USP manufacturing Engineer
Key Skills
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
DESCRIPTION:
Join Thermo Fisher Scientific as a Manufacturing Planner/Scheduler II and contribute to global healthcare and scientific advancement. You will be supporting the USP team with the following tasks:
- Writing and updating of batch records for new and existing processes.
- Owning, writing and completing of quality records of the USP department.
- Updating of SOP’s for improvements or quality records
- Ownership of CCR’s for PPI improvements.
These tasks are performed by a team of three Manufacturing Engineers who each have a primary responsibility and support with the other responsibilities.
REQUIREMENTS:
• Minimal MBO level or equivalent
• Preferred Fields of Study: Biotechnology, Process technology
• Demonstrated experience with quality systems
•Demonstrated expericane with SOP updates or technical writing.
Core Responsibilities
Write and update batch records for new and existing processes, and own, write, and complete USP department quality records. Update standard operating procedures and manage change control requests related to process improvements, while supporting the other responsibilities shared across the manufacturing engineering team.
Requirements
A minimum MBO-level qualification or equivalent is required, with biotechnology or process technology preferred. Candidates should have demonstrated experience with quality systems and with updating standard operating procedures or technical writing.
About Thermo Fisher Scientific
Industry: Biotechnology Research
Company size: 10,001+ employees
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 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, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team 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, Patheon and PPD. For more information, please visit www.thermofisher.com.