Quality Control Technician I - III

BioSpace; West Lebanon (NH); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading biopharmaceutical company is seeking a Quality Control Technician I - III at their West Lebanon, NH location. The role involves supporting QC operations, ensuring compliance with quality regulations, and performing various laboratory tasks. Candidates should possess a High School Diploma and ideally have relevant work experience in pharmaceuticals or biotechnology.

Benefits

Leading pay and annual performance bonus

36 paid days off including vacation and sick days

Health, dental, and vision insurance

401K contribution plus company match

14 weeks paid parental leave

Free access to pharmaceutical products

Qualifications

• High School Diploma with 3 years of relevant work experience.
• Associate’s degree with 0 years of relevant work experience preferred.
• Pharmaceutical or Biotechnology experience preferred.

Responsibilities

• Performs routine QC support activities including housekeeping and sanitizations.
• Identifies deviations and supports systematic problem-solving.
• Documents work in accordance with Good Documentation Practice.

Skills

Organizational skills

Time management

Attention to detail

Basic computer skills

Education

High School Diploma

Associate’s degree in a scientific field

Job description

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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.

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
• 14 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 has primary responsibility to support operations for the given area. This position requires strict adherence to cGMPs, established manufacturing practices and procedures, and compliance with quality regulations and guidelines.

This role is onsite based Monday through Friday, during standard office hours at our West Lebanon, NH bioproduction facility.

Relationships

Reports to: QC Supervisor

Essential Functions

• Performs routine QC support activities (e.g. housekeeping, sanitizations, glassware cleaning, sample receipt)
• Performs sampling with minimal support
• Support of low complexity tasks (e.g. Spectroscopy, Bioburden Testing, Incoming Inspection of Consumables)
• Performs routine equipment maintenance with support
• Identifies deviations and may support systematic problem solving and laboratory investigations
• Documents and archives work in accordance with Good Documentation Practice
• May support report writing activities
• 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
  
  
  

Qualifications

• Education and Certifications:
• High School Diploma required
• Associate’s degree in a scientific field preferred

• Work Experience:
• High School Diploma with three (3) years of relevant work experience required
• Associate’s degree with zero (0) years of relevant work experience preferred
• Pharmaceutical, Biotechnology or other regulated industry experience preferred

• Knowledge, Skills, and Abilities:
• The ability to understand and execute established written instructions is essential
• Good organizational, time management and documentation skills
• Attention to detail and ability to prioritize tasks
• Basic computer skills (e.g. email, MS Word, database management)
• Knowledge of laboratory or manufacturing operations preferred
  
  
  

Physical Requirements

0-5% overnight travel required. The ability to climb, balance, stoop, reach, stand and walk. The ability to push, lift, grasp, and feel. The ability to speak, listen, and understand verbal and written communication. Repetition including substantial movement of wrists, hands, and or fingers. Lifting up to 10 pounds of force occasionally to lift, carry, push, pull, or otherwise 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: noise, close proximity to moving parts and equipment, use of ladders, and exposure to chemicals; atmospheric conditions including: odors, fumes, and dust.

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.

Seniority level

• Seniority level

  Entry level

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  Full-time

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  Quality Assurance

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