Offers “Abbott”

days ago Abbott

Intern (New Product Introduction), Abbott Point of Care, Ottawa

  • Internship
  • Ottawa (Ottawa)

Job description

     

JOB DESCRIPTION:

At Abbott, we're committed to helping you live your best possible life through the power of health. For more than 130 years, we've brought new products and technologies to the world -- in nutrition, diagnostics, medical devices and branded generic pharmaceuticals -- that create more possibilities for more people at all stages of life. Today, 107,000 of us are working to help people live not just longer, but better, in the more than 160 countries we serve.

Abbott Point of Care is a worldwide leader in providing with-patient care solutions that are intuitive, reliable, and cost-effective for our customers. By delivering lab-quality results in minutes, our i-STAT® System family of with-patient products and services fosters a collaborative, patient-centred environment while driving operational performance.

We are headquartered in Princeton, New Jersey, with more than 1,500 global employees and a presence in 84 countries. Our 46,500 square metre manufacturing facility, Abbott Pointe, is located in Ottawa, Ontario, Canada

There is a critical need to develop and launch a high-sensitivity cardiac test which can detect an extremely small quantity of Troponin in blood.  Troponin is a protein released by the heart when it is in distress.  The new Point-of-Care Troponin test will be several times as sensitive as Abbott’s current on-market cTnI cartridge.

Status: 4 Month Contract/Full Time Hours

Position Overview:

Your particular focus will be on the TnI-Nx cartridge, developing and validating processes involved in the manufacture of our new TnI-Nx product.

As a member of our New Product Introduction Team, you will play a key role in improving product performance by building expertise on the product’s fluidic systems and reagent-based assays.  You will use engineering principals to work with R&D, Design Transfer, and Product Engineering staff in a collaborative environment to develop, validate and implement improved processes and designs.

Job Description: 

Create and execute efficient experimental strategies using DOE methods to identify potential design improvements

Independently execute assigned tasks by applying standard engineering theories, concepts and techniques

Document results of experiments in a manner consistent with the Quality System

Create verification, validation and engineering file protocols and reports consistent with the Quality System

Attend cross-functional team meetings to share information

Keep up-to-date with the latest technical developments in related areas, assess and integrate appropriate changes to work practices

Experience with GMP and in working in an ISO and FDA regulated environment is an asset.  Experience with LEAN Six Sigma manufacturing principles is an asset

Superior analytical and problem solving skills: experience with statistics.

Organizational and leadership skills. Project management experience is an asset

Excellent oral and written communication skills and ability to interact effectively with all levels in the organization

Required Education and Experience:

  • Enrolled in Bachelor’s degree program in Science or Engineering with Chemical, Biochemical, Biomedical or Mechanical Engineering focus;
  • Demonstrated initiative and problem-solving skills; critical thinking skills;
  • Ability to design experiments, analyze and interpret data, and document conclusions;
  • Analytical skills, creativity and innovative approach to problem solving;
  • Ability to collaborate effectively with multidisciplinary team members, and work independently;
  • Willingness to work in labs, manufacturing areas, and office environments;
  • Very strong investigation skills, drive to understand and solve problems;
  • Propensity for continuous learning and experimentation.
  • Ability to apply mathematical concepts and statistics.
  • Effective at dealing with a variety of people and understanding/communicating their requirements.
  • Self-directed, proactive and not easily discouraged.
  • Excellent organizational, planning and scheduling skills.
  • Good oral/written communication skills.
  • Experience in a manufacturing environment is considered an important asset.
  • Experience working in an ISO and FDA regulated environment is an asset.
  • Experience with LEAN Six Sigma manufacturing principles is an asset.

Abbott Canada is committed to the hiring, advancement and fair treatment of individuals without discrimination based on factors such as race, sex, colour, ethnic or national origin, religion, disability, age, citizenship, family or marital status, political beliefs, sexual preference or other factors included in human rights legislation.

Our diversity goals for recruitment, hiring, and retention are embedded in our corporate goals, and our diversity initiatives are supported by the highest level of the organization.

We strongly believe that a diverse workforce fosters more creative and innovative thinking throughout the organization. Creating an inclusive environment, where everyone is respected and valued, enables us to leverage our diversity as a business driver and strengthens our position as a global leader.

Abbott strives to promote and maintain an inclusive, high-performing culture that allows all employees to reach their full potential and contribute to Abbott’s success.

Join Our Talent Community to learn about upcoming job opportunities or connect with us at Abbott Canada, on LinkedIN, on Facebook and on Twitter @AbbottNews and @Abbott Global.

     

JOB FAMILY:

Product Development

     

DIVISION:

APOC Point of Care

        

LOCATION:

Canada > Ottawa : 185 Corkstown Road

     

ADDITIONAL LOCATIONS:

     

WORK SHIFT:

M-F (Canada)

     

TRAVEL:

Not specified

     

MEDICAL SURVEILLANCE:

Not Applicable

     

SIGNIFICANT WORK ACTIVITIES:

Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day)