Quality Assurance Specialist, Computer Software Validation

The estimated salary range for this position is $78,000 to $86,000 USD / year. The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. What We Offer Competitive pay and medical, dental, and vision insurance Flexible spending accounts Long- and short-term disability insurance, as well as life insurance 401(k) plan with employer contribution Competitive PTO and company-paid holidays Paid parental leave (maternity & paternity) Onsite gym (Chicago office) Position Summary The Quality Assurance Specialist - CSV is responsible for Computer Software Validation and Assurance activities for Meitheal's GMP Computer Systems. This individual will be responsible for developing, updating and executing Software Lifecycle documents [Validation Plan, Qualification Protocols/Test Scripts, Risk Assessments, Validation Reports, Procedures, etc.] in accordance with their specified requirements and validated in accordance with FDA and other agency requirements. Essential Duties and Responsibilities Author/Update Computer System Validation deliverables, including Validation Plans, User Requirements Specifications, Functional Specifications, Testing Protocols (IQ/OQ/PQ), User Acceptance Testing, Traceability Matrix, Validation Reports, SOP's and Change Control Documentation. Review of vendor provided validation documentation to determine suitability and alignment with company CSV SOPs and GAMP5. Support the release updates for all GMP related computer systems. Thorough knowledge of 21 CFR Part 11 (210, 211, 600, and 820), Data Integrity, GAMP5 requirements and FDA industry regulations. Collaborate with the Process Owners SMEs to determine, and document, appropriate user requirements. Apply FDA's new CSA guidelines to leverage risk-based strategy for testing to reduce documentation burdens while maintaining product quality and safety. Participate in the development, implementation, and modification of Computer System Validation Standard Operating Procedures (SOP) based on current regulations and industry standards. Work with QA to resolve any discrepancies or issues encountered during the validation of a computer system. Support QA in periodic audits and inspections, ensuring that all validation documentation is audit ready. Other duties, as assigned. Competencies Code of Federal Regulations and cGMP's relating to the field of Computer System Validation. Ability to write technical documents (like Validation Plan, URS, FRS, Traceability Matrix, IQ/OQ protocol and report, etc.). Strong verbal and written communication skills, good decision-making skills and time management skills are a must; ability to interface with all levels of the organization. Ability to establish clear priorities quickly, work effectively under pressure, handle multiple projects and meet deadlines. Ability to quickly learn and understand multiple types of software programs and/or SaaS applications including but not limited to QMS, ERP, Serialization, eCTD, Software Testing Tools ValGenesis) etc. Position Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Previous experience in writing, reviewing and executing computer validation documentation (VP, IQ, OQ, PQ, VSR). Knowledge of cGMP, GDP, GAMP, 21CFR Part 11, Data Integrity and industry best practices. Ability to understand existing and new business processes and requirements, to ensure proper implementation and validation of systems. Experience with SaaS systems in GxP environment preferred. ASQ, ISTQB Certification relevant to Software Quality Assurance is a plus. Education and/or Experience Degree (Bachelor's or Masters) in Computer Science, Software Engineering or other relevant Science Field or equivalent relevant experience. 3+ years in a cGMP-related industry with Computer System Validation and 21 CFR Part 11 compliance. Travel No travel expected. Physical Demands While performing the duties of this Job, the employee is frequently required to stand; walk; sit and talk or hear. The employee must occasionally lift and/or move up to 20 pounds. Computer Skills Microsoft Office, Adobe Systems (Pro, Acrobat DC), TrackWise/TrackWise Digital, SAP, Docubridge, Software Testing Tools. AAP/EEO Statement Meitheal Pharmaceuticals is an Equal Opportunity Employer. We welcome and encourage applications from all qualified individuals, including minorities, women, veterans, and individuals with disabilities. #J-18808-Ljbffr Meitheal Pharmaceuticals