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.
Join us at Thermo Fisher Scientific as a QC Scientist I to contribute to global health through quality control testing that ensures the safety and efficacy of pharmaceutical products. You will perform chemical, physical, and microbiological analyses in support of manufacturing operations while following Good Manufacturing Practices (GMP). Working with advanced analytical instruments, you'll conduct testing of raw materials, in-process samples, finished products, and stability samples. Our collaborative environment provides opportunities for continuous learning and career growth as you help deliver vital therapies to patients.
Preferred: Bachelor's degree in Chemistry or related scientific field
Experience in a GLP regulated laboratory environment performing analytical testing is desirable but not essential
Exposure to classical wet chemistry techniques for the analysis, separation, and quantification of chemical substances, including auto titrators, Karl Fischer titration, colorimetric assays, pH and buffer analysis, nitrogen determination, and dissolution testing
Some working knowledge of spectroscopic techniques, including FTIR, UV-Visible spectrophotometry, and fluorescence spectroscopy
Experience with laboratory information management systems (LIMS) and quality management systems (training provided)
Work safely, adhering to company EHS policies, prescribed safety instructions, and wearing prescribed personal protective equipment
Review COSHH documents and carry out risk assessments as required (training provided)
Calibrate analytical instrumentation before commencing work as the need arises by methods and quality systems (training provided)
Maintain instruments in good order, report defects, and repairs as advised to Process Leader and QC Manager
Analyse materials with accuracy and precision in line with approved analytical test methods while meeting department target times
Order and manage stock levels of laboratory reagents in accordance with the chemical database system
Raise purchase orders for instrument service requirements and coordinate equipment for external calibration
Basic understanding of GLP practices and quality control requirements
Excellent documentation practices and attention to detail
Strong problem-solving and analytical skills
Ability to work both independently and collaboratively
Proficiency with Microsoft Office applications
Strong written and verbal communication skills
Mandatory requirement to wear PPE including lab coat, safety glasses, and gloves
May require flexible scheduling including occasional weekend work
Knowledge of data integrity requirements
Maintain 6S housekeeping standards, keeping work areas clean, tidy, and safe
Tagged as: Life Sciences
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