Pharma Manufacturing Process Improvement Associate

BioSpace; Clayton (NC); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Health Insurance

Dental Insurance

Vision Insurance – effective day one

401K with company match

Paid holidays and PTO

Parental & family leave

Life & Disability Insurance

Job summary

Novo Nordisk in Clayton, NC is seeking a manufacturing operations support role to assist with production and QA, focusing on deviation investigations and root-cause analysis. You will help ensure regulatory compliance and drive process improvements in a fast-paced environment.

The position requires at least an associate degree in technology or equivalent experience, with GMP knowledge and strong written communication.

Qualifications

• Excellent written communication skills required.
• GMP knowledge preferred.
• System knowledge preferred.
• Manufacturing experience preferred, pharmaceutical focus a plus.
• 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 & environmental requirements in the performance of duties
• Other duties, as assigned

Skills

Written communication

GMP knowledge

System knowledge

Manufacturing experience

Pharmaceutical manufacturing

Education

Associate’s degree in technology

High School Diploma with manufacturing experience

Job description

Novo Nordisk in Clayton, NC is seeking a manufacturing operations support role to assist with production and QA, focusing on deviation investigations and root-cause analysis. You will help ensure regulatory compliance and drive process improvements in a fast-paced environment.

The position requires at least an associate degree in technology or equivalent experience, with GMP knowledge and strong written communication.