UNKNOWN

FEED

Job expectations include supporting the implementation of quality assurance and quality control processes within the LOB or ECF through ongoing monitoring and testing of controls, identifying issues and control improvements for remediation, and building out actions plans and milestones. Run regular routines with key stakeholders across GBGM AML Operations, Global Financial Crimes, Risk and Technology Demonstrate strong collaboration, influencing, and relationship management skills.

Bank of America

Global AML Operations - Business Control Mgr

With ~100,000 dedicated employees in more than 90 countries, we develop the energy systems of the future, ensuring that the growing energy demand of the global community is met reliably and sustainably. This role offers a unique opportunity to accelerate your technical development through hands-on training and collaboration with experienced manufacturing teams across Siemens Energy's global network.

Siemens Energy AG

Manufacturing Supervisor - Large Power Transformers (P)

Required to travel regularly to local and regional project sites (typically within South Carolina and surrounding states), potentially including overnight stays and perform extensive fieldwork under varying environmental conditions, including adverse weather, uneven terrain, and potentially hazardous environments, while adhering strictly to health and safety protocols. These projects span a multitude of quality assurance support roles, from geotechnical exploration in support of design development to quality assurance testing and documentation during construction, as well as some longer-term monitoring of containment systems, groundwater and gas monitoring support, stability analysis, and more.

BUNNELL LAMMONS ENGINEERING

Staff Associate - Regional Quality Assurance

clearcompany

FULL_TIME

The Quality Manager is expected to maintain sufficient technical proficiency to provide hands-on training, troubleshoot analytical and manufacturing issues, and perform Quality Control testing when operational needs require, while maintaining primary responsibility for leadership, quality systems, and departmental performance. Primary Duty: The Quality Manager is responsible for the daily execution, maintenance, and continuous improvement of the facility's Quality Management System (QMS), ensuring that raw materials, manufacturing processes, and finished products meet established quality and regulatory requirements.

Next Century Spirits Inc

Quality Manager

YEAR

High School Diploma or equivalent required; industrial engineering, manufacturing engineering, quality engineering, technical degree, engineering background preferred, but not required. 3+ years of experience in quality assurance or quality control roles, with supervisory experience preferred.

Quick Hire Staffing

Quality Supervisor 60k (Concord, NC)

Workable

Clinical Trial Management System (CTMS), Electronic Data Capture (EDC), eDiary, Electronic Patient Reported Outcomes (ePROs), Trial Master File (TMF), IVRS/IWRS, Central Monitoring dashboards), to oversee site and patient activities, study team conduct and to ensure the data has been updated to reflect timely execution of all operational aspects (required visits/calls, duration, and frequency) according to plan. Reviews the content and quality of site and central monitoring documentation (site monitoring calls, site visit reports, site letters, central monitoring reports and pertinent correspondence), to ensure they represent site management activities and conduct and that they appropriately convey any risks to protocol/GCP compliance, trial conduct, patient safety or data integrity.

Syneos Health

Sr CTM

Author, review, and approve computerized system validation deliverables, including protocols, test scripts, reports, risk assessments, deviations, and technical documentation, using a risk-based approach and ensure laboratory computerized systems comply with data integrity and electronic records and electronic signatures requirements, including 21 CFR Part 11, EU Annex 11, ALCOA++, and applicable global, regional, and site procedures. Monitor and communicate system health, compliance risks, project status, service performance, and quality metrics to Quality leadership and relevant stakeholder and serve as a subject matter expert during regulatory inspections, client audits, and internal audits for LIMS, analytical instrument systems, computerized system lifecycle controls, and laboratory data integrity.

Kyowa Kirin

Senior Specialist, Digital Quality (Quality Systems & Compliance)

ea_via_bold

The role will act as a Subject Matter Expert (SME), technical expert, and mentor, to oversee several concurrent workstreams including: all production and purification aspects of small-scale plasmid production and supply, small-scale (10L) supply of high-quality recombinant AAV vectors for research purposes, medium (50L-250L) vector supply laboratory supply for Toxicology-quality AAV vector supply, and building-wide solutions and lab consumables supply. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease.

Asklepios BioPharmaceutical, Inc. (AskBio)

Director, Pre-Clinical Manufacturing

About the role: We are seeking a Manager or to play a critical role within our growing R&D strategy team to focus on R&D reinvention across the value chain: helping clients move beyond incremental improvement to AI-enabled transformation of how they discover, develop, and deliver medicines. We work with R&D leaders - Chief Scientific and Medical Officers, Heads of R&D Functions, SVP and VP-level capability owners - to shape R&D strategy, accelerate pipeline decisions, and build the capabilities needed to compete in the age of AI-driven drug discovery and development.

