Aseptic Processing Technician I [Contract to Hire]

Iovance Biotherapeutics • Philadelphia, PA

2d • Onsite

About The Position

Iovance Biotherapeutics aims to be the 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. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.

As an Aseptic Processing Technician, you will focus on the documentation for our processes. The ideal candidate will have a background in cell culture, aseptic gowning and qualification, and ISO class 5 cleanroom operations. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to ensure the manufacturing process is completed.

Shift: 10 Hour Day Shift, Tuesday - Friday; 7:00am - 5:30pm

Requirements

• Minimum B.S. degree in biology, biochemistry, bioengineering, or related technical field, or equivalent industry experience.
• 0-2 years of experience in biopharmaceutical-based GMP manufacturing operations, including experience in cell culture and associated downstream processing.
• Able to read, write and understand English, and be proficient in Microsoft (Excel, Word, Outlook).
• Able to accurately perform basic math, including fractions, decimals, and percentages.
• Able to work effectively with team members and show initiative to assist others on the team.
• Able to work successfully in a fast-paced, team-oriented environment.
• Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations.

Nice To Haves

• Demonstrated technical knowledge of aseptic processing in cleanroom environments.
• Must not be color blind
• Must have 20/20 near vision in both eyes (can be corrected)

Responsibilities

• Complete training sessions and ensure training documentation is maintained.
• Proficiently carry out procedures to achieve a consistent, error-free execution of daily job assignments
• Work as part of a team to produce each lot accurately and fully complete batch records, forms, and documentation.
• At all times, understand and comply with quality standards and safety guidelines.
• Perform materials stocking, kit preparation, reagent preparation, cleaning activities, and equipment maintenance.
• Identify errors and report them promptly to lab management. Participate in root cause analysis and implement corrective actions.
• Adheres to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP).
• 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.
• Up to 5% of travel

Benefits

• Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level