USP manufacturing Engineer

Make it in the North; Groningen; Hybrid; EUR 52,000 - 72,000; Full time

Job summary

Thermo Fisher Scientific in Groningen, Netherlands, is seeking a Manufacturing Planner/Scheduler II to support the USP team and ensure smooth production workflows. You will contribute to quality assurance by writing batch records and maintaining quality documentation.

You should have an MBO level or equivalent and experience with quality systems, SOP updates, and technical writing. This role offers on-site work and opportunities to contribute to global healthcare advancements.

Qualifications

• Experience with quality systems is required.
• Experience with SOP updates or technical writing is preferred.
• Strong documentation and record-keeping abilities.

Responsibilities

• Write and update batch records for new and existing processes.
• Own, write, and complete quality records for the USP department.
• Update SOPs for improvements or quality records.
• Own CCRs for PPI improvements.

Skills

Quality systems experience

SOP updates / technical writing

Documentation and record-keeping

Education

MBO level or equivalent

Biotechnology

Process technology

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.