Job Description

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Quality Control Microbiology Associate Scientist

Facility: Quality

Location:

West Lebanon, NH, US

About the Department

Site New Hampshire, located in West Lebanon, is where Novo Nordisk\'s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It\'s not your average production site - it\'s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We\'re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?

The Position

This position is the subject matter expert on industrial/pharmaceutical microbiology for the facility. Ensures facility program is in line with industry, regulatory and corporate practice. This individual exercises judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions, while maintaining a high level of compliance with cGMP\'s. Normally receives no instructions on routine work, and general instructions on new assignments.

Relationship

Reports to: According to the organizational chart.

Number of subordinates with direct/indirect referral: n/a.

Essential Functions

• Key lead for microbial identification program. Responsible for introduction of new technology/equipment as needed
• Technical subject matter expert on microbiological assays, techniques and industry practices
• Conducts routine and specialized microbiological assays in standard techniques
• Reviews microbiological trending data and writes reports summarizing the trends, independently
• Investigates and resolves issues related assay failures, system deficiencies, deviations, and equipment / assay troubleshooting, with no assistance
• Performs other routine laboratory activities and peer data review as needed
• Conducts routine and specialized assays following SOP\'s
• Schedules laboratory work
• Review and amend test method and instrumentation SOPs as needed
• Updates and maintains trending files, and provides routine summaries of trending to support investigations
• Assists with other routine laboratory investigations including analyst training
• Determines methods and procedures on new assignments as required
• Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes
• Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others

Physical requirements

The ability to climb, balance, stoop, crouch, reach, stand, and walk. The ability to push, pull, lift, finger, and grasp. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 33lbs/15kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. Visual acuity to perform close activities such as: reading, writing, and analyzing; and to determine the accuracy, neatness, and thoroughness of work assigned or to make general observations. The working environment includes a variety of physical conditions including: inside and outside conditions including temperature changes; proximity to moving mechanical parts, moving vehicles, electrical current, working on scaffolding and high places, exposure to high heat or exposure to chemicals. Local and International travel: 0-5%.

Qualifications

• A Bachelor\'s degree in microbiology, biological sciences or related field with a minimum of five (5) years\' related experience or a Master\'s/PhD with a minimum two (2) years of related experience
• Experience:

• Must have a minimum two (2) years\' experience in a lead role within a biotech/pharmaceutical microbiology laboratory
• Experience with environmental monitoring is a plus

• Skills & abilities:

• Must be able to work independently in a team based setting and function in a rapidly changing environment while balancing multiple priorities simultaneously
• Able to perform Sterility, Bacterial Endotoxin, Bioburden and Microbial Identification testing. Basic troubleshooting for laboratory equipment
• Excellent analytical and writing skills are also required with the ability to author/review scientific and technical reports

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we\'re life changing.

Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.

If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.

Novo Nordisk