Quality Systems Specialist
3 weeks ago
Quality Systems SpecialistAs a Quality Systems Specialist, you will contribute in the following areas:Conduct receipt and processing of field returned productReview and approve quality records to ensure accuracy, completeness, and compliance with regulatory requirementsSupport document control processes in compliance with established SOPs and regulatory requirements and maintain systems for document control, reviews, approvals, and QA functionsSupport continuous improvement initiatives within document control workflows and the broader Quality Management System (QMS)Develop a comprehensive understanding of DEKA's products and processes, leveraging this knowledge to enhance QMS effectivenessSupport collection, analysis, and trending of QMS dataSupport internal and external auditsSkills & Attributes:Aptitude for Learning: Quickly grasp and apply a variety of processesEffective Communication: Articulate problems and solutions clearly to diverse, cross-functional teams with varying technical backgroundsProject Coordination/Management: Plan, execute, and oversee projects with varying timelinesProblem Solving: Tackle challenges with creative, practical solutionsCollaboration: Work effectively across teams, share ideas, take initiative, and contribute to common objectives while fostering a positive work environmentAttention to Detail: Demonstrate exceptional accuracy and precision in all tasksReliability: Deliver consistently high-quality work and demonstrate dedication to your roleTechnical Proficiency: Excel inor rapidly learntools including Excel, Word, and VisioTraining / Knowledge:Required: Bachelor's degree in Science, Engineering, or a related field. 1+ years of experience administering processes within a database. Strong written and verbal communication skills. Advanced proficiency in Microsoft Word, including manipulation of headers/footers, page layout control, document sections, orientation, styles, and tracked changes. Strong computer skills with databases and software applications. Project coordination and/or project management experience. Demonstrated aptitude for learning technical information quickly and accurately.Preferred: 1+ years of experience in a QMS or document-centric environment. Experience with document management systems such as Intellect, Veeva, ETQ, and requirements-tracing programs (e.g., DOORS).About DEKA: One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age. Behind DEKA's brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
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Quality Systems Specialist
2 weeks ago
Manchester, New Hampshire, United States Merrimack Manufacturing Full time $60,000 - $80,000 per yearCOMPANY OVERVIEW:Merrimack Manufacturing is a medical device manufacturer located in the Manchester Millyard. We are a growing manufacturing company that will play a crucial part in bringing innovative and life changing products to life. POSITION OVERVIEW:The Quality Systems Specialist is responsible for assisting the in managing and maintaining the...
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Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeDEKA R&D has an immediate opening for a Quality Specialist to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Director of Quality. The Quality Specialist is actively involved with everyday quality assurance operational tasks for ongoing product development projects and...
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Quality Specialist
7 days ago
Manchester, United States DEKA Research & Development Full timeDEKA R&D has an immediate opening for a Quality Specialist to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Director of Quality. The Quality Specialist is actively involved with everyday quality assurance operational tasks for ongoing product development projects and commercially...
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Quality Specialist
4 days ago
Manchester, New Hampshire, United States DEKA Research & Development Full timeDEKA R&D has an immediate opening for a Quality Specialist to work in the Quality Department in a dynamic Medical Device Research and Development environment. The position reports to the Director of Quality. The Quality Specialist is actively involved with everyday quality assurance operational tasks for ongoing product development projects and commercially...
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Specialist, Quality Engineer
4 weeks ago
Manchester, United States Clearance Jobs Full timeSpecialist, Quality EngineeringL3Harris Technologies is the Trusted Disruptor in the defense industry. With customers' mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security.Job Title: Specialist, Quality EngineeringJob Code:...
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NPI Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeThe New Product Introduction (NPI) Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other...
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NPI Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeThe New Product Introduction (NPI) Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other...
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NPI Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeThe NPI Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other QMS documentation to...
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NPI Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeThe NPI Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other QMS documentation to...
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NPI Quality Specialist
2 weeks ago
Manchester, United States DEKA Research & Development Full timeThe NPI Quality Specialist supports design transfer activities and quality operations in an innovative, fast-paced, medical device-manufacturing environment. This role focuses on coordinating the development, review and maintenance of control plans, risk management files, validation protocols, process capability studies; and other QMS documentation to...
