About the Department
Our Research & Development organization brings together the best minds in life science innovation. The teams located in facilities in Lexington, Watertown, Cambridge and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct R&D community based on collaboration, partnerships, and cutting-edge research across multiple modalities and therapeutic areas. We recognize that improving human health starts here and that patients rely on us. Our R&D hub merges biotech speed and agility with large pharmaceutical company quality, resources, and stability, uniting the best of both worlds to develop new medicines for patients.
The Position
The Specialist, API Manufacturing works in Novo Nordisk's Boulder, Colorado manufacturing facilities and is responsible for the production oligonucleotide API to support toxicology studies or clinical trials. In addition to ensuring the supply of API and meeting production goals, the Specialist actively supports continuous improvement initiatives and identifies wherever possible improvements that reduce risk and cost to the overall operation.
Relationships
Specialist, API Manufacturing reports to the Senior Manager, API Manufacturing. The Specialist, API Manufacturing works with Chemical Development, Analytical Services, Engineering, Facilities, EH&S, Program Management and Quality Assurance.
Essential Functions
Responsible for the manufacture of oligonucleotide API ensuring compliance to cGXP, safety, regulatory, and business processes and/or procedures
Commission, operate, maintain, and troubleshoot pilot plant equipment such as oligonucleotide synthesizers, purification systems, lyophilizers, and analytical instrumentation
In collaboration with Chemical Development, transfer and scale-up processes from laboratory to manufacturing scale
Author and/or review batch documentation, operational procedures, forms, and other required documents. Generate automated equipment methods
Maintains a clean, safe, and well-organized work environment
Execute manufacturing schedule to achieve manufacturing goals
Safely handle hazardous materials/waste including organic solvents, strong acids and bases
Identify and troubleshoot technical issues with the process and equipment
Investigate unexpected or aberrant results during production to provide suitable root cause investigation analysis
Responsible for routine communication to all levels of the organization on manufacturing activity
Provides cross-functional site support as needed, including facility maintenance, equipment maintenance and calibration, and inventory control.
Support equipment calibration and maintenance programs
Provides training to other staff members
Perform other tasks as necessary or assigned
Physical Requirements
Ability to sit, stand, reach, bend, climb, balance, walk, and use hands/fingers. Ability to lift up to 50lbs 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 determine accuracy, neatness, and thoroughness of work and to make general observations.
Qualifications
Bachelor's degree in Life Science, Chemistry, or Engineering with at least four (4) years of relevant experience or eight (8) years of relevant experience with a High School diploma
Strong background in oligonucleotide-based drug substance development and manufacturing including knowledge of nucleic acid synthesis, purification, ultrafiltration, annealing and lyophilization techniques and equipment is highly desired
Requires a proficient understanding of cGXP and applicable regulations and guidelines
Working knowledge of control software for automated oligonucleotide synthesizers and/or chromatography systems is highly desired
Mechanical aptitude with ability to use tools to perform tasks, basic troubleshooting of mechanical components and systems
Ability to work independently and within teams that consist of members with different degrees of knowledge or ability
Possess excellent written and verbal communication skills
Excellent organizational and multi-tasking skills, attention to detail, and the ability to adapt to changing priorities
Basic computer literacy including, but not limited the use of MS Office suite programs (Word, Excel, Outlook)
Experience using NN software systems (SCADA, SAP, LIMS, Veeva) is preferred
Experience with new plant start-up and operation is desired
Familiarity with the transfer and scale-up of development processes to the manufacturing scale is preferred
The base compensation range for this position is $81,000 to $140,000. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.
Novo Nordisk offers long-term incentive compensation and or company vehicles depending on the position's level or other company factors.
Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex-able vacation policy, and parental leave policy.
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
We're not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.
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.
