QA Engineer Visa Sponsorship Jobs in Delaware
Delaware's QA engineer job market centers on Wilmington and Newark, where financial services giants like JPMorgan Chase, Bank of America, and Chemours, along with biotech firms near the University of Delaware, drive consistent demand. International candidates with software testing, automation, and quality assurance expertise will find employers here with established visa sponsorship programs.
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A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
SUMMARY
This position is responsible for providing GCP oversight of Clinical development teams to the Head of Incyte Global R&D QA. This role will also include the execution and management of Incyte QA GCP audits and the provision of GCP guidance and advice across assigned Clinical Development programs.
The Senior Manager Clinical R&D QA is also the QA lead for clinical inspection activities related to the clinical programs under its quality oversight.
DUTIES AND RESPONSABILITIES
- Provide QA GCP advice and support to Incyte Clinical Development/Operations functions and other relevant functions as assigned.
- Plan, schedule and conduct audits of Clinical Investigator Sites, Vendors, Trial Master Files and Clinical submission documents.
- Assist with the management of QA consultants performing audits on behalf of Incyte QA.
- Lead regulatory authority inspections activities for development programs assigned including conducting pre-inspection audits, inspection readiness activities and coordination/hosting inspection role, as assigned.
- Coordinate responses and corrective/preventative actions from deviations, audit and regulatory findings.
- Assist with the maintenance of the clinical Quality Management System including QA support for change control, deviations, review/revision of SOPs with ensuring continuous process improvement.
- Stay abreast of clinical trial requirements, ICH GCP, and guidelines from other regulatory agencies for the management of clinical trials as appropriate.
- Alert Global Clinical R&D QA Upper Management of internal and external GCP compliance and clinical trial issues in a timely manner.
- Mentoring Junior Clinical QA as assigned.
- Promote Quality Culture with external R&D stakeholders, as assigned.
- Stay abreast of local/country clinical activities/initiatives from Regional Clinical Operations members and ensure necessary QA oversight in place as Clinical R&D QA Point of contact.
- Conduct GCP training for Incyte staff.
- Be knowledgeable and be able to understand advanced operational, scientific and/or clinical research areas.
- Be thoroughly familiar with assigned Incyte Compounds and protocol.
REQUIREMENTS
- Bachelor’s degree in a science or healthcare related discipline, or similarly conferred degree from a university.
- 5 to 7 years’ experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
- Minimum of 5 years’ experience performing GCP audits of investigator sites and/or CROs.
- English fluency written and spoken (the company language).
- Regulatory inspection experience as coordinator or key role.
- Ability to travel up to 30%.
- Excellent written and oral communication skills.
- This role is office-based.
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.
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.
Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity.
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
SUMMARY
This position is responsible for providing GCP oversight of Clinical development teams to the Head of Incyte Global R&D QA. This role will also include the execution and management of Incyte QA GCP audits and the provision of GCP guidance and advice across assigned Clinical Development programs.
The Senior Manager Clinical R&D QA is also the QA lead for clinical inspection activities related to the clinical programs under its quality oversight.
DUTIES AND RESPONSABILITIES
- Provide QA GCP advice and support to Incyte Clinical Development/Operations functions and other relevant functions as assigned.
- Plan, schedule and conduct audits of Clinical Investigator Sites, Vendors, Trial Master Files and Clinical submission documents.
- Assist with the management of QA consultants performing audits on behalf of Incyte QA.
- Lead regulatory authority inspections activities for development programs assigned including conducting pre-inspection audits, inspection readiness activities and coordination/hosting inspection role, as assigned.
- Coordinate responses and corrective/preventative actions from deviations, audit and regulatory findings.
- Assist with the maintenance of the clinical Quality Management System including QA support for change control, deviations, review/revision of SOPs with ensuring continuous process improvement.
- Stay abreast of clinical trial requirements, ICH GCP, and guidelines from other regulatory agencies for the management of clinical trials as appropriate.
- Alert Global Clinical R&D QA Upper Management of internal and external GCP compliance and clinical trial issues in a timely manner.
- Mentoring Junior Clinical QA as assigned.
- Promote Quality Culture with external R&D stakeholders, as assigned.
- Stay abreast of local/country clinical activities/initiatives from Regional Clinical Operations members and ensure necessary QA oversight in place as Clinical R&D QA Point of contact.
- Conduct GCP training for Incyte staff.
- Be knowledgeable and be able to understand advanced operational, scientific and/or clinical research areas.
- Be thoroughly familiar with assigned Incyte Compounds and protocol.
REQUIREMENTS
- Bachelor’s degree in a science or healthcare related discipline, or similarly conferred degree from a university.
- 5 to 7 years’ experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
- Minimum of 5 years’ experience performing GCP audits of investigator sites and/or CROs.
- English fluency written and spoken (the company language).
- Regulatory inspection experience as coordinator or key role.
- Ability to travel up to 30%.
- Excellent written and oral communication skills.
- This role is office-based.
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.
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.
QA Engineer Job Roles in Delaware
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Search QA Engineer Jobs in DelawareQA Engineer Jobs in Delaware: Frequently Asked Questions
Which companies in Delaware sponsor visas for QA engineers?
Financial services and pharmaceutical companies are the most active visa sponsors for QA engineers in Delaware. JPMorgan Chase, Bank of America, and Capital One have sponsored H-1B visa workers in technology quality roles from their Wilmington operations. Incyte, a biopharmaceutical company headquartered in Wilmington, also sponsors QA engineers in regulated environments. Larger technology contractors and consulting firms operating in the state round out the sponsoring employer pool.
Which visa types are most common for QA engineers in Delaware?
The H-1B is the most common visa for QA engineers in Delaware, as most roles require a bachelor's degree in computer science, engineering, or a related field, satisfying the specialty occupation requirement. Candidates already holding H-1B status at another employer can transfer to a Delaware-based company without waiting for a new lottery cycle. F-1 OPT and STEM OPT extension holders are also commonly hired by larger employers in the state before transitioning to H-1B sponsorship.
Which cities in Delaware have the most QA engineer sponsorship jobs?
Wilmington is Delaware's primary employment hub for QA engineers, driven by its concentration of financial services and pharmaceutical headquarters. Newark is the second-strongest market, partly because of its proximity to the University of Delaware and a cluster of technology and biotech employers along the Route 1 corridor. Dover has a smaller but present market, mainly through state government IT contractors and regional healthcare organizations that occasionally sponsor qualified candidates.
How to find qa engineer visa sponsorship jobs in Delaware?
Migrate Mate filters job listings specifically by visa sponsorship, so you can search for QA engineer roles in Delaware without sorting through positions that won't support international candidates. The platform surfaces openings from financial services, biotech, and technology employers concentrated in Wilmington and Newark. Filtering by location and role on Migrate Mate saves significant time compared to reviewing unfiltered postings where sponsorship willingness is unclear.
Are there state-specific considerations for QA engineers seeking sponsorship in Delaware?
Delaware's QA engineer market is heavily shaped by its financial services sector, meaning many roles involve regulated systems, compliance testing, or fintech platforms where domain knowledge can strengthen a sponsorship case. The University of Delaware also feeds a steady pipeline of engineering graduates into the local market, so international candidates benefit from demonstrating specialized skills in test automation frameworks like Selenium or Cypress that entry-level graduates typically lack. Delaware has no state income tax on non-wage income, though this does not affect the sponsorship process itself.
What is the prevailing wage for sponsored qa engineer jobs in Delaware?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.