Pharmaceutical Deviation Investigator

Cynet Systems • Clayton, NC

6d • Onsite

About The Position

Support people, equipment, and processes for operations areas to meet business and regulatory requirements. This role involves working directly with production and QA to support deviation investigations, quick containments, and root cause analysis. The position ensures compliance with standards, identifies process needs and improvement opportunities for routine to minimally complex matters, and performs process confirmations to ensure compliance and process improvements. The investigator is also responsible for reviewing Batch Production Records (BPRs) as necessary and must follow all safety and environmental requirements in the performance of duties.

Requirements

• Associate's degree in technology (engineering, technology, or related field of study preferred) from an accredited university required.
• May consider a High School Diploma or equivalent with a minimum of 2+ years of manufacturing experience required, preferably in a pharmaceutical manufacturing environment.
• Strong verbal and written communication skills required.

Nice To Haves

• 1+ years of manufacturing experience in a pharmaceutical manufacturing environment preferred.
• GMP knowledge preferred.
• System knowledge preferred.
• Manufacturing experience preferred.
• Pharmaceutical manufacturing experience a plus.

Responsibilities

• Work directly with production and QA to support deviation investigations, quick containments, and root cause analysis.
• Ensure compliance with standards.
• Identify process needs and improvement opportunities for routine to minimally complex matters.
• Perform process confirmations to ensure compliance and process improvements.
• Responsible for reviewing BPRs as necessary.
• Follow all safety and environmental requirements in the performance of duties.
• Other duties, as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree