QC Scientist II

Job Description

Job Summary:

• You’ll perform sophisticated analyses to ensure product quality and safety in our laboratories.
• As a QC Scientist II, you’ll conduct complex analytical testing to support the analysis of raw materials and other production samples using approved analytical methods.
• You’ll assist in quality investigations of manufactured products and incoming raw materials for the QC laboratory in accordance with Client procedures.
• You’ll work with analytical instruments and technologies while making a meaningful impact on patient health through precise quality control testing.
• Working with cross-functional teams, you’ll execute validated test methods, participate in method development and validation activities, investigate out-of-specification results, and maintain detailed documentation of analyses.
• You’ll contribute to continuous improvement initiatives and help establish robust analytical processes while adhering to GLP requirements and safety standards.

Requirements:

• Advanced degree or Bachelor’s degree with at least 2 years of experience in a GLP regulated laboratory environment performing analytical testing.
• Preferred Fields of Study: Chemistry or related scientific field.
• Strong expertise in analytical techniques, including classical wet chemistry methods for the analysis, separation, and quantification of chemical substances.
• Hands-on experience in the use of auto titrators, , pH and buffer analysis, and Karl Fischer titration
  Spectrophotometry techniques including FTIR, UV-Vis Spectrometry, and Fluorescence analysis.
• Desired expertise in chromatographic techniques including GC, HPLC, and LCMS.
• Experience with laboratory information management systems (LIMS) and quality management systems.
• 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.
• Calibrate analytical instrumentation before commencing work as the need arises by methods and quality systems.
• Maintain instruments in good order, report defects, and repairs as advised to Process Leader and QC Manager.
• Analyze materials with accuracy and precision in line with approved analytical test methods while meeting department Client times.
• Strong knowledge 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.
• Experience with method validation and transfer activities preferred.
• Knowledge of data integrity requirements and good documentation practices.
• Demonstrated ability to investigate out-of-specification results and author technical reports.
• Maintain 6S housekeeping standards, keeping work areas clean, tidy, and safe.