Job Description

Job Description

Position: Document Control Associate

Overview:

We are seeking a highly organized and detail-oriented Document Control Associate to support the Quality Document Control team. This role is responsible for ensuring control, security, integrity, and availability of documentation, while maintaining compliance with applicable regulations.

Responsibilities:

• Review and approve change orders in PLM.
• Create and update documentation master files.
• Perform filing, record retention, and organizational tasks.
• Maintain supplier data in PLM.
• Retrieve historical paper documentation from offsite storage.
• Support global document control and record retention activities.
• Perform additional duties as assigned.

Qualifications:

• 0–2 years’ experience in a QC or GMP/ISO-certified environment preferred.
• Proficiency in Microsoft Office; advanced knowledge of Word.
• Strong clerical, organizational, and record-keeping skills.
• Excellent attention to detail and ability to prioritize.
• Strong verbal and written communication skills.
• Ability to work effectively in a team environment.
• Experience in a medical device or regulated environment a plus.

Why Apply:

This is an excellent opportunity to build experience in a regulated environment and contribute to a critical function within Quality. If you are detail-driven, organized, and eager to grow, we encourage you to apply today.

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