Process Engineer
2 weeks ago
Iovance Biotherapeutics, Inc. is seeking a highly skilled Process Engineer to join our team. As a Process Engineer, you will play a critical role in providing oversight and review of design and construction work related to process improvements within our cGMP manufacturing facility.
Key Responsibilities:- Implement process improvements, including the selection and modification of new equipment and facilities.
- Write, review, and edit technical documents, including equipment specifications, test protocols, SOPs, CAPAs, and change controls.
- Participate in technology transfer, conference calls, and sharing of technical information.
- Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and Good Documentation Practices (GDP).
- Manage projects to ensure timely initiation and completion of work.
- BS or MS in Chemical, Mechanical, Biochemical Engineering, or a related field.
- 2+ years of related BioPharma Life Sciences experience.
- Experience with GMP procedures, including change controls, deviation management, and CAPAs.
- Extensive knowledge of small-scale cell culture processes and techniques.
- Excellent oral and written communication skills.
This position will work in both an office and a manufacturing lab setting. The successful candidate will be able to work in a lab setting with various chemical/biochemical exposures, including latex and bleach. The position requires the ability to work in a cleanroom with biohazards, human blood components, and chemicals.
Iovance Biotherapeutics, Inc. is an equal-opportunity employer and welcomes applications from diverse candidates. If you need assistance or accommodation to apply to this opportunity, please contact us.
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