Job Description:
When you join us at Thermo Fisher Scientific, youll be part of a smart, driven team that shares your passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
Key Responsibilities:
Perform/Assist with Quality Assurance core activities including:
* Batch Record/document review
* Lot release/Disposition using ERP system (Made2Manage).
* In-Line Batch Record/document scanning and archiving.
* Data collection and presentation document control.
* Computer skills including Microsoft office (Word, Excel, etc.).
* Assist/Lead Process Improvement initiatives which support quality objectives.
* Other duties as required.
Preferred Qualification:
* Medical Device exposure
* ISO 13485 Knowledge
Minimum Qualifications:
* High School Diploma or GED
Waltham, MA
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of more than $24 billion and approximately 70,000 employees globally. Our mission is to enable our customers to make the world healthier, cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity. Through our premier brands - Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services - we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services.
To serve science, Thermo Fisher Scientific needs to stay ahead of it. To be the world leader in serving science, we need to anticipate (pre-empt) customer needs. We need to constantly think about advancing science, so customers have the freedom to be bolder and more innovative – we are committed to pushing science and technology a step beyond where it is today.