What are the responsibilities and job description for the Document Specialist I position at Thermo Fisher Scientific?
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
About Us
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 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 80,000 colleagues delivers an outstanding 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.
All our employees share a common set of values - Integrity, Intensity, Innovation, and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve humankind by enabling our customers to make the world healthier, cleaner, and safer.
If you share in our values and if you are looking for an employer who is strongly committed to developing talent and rewarding achievement, come grow with us at Thermo Fisher Scientific.
Position Summary
The position has the assignment under the direction of a product engineering supervisor to create specifications, item masters, routings, and bills of material. The position will also launch documentation tasks in Master Control for approval. This will require interacting with other department members to ensure product and processes meet customer and regulatory requirements. Attention to detail is critical!
Key Responsibilities
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
About Us
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $30 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 80,000 colleagues delivers an outstanding 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.
All our employees share a common set of values - Integrity, Intensity, Innovation, and Involvement. Our ability to grow year after year is driven by our ability to attract, develop and retain world-class people who will thrive in our environment and share in our desire to improve humankind by enabling our customers to make the world healthier, cleaner, and safer.
If you share in our values and if you are looking for an employer who is strongly committed to developing talent and rewarding achievement, come grow with us at Thermo Fisher Scientific.
Position Summary
The position has the assignment under the direction of a product engineering supervisor to create specifications, item masters, routings, and bills of material. The position will also launch documentation tasks in Master Control for approval. This will require interacting with other department members to ensure product and processes meet customer and regulatory requirements. Attention to detail is critical!
Key Responsibilities
- Create Item Masters, Bills of Material, and Routings
- Transact tasks in Master Control to add specifications
- Create specifications
- Create pre-populated cut sheets
- Participate in PPI and other lean initiatives
- Support global operations
- Work on projects as advised by Product Engineering leadership.
- High School Diploma Required.
- 3 years' experience with Microsoft and other office application software.
- 1 years of experience with the manufacturing and quality processes of Bioprocess Containers preferred.
- Must have good computer skills and be familiar with GMP and ISO principles.
- Demonstrated organizational, writing, and communication skills.
Salary : $30
