D, PDCA, DMAIC) • Demonstrated advanced problem-solving and training skills (Certified 6S Master Black Belt or equivalent) • Demonstrated knowledge of advanced Lean principles and methods (Certified Lean/6-Sig, Value Stream Mapping, RIE, Status Display) • Demonstrated basic understanding and training in at least three of the following areas: • Probability and Statistics • Industrial statistics (Cpk, MSA, SPC) • QA Tools (PPAP, FMEA, Control Plans) • Design of Experiments • Able to read, understand, and interpret technical drawings/documentation from three and able to create technical drawings/documentation in at least one of the following disciplines: • Pneumatics • Data acquisition/Gauging • Mechanical Design • Electronics and sensors • Chemical formula preparation. • Working knowledge of Injection Molding equipment and processes • Working knowledge of machined part equipment and processes • Working knowledge of advanced Lean principles and methods (Value Stream Mapping, RIE, Status Display, 6S, Continuous Flow) • Certified Six Sigma Green Belt/Black Belt • Certified quality engineer/Certified manager of quality/Organizational Excellence (CMQ/OE) • Demonstrates a passion and a responsibility for consumer • Exhibit a passion for the company's Essence, Global Imperatives, Corporate Direction • Desire to own decisions and take responsibility for outcomes • Willingness to continually embrace personal and professional development • Demonstrated exceptional written and oral communication skills • Experience in quality management systems • Experience in quality system audits.
p>As a Manager, Product Quality Clinician, you will be a member of Complaint Handling and Post Market Surveillance/Risk Management team to provide clinical guidance/clinical expert knowledge to Quality, Engineering and other cross functional teams to understand the nature of complaints and possible health risks. How you will make an impact:
Partnering closely with manufacturing, Central Quality, and key stakeholders, the Manager of Quality strengthens existing systems, launches new processes, and resolves manufacturing and product issues through data-driven insights. This role inspires and develops a team of Quality professionals, fostering a culture of accountability, high performance, and continuous learning while driving initiatives aligned with business objectives.
p>Lead and continuously improve the site Quality Management System (QMS) to support business strategy and operational excellence. Champion continuous improvement initiatives using Lean, Six Sigma, and structured problem-solving tools.
5-8 years of people management - food industry required (meat industry highly preferred) Working knowledge of USDA and FDA regulations Knowledge of Quality Management System (QMS), Total Quality Management (TQM) a plus Excellent communication skills (both oral and written) required Bilingual in Spanish or Portuguese a plus Proficient in Microsoft Office products required. OVERVIEW OF ROLE: As part of the management team, the Manager, Food Safety & Quality Assurance (FSQA) develops and implements food safety and quality assurance strategies, programs, policies, and procedures to ensure the highest levels of food safety and quality.
The Senior Manager leads managers and/or advanced individual contributors and partners with senior leadership to embed data‑driven decision‑making across the organization. This role is responsible for scaling analytics solutions that enable proactive Quality Compliance, regulatory readiness, and enterprise‑level risk management across the medical device lifecycle.
Unsolicited resumes or candidate information submitted to Emergent BioSolutions by search/recruiting agencies not already on Emergent BioSolutions' approved agency list shall become the property of Emergent BioSolutions and if the candidate is subsequently hired by Emergent BioSolutions, Emergent BioSolutions shall not owe any fee to the submitting agency. The incumbent serves as a key member of Site Quality Management, providing independent quality oversight, risk-based decision making, and leadership to ensure reliable supply of compliant vaccine drug substance.
li>Contribute to regulatory and technical documentation by reviewing QC data for accuracy, completeness, and traceability; verifying data transcription and data checks supporting regulatory submissions; and ensuring information is ready for inclusion in internal reports, APQRs, Module 3 submission-supporting documents, and responses to regulatory authorities. The selected candidate will work collaboratively with Analytical Quality Control leaders to assess laboratory conformance with cGMPs, and with CMC Regulatory Affairs and Quality Assurance to ensure the translational accuracy and integrity of data incorporated into Module 3 sections of CTD regulatory submissions and written responses to regulatory authorities.
Developing and managing sites' project plans for implementation of ECMP workstream outputs; + Tracking progress and ensuring execution according to plan; + Reporting sites' progress to ECMP Program Management Office (PMO); + Being responsible for ECMP documentation and schedule at sites; + Coordinating collaborative activities between sites' local activities; + Periodically reviewing the outputs from the sites' work stream activities to ensure it is aligned with requirements of the ECMP and individual site's project plan; + Facilitating resolution to issues. The Quality Compliance Manager, ECMP Site Facilitator will be traveling between our three (3) sites as needed (Añasco, Puerto Rico; Mansfield,MA; Cincinnati, OH occasionally) and the established on-site primary location needs to be Mansfield, MA.
li>Develop and support a culture of reflective practice among teachers;
This role is responsible for ensuring compliance with AS9100, ISO 9001, and applicable regulatory requirements while driving continuous improvement across manufacturing, inspection, supplier quality, and customer satisfaction. The ideal candidate will be a hands-on leader with strong aerospace quality experience who can balance compliance, execution, and process improvement in a fast-paced, regulated manufacturing environment.
p>ESSENTIAL DUTIES AND RESPONSIBILITIES. Lead and manage global Supplier Quality projects, ensuring structured planning, execution, tracking, and on-time delivery of key initiatives. The Project Manager partners with Quality, Regulatory, Operations, and IT to ensure effective execution, compliance, and continuous improvement of supplier quality processes.
Program Manager partners with Quality, Regulatory, Operations, Procurement, Supply Chain, and IT to ensure effective execution of strategic supplier quality initiatives, regulatory compliance, operational resilience, and continuous improvement across the supplier network. Program Manager, Supplier Quality Risk Management is responsible for leading and executing enterprise-wide supplier quality risk management initiatives across the global organization.
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