- Performs root cause analysis and investigations in response 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.
- Bachelor's degree in a relevant discipline (biological sciences or equivalent)
- 3-5 years of experience in the biopharmaceutical industry within a cGMP Quality Control role
- Basic knowledge of biological drug development with respect to Quality Control
- Extremely detail-oriented with strong analytical, written, and verbal communication skills
- Demonstrate sense of urgency; ability to recognize time sensitivity
- Flexible and adaptable style with an eagerness to take on challenges
- Experience with cell and/or gene therapy products
- GMP regulated laboratory experience
- Knowledge of investigation writing
- Must be able to Sit for an extended amount of time in front of the computer or biological safety cabinet
- 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
- 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.
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Quality Control Compliance Investigator II Contract to Hire - Philadelphia, United States - Iovance Biotherapeutics Inc
Description
Job Description
Job DescriptionSalary: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 Quality Control (QC) Compliance Investigator II will assist the QC Compliance Manager in advancing and closing QC related investigations. Strong technical writing skills are required. 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.
Essential Functions and Responsibilities
Required Education, Skills, and Knowledge
Preferred Education, Skills, and Knowledge
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:
Mental:
Work Environment:
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.
Iovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal-opportunity employer, our employees and applicants will be considered without regard to an individual's race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact
By voluntarily providing information and clicking "Submit Application", you explicitly consent to the collection and use of your personal information for the purposes described above and in our Candidate Privacy Notice.
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