About this role
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 CompensationMedical and Prescription Drug CoverageDental and Vision InsuranceShort and Long-Term Disability Insurance401(k) With Company Match401(k) Annual Student Loan Match ProgramPaid HolidaysPaid Time OffFlexible Spending Accounts (Health Care & Dependent Care)Health Savings AccountEmployee Assistance Program & Benefits Concierge AppAD&D and Life InsuranceWellness Rewards ProgramValidation (CSV) AssociatePittsburgh, PAFull TimeInformation TechnologyMid LevelShareAbout 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 SummaryKrystal Biotech is seeking a highly motivatedComputer System Validation (CSV) Associateto support validation and compliance activities for GxP computerized systems used in Manufacturing, Quality Control laboratories, and other regulated business areas. This role will support the implementation, qualification, maintenance, and lifecycle management of GxP systems to ensure compliance with applicable regulatory requirements and company procedures.The ideal candidate will have experience supporting CSV activities in a regulated environment and possess strong technical writing, organizational, and problem-solving skills.Primary Responsibilities:Support Computer System Validation (CSV) activities for GxP computerized systems, analytical instruments, laboratory systems, manufacturing systems, and software applications.Develop, review, execute, and maintain validation documentation including Validation Plans, User Requirements Specifications (URS), Functional/Design Specifications, Risk Assessments, IQ/OQ/PQ Protocols, Traceability Matrices, and Validation Summary Reports.Support system implementations, upgrades, configuration changes, and periodic reviews in accordance with established procedures.Ensure computerized systems remain in a validated and compliant state throughout the system lifecycle.Support compliance with FDA 21 CFR Part 11, EU Annex 11, GAMP 5, and Data Integrity requirements.Author, revise, and review SOPs, work instructions, forms, and policies related to CSV, IT compliance, data integrity, and computerized systems.Collaborate with cross-functional teams including QA, QC, Manufacturing, IT, Engineering, Regulatory Affairs, R&D, Supply Chain and vendors to support project execution and compliance activities.Participate in discrepancy investigations, CAPAs, deviations, and change control assessments related to computerized systems.Support audit and inspection readiness activities and assist during internal and external audits.Perform and document periodic reviews of computerized systems per established procedures.Assist with user access reviews, backup verification activities, and system administration support as applicable.Support vendor assessments and leverage vendor documentation packages where appropriate.Maintain validation documentation and records within electronic document management systems (e.g., Veeva Vault).Support data migration, disaster recovery, and system retirement activities as needed.Perform additional duties as assigned.Minimum Qualifications & Desired Competencies:Bachelor’s degree in Computer Science, Information Systems, Engineering, Life Sciences, or a related discipline.2+ years of experience in Computer System Validation (CSV), Quality Systems, or IT compliance within a regulated environment.Experience supporting computerized systems in pharmaceutical, biotechnology, medical device, or other regulated industries preferred.Working knowledge of FDA 21 CFR Part 11, EU Annex 11, GAMP 5, Data Integrity principles (ALCOA+), and Change Management and SDLC methodologies.Experience developing and executing validation documentation and test protocols.Familiarity with laboratory and manufacturing systems such as LIMS, QMS, MES, Veeva Vault, TrackWise, analytical instruments, and standalone systems.Knowledge of IT infrastructure concepts including backups, disaster recovery, Active Directory, networking, cybersecurity, and system security is a plus.Familiarity with audit trail review, electronic signatures, and security/access management.Experience supporting cloud-based or SaaS applications in regulated environments.Strong technical writing, documentation, and communication skills.Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment.Ability to work independently and collaboratively within cross-functional teams.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.ShareApplyApply for this positionRequiredFirst NameLast NameEmail AddressPhoneAddressResumeWe've received your resume. Clickhereto update it.Attach resumeorPaste resumeAttach resume as .pdf, .doc, .docx, .odt, .txt, or .rtf (limit 5MB) orPaste resumePaste your resume here orAttach resume fileCover LetterAre you willing to relocate?No answerYesNoWhat's your citizenship / employment eligibility?No answerI am a U.S. Citizen/Permanent ResidentNon-citizen allowed to work for any employerNon-citizen allowed to work for current employerNon-citizen seeking work authorizationI am a Canadian Citizen/Permanent ResidentOtherDesired salaryEarliest start date?Are you currently in a commutable distance to our Pittsburgh facilities?*-- No answer --YesNoPlanning to RelocateThe following questions are entirely optional.To comply with government Equal Employment Opportunity and/or Affirmative Action reporting regulations, we are requesting (but NOT requiring) that you enter this personal data.
This information will not be used in connection with any employment decisions, and will be used solely as permitted by state and federal law. Your voluntary cooperation would be appreciated.Learn more.GenderDecline to answerFemaleMaleRace/EthnicityDecline to answerHispanic or LatinoWhite, not Hispanic or LatinoBlack or African-American, not Hispanic or LatinoAsian, not Hispanic or LatinoNative Hawaiian or Other Pacific Islander, not Hispanic or LatinoAmerican Indian or Alaskan Native, not Hispanic or LatinoTwo or More Races, not Hispanic or LatinoMENA (Middle Eastern and North African)Human Check*Submit Application