Senior Quality Control Analyst Philadelphia, PA

Iovance Biotherapeutics, Inc.; Philadelphia (Philadelphia County); On-site; USD 80,000 - 120,000; Full time

Job summary

Iovance Biotherapeutics is seeking a Senior Quality Control Analyst to join their team at the integrated Cell Therapy Center. The role involves conducting quality control testing for cell therapy products, ensuring compliance with GMP regulations while mentoring new staff members and performing data analysis for product release. Ideal candidates will have extensive experience in a GMP Quality Control environment, with hands-on experience in flow cytometry and ELISA platforms.

Qualifications

• Minimum 8 years of experience in a GMP Quality Control role.
• Experience in the pharmaceutical industry.
• Strong technical skills and the ability to manage multiple priorities.

Responsibilities

• Conduct GMP Quality Control testing activities with minimal errors.
• Analyze data for product lot release adhering to turnaround times.
• Mentor and train new laboratory personnel.

Skills

Attention to detail

Technical skills

Data analysis

Problem solving

Education

Bachelor’s degree with 8 years of experience

Master’s degree with 6 years of experience

PhD with 3 years of experience

Tools

Flow Cytometry platforms

Cell-based ELISA platforms

NC-200 platform

Job description

Iovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. The Senior Quality Control Analyst will support quality control testing operations at Iovance’s integrated Cell Therapy Center (iCTC). The Quality Control testing programs include, but are not limited to, in-process, final drug product, and stability testing with a focus on cell therapy products.

The Senior Quality Control Analyst will support quality control testing operations at Iovance’s integrated Cell Therapy Center (iCTC). The Quality Control testing programs include, but are not limited to, in-process, final drug product, and stability testing with a focus on cell therapy products. We are looking for an individual that has hands-on laboratory experience handling primary and/or continuous cell lines and the execution of cell-based potency and identification assays using various immunoassay (ELISA, etc.), flow cytometry platforms, as well as cell count/viability determinations using the NC-200 platform. This position will support the ramp up of QC and other activities in a newly built facility for cell therapy products. This position works across different shifts. Depending on your assigned shift, you may be required to work weekends and holidays to meet target turnaround times.

Shift: Tuesday – Saturday, Day shift 8am – 5pm

Essential Functions and Responsibilities:

• Act as a technical subject matter expert (SME) for potency and/or flow testing activities
• Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuringtesting is completed in compliance with all applicable procedures, standards, and GMP regulations
• Mentor and train new laboratory personnel
• Perform data analysis and final result reporting to support product lot release with adherence to turnaround times
• Perform all activities with respect to GMP/GDP compliance.
• Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs and change controls
• Support QC Compliance to conduct thorough GMP investigations for out of specification test results and other quality events (DRs and LIRs)
• Support technical problem solving for issues pertaining to GMP Quality Control
• Support product stability programs including execution of stability testing and stability data analysis
• Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results.
• Perform peer and/or technical review of laboratory data and logbooks
• Analysis of assay-specific analytical performance trending
• Contribute to Health Authority inspections
• Provide input to functional laboratory and cross functional team meetings
• Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results
• 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
• Other responsibilities as assigned

Required Education, Skills, and Knowledge

• Minimum of 8 years of related experience with a Bachelor’s degree; or 6 years and a Master’s degree; or a PhD with 3 years experience; or equivalent experience.
• Minimum four (4) years of experience in the pharmaceutical industry within a GMP Quality Control role
• Experience with Flow Cytometry and/or Cell based ELISA platforms
• Successfully interface with multi-disciplined teams.
• Extremely detail-oriented with strong technical skills.
• Ability to effectively manage multiple priorities involving aggressive, changing timelines at a high level of productivity.
• High level of ownership and accountability.
• Demonstrate sense of urgency; ability to recognize time sensitivity.

Preferred Education, Skills, and Knowledge

• Experience with cell therapy products
• Experience with cell therapy products is a plus and/or relevant technical skills (NC 200, ELISA, and/or Flow).

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 wear all appropriate Personal Protective Equipment (PPE), including but not limited to: lab coat, half face respirator as applicable, safety glasses/goggles, and nitrile gloves.
• Able to stand and/or walk 90% (and sit 10%) of the scheduled workday which may include climbing ladders or steps.
• Must be able to use near vision to view samples at close range.
• Able to crouch, bend, twist, reach, and perform activities with repetitive motions.
• Must be able to lift and carry objects weighing 20 pounds.

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.

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.

#LI-onsite

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 [e-mail] .

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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