Aseptic Manufacturing Technician II - Night Shift [Contract to Hire]

Society for Conservation Biology; Philadelphia (Philadelphia County); On-site; USD 50,000 - 80,000; Full time

Job summary

An innovative firm in the biopharmaceutical sector is seeking a dedicated Aseptic Manufacturing Technician II for their night shift team. This role is pivotal in the autologous cell therapy manufacturing program, where you'll engage in hands-on cell processing using advanced bioreactors and aseptic techniques. The position offers a dynamic work environment, requiring adherence to strict GMP standards while collaborating with a diverse team. If you are passionate about contributing to groundbreaking cancer therapies and thrive in a fast-paced setting, this opportunity is perfect for you.

Qualifications

• 1+ years in GMP biopharmaceutical manufacturing, focusing on aseptic techniques.
• Knowledge of GMP regulations and ability to mentor others.

Responsibilities

• Execute GMP cell therapy manufacturing processes proficiently.
• Conduct environmental monitoring and biosafety cabinet duties.

Skills

Aseptic Techniques

GMP Regulations

Cell Processing

Microsoft Office

Education

Bachelor's Degree in Biology or related field

Tools

Bioreactors

Biosafety Cabinets

Cell Count Machines

Job description

Aseptic Manufacturing Technician II - Night Shift [Contract to Hire]

Employer: Iovance Biotherapeutics Inc | Location: Philadelphia, Pennsylvania, US | Salary: Competitive | Closing date: May 9, 2025

Sector: Consultancy/Private Sector | Field: Conservation science | Discipline: Biology | Salary Type: Salary | Employment Type: Contract

Job Description

Overview: Iovance Biotherapeutics is an immuno-oncology company focused on developing and commercializing novel cancer immunotherapies based on tumor infiltrating lymphocytes (TIL). The Aseptic Manufacturing Technician II plays a crucial role in the autologous cell therapy manufacturing program, requiring a broad understanding of manufacturing processes.

Responsibilities include hands-on cell processing using high-density bioreactors, BSCs, cell count machines, and other equipment for clinical and commercial use. Tasks involve environmental monitoring, cell culturing, and liquid transfers within ISO Grade A and B cleanrooms. The role requires working across different shifts, including overtime, weekends, and holidays, especially after onboarding training.

Shifts:
- Shift A: Sunday to Tuesday or Wednesday to Saturday, with specific hours.
- Shift B: Wednesday to Saturday or Thursday to Saturday, with specific hours.

Essential Functions:

• Execute GMP cell therapy manufacturing processes proficiently.
• Complete and maintain training documentation.
• Comply with quality standards, GMP, SOPs, and GDP.

Primary Responsibilities:

Perform cell counts, operate cell processing equipment, and perform aseptic procedures in Grade B/ISO7 and Grade A/ISO5 environments.

Train and pass APQs, perform media preparation, tumor processing, and final product formulation and inspection.

Conduct environmental monitoring and biosafety cabinet duties.

Handle material transfer, sample collection, and final product cryopreservation.

Review documentation, maintain gowning qualifications, and participate in daily meetings.

Qualifications:

• Bachelor’s degree or equivalent experience.
• At least 1+ years in GMP biopharmaceutical manufacturing, including aseptic techniques.
• Knowledge of aseptic processing, GMP regulations, and ability to mentor others.
• Proficient in Microsoft Office and capable of performing complex operational tasks.

Physical and Work Environment:

Must meet visual and physical requirements, wear PPE, and work in a cleanroom environment with potential chemical exposures. Ability to lift 50 pounds and stand for extended periods is essential.

Iovance promotes diversity and is an equal-opportunity employer. Accommodations are available upon request. By applying, you consent to the use of your personal information as described in our privacy notice.