Associate Documentation Support

Associate Documentation Support role at Insulet, a medical device company. Responsible for maintaining document control systems under GMP/ISO regulations in Waalwijk, Netherlands. Requires 2 years of experience in a QC or GMP/ISO environment.

On-siteFull-timeMid LevelMicrosoft OfficeMicrosoft Access

Associate Documentation Support

Associate Documentation Support role at Insulet, a medical device company. Responsible for maintaining document control systems under GMP/ISO regulations in Waalwijk, Netherlands. Requires 2 years of experience in a QC or GMP/ISO environment.

Apply

On-siteFull-timeMid LevelMicrosoft Office

Salary

Not specified

Work Location

Waalwijk, North Brabant, Netherlands, NL

Work Model

On-site

Experience Required

2 years

Employment Type

Full-time

Experience Level

2 years of experience maintaining documents within a QC or GMP/ISO-certified environment preferred

Core Qualifications

Technical (Must-have)

Microsoft OfficeMicrosoft AccessMicrosoft WordGMPISO

Soft Skills

written communicationverbal communicationorganizational skillsability to generate accurate records

Preferred Qualifications

Technical (Nice-to-have)

Configuration Data ManagementERPMFG/Pro

Key Responsibilities

•Maintain DHR documentation database.
•Control the flow of DHR documents to support lot release.
•Create and update documentation for DHR files & logs.
•Perform Lot Release.
•Conduct internal quality audits.
•Data input into the Insulet computer system.
•May provide guidance to other staff.

Document ControlQuality AssuranceMedical DeviceGMPISOWaalwijk