Quick Info
Experience Level
Mid LevelMinimum Degree
BachelorDepartment
Manufacturing ProductionJob Type
Full TimeSpecialty Skills
Biologics ManufacturingGene Therapy ManufacturingUpstream ProcessingDownstream ProcessingAseptic FillGMPBioreactorsFiltrationPurificationCell CulturingAseptic TechniqueCleanroom Operations
About the Role
Krystal Biotech, Inc is seeking a highly motivated and dynamic Bioprocess Engineer to support our product manufacturing at our Pittsburgh GMP facility. This role is critical to our make a meaningful difference in the lives of underserved patient populations having rare diseases. Quality, safety and on-time delivery is a must to be successful in this role! The ideal candidate will have foundational experience in upstream and/or downstream biologics or gene therapy manufacturing.
Primary Responsibilities:
* Perform/support/monitor the process steps/activities – buffer preparation, upstream, downstream, Aseptic Fill
* Document/record data following standard operating procedures or GMP documents for process steps and/or equipment activities
* Maintain equipment and operate – facilitate/perform qualifications, cleaning, logbooks
* Clean, maintain, and monitor the GMP facility
* Collaborate with Quality assurance, Quality control, Facilities, Materials and others
* Participate in learning and training to be competent in above functions
* Other duties as assigned
Requirements and Preferred Qualifications:
* Bachelor’s degree, preferably in life sciences
* Expertise working in a clean room facility, 1+ years of professional experience demonstrating proper cleanroom behavior/technique
* Cell culturing / Aseptic technique
* Familiarity with large scale bioreactors highly preferred
* Downstream processing experience
* Filtration/Purification
* Highly organized and detail oriented, while also demonstrating the ability to synthesize information and demonstrate strategic thinking
* Highly self-motivated, flexible, proactive, able to follow through in an ambiguous, fast-changing environment, and proven ability to meet deadlines under pressure
* A demonstrated understanding of the drug development process, biopharmaceutical industry and/or related life sciences industry
* Demonstrated ability to prioritize and manage multiple projects simultaneously
* Demonstrated ability to work effectively with many different types of personalities at all levels of the organization
* Excellent interpersonal, collaboration and stakeholder management skills
* Excellent communication skills (written/verbal)
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