QC Scientist

Job Title:

QC Scientist IJob Description

• Perform routine analytical testing using HPLC, ICP-MS, UV-Vis spectroscopy, dissolution testing, and other laboratory techniques to support quality control operations.

• Conduct microbiological testing and support aseptic laboratory operations in accordance with established procedures.

• Follow all applicable SOPs and adhere to cGMP, GLP, and GDP requirements to ensure regulatory compliance and robust quality standards.

• Accurately document testing results, maintain complete laboratory records, and uphold data integrity standards at all times.

• Perform routine equipment maintenance, calibration, and basic troubleshooting for analytical instruments and laboratory equipment.

• Utilize LIMS and other laboratory software systems to manage, track, and report testing data efficiently and accurately.

• Investigate and report deviations, out-of-specification (OOS) results, and atypical findings in accordance with quality procedures.

• Support continuous improvement initiatives and quality enhancement projects within the laboratory and broader quality organization.

• Collaborate closely with laboratory and quality teams to support production schedules, testing priorities, and product release timelines.

• Maintain a clean, organized, and compliant laboratory workspace that supports safe and efficient operations.

• Experience working in a regulated quality control laboratory environment following cGMP and GLP requirements.

• Proficiency with analytical instrumentation, particularly HPLC, and familiarity with common laboratory testing techniques.

• Strong understanding of SOP adherence, GDP documentation practices, and quality management systems.

• Ability to investigate test results, maintain data integrity, and support overall quality operations.

• Experience with LIMS and other laboratory software systems for data entry, tracking, and reporting.

• Knowledge of aseptic technique and microbiological testing principles.

• Bachelors degree in Chemistry, Biochemistry, Biology, Molecular Biology, or a related scientific field.

• Strong computer proficiency, including Microsoft Office applications and laboratory informatics tools.

• Excellent organizational skills with the ability to manage documentation and multiple tasks effectively.

• Clear and professional communication skills, both written and verbal.

• High level of attention to detail and accuracy in all aspects of laboratory work.

• Strong analytical and troubleshooting skills for interpreting data and resolving technical issues.

• Biotech or pharmaceutical industry experience.

• Hands‑on experience with microbiological testing in a QC or regulated laboratory environment.

• Experience using LIMS for sample management and data reporting.

• Practical experience with ICP-MS, dissolution testing, and UV-Vis spectroscopy.

• Knowledge of pharmacopeia requirements and relevant regulatory standards.

• Ability to manage multiple priorities and adapt to changing project needs.

• Self‑motivated and accountable, with a strong sense of ownership for assigned tasks.

• Effective interpersonal skills and the ability to collaborate as a supportive team player.

• Adaptable and flexible mindset suited to a dynamic, quality‑focused environment.

This role is based in a regulated quality control laboratory environment that emphasizes accuracy, compliance, and collaboration. You will work daily with advanced analytical instruments such as HPLC, ICP-MS, UV-Vis spectrophotometers, dissolution testers, and microbiological testing equipment, as well as LIMS and other laboratory software systems. The work involves following cGMP, GLP, GDP, and established SOPs, with a strong focus on data integrity and quality management.

The…