Qc Technician

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.

**The job**

The job holder should be practically and theoretically good in the field of expertise (Analytical methods). Knowledge of analytical methods and processes according to cGMP and EH&S guidelines and quality systems is achieved by keeping training status up to date and increasing own knowledge related to own activities. The job holder delivers reliable results and reports and communicates this in a correct way.

The job holder organizes own work in an optimal way to meet the expectations. The job holder works in a team and needs good communication and interpersonal skills to achieve to team result.

Quality and EH&S: Work according to the local EH&S and Quality guidelines and take initiative for continuous improvement on EH&S and Quality issues within the work environment activities.

**What will you do?**
- Performs sampling and testing of samples for the monitoring programs, general QC-activities like clerical
- and administrative tasks, generic tests for cGMP projects, development, validation or stability programs
- Assist in the improvement of Quality Control procedures, quality and quantity of output.
- Execution of generic tests for monitoring activities, raw material testing, GMP- and PD projects in the (bio)chemical laboratory and the microbiological laboratory and execution of general QC activities
- Train (new) colleagues in the relevant QC procedures and use of specific equipment
- Support in validation, development and stability testing (generic tests);
- Write documentation for the work carried out for: generic analysis (analytical methods and equipment (manuals), data logging (analytical protocols and logbooks) raw material testing (specification sheets and article information sheet), generic validations studies (e.g. PQ )
- Responsible for the proper functioning of specific equipment, as equipment owner expert user and/or trouble shooter, as agreed upon with the line manager. Execution of limited calibration and maintenance of equipment. Assure Equipment file is up to date with procedures, manuals and logbooks.

**Required Education**:

- (K)MLO - laboratory education
- Verbal and written English at MLO level is required
- Excellent knowledge and working in cGMP environment is desired

**Experience**

Experience in analytical techniques in the bio(pharmaceutical) fields is desired.

**Knowledge Skills and Abilities**
- Discipline;
- Communication;
- Planning and organization of own work;
- Dedication;
- Ability to learn;
- Result orientation;