Microbiologist I – Novo Nordisk in Petersburg, VA | Apply Now
Are you passionate about microbiology and ready to make a meaningful impact in global healthcare? Novo Nordisk invites you to join our state-of-the-art facility in Petersburg, Virginia as a Microbiologist I. In this vital role, you will help ensure the safety and quality of our pharmaceutical products by performing essential microbiological testing and contributing to our mission of improving lives. This is your opportunity to be part of a company that values innovation, integrity, and scientific excellence.
About Novo Nordisk:
Novo Nordisk is a global healthcare leader with more than 100 years of innovation and dedication to addressing the unmet medical needs of people living with serious chronic diseases, including diabetes, obesity, and other rare disorders. Headquartered in Denmark, we operate in over 80 countries and employ more than 60,000 people worldwide. Our new facility in Petersburg, VA marks a strategic expansion in Emerging Technologies (ET) and Chemical API development, underscoring our commitment to delivering high-quality, life-saving treatments efficiently and sustainably. At Novo Nordisk, we are driven by a core purpose—to discover better treatments and ensure a healthier future for millions.
Job Details:
Position: Microbiologist I
Department: Quality
Location: Petersburg, VA, US
Responsibilities:
- Perform routine and non-routine microbiological assays on raw materials, water, in-process samples, packaging materials, and finished products to detect the presence of microorganisms
- Sample and analyze air, surfaces, and water within the manufacturing facility to monitor for microbial contamination
- Provide support in establishing, validating, and maintaining standard operating procedures (SOPs) and equipment for microbiological testing methods
- Ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements related to microbial testing
- Isolate and identify microorganisms using various techniques like culture-based methods, molecular biology, and automated systems
- Perform sterility tests on sterile pharmaceutical products to ensure their freedom from viable microorganisms
- Provide training as directed to laboratory technicians on proper microbiological techniques and ensuring accurate documentation of all testing activities
- Identify improvements to ensure a better and faster execution of QC Micro development and transfer activities
- Ensure GMP compliance in work processes and implementation of new or revised requirements affecting the departments processes
- Ensure working in compliance with QMS and OHS standards
- Provide sufficient quality for scientific and regulatory documentation
- Participate in multidisciplinary project groups
- Contribute proactively to cLEAN process improvement activities
- Perform general laboratory duties including cleaning and maintenance of equipment, work areas, and cleaning of the microbiology laboratory
- Follow all safety & environmental requirements in the performance of duties
- Other duties as assigned
Requirements:
- Bachelor’s degree in microbiology or science-related field from an accredited university required
- May consider an associate’s degree in microbiology or related field from an accredited college with a minimum of two (2) years of experience performing routine and non-routine microbiological assays on raw materials, water, in-process samples, packaging materials, and finished products or related experience required
- May consider a High School Diploma/GED with a minimum of four (4) years of experience performing routine and non-routine microbiological assays on raw materials, water, in-process samples, packaging materials, and finished products or related experience required
- Minimum of two (2) years of experience performing routine and non-routine microbiological assays on raw materials, water, in-process samples, packaging materials, and finished products or related experience preferred
- Strong understanding of microbiology principles, including microbial identification, culture techniques, and sterilization methods preferred
- Experience with GMP regulations and quality control procedures preferred
- Proficiency in laboratory techniques such as aseptic technique, microbial enumeration, and molecular biology methods preferred
- Excellent analytical and problem-solving skills preferred
- Detail-oriented with strong documentation and record-keeping abilities required
- Ability to work independently and as part of a team required
- Excellent communication skills to effectively report findings and collaborate with other departments required
- Ability to set scientific direction and mobilize a project work and activities a plus
- Good collaboration skills with and interaction with many departments required
Benefits:
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance, Dental Insurance, Vision Insurance – effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14 weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
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