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Iovance Biotherapeutics
Philadelphia, PA, United States
Iovance is hosting an onsite Job Fair. Where : Iovance Cell Therapy Center (iCTC) Location : 300 Rouse Blvd Philadelphia, PA 19112 Date : Monday, June 24, 2024 Time : 12pm to 6pm (EDT) What to bring: U pdated resume We are Hiring! We look forward to seeing you at the Job Fair. Overview The Quality Control Specialist II, Compliance I
Job Source: Iovance BiotherapeuticsIovance Biotherapeutics Inc
Philadelphia, PA, United States
Job Description Job Description Salary: Iovance is hosting an onsite Job Fair. Where : Iovance Cell Therapy Center (iCTC) Location : 300 Rouse Blvd Philadelphia, PA 19112 Date : Monday, June 24, 2024 Time : 12pm to 6pm (EDT) What to bring: U pdated resume We are Hiring! We look forward to seeing you at the Job Fair. Overview The Qualit
Job Source: Iovance Biotherapeutics IncIovance Biotherapeutics Inc
Philadelphia, PA, United States
Job Description Job Description Salary: Iovance is hosting an onsite Job Fair. Where : Iovance Cell Therapy Center (iCTC) Location : 300 Rouse Blvd Philadelphia, PA 19112 Date : Monday, June 24, 2024 Time : 12pm to 6pm (EDT) What to bring: U pdated resume We are Hiring! We look forward to seeing you at the Job Fair. Overview Iovance Bi
Job Source: Iovance Biotherapeutics IncIovance Biotherapeutics Inc.
Philadelphia, PA, United States
Iovance is hosting an onsite Job Fair. Where: Iovance Cell Therapy Center (iCTC) Location: 300 Rouse Blvd Philadelphia, PA 19112 Date: Monday, June 24, 2024 Time: 12pm to 6pm (EDT) What to bring: Updated resume We are Hiring! We look forward to seeing you at the Job Fair. Overview The Supervisor, Quality Control Compliance is a part of the
Job Source: Iovance Biotherapeutics Inc.TD Bank Group
Mount Laurel Township, NJ, United States
Compliance, Quality Control & Assurance Manager Work Location: Mount Laurel, New Jersey Hours: 40 Pay Details: $86,840 - $139,360 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. The included salary range for this role takes into account multiple factors that are considered in making compensati
Job Source: TD Bank GroupTD Bank
Mount Laurel Township, NJ, United States
Compliance, Quality Control & Assurance Manager page is loaded Compliance, Quality Control & Assurance Manager Apply remote type Hybrid locations Mount Laurel, New Jersey 11325 North Community House Road, Suite 500 & 575 Mount Laurel - 12000 Horizon Way 5900 North Andrews Avenue time type Full time posted on Post
Job Source: TD BankBank of New York Mellon Corporation
, PA, United States
At BNY, our culture empowers you to grow and succeed. As a leading global financial services company at the center of the world’s financial system we touch nearly 20% of the world’s investible assets. Every day around the globe, our 50,000+ employees bring the power of their perspective to the table to create solutions with our clients that benefit
Job Source: Bank of New York Mellon CorporationBank of New York Mellon Corporation
, PA, United States
At BNY, our culture empowers you to grow and succeed. As a leading global financial services company at the center of the world’s financial system we touch nearly 20% of the world’s investible assets. Every day around the globe, our 50,000+ employees bring the power of their perspective to the table to create solutions with our clients that benefit
Job Source: Bank of New York Mellon CorporationPhiladelphia, PA, United States
OverviewThe Quality Control (QC) Compliance Investigator II will assist the Laboratory Manager in advancing and closing QC related investigations. Strong technical writing skills are required with flow cytometry and ELISA experience. Experience in a CAR-T or TIL environment is a plus.The ideal candidate will have experience working in a GMP-regulated laboratory with knowledge of writing investigations but is not required. The position will be on-site at the Philadelphia location.
Essential Functions and ResponsibilitiesAssists Lab Support Manager and other investigators with responses to audits, deviations, out of specification/lab investigations, and corrective/preventative actions (CAPA).Work cross-functionally to support deviations and Out of Specification investigations with an emphasis on analytical assays (flow cytometry, ELISA, and other cell-based assays) and Microbiology assays.Gather data in support of deviations and maintain a trending database of applicable metrics.Revise Quality documents in support of deviation mitigation and/or CAPAs.Other responsibilities as determined.
Required Education, Skills, and KnowledgeBachelor’s degree in a relevant discipline (biological sciences or equivalent)1-5 years of experience in the biopharmaceutical industry within a cGMP Quality Control roleBasic knowledge of biological drug development with respect to Quality ControlExtremely detail-oriented with strong analytical, written, and verbal communication skillsDemonstrate sense of urgency; ability to recognize time sensitivityFlexible and adaptable style with an eagerness to take on challenges
Preferred Education, Skills, and KnowledgeExperience with cell and/or gene therapy productsGMP regulated laboratory experienceKnowledge of investigation writing
The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation.
Physical Demands and Activities Required:Must be able to Sit for an extended amount of time in front of the computer or biological safety cabinet
Mental:Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadline
Work Environment:This position will work in both an office and a manufacturing lab setting.When in the lab, must be able to work in Lab setting with various chemical/biochemical exposures, including latex and bleach.Able to work in cleanroom with biohazards, human blood components, and chemicals.Potential exposure to noise and equipment hazards and strong odors.The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.
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Email Alert for Quality Control Compliance Investigator II jobs in Philadelphia, PA, United States
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