Quality Control Support Technician

Thanks for visiting our Career Page. Please review and apply to our positions which match your qualifications.Krystal Biotech, a Pittsburgh-based company founded in 2016, has quickly emerged as a global leader in gene therapy.

In May 2023, Krystal Bio received FDA approval for the first-ever redosable gene therapy, VYJUVEK™, for the treatment of Dystrophic Epidermolysis Bullosa. Krystal continues to leverage their proprietary platform to develop new treatments throughout its clinical pipeline.

Additionally, the company has developed innovative commercial- and clinical-stage manufacturing processes, deployed across two state-of-the-art GMP facilities.BenefitsWe make every effort to provide essential and desirable benefits that make each employee's life that much easier. In addition to benefits listed below, we also offer competitive compensation that rewards you for your contributions toward achieving company goals.Benefits include:Equity / Stock OptionsMedical and Prescription Drug CoverageDental and Vision InsuranceShort and Long-Term Disability Insurance401(k) With Company MatchPaid HolidaysPaid Time OffFlexible Spending Accounts (Health Care & Dependent Care)Employee Assistance Program & Benefits Concierge AppAD&D and Life InsuranceWellness Rewards ProgramQuality Control Support TechnicianPittsburgh, PAFull TimeQuality ControlEntry LevelShareQuality Control Support TechnicianAbout Krystal Bio:At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs.Founded in 2016, Krystal is distinguished in three powerful ways: science and technology using our patented gene therapy platform, innovative manufacturing supported by our commercial scale facilities, and a unique commercialization model that focuses on the patient’s end-to-end experience.Krystal received U.S.

FDA approval for the first and only redosable gene therapy treatment, VYJUVEK®, for the treatment of Dystrophic Epidermolysis Bullosa (DEB). Krystal continues to leverage our proprietary platform to rapidly advance a robust pipeline of investigational genetic medicines in respiratory, oncology, dermatology, and ophthalmology.Krystal is headquartered in Pittsburgh, PA, which is home to our two state-of-the-art CGMP manufacturing facilities with teams around the world and satellite offices in Switzerland, Germany, and Japan.

We are a company built and run by people who care, are fearless in the face of a challenge, love the work they do, and practice the highest level of scientific integrity. As we grow, we are seeking team members that embody these values.Job Description Summary:The QC Support Technician provides operational, administrative, and laboratory support within the Quality Control department in a GMP-regulated environment.

This role is responsible for supporting routine laboratory operations, sample management activities, inventory control, documentation organization, and general laboratory upkeep to improve overall laboratory efficiency.The ideal candidate is highly organized, detail-oriented, able to work independently, and capable of following established procedures while supporting a fast-paced laboratory environment.Responsibilities will include, but are not limited to, the following:Sample & Material SupportPerform sample receipt and sample request fulfillment activitiesSupport aliquoting activities including batch samples, reference standards, and CQP samplesCoordinate sample shipments, including stability and manufacturing-related shipmentsAssist with reagent preparation activitiesLaboratory Operations SupportMaintain laboratory inventory and consumable stockingSupport equipment cleaning and general laboratory organizationPerform waste removal and laboratory housekeeping activitiesSupport autoclave and dishware activities, as applicablePerform routine safety checks including safety shower and eyewash inspectionsCoordinate equipment send-outs and service support activitiesDocumentation & Administrative SupportScan, organize, and file laboratory documentationMaintain spreadsheets, trackers, and laboratory support logsAssist with data collection and trending activities for laboratory metrics and reportsSupport meeting scheduling and note-taking activitiesAssist with ad hoc laboratory studies and operational initiativesCompliance & Quality SupportFollow all GMP, safety, and laboratory proceduresMaintain accurate and complete documentation practicesSupport inspection readiness through organization and maintenance of laboratory records and workspacesAdhere to standard operating procedures and departmental expectationsRequirements and Preferred Qualifications:High school diploma or equivalent required; Associate degree in life science or related field preferredValid driver’s license required for occasional travel between company sitesExperience working in a regulated environment (GMP, GLP, ISO, or similar)Familiarity with laboratory inventory systems and sample trackingExperience supporting laboratory operations or scientific teamsExperience with documentation scanning, filing, and archival processesKrystal Biotech, Inc. is anEqual 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.ShareApplyApply for this positionRequired*First Name*Last Name*Email Address*Phone*AddressResume*We've received your resume.

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