Supervisor, Quality Operations
4 weeks ago
**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**
This individual will be responsible for supporting day-to-day Quality Operations activities relating to support manufacturing and release of products manufactured at the iCTC. The individual will be collaborative, organized, innovative, flexible, with a strong desire to learn and take ownership and accountability.
**Essential Functions and Responsibilities**
- Supervision and Development direct reports, mentoring/coaching to motivate and mentor peers/staff to foster a culture of continuous improvement, quality, and excellence.
- Perform real-time, on-the-floor support for escalations to ensure compliance with GMP and GDP quality initiatives.
- Schedule and coordinate daily activities ensuring conformance to the daily schedule.
- Helps to 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 escalate if not resolved as appropriate to management.
- Review batch records and related production documentation, ensuring resolution of all identified issues prior product disposition. Work with internal functions to address all identified issues in a timely manner. Reports errors, deficiencies, discrepancies, and observations to management.
- Support release of drug product and materials during the shift
- Issuance of lot numbers and supporting documentation as needed for the shift.
- Initiate and participate in standard operating procedure (SOP) revisions to improve compliance.
- Review of Quality System records for compliance.
- Work in a cleanroom with biohazards, human blood components, and chemicals
- Must adhere to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations.
- Perform miscellaneous duties as assigned.
**Required Education, Skills, and Knowledge**
- Minimum B.S. in biology, biochemistry, bioengineering, related technical field, or equivalent industry and technical experience.
- Minimum of 5 years of experience in biopharmaceutical-based GMP aseptic manufacturing. A minimum of 2 years in a Lead/Leadership/Supervisory Role is desired**.**:
- Detailed knowledge of Code of Federal Regulations 21 CFR 210/211 and International Council for Harmonization Guidelines governing current Good Manufacturing Practices for Pharmaceuticals; 21 CFR 1271 is a plus
- Excellent oral and written communication skills
- Ability to identify and resolve quality issues with others in a proactive, diplomatic, flexible, and constructive manner
- Must be comfortable in a fast-paced environment and changing priorities
- Experience with use of an electronic QMS, MasterControl
**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.
**For the Visual Inspection Program, the technician must be able to pass a Vision Exam that includes the following**:
- Must not be color
- Must have 20/20 near vision in both eyes (can be corrected)
**Physical Demands and Activities Required**:
- Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc.
- Must be able to work in a cleanroom lab setting with biohazards / various chemicals.
- Must meet requirements for and be able to wear a half-face respirator.
- Able to stand and/or walk 90% (and sit 10%) within your scheduled workday, which may include climbing ladders or steps.
- Ability to crouch, bend, twist, reach, and perform activities with repetitive motions.
- Must be able to lift and carry objects weighing up to 45
**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 deadlines.
**Work Environment**:
This position will work in both an office and a manufacturing setting. When in the lab, you may be exposed to various chemicals/biochemical, including latex and bleach. Additionally, there is potential for variable noise levels, equipment hazards, strong odors, and other detergents/sanitizers.
The statements contained in this document are intended to describe the general natur
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