Manufacturing / Bioprocess Support Technician

Bioprocess Support Technician

About Krystal Bio:

At Krystal Biotech, Inc., we bring together the brightest and most eager minds to relentlessly pursue the discovery, development and delivery of transformative medicines for people with serious and life-threatening genetic diseases. Founded in 2016, the Company is the leader in redosable gene therapy with prominent clinical and pre-clinical stage programs for dystrophic epidermolysis bullosa, TGM1-deficient ARCI, Netherton Syndrome, Cystic Fibrosis, alpha-1 antitrypsin deficiency, and is advancing research to apply our technology to these and other diseases. The Company’s innovation is fueled by visionary leadership within an entrepreneurial organizational structure with a robust pipeline of investigational medicine.

Our US headquarters is in Pittsburgh, PA with other offices located in Boston, MA and in Zug, Switzerland. For more information about the Company’s platform, commitment to patients and pipeline, please visit and engage with us on

We have an exciting journey ahead and a tremendous opportunity for growth, and now is the time to make a meaningful impact on the lives of our patients!

Summary:

Krystal Biotech, Inc is seeking a highly motivated Bioprocess Support Technician to support the growing Manufacturing team in Pittsburgh, PA. This role will perform a wide range of duties to support manufacturing processes in a GMP environment.

Primary Responsibilities:

• Perform other tasks, as assigned
• Collaborate with Manufacturing team as well as Quality assurance, Quality control, Facilities, Materials and others
• Support a standard 40-hour work week with flexibility to support occasional off-shift hours and/or weekends
• Maintain clean room areas and ensure that all equipment and materials are clean, sanitized and consistently meeting requirements for sterile drug product manufacturing
• Maintain accurate documentation and data, showing proficiency across computer-based systems used within manufacturing
• Support the maintenance of process gas levels, calibration of equipment, and preventative maintenance schedules
• Overall upkeep of facility and materials, ensuring resources are in place to meet production demands
• Assist with movement of materials; work with EHS/Materials Teams for collection and dispensing of biohazardous waste
• Support bioprocessing activities (buffer preparation, upstream, downstream, aseptic fill) in a cGMP cleanroom setting

Requirements and Preferred Qualifications:

• Knowledge of upstream/downstream processing, cell culture, or bioreactor operations is highly preferred
• Minimum of HS Diploma; BS Degree in Biology, Engineering or related field is preferred
• Experience in GMP or cleanroom/aseptic manufacturing environment is desired
• High level of interpersonal skills with a collaborative mindset
• Strong communication skills, both verbally and written

Krystal Biotech, Inc. is an Equal Employment Opportunity and Affirmative Action Employers. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. Headhunters and recruitment agencies may not submit resumes/CVs through this Web site or directly to managers. Krystal Biotech, Inc. does not accept unsolicited headhunter and agency resumes. Krystal Biotech, Inc. will not pay fees to any third-party agency or company that does not have a signed agreement with Krystal Biotech, Inc.

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