Accenture Plc

Life Sciences R&D Strategy Manager

Manage and maintain the repair station's QMS (Quality Management System) in accordance with 14 CFR Part 145, including the Repair Station Manual (RSM) and Quality Control Manual (QCM); prepare revisions, obtain FAA acceptance with working with the Chief Inspector, and ensure changes are implemented and trained across the site. We are seeking a dynamic Quality Assurance Manager to lead the quality system at our FAA 14 CFR Part 145 repair station, which supports Part 121 air carrier customers and holds multiple foreign authority approvals.

TAT Technologies Ltd

Quality Assurance Manager

Demonstrated expertise in Regulations & quality systems in one or more of the following: product disposition, DV/CAPA, Change Control, Audits, Supplier Management, Project Management, Validation, laboratory method and equipment validation, warehouse/logistics, and IT preferred. Our Product Supply Aseptic Manufacturing (PS AM) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments.

<h1><strong>Working at Novo Nordisk</strong></h1>
<p> </p>
<h3><strong>Life-changing careers</strong></h3>
<p>Starting a career at Novo Nordisk is more than getting a job. It is an opportunity to improve the lives of millions of people living with a serious chronic disease.</p>
<p>Whether you are a part of supplying insulin for patients around the world, discovering the next breakthrough at one of our state-of-the-art research centres, working with us is truly life-changing.</p>
<p> </p>
<h3><strong>We are inspired by life</strong></h3>
<p>We are a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. Millions rely on us.</p>
<p>We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. From our colleagues in the lab, working to change lives through pioneering break-through treatments, to our colleagues putting sustainability at the core of our processes and working to prolong the life of our planet, this mission to improve lives is at the core of our every action.</p>
<p> </p>
<h3><strong>Together we drive change</strong></h3>
<p>Change is a constant — change in lifestyle, change in technology, change all over. At Novo Nordisk, we don’t wait for change. We drive it.</p>
<p>We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future.</p>
<p>That’s why we continuously push to improve the way we work and the lives of the patients we serve, creating innovative solutions that fit the way people want to live. To accomplish this, we embrace a spirit of open-mindedness and experimentation, striving for excellence without fixating on perfection.</p>
<p> </p>
<h3><strong>Together, we are life-changing</strong></h3>
<p>Our company is our people. We know that life is anything but linear and balancing what is important at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We want to ensure that every employee can achieve a work-life balance that supports their current priorities and where they want to go next.</p>
<p> </p>
<h3><strong>Your development starts here</strong></h3>
<p>We value our employees for the unique skills, backgrounds and perspectives they bring to the table. We work continuously to help bring out the best in all of our people, offering opportunities for development and creating an environment of mobility within the company. We strive to offer a workplace that’s great to be in and to be from.</p>
<p>It is very important to us that anyone working with us feels empowered as an employee and as a person. We all should have the opportunity to act fast, make decisions and be agile. </p>
<p>With a career at our company, you will feel a difference right from the start. A sense of inspiration that comes from a shared belief in driving positive change for people, families and communities everywhere, and it’s a collective effort. We rely on the joint potential and collaboration of our more than 45,000 employees.</p>
<p>In the video above, meet  Marie Darting, one of our scientists, and hear more about her work as a formulation scientist, her perspective on development plans and the impact she feels her work has on people living with a chronic disease.</p>
<p> </p>
<h3><strong>Who we are</strong></h3>
<p>We were founded in 1923 and today we are a global healthcare company headquartered just outside Copenhagen, Denmark.</p>
<p>Our purpose is to drive change to defeat diabetes and other serious chronic diseases, such as obesity and rare blood and endocrine disorders. We do so by pioneering  scientific breakthroughs, expanding  <a href="https://www.novonordisk.com/sustainable-business/access-and-affordability.html">access to our medicines</a> , and working to <a href="https://www.novonordisk.com/sustainable-business/preventing-chronic-diseases.html">prevent</a> and <a href="https://www.novonordisk.com/disease-areas/type-1-diabetes.html">ultimately cure diabetes</a>.</p>
<p>With almost 100 years of experience, one of the broadest diabetes product portfolios in the healthcare industry, as well as an award-winning pipeline of innovative products, our success is built on our company values – <span style="text-decoration: underline"><a href="https://www.novonordisk.com/about/who-we-are.html">the Novo Nordisk Way.</a></span></p>

Novo Nordisk AS

Quality Assurance Area Specialist III

Our company is seeking an experienced Dental CAD/CAM Manager to lead and support a growing digital production team focused on implant restorations, custom abutments, metal manufacturing, and advanced restorative workflows. The ideal candidate will be comfortable overseeing design quality, managing production workflow, troubleshooting digital and manufacturing challenges, and helping build a team as the operation continues to expand.

