Job Description

Job Title: Document Control Technician

Reports To: Quality Manager / Document Control Supervisor

Group/Division: Laboratory Products Group/Laboratory Equipment Division

Position Location: Marietta, OH

How will you make an impact?

Facilitate the management and improvement of quality records created and maintained by the Marietta Manufacturing Center of Excellence. Measure and report operational performance on GDP compliance. Control records according to written procedures within a manual or electronic document management system. Perform other related duties as assigned by the Quality Manager / Document Control Supervisor.

What will you do?

* Identify error-check, log and file documents critical to GMP compliance.
* Inspect measure and report GDP performance of reviewed records.
* Perform and record inspections / acceptance, control and release of manuals and other labeling.
* Provide guidance and training to coworkers as it relates to GDP.
* Serve as a critical function in facilitating internal and external audits of the facility by retrieving, reviewing, and copying records as needed.
* File records (electronic or hard-copy) in designated locations; retrieve as necessary to support the business.
* Performs all job duties within ISO standards, regulatory or statutory requirements

Education

* High school diploma or GED required

Minimum Requirements

* 2 years experience in Quality Systems, document control administration is desired.

Knowledge, Skills, Abilities

* Strong verbal and written communication skills.
* Unwavering attention to detail, able to identify GDP errors.
* Proficient in use of Microsoft Office Suite.
* Working experience with Good Manufacturing Practices, FDA, ISO 13485 and Good Documentation Practices is a plus

At Thermo Fisher Scientific, quality is inherent in all that we do, earning our Customers loyalty through their trust in our products and services. All employees are required to understand and adhere to site quality requirements, stemming from ISO 13485, and any other applicable regulatory requirements (e.g. FDA CFR). Employees will undergo Quality training during onboarding and annually through our internal learning management system