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.


Manager, Technical Operations

Department: Global Pharma Development
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 Global Process Chemistry Development organization is looking for a Manager, Technical Operations.  This role provides analytical support for assigned projects while working collaboratively with cross-functional teams in support of drug development activities.  The role has responsibilities for management of data input in LIMS, oversight of the standard management system, and contributions to overall systems improvement initiatives. The Manager has some responsibilities for the generation of analytical data and collaborates with colleagues in Process Chemistry, Formulation Development, Quality Assurance and Regulatory Affairs to ensure high quality, on time delivery of GTO deliverables to ensure on-time progression of Pre-Clinical, Clinical and Commercial programs.

Essential Functions of the Job  (Key responsibilities):

  • Contribute to drug development Analytical activities to address key issues.
  • Monitor, review, and guide the analytical activities at external laboratories to ensure timely delivery of quality analytical work packages.
  • Contribute to and coordinate improvement initiatives within Analytical Development.
  • Track stability studies across projects, collate the associated data and summarize/tabulate results.
  • Contribute to implementation of data management systems.
  • Ensure consistency in documentation of shelf lives and retest dates that ensure the quality and safety of drug substances and drug products.
  • Ensure consistency in drug substance and drug product specifications, incorporating batch data and regulatory expectations to ensure drug substance and drug product quality.
  • Writes and reviews technical documentation for regulatory submissions.
  • Authors and reviews SOPs to ensure quality and compliance within GTO.

Qualifications (Minimal acceptable level of education, work experience, and competency):

  • Must have at least a BS in analytical chemistry or other relevant field.
  • Experience with key analytical technology such as HPLC and GC.
  • Experience with electronic lab data management systems.
  • Experience in GMP, Industry and Regulatory requirements.
  • Three years of pharmaceutical R&D analytical experience.
  • Must have thorough knowledge of GMP, Industry and Regulatory requirements.
  • Previous experience of working on several projects running simultaneously while working independently as well part of a team is preferable.

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.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

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