Quality Control Compliance Investigator I

4 weeks ago

Philadelphia, United States Iovance Biotherapeutics Inc Full time

**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 Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. Iovance is seeking a Quality Control (QC) Compliance Investigator who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus.

**Essential Functions and Responsibilities**
- Performs deviation investigations for all areas within Quality Control
- Perform out of specification investigations with an emphasis on QC analytical assays (flow cytometry, ELISA, and other cell-based assays) and microbiology assays
- Work cross-functionally to create relevant corrective/preventative actions (CAPA).
- Support maintenance of a database in support of QC metrics and KPI’s.
- Revise quality documents in support of deviation mitigation and/or CAPAs.
- Support programs to improve on-time closure rates for all quality records
- Other responsibilities as determined.

**Required Education, Skills, and Knowledge**
- Bachelor’s degree in a relevant discipline (biological sciences or equivalent)
- 1-3 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

**Preferred Education, Skills, and Knowledge**
- Experience with cell and/or gene therapy products
- GMP regulated laboratory experience
- Knowledge 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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