Not specified; benefits: competitive medical benef...
Bachelor's degree in science or related field
Minimum three years qa pharmaceutical manufacturing experience
Prior experience with investigation writing and root cause analysis
The Quality Assurance Specialist is responsible for managing events, discrepancies, and investigations associated with product or process while ensuring compliance with current Good Manufacturing Practices
Job Summary
The Quality Assurance Specialist is responsible for managing events, discrepancies, and investigations associated with product or process while ensuring compliance with current Good Manufacturing Practices.
This position requires a rotating 2-2-3 shift schedule from 7 pm to 7 am at the St. Petersburg facility, which is the primary soft gel development and manufacturing site in North America.
Catalent offers competitive medical benefits, a 401K plan, 152 hours of PTO plus 8 paid holidays, and opportunities to work on continuous improvement processes within a global drug development leader.
Matching Summary
The Quality Assurance Specialist is responsible for managing events, discrepancies, and investigations associated with product or process while ensuring compliance with current Good Manufacturing Practices.
Salary
Not specified; Benefits: Competitive medical benefits and 401K; Time Off: 152 hours PTO + 8 Paid Holidays
Skills & Requirements
Must-have
Bachelor's Degree in Science or related field
Minimum three years QA pharmaceutical manufacturing experience
Prior experience with investigation writing and root cause analysis
Working knowledge of cGMPs and OSHA regulations
Ability to work rotating 2-2-3 shift schedule
Nice-to-have
Experience preparing annual product reviews
Dynamic fast-paced work environment
Opportunity for continuous improvement processes
Collaborative team culture across operations and quality
Personal initiative and ability to meet deadlines
Key Requirements
Bachelor's Degree in Chemistry, Microbiology, or Biology
3+ years related experience in QA pharmaceutical manufacturing
Must have prior experience with investigation writing
Required working knowledge of cGMPs and OSHA regulations