Job Description

Job Title: Sr QA Technician, Document Management

Requisition ID: 143634BR

When youre part of a team at Thermo Fisher Scientific, youll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and youll be supported in achieving your career goals.

Location/Division Specific Information

Greenville, NC

How will you make an impact?

Ensures work is performed in a safe and responsible manner striving to create an injury-free and incident-free workplace. Provides Area oversight and execution of creation, routing, approval and issuance of critical documents and records that support all phases of product operations. This is a 1st shift role working Monday through Friday.

What will you do?

* Ensures authors are advised of documents requiring periodic review and conduct follow-up to ensure requirements are met per procedure and compliance requirements.
* Serves as a subject matter and technical expert in support of multiple departments and ensure documents and records are accurate to meet specifications, business rules and compliance requirements.
* Represents Department as a technical resource on systems and transactions used to process critical documents/records by working closely with area supervision and management, and with appropriate technical resources to implement system changes and enhancements.
* Trains with other employees internally (receiving and providing training as appropriate) to ensure ongoing support in documentation and record-keeping systems.
* Tracks and coordinates change controls with customers and ensure documentation/record changes are approved by customers per quality agreements.
* Monitors production schedules and work requests for multiple departments and ensures specifications, changes controls, BOMs, labeling and other documents/records are prepared, implements on time and are accurate for use in production and QC areas.
* Provides 2nd verification as assigned to support critical steps within departmental processes.
* Authors and/or provides review of Standard Operating Procedures (SOPs) and training materials and participates in user testing of systems to support projects and ongoing maintenance of Document/Records Management or Change Control systems

How will you get here?

Education:

High school diploma or equivalent is minimally required.

Experience:

At least 3 years of experience in office management and use of business computers. Similar experience in managing documents and record in a regulatory or controlled environment. At least three years in the use of office applications such as Microsoft Word, Excel, and PowerPoint.

Equivalency:

Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities:
* Microsoft Word, Excel and PowerPoint
* Document Management Systems
* Change Control Management System

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.