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18 Days Ago
Manchester, NH, USA
670 Employees
3-5 Years of Experience
670 Employees
3-5 Years of Experience
Healthtech • Biotech
The Junior Engineering Project Manager will assist with project activities, manage resources, solve technical challenges, and help to implement process improvements, ensuring product quality in accordance with DEKA's standards.
18 Days Ago
Manchester, NH, USA
670 Employees
5-7 Years of Experience
670 Employees
5-7 Years of Experience
Healthtech • Biotech
The Product Complaint Manager oversees a team of Complaints Specialists, ensuring proper handling of product complaints and compliance with regulations. This role involves conducting training, managing complaint records, escalating serious issues, and providing support during audits to enhance customer satisfaction.
18 Days Ago
Manchester, NH, USA
670 Employees
5-7 Years of Experience
670 Employees
5-7 Years of Experience
Healthtech • Biotech
The Engineering Project Manager at DEKA Research & Development will lead cross-functional teams in the development of innovative products and solutions in medical device technology. Responsibilities include managing project schedules and resources, translating project goals into technical requirements, and ensuring effective communication with stakeholders. The role requires technical leadership and the ability to solve complex project challenges.
18 Days Ago
Manchester, NH, USA
670 Employees
3-5 Years of Experience
670 Employees
3-5 Years of Experience
Healthtech • Biotech
The Cybersecurity Software Technical Writer is responsible for creating and reviewing FDA documentation for eSTAR materials concerning cybersecurity, including threat models, risk management plans, and architecture diagrams. This role requires technical writing skills in a medical device context and basic scripting skills.
18 Days Ago
Manchester, NH, USA
670 Employees
1-3 Years of Experience
670 Employees
1-3 Years of Experience
Healthtech • Biotech
As a Quality Systems Engineer at DEKA, you will focus on improving quality and compliance in software development by refining SOPs, leading internal investigations, ensuring compliance with FDA and ISO standards, and collaborating with cross-functional teams. Your role also involves technical writing and project management.
18 Days Ago
Manchester, NH, USA
670 Employees
3-5 Years of Experience
670 Employees
3-5 Years of Experience
Healthtech • Biotech
As a Quality Engineer at DEKA, you will provide quality guidance in the medical device R&D environment, ensure compliance with regulatory standards, lead risk management activities, conduct investigations, and drive process improvements.
18 Days Ago
Manchester, NH, USA
670 Employees
5-7 Years of Experience
670 Employees
5-7 Years of Experience
Healthtech • Biotech
The Quality System Implementation Analyst will analyze organizational needs, design and implement modules within DEKA's eQMS (Intellect system), conduct data analysis, drive project implementations, and facilitate collaboration across departments to enhance operational efficiency and compliance.
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