Conduct experiments using common as well as novel ELISA/cell/SPR-based assays to support cell line development, process and formulation development, comparability and structure-function elucidation ...
Conduct experiments using common as well as novel ELISA/cell/SPR-based assays to support cell line development, process and formulation development, comparability and structure-function elucidation ...
Research Investigator, Biologics Analytical Development
Wilmington, DE · On-site
$45K - $45K/yr
Conduct experiments using common as well as novel ELISA/cell/SPR-based assays to support cell line development, process and formulation development, comparability and structure-function elucidation ...
Research Investigator, Biologics Analytical Development
Wilmington, DE · On-site
$45K - $45K/yr
Conduct experiments using common as well as novel ELISA/cell/SPR-based assays to support cell line development, process and formulation development, comparability and structure-function elucidation ...
Senior Staff Quality Engineer
$86K - $117K/yr
... End of Line Testing performance data of the Fuel Cell Power Module's and identify product performance excursions in the data to support KPI objectives. * Work closely with product development ...
Senior Staff Quality Engineer
$86K - $117K/yr
... End of Line Testing performance data of the Fuel Cell Power Module's and identify product performance excursions in the data to support KPI objectives. * Work closely with product development ...
... End of Line Testing performance data of the Fuel Cell Power Module's and identify product performance excursions in the data to support KPI objectives. * Work closely with product development ...
... End of Line Testing performance data of the Fuel Cell Power Module's and identify product performance excursions in the data to support KPI objectives. * Work closely with product development ...
Director Feasibility, SMM CTCO
Wilmington, DE · On-site
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Director Feasibility, SMM CTCO
Wilmington, DE · On-site
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Director Feasibility, SMM CTCO
Wilmington, DE · On-site
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Director Feasibility, SMM CTCO
Wilmington, DE · On-site
Minimum 5 years experience in Pharmaceutical Industry in Clinical Development and Study Operations ... Line manager to and oversight of Local Feasibility Lead (LFL) within Cell Therapy markets globally ...
Review site plan and one-line diagrams for fuel cell installation projects for accuracy and ... development. * Performance tracking to track and summarize estimate performance collaborating with ...
Review site plan and one-line diagrams for fuel cell installation projects for accuracy and ... development. * Performance tracking to track and summarize estimate performance collaborating with ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. Good understanding of Clinical Study ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. Good understanding of Clinical Study ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. * Good understanding of Clinical Study ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. * Good understanding of Clinical Study ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. Good understanding of Clinical Study ...
Collaborates with local Medical Science Liaisons (MSLs) as directed by LSAD or line management ... Basic understanding of the drug development process. Good understanding of Clinical Study ...
With more than 30,000 fuel cell modules deployed worldwide, we are the trusted partner for Fortune ... Lead development of realtimevisual analytics dashboardsthat provide insights into cycle times, OEE ...
With more than 30,000 fuel cell modules deployed worldwide, we are the trusted partner for Fortune ... Lead development of realtimevisual analytics dashboardsthat provide insights into cycle times, OEE ...
With more than 30,000 fuel cell modules deployed worldwide, we are the trusted partner for Fortune ... Ensure Skid line manufacturing has 100% Quality assurance through inspection, testing, and sub ...
With more than 30,000 fuel cell modules deployed worldwide, we are the trusted partner for Fortune ... Ensure Skid line manufacturing has 100% Quality assurance through inspection, testing, and sub ...
Correctional Staff Sergeant
New Castle, DE · On-site
$71K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... Conducts periodic shakedowns of inmates and searches inmates, visitors, employees, cell blocks and ...
Correctional Staff Sergeant
New Castle, DE · On-site
$71K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... Conducts periodic shakedowns of inmates and searches inmates, visitors, employees, cell blocks and ...
Correctional Staff Sergeant
Dover, DE · On-site
$50K - $60K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... This course is administered by the Department of Correction at the Employment Development Center.
Correctional Staff Sergeant
Dover, DE · On-site
$50K - $60K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... This course is administered by the Department of Correction at the Employment Development Center.
Correctional Staff Sergeant
Dover, DE · On-site
$50K - $60K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... This course is administered by the Department of Correction at the Employment Development Center.
