Quality Assurance Release Coordinator

5 days 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 global leader in innovating, developing, and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient.

We are a patient-centric, collaborative organization that is driven to change the way cancer is treated. We are agile in our thinking and strive for excellence and innovation while acting with high integrity to create value for all stakeholders.

The Quality Assurance, Lot Release Coordinator will play a key role in the compilation of information and documentation required to release materials and products. This role will work collaboratively to assemble information.

**Essential Functions and Responsibilities**
- Preparation of information and management of attendees and distribution of the Material Review Board meeting for internally and externally manufactured Drug Product lots.
- Coordinating with Quality Systems for investigations related to product complaints and BDPR related to internally manufactured Drug Product lots.
- Coordinating release tasks as assigned to the Quality Release team by the schedule.
- Coordinating lot release with cross functional teams for clinical release.
- Ensure compliance to cGMPs and facility procedures. Interface with functional groups, such as Manufacturing, Quality Control, and Document Control, to determine events (errors, deficiencies, discrepancies, deviations, and other observations) and report to management.
- Update, review, and maintain documentation related to quality assurance activities.
- Review batch records and related production documentation, ensuring resolution of all identified issues prior product disposition.
- Collaborate with internal functions to address all identified issues in a timely manner. Determine if the issue needs to be documented in the Quality System.
- Reports errors, deficiencies, discrepancies, and observations to management that could impact product Quality on release.
- Perform disposition of incoming materials and finished product.
- Issuance of labels.
- Support generation of Quality Metrics.
- Verification of data in data management systems
- Ensure timely lot closure.
- Support and review deviations, CAPAs, Laboratory Investigations, temperature excursions and other non-conformances.
- Perform miscellaneous duties as assigned.
- Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Perform miscellaneous duties as assigned.

**Required Education, Skills, and Knowledge**
- A Bachelor’s Degree in Science, Engineering, or a related technical discipline.
- At least three years of experience in a regulated industry.
- Proficient knowledge of cGMP regulations.
- Perform routine activities with mínimal oversights.
- Prior experience with review of QC data specific to cell therapy testing.
- Strong administrative skills including use of Microsoft Word, Excel, and PowerPoint.
- Extremely detail oriented with strong technical skills.
- Knowledge of MasterControl is preferred.
- High level of accountability and ownership.
- Demonstrate a sense of urgency ability to recognize time sensitivity.
- Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity.
- Successfully interface with multi disciplined teams.

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 remain in a stationary position standing or sitting for prolonged periods of time.
- Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.
- Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.
- This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.
- Must be able to communicate with others to exchange information.

**Mental**:

- Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion
- Ability to handle work-related stress
- Ability to handle multiple prioriti

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