Aseptic Manufacturing Process Associate

Novo Nordisk A/S; Clayton (NC); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Competitive pay and annual bonus

14 paid holidays

Health insurance from day one

401K with company match

Parental and family leave

Job summary

Novo Nordisk in Clayton, NC, is seeking to support people, equipment and processes for operations to meet business and regulatory requirements. The role reports to a Manager and collaborates with stakeholders in the assigned area.

Responsibilities include deviation investigations with QA, ensuring standards compliance, identifying improvement opportunities, conducting process confirmations, and reviewing BPRs while adhering to safety and environmental requirements.

Qualifications

• Associate's degree in technology from an accredited university required.
• May consider a High School Diploma or equivalent with a minimum of two years of manufacturing experience.
• Minimum of one year of manufacturing experience in a pharmaceutical environment preferred.
• GMP knowledge preferred.
• System knowledge preferred.
• Manufacturing experience preferred.
• Pharmaceutical manufacturing experience is 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.

Skills

GMP knowledge

System knowledge

Manufacturing experience

Education

Associate's degree in technology

High School Diploma or equivalent with 2 years manufacturing experience

Job description

Novo Nordisk in Clayton, NC, is seeking to support people, equipment and processes for operations to meet business and regulatory requirements. The role reports to a Manager and collaborates with stakeholders in the assigned area.

Responsibilities include deviation investigations with QA, ensuring standards compliance, identifying improvement opportunities, conducting process confirmations, and reviewing BPRs while adhering to safety and environmental requirements.