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. What we offer you:
Leading pay and annual performance bonus for all positions
36 Paid days off including vacation, sick days & company holidays
Health Insurance, Dental Insurance, Vision Insurance
Guaranteed 8% 401K contribution plus individual company match option
12 weeks Paid Parental Leave
Free access to Novo Nordisk-marketed pharmaceutical products
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 will support commissioning activities providing analysis, authoring protocols, and commissioning new and existing equipment, processes, and instrumentation in accordance with science and risk-based validation (SRV). This role will provide input to project team members through all stages of specification setting, supplier selection, and commissioning / qualification /verification. This role will also help develop requirements, build/construct, design, commission, perform SAT and FAT verification activities for projects according to (SRV) and approved timelines. This work may include commissioning within pharmaceutical manufacturing such as: requalification, cleaning, sterilization, and utilities. Collaboration with production, production support groups and other stakeholders to ensure completion of deliverables. Commissioning projects will primarily consist of Brownfield projects including: installations, modifications, and ugrades to existing systems & equipment.
This position can be considered for Commissioning Engineer Levels I-III dependent on candidate meeting minimum qualifications for such role.
This role is a full-time onsite based role at our West Lebanon, NH site. Relocation assistance is available for selected candidate.
Relationships
Reports to: Senior Manager - Facilities Engineering & Metrology.
Number of subordinates with direct/indirect referral: none, this is an individual contributor role.
Essential Functions
Maintains proficiency and understanding of Facilities, Utilities, Systems and equipment operations
Author and participate to complete commissioning protocols and execution, data analysis and final report preparation for utilities, equipment, and instrumentation. This may include site acceptance testing (SAT) and factory acceptance testing (FAT)
Supports consistent and best practices for creating and executing commissioning protocols
Ensures accuracy and compliance of commissioning and system records
Partner with the Validation Department to participate and provide feedback to NN validation process group
Ability to work and communicate effectively across multiple local departments. multiple international production sites
Support the creation and review of documentation (Specifications, SOPs, etc.) in accordance with local, NN and regulatory requirements
Supports Deviations (DV) and Change requests (CR) related to commissioning activities
Maintain effective communication and ensure alignment in coordination with appropriate teams
Support facility certification for new or upgraded Pharmaceutical Manufacturing (process equipment and facility-support equipment) and Quality Control facilities as needed and the continued operation of such facilities
Ensures systems and processes are commissioned in a compliant manner in accordance with FDA, EMA and NN requirements
Represent Facilities Engineering and actively participate with cross-functional teams (Validation, Manufacturing, Engineering, Facilities and Quality groups) related to commissioning and validation
Provide data for assessments associated with change control activities
Review protocols, summary reports and other documentation associated with commissioning
Serves as Subject Matter Expert (SME) for commissioning activities within Facilities Engineering and primary point of contact with site Validation Team
Present and support commissioning concepts, data and approaches for audits and inspections
Maintains technical knowledge and current trends within the commissioning process and science and risk-based validation (SRV) programs
Other job duties as assigned
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
Qualifications
Bachelor’s degree or equivalent experience in life sciences or engineering
A minimum of three (3) years related experience with a Bachelor’s degree
Experience with data analysis and report writing
Entry level understanding of:
Concepts of Validation and commissioning
Change control processes
Root cause analysis techniques and cGMP documentation practices
cGMP regulations
Excellent written and verbal communication skills a must
A strong work ethic (self-motivated) and demonstrated ability to work in teams as well as independently
Physical Requirements
The ability to climb. stoop, kneel, crouch, crawl, reach, stand, and walk. The ability to push, pull, lift, finger, feel, 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 visual inspection. The working environment includes a variety of physical conditions including: noise, inside and outside conditions, working in narrow aisles, and temperature changes; atmospheric conditions including: odors, fumes, and dust. Local and International Travel: 0-10%.
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.