The Drive to Discover. The Experience to Deliver.

Careers At Incyte Corporation

Looking for a challenge and a chance to grow your career?

Then Incyte is the pharmaceutical company for you. While our pipeline demonstrates the ability to compete with much larger pharmaceutical companies in selecting compelling targets and creating high-quality drug candidates, our smaller size enables employees to see the direct impact of their contributions on the direction of the company. Due to our smart, agile culture and cutting-edge science, we delivered a novel, first-to-market product in an unmet medical need in 2011 - the first in the company's history.

Opportunities for taking on new and/or additional responsibilities, in addition to advancement, are a key element in our culture. Add to that a science-based, fast-paced work environment and you’ve got an exciting company in which to work.

In addition to opportunities for growth, we offer an outstanding benefits andcompensation package to help meet personal needs as well.

Take a look at our current openings to find the match that’s right for you!

Incyte Corporation values the talents of our diverse workforce and is proud to be an Equal Opportunity Employer.


Coordinator, QA

Department: Quality Assurance and Control
Location: Incyte Corporate Headquarters

Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rigorous pursuit of research and development excellence to improve the lives of patients, make a difference in health care, and build sustainable value. 

The Company strives to discover and develop first-in-class and best-in-class medicines—advancing a diverse portfolio of large and small molecules. 

Our Quality Assurance group is looking for an experienced Coordinator.  

Job Summary: 

The Quality Assurance Coordinator handles a wide range of administrative and support related tasks for the Global R&D QA group and the Global Quality Systems group.

Responsibilities:

  • General Administration:
    • Coordinate and arrange team/working group meetings, video conferences, rooms and schedules.
    • Issue  and follow-up PO’s and invoices.
    • Memo generation/mailing.
    • Share Point/Shared Drive Administration support.
    • Ensure adequate level of office supplies are maintained.
    • General visitor support.
  • Operations support:
    • Management of Documentation Requests & Document Storage in paper or electronic format.
    • Track project timelines & provide regular updates.
    • Organize incoming information and triage to associated functional areas/team members.
    • Collate metrics to be used for management review. 
    • Assist in the preparation of routine reports.
    • Create, maintain, and monitor databases or communications as required.

Qualifications:

  • High School diploma/GED required, college degree preferred.
  • 5 or more years of related administrative support.
  • Excellent oral and written communication skills and is able to communicate effectively through all levels of the organization.
  • Detail oriented; Must possess excellent organizational skills and the ability follow complex processes, procedures and systems.
  • Ability to work in collaborative and independent work situations and environments with minimal supervision.
  • Demonstrate critical thinking and ability to execute goals set by Department Leaders and managers.
  • Maintain composure and competence under stressful situations; flexibility and adaptability.
  • High level of proficiency with Microsoft Office; comfortable with other software programs.


Disclaimer:  The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications.   Management reserves the right to change or modify such duties as required.

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