Correctional Staff Sergeant
Dover, DE · On-site
$50K - $60K/yr
Summary Statement This is the first line supervisor responsible for supervising and participating ... This course is administered by the Department of Correction at the Employment Development Center.
Open Rank Professor (Continuing Track) Biomedical Engineering Quantitative Systems Pharmacology
Newark, DE · On-site
The candidate will also support the growth and development of the QSP program and foster industry ... The continuing track (CT) is UD's full-time, continuing faculty line. CT faculty enjoy contracts ...
Open Rank Professor (Continuing Track) Biomedical Engineering Quantitative Systems Pharmacology
Newark, DE · On-site
The candidate will also support the growth and development of the QSP program and foster industry ... The continuing track (CT) is UD's full-time, continuing faculty line. CT faculty enjoy contracts ...
Open Rank Professor (Continuing Track) Biomedical Engineering Quantitative Systems Pharmacology
Newark, DE · On-site
The candidate will also support the growth and development of the QSP program and foster industry ... The continuing track (CT) is UD's full-time, continuing faculty line. CT faculty enjoy contracts ...
Open Rank Professor (Continuing Track) Biomedical Engineering Quantitative Systems Pharmacology
Newark, DE · On-site
The candidate will also support the growth and development of the QSP program and foster industry ... The continuing track (CT) is UD's full-time, continuing faculty line. CT faculty enjoy contracts ...
Director, Enterprise Access and Reimbursement Manager (ARM) Team - Mid-Atlantic Region
Wilmington, DE · On-site
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that ... The successful candidate is responsible for supporting the development and management of our broad ...
Director, Enterprise Access and Reimbursement Manager (ARM) Team - Mid-Atlantic Region
Wilmington, DE · On-site
From optimizing a production line to the latest breakthroughs in cell therapy, this is work that ... The successful candidate is responsible for supporting the development and management of our broad ...
Correctional Lieutenant
Georgetown, DE · On-site
$76K/yr
Conducts periodic shakedowns of inmates and searches inmates, visitors, employees, cell blocks and ... Appointees other than in-line promotions must successfully complete a Department training course in ...
Correctional Lieutenant
Georgetown, DE · On-site
$76K/yr
Conducts periodic shakedowns of inmates and searches inmates, visitors, employees, cell blocks and ... Appointees other than in-line promotions must successfully complete a Department training course in ...
Freelance Cell Line Development information
$45K - $45K/yr
Other
Posted 29 days ago
Job description
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.
Job Summary (Primary Function)
The Research Investigator, Biologics Analytical Development is responsible for designing and conducting experiments to develop new analytical methods to support release testing, stability, and characterization of a growing biologics pipeline. This role requires scientific knowledge of a variety of analytical methods, experience in biologics development from early stage to late stage, and familiarity with ICH guidance. Strong interpersonal and communication skills are required.
Essential Functions of the Job (Key responsibilities)
- Design experiments, generate and interpret data to support CMC analytical activities. Conduct experiments using common as well as novel ELISA/cell/SPR-based assays to support cell line development, process and formulation development, comparability and structure-function elucidation towards regulatory filings.
- Perform routine sample testing using analytical methods such as ELISA, PCR, SPR, etc.
- Author notebooks, protocols, SOPs, and reports.
- Present data summaries and study conclusions at internal scientific meetings.
- Participate in analytical method transfer/qualification.
- Operate and maintain analytical instrumentation in compliance with all safety rules and procedures.
Qualifications (Minimal acceptable level of education, work experience, and competency)
- Master's degree with 5 to 7 years or Ph.D. degree in biochemistry, biological sciences, or pharmaceutical sciences, or equivalent experience, with relevant laboratory experience in a variety of analytical techniques in a pharma/biotech or academic setting.
- Experience with biophysical and biochemical methods including protein assays, ELISA, PCR, SPR, higher order structure analysis, etc.
- Experience with analytical method development, qualification, method transfer, and validation is valued.
- Familiarity with SoftMax Pro, LIMS, and/or ELN systems is preferred, but not required, as training will be provided.
- Excellent written, verbal, and organizational skills are 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.
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.
About Incyte
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Wilmington, DE, US
Year founded
1991