CMM Quality Specialist - Hudson, NH USA
1 week ago

Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
We are seeking a dedicated Supplier Quality Specialist to join our team. As a Supplier Quality Specialist, you will be an essential part of the Quality Department supporting the qualification and approval of new dietary ingredients. · Collect, organize, and maintain documentation ...
1 week ago
Our client, a leading organization in the dietary supplement industry, is seeking a dedicated Supplier Quality Specialist to join their team. · ...
1 week ago
About Commonwealth Fusion Systems: · Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy. · Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And we're ...
3 days ago
About Commonwealth Fusion Systems: · Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy. · Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And we're ...
3 days ago
About Commonwealth Fusion Systems: · Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy · Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And we're ...
2 days ago
· About Commonwealth Fusion Systems: · Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy. · Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And we' ...
1 day ago
This is a hands-on, high-impact role in a fast-moving environment where quality must keep pace with innovation. The Quality Specialist will own the day-to-day execution and continuous improvement of SiPhox's Quality Management System (QMS), supporting the development, validation, ...
1 month ago
About Commonwealth Fusion Systems: · Commonwealth Fusion Systems is on a mission to deliver the urgent transition to fusion energy. · Combining decades of research, top talent, and new technologies, we're designing and building commercially viable fusion power plants. And we're w ...
3 days ago
The Quality Assurance Product Disposition Specialist is responsible for supporting quality and disposition activities at the Devens MA Cell Therapy manufacturing facility in accordance with Client policies standards procedures and Global cGMP The role will aid in the routine and ...
4 weeks ago
Supports end-of-line product testing, in-process inspection, receiving inspection, and failure analysis within the Quality Control department. Ensures reliable testing in accordance with ISO, MED, MER, CE and internal standards. · ...
1 week ago
As a Quality Specialist you will own the day-to-day execution and continuous improvement of SiPhox's Quality Management System (QMS). You will work closely with engineering, operations, and clinical teams to ensure that products meet internal requirements and applicable regulator ...
1 month ago
· At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. · Are you interested in joining o ...
4 days ago
Inspect incoming materials and parts from suppliers using visual and mechanical tools review and verify First Article Inspection (FAI) from suppliers use conventional and advanced inspection devices to verify dimensions to drawing specifications manage or assist in managing the c ...
2 weeks ago
Supports end-of-line product testing, · inspects products in process and upon receipt, · and performs failure analysis within quality · control. Ensures reliable testing to ISO standards. · Aids Quality Control Section activities. · ...
2 weeks ago
The Quality Assurance Specialist is part of the QA/QC department at Plenus Group and is responsible for ensuring that all products and processes meet the company's high-quality standards and regulatory requirements. · Product Testing and Inspection: Perform regular routine quanti ...
3 weeks ago
The Quality Document Control Specialist implements and maintains the Engineering Change Notice (ECN) System. · Key Responsibilities:Responsible for issuing part numbers, ECNs, · ...
1 month ago
We are seeking an Analytical Quality & Compliance Specialist to join our team in Devens, MA. The successful candidate will be responsible for reviewing and approving qualification documents, supporting the Network QC team in developing and implementing a strategy to standardize Q ...
4 weeks ago
Quality System Specialist/Senior Quality System Specialist
Only for registered members
The Quality System Specialist / Senior Quality System Specialist plays a key role in supporting and enhancing Vaxess Technologies' Quality Management System (QMS) to ensure compliance with applicable GMP/GLP standards. · ...
4 weeks ago
This role involves ensuring quality assurance of products through execution of label control tasks, logbook management, floor operations and gowning in compliance with GMP standards. · Execution of label control tasks and logbook management. · Floor operations (70-80% of their sh ...
1 month ago
The QA Investigation Reviewer is responsible for the independent review and approval of GMP investigations within the Andover biopharma manufacturing facility. · This role ensures non-conformances/deviations, OOS/OOTs, and other quality events are thoroughly investigated, · and c ...
3 weeks ago