EDUCATION:

High school diploma or equivalent required.

EXPERIENCE:

• Required: Minimum of 2 years of work experience in QA or QC or related field
• Required: Experience in a cGMP environmen

KNOWLEDGE, SKILLS, ABILITIES:

• Computer literate
• Knowledge of automatic inspection equipment: Possesses a solid understanding of the operation and uses automatic inspection equipment specific to pharmaceutical labeling manufacturing. Capable of setting up and calibrating equipment, interprets, and analyses inspection results, and troubleshoots any equipment-related issues. Familiarity with automatic inspection equipment and its capabilities is crucial for effective quality control.
• Ability to follow pacing and maintain production flow: Possesses the ability to follow pacing and maintains the production flow including effectively managing their time, ensuring inspections are conducted in a timely manner, and keeping up with the production schedule. Maintains attention to detail to prevent any bottlenecks in the manufacturing process.
• Problem tracking and troubleshooting skills: Possesses strong problem tracking and troubleshooting skills and the ability to identify and track issues or deviations during inspections. Investigates root causes, and propose appropriate corrective actions. Applies analytical thinking and problem-solving abilities to address quality-related problems promptly and effectively to maintain quality standards, minimizes disruptions, and ensures smooth operations in pharmaceutical trial labeling manufacturing.

PHYSICAL REQUIREMENTS / WORK ENVIRONMENT

• Fast-paced environment which relies on teamwork to ensure jobs are completed within established timelines.

Please refer the Job description for details