Step into the pharmaceutical industry as a Quality Assurance Associate at Catalent's Adair facility. Play a key role in product quality assurance and compliance for cutting-edge oral dosage forms.
Catalent is seeking a detail-oriented individual for the Quality Assurance Associate role to ensure compliance with regulations and company standards. You'll be integral to the startup of an cutting-edge manufacturing site, conducting audits and training staff on compliance practices. This role offers the chance to significantly impact pharmaceutical manufacturing quality.
Key Responsibilities:
• Audit production processes and documentation practices • Ensure compliance with cGMP and SOPs • Train and coach production personnel on quality standards • Perform compliance audits and generate reports • Oversee finished product inspections prior to release
Requirements: • Bachelor’s Degree in relevant science or engineering field • Ability to handle physical tasks and manual duties • Strong attention to detail and problem-solving skills • Excellent communication skills in both written and verbal forms • Capable of working with minimal supervision
Join Catalent and help maintain the highest standards in pharmaceutical quality and compliance. #J-18808-Ljbffr