Science & Research H-1B1 Singapore Sponsorship Jobs in Delaware
Science and research H-1B1 Singapore sponsorship jobs in Delaware are concentrated around Wilmington and the broader New Castle County corridor, where employers in pharmaceutical research, chemical sciences, and life sciences maintain active hiring. Companies such as DuPont and Corteva Agriscience have historically supported specialty occupation filings, making Delaware a notable state for Singapore nationals pursuing research-focused careers in the U.S.
See All Science & Research JobsOverview
Showing 5 of 6+ Science & Research H-1B1 Singapore Sponsorship Jobs in Delaware
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all Science & Research H-1B1 Singapore Sponsorship Jobs in Delaware
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Science & Research H-1B1 Singapore Sponsorship Jobs in Delaware.
Get Access To All JobsINTRODUCTION
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for a Research Scientist in our Bioanalytical (GBA) department. GBA is comprised of three laboratory operation units: Small Molecules, Proteins, and Oligonucleotides, and each unit has their own Method Development/Method Validation/Sample Analysis (MD/MV/SA) group. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support drug development of small molecules, antibody drug conjugates, protein, and genetic medicines.
The GBA department expertise lies in the quantitation of small molecules, peptides, proteins, oligonucleotides, and biomarkers by various chromatographic (standard flow LC, microflow LC, SFC) coupled to tandem mass spectrometric (MS/MS, MS/HRMS, hybrid/immunocapture mass spec) techniques. We have been pivotal in supporting most of the HIV drugs, most of the HBV/HCV drugs, 2 of the 15 ADCs, and 7 of the 24 oligonucleotide therapeutics approved by FDA/EMA.
We are currently looking for Research Scientists for our Sample Analysis groups. This position will serve as Principal Investigator (PI) on Bioanalytical studies and be responsible for study management, interpretation and reporting of study data, and in concert with team members and peers, will participate in method validation when needed.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology, and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical, and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring, and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork, and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
THE JOB
- Independently manage multiple sample analysis projects/studies at the same time with minimum supervision.
- Prepare, and/or review and understand study protocols.
- Coordinate with client and internal resources to plan, design, and conduct studies.
- Evaluate significance of data and report findings.
- Prepare study summaries and/or reports.
- Set up, utilize, and maintain complex instrumentation.
- Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.
- Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.
- Maintain schedule of projects and timelines.
- Supervise, train, and/or mentor junior scientific staff.
- Develop, validate, and run sensitive, reliable, and efficient LC/MS/MS assays for TK/PK assessment.
- Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.
WORK LOCATION
- This job will be 100% QPS-office/facility based.
REQUIREMENTS
The successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:
- Ph.D. degree
- Recent graduates must have direct experience in LC-MS/MS analysis.
- If more than 2 years since graduation, candidates must have direct experience in method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience.
- Understanding of experimental design and planning, and data collection and analysis software.
WHY YOU SHOULD APPLY
- Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
- Structured Career Ladders that provide excellent growth based on your personal aspirations.
- Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team, and company performance.
- Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance.
- Park-like setting in Newark, Delaware.
- Internal committees designed with the needs and enjoyment of QPS employees in mind.
QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote, and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
INTRODUCTION
Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for a Research Scientist in our Bioanalytical (GBA) department. GBA is comprised of three laboratory operation units: Small Molecules, Proteins, and Oligonucleotides, and each unit has their own Method Development/Method Validation/Sample Analysis (MD/MV/SA) group. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support drug development of small molecules, antibody drug conjugates, protein, and genetic medicines.
The GBA department expertise lies in the quantitation of small molecules, peptides, proteins, oligonucleotides, and biomarkers by various chromatographic (standard flow LC, microflow LC, SFC) coupled to tandem mass spectrometric (MS/MS, MS/HRMS, hybrid/immunocapture mass spec) techniques. We have been pivotal in supporting most of the HIV drugs, most of the HBV/HCV drugs, 2 of the 15 ADCs, and 7 of the 24 oligonucleotide therapeutics approved by FDA/EMA.
We are currently looking for Research Scientists for our Sample Analysis groups. This position will serve as Principal Investigator (PI) on Bioanalytical studies and be responsible for study management, interpretation and reporting of study data, and in concert with team members and peers, will participate in method validation when needed.
