Junior Quality Systems Engineer
Company: DEKA Research & Development
Location: Manchester
Posted on: April 1, 2026
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Job Description:
Join our dynamic team at DEKA and be at the forefront of driving
quality excellence! As our Junior Quality Systems Engineer , you'll
be a key player in our collaborative environment, working
hand-in-hand with cross-functional teams to ensure the highest
standards of quality and compliance. As a key contributor to our
team, the following skills are required: Technical Writing:
Proficient in conveying complex technical information clearly and
concisely to as variety of audiences. Aptitude for Learning
Technical Information: Ability to comprehend and apply technical
concepts effectively. Effective Communication: Ability to
articulate problems and solutions with clarity and precision to a
diverse, cross-functional team with varying levels of technical
aptitude. Project Coordination/Management: Skilled in planning,
executing, and managing projects with varying timelines. Problem
Solving: Embrace challenges and find creative solutions.
Collaboration: Effectively collaborate with various teams and
departments, sharing ideas, taking initiative and proactively
contribute to achieve common objectives. Work to maintain a
positive attitude, fostering a supportive and productive work
environment. Attention to Detail: Display exceptional accuracy and
precision in all tasks. Reliability: Consistently delivering
high-quality work and demonstrating dedication to your role.
Excellent at utilizing or the ability to quickly learn
applications, including Excel, Word, and Visio. As a Jr. Quality
Systems Engineer, you will contribute in the following areas:
Champion continuous improvement initiatives within the Quality
Management System (QMS), actively seeking opportunities to enhance
product quality and operational efficiency. Attain a comprehensive
understanding of DEKA's products and processes, leveraging this
knowledge to drive investigations and improvements within the QMS.
Lead collaborative efforts in driving root cause investigations for
Corrective and Preventive Actions (CAPAs), ensuring comprehensive
analysis and appropriate solutions are implemented by
cross-functional teams, while fostering a culture of technical
understanding and problem-solving excellence. Support change
management processes by developing and revising Standard Operating
Procedures (SOPs) and associated change controls, ensuring
alignment with regulatory requirements. Ensure compliance with FDA
Part 820 and ISO 13485 regulatory standards, maintaining the
integrity and effectiveness of the DEKA QMS. Review and approve
quality records to ensure accuracy, completeness, and compliance
with regulatory requirements. Required Training / Knowledge: BS/MS
in Science or Engineering Preferred 1 years’ experience in quality
systems management, CAPA, quality assurance or a similar regulated
environment Strong written/verbal communication skills Excel, Word,
Visio skills Technical Writing experience Project
coordination/management skills Aptitude for learning technical
information Nice to have: Knowledge of FDA’s Quality System
Regulation Knowledge of ISO 13485 and related standards Experience
with Corrective and Preventive Action (CAPA)
Keywords: DEKA Research & Development, Lynn , Junior Quality Systems Engineer, Engineering , Manchester, Massachusetts