Job Summary:
Novo Nordisk is hiring a dedicated 3rd Shift Scientist, Quality Control in Bloomington, USA. This role involves routine GMP laboratory testing, data analysis, deviation investigations, and continuous process improvements in a cutting-edge pharmaceutical manufacturing environment. Ideal for professionals with experience in QC testing and compliance in cGMP settings.
Key Responsibilities:
Independently execute and document cGMP Quality Control testing.
Operate QC lab equipment and perform routine maintenance.
Author SOPs, reports, and technical documents.
Prioritize lab activities to meet production and testing deadlines.
Contribute to deviation investigations and CAPA (Corrective and Preventive Actions) processes using problem-solving tools.
Perform data entry and review in LIMS and TrackWise systems.
Support continuous process improvement and lab housekeeping following 5S principles.
Participate actively in team meetings and training sessions.
Comply with all environmental, health, and safety (EHS) standards.
Required Skills & Qualifications:
Bachelor’s in science with 3+ years’ experience (including 1 year in GMP environment), or
Master’s/PhD with relevant experience in GMP or regulated industries.
Knowledge of analytical chemistry and QC lab equipment.
Experience in deviation handling, investigations, and CAPA implementation.
Proficiency with cGMP, GLP, GDP, SOPs, and clean room procedures.
Excellent problem-solving, decision-making, and multi-tasking abilities.
Strong written and verbal communication skills.
Ability to work in high-pressure, deadline-driven environments.
Perks & Benefits:
Competitive pay and annual performance bonus.
14 paid holidays and generous PTO.
Health, Dental & Vision insurance effective from day one.
Guaranteed 8% 401K contribution plus company match option.
14 weeks paid parental & 6 weeks family medical leave.
Free access to Novo Nordisk pharmaceuticals.
Tuition assistance, Life & Disability Insurance.
Employee Referral Awards.
Company Description:
Novo Nordisk is a globally recognized leader in healthcare with over 100 years of innovation in diabetes, biopharma, and chronic disease treatment. Its Bloomington site is an advanced pharmaceutical manufacturing facility committed to quality, compliance, and life-changing innovation.
Work Mode:
On-site (Bloomington, USA) – 3rd Shift (11:00 PM to 7:30 AM, Sunday–Thursday)
Call-to-Action:
Ready to advance your pharmaceutical career with a global leader? Apply now to join Novo Nordisk's QC team and make a difference in global healthcare.
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