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Quality Assurance Release Coordinator

4 months ago

Philadelphia, United States Iovance Biotherapeutics Inc Full time
Job DescriptionJob 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

 

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 minimal 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 priorities simultaneously
  • Ability to meet deadlines


Work Environment


  • This job works in a professional office environment and a manufacturing lab setting.
  • Potential exposure to latex, bleach, loud noise, lab equipment hazards, strong odors, and chemical/biochemical is possible.
  • Requires operating standard office equipment and keyboards.

 

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 careers@iovance.com.

 

 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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