The position has two available shifts: 1st Shift: Monday–Friday, 6:00 AM – 2:30 PM 2nd Shift: Monday–Friday, 2:00 PM – 10:30 PM In this role, you’ll be part of the team responsible for supporting visual inspection and manufacturing operations for drug products in a multi-product facility. The work includes performing hands-on production activities such as visual inspection, cleaning, palletizing, and documentation in accordance with cGMP and cGDP standards. You’ll also support areas like batch record execution, equipment use logs, logistics coordination, and continuous improvement projects. What we’re looking for: At least 1 year of experience in a GMP-regulated environment (pharma, biotech, or similar) Strong attention to detail and ability to follow written procedures accurately Comfortable working with computer-based systems and manufacturing execution systems (MES) Team-oriented mindset with strong communication skills Ability to meet visual inspection standards and perform light physical work (up to ~25 lbs) This is a fantastic opportunity to gain hands-on experience with a respected global company known for quality, innovation, and career development in the biopharmaceutical industry.