Life-Changing
Careers

BRIAN PERRELLA
CHERYL PEDOTA
Prabhdeep Singh
USA

Share this Job

Validation Engineer Job

Date: Jul 31, 2019

Location: West Lebanon, NH, US

Company: Novo Nordisk

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?
We're looking for a detail oriented, team player, to join our Manufacturing Engineering group as a Validation Engineer. This position will work on validation activities where in-depth analysis, authoring protocols, teamwork and flexibility are required. The person in this role will also be responsible for validation activities in several areas of pharmaceutical manufacturing including, but not limited to, DQ, IQ, OQ, PQ, requalification, cleaning, sterilization and utilities. We're looking for candidates with the following knowledge, skills & abilities and experience:

Education:
  • Bachelors degree or equivalent experience in life sciences or engineering
Experience:
  • A minimum of three (3) years validation experience in the pharmaceutical or biotechnology industry
  • Experience preparing protocols, executing data analysis, and report writing
Skills & abilities:
  • Experience preparing protocols, executing data analysis, and report writing
  • Ability to demonstrate broad understanding of:
    • Concepts of Validation
    • Change control processes
    • Root cause analysis techniques and cGMP documentation practices
    • cGMP regulations, GMP and other industry standards pertaining to validation.
    • Technical requirements for Validation and of biopharmaceutical equipment, facilities and/or instrumentation.
  • Excellent written and verbal communication skills a must
  • A strong work ethic (self-motivated) and demonstrated ability to work in teams
Physical requirements and working environment:
  • 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%
Title and pay are commensurate with experience.

Relocation assistance available for candidates outside open to moving to the area.


Novo Nordisk is an Equal Opportunity Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity.

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.


Requisition ID: 59971BR
State/Provinces: West Lebanon
Job Category: Quality


Nearest Major Market: Hanover

Job Segment: Developer, Biotech, Manufacturing Engineer, Engineer, Pharmaceutical, Technology, Science, Engineering