Engineer II QC

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
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 our Quality Control team at Thermo Fisher Scientific where you'll make meaningful contributions to our mission of enabling customers to make the world healthier, cleaner and safer. As an Engineer/Scientist II, QC, you'll perform testing and analysis to ensure product quality while working with state-of-the-art analytical equipment in a GMP environment. You'll conduct testing of raw materials, in-process samples, and finished products using various analytical techniques, evaluate test data, document results, and participate in continuous improvement initiatives. This role offers excellent opportunities for professional growth while working alongside colleagues who share your commitment to science and quality.

REQUIREMENTS

Bachelor's Degree plus 8 to 12 years of experience, preferably in pharmaceutical/biotech industry
Preferred Fields of Study: Chemistry, Biochemistry, Biology, Molecular Biology or related scientific field
Additional certifications in Quality Control/GMP practices beneficial
Strong knowledge of GMP regulations and quality systems requirements
Proficiency in analytical techniques including HPLC, GC, MS, spectrophotometry
Experience with microbiological and biochemical testing methods
Demonstrated expertise in data analysis and investigation of out-of-specification results
Strong documentation skills and proficiency with laboratory information management systems
Knowledge of relevant regulatory standards (ISO, FDA, USP, EP)
Excellent attention to detail and ability to follow written/verbal procedures accurately
Strong organizational and time management skills
Ability to work both independently and collaboratively in a team environment
Proficiency in Microsoft Office applications
Clear written and verbal communication skills in English
Experience with laboratory automation systems preferred
Knowledge of Lean/Six Sigma principles beneficial