QPS’ Story:
Since its inception, QPS has been assisting pharmaceutical, biotechnology, and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical, and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring, and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.
Team members enjoy challenging and rewarding work and are encouraged to achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, teamwork, and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.
If this sounds like your ideal work environment, then we would love to speak with you, so apply today!
THE JOB
- Independently manage multiple sample analysis projects/studies at the same time with minimum supervision.
- Prepare, and/or review and understand study protocols.
- Coordinate with client and internal resources to plan, design, and conduct studies.
- Evaluate significance of data and report findings.
- Prepare study summaries and/or reports.
- Set up, utilize, and maintain complex instrumentation.
- Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.
- Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.
- Maintain schedule of projects and timelines.
- Supervise, train, and/or mentor junior scientific staff.
- Develop, validate, and run sensitive, reliable, and efficient LC/MS/MS assays for TK/PK assessment.
- Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.
WORK LOCATION
- This job will be 100% QPS-office/facility based.
REQUIREMENTS
The successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:
- Ph.D. degree
- Recent graduates must have direct experience in LC-MS/MS analysis.
- If more than 2 years since graduation, candidates must have direct experience in method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience.
- Understanding of experimental design and planning, and data collection and analysis software.
WHY YOU SHOULD APPLY
- Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
- Structured Career Ladders that provide excellent growth based on your personal aspirations.
- Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team, and company performance.
- Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance.
- Park-like setting in Newark, Delaware.
- Internal committees designed with the needs and enjoyment of QPS employees in mind.
QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote, and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.
Science & Research Job Roles in Delaware
See all Science & Research Jobs in Delaware
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Science & Research Jobs in DelawareScience & Research Jobs in Delaware: Frequently Asked Questions
Which science and research companies sponsor H-1B1 Singapore visas in Delaware?
Delaware's science and research sector includes employers such as DuPont, Corteva Agriscience, and various contract research organizations operating in the Wilmington area. Pharmaceutical and chemical companies in New Castle County have filed Labor Condition Applications for specialty occupation roles. Sponsorship decisions depend on the specific role, the employer's workforce needs, and whether the position meets the H-1B1 visa specialty occupation definition. Reviewing DOL LCA disclosure data gives the most accurate picture of which Delaware employers have recent filing history.
Which cities in Delaware have the most science and research H-1B1 Singapore sponsorship jobs?
Wilmington and Newark are the primary hubs for science and research employment in Delaware. Wilmington anchors the state's chemical and life sciences industry, with a concentration of corporate research facilities and laboratory operations. Newark, home to the University of Delaware, supports research activity in materials science, environmental science, and biotechnology. New Castle County overall accounts for the majority of specialty occupation roles in the state, making it the most practical geographic focus for H-1B1 Singapore job seekers.
How do I find science and research H-1B1 Singapore sponsorship jobs in Delaware?
Migrate Mate is built specifically for this search, filtering science and research roles in Delaware by employers with verified H-1B1 Singapore LCA filing history. Rather than sorting through broad job listings and guessing at sponsorship willingness, Migrate Mate surfaces positions from companies that have already demonstrated they file for Singapore nationals in specialty occupation categories. This saves significant time for researchers, scientists, and lab professionals evaluating Delaware employers before applying.
What types of science and research roles typically qualify for H-1B1 Singapore sponsorship in Delaware?
Roles that typically qualify are those requiring at least a bachelor's degree in a directly related scientific discipline. In Delaware, this includes research chemists, materials scientists, environmental scientists, biologists, and research and development engineers, particularly in chemical and agricultural science sectors. The H-1B1 specialty occupation standard requires that the specific degree field is directly tied to the duties performed. Generalist roles or positions where multiple unrelated degree fields are accepted are less likely to meet the definition.
Are there state-specific or industry-specific considerations for H-1B1 Singapore sponsorship in Delaware?
Delaware's science sector is heavily weighted toward chemical sciences, agricultural research, and materials science, reflecting the legacy of major corporate research campuses in the state. Employers in these fields are generally familiar with specialty occupation filings, though H-1B1 sponsorship decisions remain employer-specific and role-dependent. Delaware has no state-level visa or immigration program, so all H-1B1 requirements are governed federally through USCIS and DOL. Singapore nationals should confirm that any prospective employer is prepared to file a Labor Condition Application before accepting an offer.
What is the prevailing wage for H-1B1 Singapore science & research 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.