Document Control Analyst – Medical Devices & Compliance

1010 Analog Devices Inc.; Wilmington (MA); On-site; USD 69,000 - 95,000; Full time

Benefits offered by this job

Discretionary bonus

Medical, vision and dental coverage

401k

Job summary

Analog Devices, Inc. is seeking a professional to manage document control and training coordination within a regulated medical device environment. You will ensure compliance with QMS and eQMS processes, review documentation, and support audits to maintain readiness.

Responsibilities include user administration, training, and process improvement to sustain system integrity and timely document lifecycle management. Strong communication and attention to detail are essential for success.

Qualifications

• 1–4 years of experience in Document Control, Quality Systems, or regulated documentation within a medical device environment.
• Working knowledge of ISO 9001, IATF, FDA QMSR, and ISO 13485 requirements and document control principles.
• Strong analytical skills, attention to detail, and professional communication capability.
• Bachelor’s degree or equivalent professional experience.

Responsibilities

• Execute document creation, revision, routing, approval, publishing, and archival activities in the eQMS in compliance with QMS requirements.
• Review documentation for completeness, format adherence, and procedural compliance prior to system release.
• Apply professional judgment to identify document discrepancies, inconsistencies, or compliance risks and recommend corrective actions.
• Administer eQMS user accounts, roles, permissions, and access.
• Provide eQMS user training and advanced support, troubleshoot system issues, and perform approved system configuration activities.

Skills

Document Control

Quality Systems

Regulated documentation

Professional communication

Education

Bachelor’s degree or equivalent

Tools

eQMS

ISO 9001

FDA QMSR

Job description

Analog Devices, Inc. is seeking a professional to manage document control and training coordination within a regulated medical device environment. You will ensure compliance with QMS and eQMS processes, review documentation, and support audits to maintain readiness.

Responsibilities include user administration, training, and process improvement to sustain system integrity and timely document lifecycle management. Strong communication and attention to detail are essential for success.