USP manufacturing Engineer
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What you'll do
- 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.
What they're looking for
- Minimal MBO level or equivalent
- Demonstrated experience with quality systems
- Demonstrated expericane with SOP updates or technical writing.
Nice to have
- Preferred Fields of Study: Biotechnology, Process technology
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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, Loud Noises (Equipment/Machinery), 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.
Company
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