Quality Control Analyst II — Tablet QC & Compliance

Biopharma Careers; North Carolina; On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Leading pay and annual performance-bon

14 paid holidays

Health Insurance

Dental Insurance

Vision Insurance – effective day one

401K with company match

Parental & family medical leave

Tuition Assistance

Life & Disability Insurance

Employee Referral Awards

Job summary

Novo Nordisk is hiring for a QC Analyst position in North Carolina. The role focuses on performing and reviewing analysis of in-process, release, and stability samples in line with cGMP and site procedures.

You will transfer technology and processes per project plans and timelines, reporting to the Senior Manager, QC – OFP. The ideal candidate holds a chemistry degree with relevant lab experience, demonstrates meticulous attention to detail, and is capable of coaching other analysts while

Qualifications

• Bachelor’s degree in Chemistry or relevant field required.
• 3+ years of experience in a clinical or industrial/pharmaceutical laboratory
• Attention to detail and ability to work in a GMP environment

Responsibilities

• Accuracy & Scientific Soundness of Lab Data
• Environmental Compliance
• GMP Compliance of Laboratory
• Maintain testing proficiency for methods
• Timeliness of Lab Results & Investigations
• Analysis of Samples
• Author Deviations
• Coaching other analysts
• Data Trending & Tracking
• Ensure departmental documents are current & standardized
• Laboratory Equipment Validation & System support
• Laboratory IT System support
• Perform deviation & change control activities
• Supports Deviations
• Systematic Problem Solving
• Follow all safety and environmental requirements in the performance of duties
• Other accountabilities, as assigned

Skills

Attention to detail

Strong communication skills

GMP knowledge

Education

Bachelor’s degree in Chemistry

Associate’s degree in Chemistry

High School Diploma or GED with 5 years lab experience

Job description

Novo Nordisk is hiring for a QC Analyst position in North Carolina. The role focuses on performing and reviewing analysis of in-process, release, and stability samples in line with cGMP and site procedures.

You will transfer technology and processes per project plans and timelines, reporting to the Senior Manager, QC – OFP. The ideal candidate holds a chemistry degree with relevant lab experience, demonstrates meticulous attention to detail, and is capable of coaching other analysts while