QC Biochemistry Technician II

Work Schedule

Flex Shifts 40 hrs/wk

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

We are looking for additional an colleague for the QC Biochemistry team to support the implementation of incoming new business (NPI).

Location/Division Specific Information

This position is within the Quality control (Biochemistry) of Thermo Fisher Scientific in Groningen.

Our site in Groningen is part of the world class Pharma Services of Thermo Fisher Scientific and we are looking for a Technician II for our QC department. We operate in a sophisticated and highly regulated environment. You’ll contribute to the work we do, like helping customers in finding cures for diseases! You will have a real-world impact, and you’ll be supported in achieving your career goals.

The Pharma Services devision of Thermo Fisher Scientific offers our clients a powerful platform for their drug development with technologies that are industry standard to state of the (including Single Use Technologies such as Single Use Bioreactors).

This type of facility has to follow rules and regulations of cGMP set by countries health and welfare ministries and with internationally harmonized guidelines that give guidance with implementing these rules and regulations.

Controlled production activities and compliance to cGMP rules, regulations and guidelines is critical for the suitability of the clients’ products and the license to operate for the site. Main contacts are within own department. The production activities have to be completed in an efficient and effective manner to assure the sites overall competitiveness. In addition, due to the very high value of intermediates and products, production activities have to be performed in a highly controlled fashion.

Discover Impactful Work:

As QC Technician II you will be supporting in the testing of Drug Substance material and it’s intermediates to ensure Quality Aspects of the product.

Do you have laboratory experience? Preferably in a cGMP environment. Primary techniques that you will work with are (but not limited to): Concentration determination, HPLC/UPLC chromatography, Capillary Electrophoresis, ELISA. Then you might be the perfect addition to our team.

A day in the Life:

• Actively participate in daily team assignments.
• Perform laboratory testing by ensuring standard operating procedures are followed.
• Actively keep training performance up to date.
• Support improvement projects in the biochemistry department and assays.
• Exemplifies professional behaviors as well as a quality culture mentality.
• Operates within company and regulatory policies and procedures.
• Good interpersonal, analytical/problem solving skills.
• Being able to work alone as well as in a team.

Knowledge, Skills, Abilities

• Capability to use diverse resources, respond quickly, understand impact of changes and decisions, facilitate agreement, and build collaborative relationships.
• Must be proficient in MS Word, Excel, PowerPoint, and Windows-based software.
• Ability to function in a dynamic work environment and balance multiple priorities simultaneously.

Education / Experience

MLO or HLO degree Affinity with (bio)chemical analyses required.

Experience in GMP not required but preferred.