Aseptic Manufacturing Technician I - Day Shift A [Contract to Hire]
Iovance Biotherapeutics · Philadelphia, PA
Posted about 2 months ago
or apply directly on Iovance Biotherapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 60 days Iovance Biotherapeutics's roles stay open a median of 83 days
- Reposted
- No
- Salary listed
- No 0% of Iovance Biotherapeutics's roles list one
- Ghost-job risk at Iovance Biotherapeutics
- high 43 stale, 1 reposted of 43 open
- Hiring momentum
- 69 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-10-25
Measured from postings appearing on and disappearing from Iovance Biotherapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Iovance Biotherapeutics.
About this role
The Aseptic Manufacturing Technician I at Iovance Biotherapeutics is responsible for supporting the autologous cell therapy manufacturing program. Daily tasks include suite preparation for cell processing, material transfer, environmental monitoring, and final product inspection and cryopreservation. The role requires adherence to Good Manufacturing Practices (GMP) and may involve working various shifts, including weekends and holidays, to ensure production schedules are met.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 3/5
- role clarity
- 4/5
- pay transparency
- 0/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Iovance Biotherapeutics as an employer.
What you need
- Bachelor’s degree or equivalent experience
- Minimum 0-1 year of experience in biopharmaceutical-based GMP manufacturing operations
- Ability to read, write and understand English for Good Documentation Practices
- Proficiency in Microsoft Excel, Word, Outlook and Teams
- Ability to perform arithmetic calculations including fractions, decimals, percentages, and basic algebraic and geometric calculations
- Quality mindset, familiar with 21 CFR Part 11 and standard GxP best practices and FDA regulations
Nice to have
- Background in cell culture
- Experience with aseptic gowning and qualifications
- Familiarity with ISO class 5 (Grade A) cleanroom operations
Worth weighing
- The position requires flexibility in working hours, including potential overtime and weekends
- The role involves working in both an office and a manufacturing setting with exposure to chemicals and equipment hazards
- The job may require physical activities such as standing for long periods and lifting heavy objects
Summarised from Iovance Biotherapeutics's posting. Read the full original.
Listed by Iovance Biotherapeutics on their greenhouse job board, last confirmed open on 2026-10-25. PitchMeAI is not the employer.
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