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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 QA Operations

Department: Global Quality Assurance
Location: Incyte Biosciences Technical Operations Sŕrl - Morges

Summary

The QA Manager will be responsible for the Quality oversight of commercial manufacturing activities for the assigned products (drug substance to Drug product).

Duties and Responsibilities

  • Manage the day-to day quality oversight of the commercial supply chain
  • Ensure compliance of Products by reviewing, approving and ensuring maintenance of Material and Product specifications,
  • Perform Batch Record Reviews and releases of commercial batches,
  • Manage & Approve deviations and investigations,
  • Ensure and monitor implementation of Changes at CMOs.
  • Ensure and monitor implementation of CAPAs at contract organizations
  • Perform external and internal audits according to Incyte audit program;
  • Collect and compile data for the preparation of Annual Product Quality Reviews
  • Maintain and Control the Product Batch records filling and databases
  • Support the CMC group for regulatory submissions and follow-ups
  • Maintain Quality and Technical Agreements with applicable commercial supply chain
  • Ensure inspection readiness at assigned CMOs
  • Interpret GMP, general regulatory requirements and Quality systems regulations in the area of manufacturing and ensure implementation as applicable,
  • Performs all responsibilities in accordance with company policies, procedures, applicable regulations and safety requirements
  • Stay current with the applicable regulations and promote Quality across the Incyte organization
  • Cooperate with the Supply Chain, CMC, QC and RA functions in matters relating to commercial Product

Company Culture

  • Contribute positively to a strong culture of business integrity and ethics
  • Act within compliance and legal requirements as well as within company guidelines

Requirements

  • Academic degree in natural or applied sciences (Pharmacy, chemistry, biotechnology, engineering);
  • Firsthand experience of min 5 years in Quality Operations for pharmaceuticals;
  • Thorough knowledge in cGMP and US regulatory requirements;
  • Qualified auditor;
  • Experience in CMO QA oversight;
  • Expertise in solid oral dosage forms and Biotechnology products
  • Strong Interpersonal skills;
  • Strong verbal and written communication skills with well-structured communication and presentation ability;
  • Ability to manage multiple on-going projects;
  • Results focused which may require negotiating skills, empathy, diplomacy, common sense
  • English fluency written and spoken (the company language);
  • Travel, up to 20%

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.

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.

We Respect Your Privacy

Learn more at: http://www.incyte.com/privacy-policy

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.

During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job.   You can learn more about this process here.

You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work. 

You can learn more about Incyte’s data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable).

Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

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