DCS Lab

CAD/CAM Manager

The Quality Assurance Manager plays a critical part in understanding and meeting internal and external customer needs by developing solutions and validating product/solution performance through: Executing quality complaint investigations, root cause analysis, troubleshooting, data collection and proposes solutions. If you are looking for a company that is thriving across various high growth industries and is innovative, customer focused, high integrity, believes in strong teamwork and collaboration, Pregis is the company for you.

Pregis LLC

Master''s degree in a discipline relative to the program from an appropriately accredited institution and three years of related experience; or Bachelor's degree in a discipline relative to the program area from an appropriately accredited institution and five years of related experience; or an equivalent combination of education and experience. It is responsible for ensuring the health, safety, and well-being of all North Carolinians, providing human service needs for special populations including individuals who are deaf, blind, developmentally disabled, and mentally ill, and helping poor North Carolinians achieve economic independence.

State of North Carolina

Human Services Program Consultant II (QA)

Avance Care is seeking an experienced Advanced Practice Provider (Nurse Practitioner or Physician Assistant) for an exciting opportunity to grow your career in a role that offers both meaningful patient connection and broader organizational impact. If you’re looking for a role where you can care for patients, influence meaningful change, and grow as a clinical leader, we invite you to join Avance Care and be part of the future of high-quality, data-driven healthcare.

Avance Care

Clinical Quality Specialist (Nurse Practitioner/ Physician Assistant)

[AW]-iCims

Leads and coordinates the execution of a clinical trial globally from sourcing strategy and study specification development for requests for proposals to fully outsourced studies and ancillary vendors, study start up through database release and inspection readiness to ensure timely delivery of quality study data. Provides leadership to the teams in setting recruitment targets and delivery milestones as the single point of accountability for detailed study start up, monitoring, and other study level plans and delivery to the agreed plans by partnering with cross functional colleagues.

Parexel

Global Study Manager/Project Leader - US or Canada - FSP

Clinical Trial Manager - Full Service

If you're passionate about helping customers develop new pharmaceuticals and biologics; have an entrepreneurial spirit; and ready to join other science, business, and operations leaders, we would love to get to learn more about how we can help each other grow. At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

Allucent

VP, Quality Assurance

Quality Assurance and Maintenance: Assists in overseeing quality assurance and instrument maintenance procedures and maintains related records according to established policies/procedures, which may include the following: Performs, verifies accuracy of results, and records both QC function checks and quality control testing within the specified time frame. Follow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test results for the following instruments/tests: Hematology.

Physicians East PA

Medical Laboratory Technician II

Analyzes quality data for accuracy and to identify areas for improvement in data throughout the organization including workflow analysis, process redesign, staff education and process documentation and efficient workflow while maintaining quality patient care and safety. Independent and analytical thinker who can function effectively in a fast-paced environment, handle multiple tasks and assignments, work through frequent interruptions and make decisions under pressure.

Air Quality Specialist Jobs in Massachusetts

Global AML Operations - Business Control Mgr Bank of America

Manufacturing Supervisor - Large Power Transformers (P) Siemens Energy AG

Staff Associate - Regional Quality Assurance BUNNELL LAMMONS ENGINEERING

Quality Manager Next Century Spirits Inc

Quality Supervisor 60k (Concord, NC) Quick Hire Staffing

Sr CTM Syneos Health

Senior Specialist, Digital Quality (Quality Systems & Compliance) Kyowa Kirin

Director, Pre-Clinical Manufacturing Asklepios BioPharmaceutical, Inc. (AskBio)

Life Sciences R&D Strategy Manager Accenture Plc

Quality Assurance Manager TAT Technologies Ltd

Quality Assurance Area Specialist III Novo Nordisk AS

CAD/CAM Manager DCS Lab

Quality Assurance Manager Pregis LLC

Human Services Program Consultant II (QA) State of North Carolina

Clinical Quality Specialist (Nurse Practitioner/ Physician Assistant) Avance Care

Global Study Manager/Project Leader - US or Canada - FSP Parexel

Clinical Trial Manager - Full Service Syneos Health

VP, Quality Assurance Allucent

Medical Laboratory Technician II Physicians East PA

Quality Improvement Coordinator Randolph Health

Similar Job Searches

Stand out to leading employers.