Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with revenues of $17 Billion and approximately 50,000 employees in 50 countries. 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 and increase laboratory productivity. Through our premier brands – Thermo Scientific, Applied Bio-Systems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive support.
This position serves as Pleasanton's primary Document Control Analyst. Responsibilities include:
- review and processing of change orders in compliance with company standards
- training system users on Agile ECO/DCO processes
- ensuring correct reviewers and approvers are assigned
- maintaining Control of Documents SOP and related forms/work instructions
- communicating new/revised documents to Pleasanton community
- implementing process for document review cycle
The position requires the ability to handle competing priorities successfully with minimal supervision, while ensuring that activities adhere to written procedures and regulations. This candidate needs to be detailed, accurate and organized since they will be managing critical quality data. The role requires effective collaboration with R&D, manufacturing, distribution, supply chain and facilities functions, records management and database entry. Since this candidate will be working closely with employees across the organization, excellent customer service skills are a must.
Minimum Qualifications (must have)
Excellent organizational and communication (verbal and written) skills required.
Ability to manage multiple priorities in a fast paced environment, and good judgment ensuring written procedures are followed.
Demonstrated ability to work cross functionally.
Requires a minimum of HS or Bachelor degree. A B.S degree in biological sciences or chemistry is preferred.
Preferred Qualifications -
Three years Quality Assurance experience is preferred. Experience with ISO 13485 or GMP manufacturing environments preferred. Previous document control experience (preferably with electronic document management systems such as Agile) is preferred.
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.