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Engineering Area Specialist (Technical Writer)

Employer
Novo Nordisk
Location
West Lebanon, NH
Start date
Sep 4, 2024
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Job Details

About the Department       

Site New Hampshire, located in West Lebanon, NH, 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

The primary responsibilities of the Engineering Area Specilist are to support technical operations. Assist in coordination and execution of processes and equipment improvement programs, investigate deviations, and implement corrective/preventative actions via change requests, document change controls, and develop training.

 

Relationships

Reports to: Lead Engineer 

 

Number of subordinates with direct/indirect referral: None

 

Essential Functions

  • Liaison between Engineering and manufacturing for the coordination of process/equipment improvements
  • Ability to investigate and write up Deviations events utilizing Root Cause Analysis
  • Utilize the quality system to implement changes associated with technical operations, engineering, and/or validation (generate, execute, and evaluate change requests)
  • Revise and create documentation (SOP, batch records, reports) associated with technical operations, production, engineering, and validation
  • Incorporate technical pre-planned process improvements and cost reduction projects into manufacturing
  • Develop training for engineering/validation or production with direction from engineers
  • Support Health Authority inspections and internal audits
  • Ability to take on and manage multi-disciplined projects, with minimal supervision
  • Work on cross-functional teams with Validation, Engineering, Manufacturing, Project Management, Quality Control, Facilities, and Quality Assurance
  • 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
  • Other duties as assigned
  •  

    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. Visual acuity to perform close activities such as: reading, writing, and analyzing. Lifting up to 33 lbs/15 kg of force occasionally, and/or up to 30 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects. 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%.

     

    Qualifications

  • Education and Certifications:
    • Associate's Degree in a Business or technicial field, or equivalent combination of education & experience required.
    • Bachelors degree preferred.
  • Work Experience:
    • 4+ years of experience in technicial writing, preferably in engineering, life sciences, software or related industries required with an Associates Degree. 
    • Two (2) years experience with a Bachelors degree preferred
  • Knowledge, Skills, and abilities:
    • Ability to follow routine work instructions for new and ongoing projects and assignments
    • Excellent communication skills and ability to work in a high-paced team-oriented environment
    • Requires functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines
    • Ability to understand and execute established written instructions is essential
    • Organizational skills and an ability to perform assignments with a high degree of attention to detail
    • Demonstrate a practical understanding of lean manufacturing principles
    • Analytical abilities and problem-solving skills
    • A strong work ethic (self-motivated), honesty, excellent communication skills, and the ability to work in teams – displays initiative and commitment
  •  

    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.

    Company

    Novo Nordisk is a leading global healthcare company, founded in 1923 and headquartered in Denmark. Our purpose is to drive change to defeat diabetes and other serious chronic diseases such as obesity and rare blood and endocrine disorders. We do so by pioneering scientific breakthroughs, expanding access to our medicines, and working to prevent and ultimately cure disease. Novo Nordisk employs about 54,400 people in 80 countries and markets its products in around 170 countries. For more information visit novonordisk.com.

    Our US Research & Development hub, located in the Greater Boston area, brings together the best talent to drive life science innovation. Located in Lexington, Watertown and Cambridge, our teams reflect the full scope of R&D, from early research through late-stage clinical development. We are building for the future by 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. By combining the speed and agility of biotech with the quality, resources, and stability of a large pharmaceutical company, our US R&D hub will benefit from the best of both worlds to develop new medicines that meet the needs of patients.

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    Company info
    Website
    Phone
    617-612-6200
    Location
    75 Hayden Avenue
    Lexington
    MA
    02421
    United States

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