Senior Validation Engineer Lead at Novartis

Job Description SummaryThe Senior Validation Engineer is a subject matter expert in the Commissioning and Qualification program and provides leadership and mentorship in the qualification of equipment utilities and processes.Job DescriptionLocation: Durham NCPlease note this role is on-site 5 days a week and does not have the ability to work remotely. This role is based in Durham NC.Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.Responsibilities:Develops a tailored approach for each project they are assigned including assessing vendor validation packages performing gap analysis to User Requirements developing plans and protocols using a risk-based approach that comply with company policies and procedures and completing trace matrices.Reports on progress and roadblocks to the project team(s).Develops Commissioning and Qualification policies and procedures to enhance the companys ability to conform to and maintain compliance with site corporate and regulatory standards.Development execution and management of small to medium size projects.Manages CQV contractors to perform tasks as required.Authors and/or manages authoring of commissioning qualification and validation plans validation protocols validation summary reports and requirement trace matrices.Validation using risk-based approach (FMEA PHA etc.). Performs risk assessments to confirm safe and compliant designs and recommend additional controls.Reviews project documentation (URS FRS Technical Specifications Functional Specifications).Participates in discussions with internal business partners on priorities timelines and transparent sharing of information.Partners with Quality to ensure a quality and compliant manufacturing environment.Manages workload to ensure timely approval of validation testing and documentation.Supports the validation department during inspections or audits as a Subject Matter Expert.Other related duties as assignedRequirements:BS/MS degree in Chemical Industrial Mechanical or other related engineering/science discipline with 7 years of relevant engineering experience supporting GMP operations.7 years of experience in the engineering design and support or qualification of commercial grade pharmaceutical or biotechnology process equipment and utilities.Ability to read/interpret engineering drawings and design documents.Excellent technical writing and verbal communication skills.People oriented and a team playerProficient in Microsoft Word Excel PowerPoint and Project.In-depth knowledge of FDA and EMEA regulations particularly 21 CFR partAnnex 1.Working knowledge of ICH Q8 Q9 Q10 and other international regulatory requirements.Familiarity with the following equipment: bioreactors centrifuges laboratory systems TFF systems chromatography skids fillers autoclaves parts washers.Experience managing 3rd parties (both in-sourcing and outsourcing).Ability to prepare contingency plans and logically work through complex issues in a high-pressure situation.Skills: Automation.Business Continuity.Change Control.General Hse Knowledge.Including Gdp.Knowledge Of Capa.Knowledge Of Gmp.Managing Performance Improvement.Manufacturing (Production).Project Commissioning.Project Engineering.Project Execution.Risk Management.Root Cause Analysis (Rca).Languages:EnglishNovartis Compensation and Benefit Summary:The salary for this position is expected to range between $103600 and $192400/year. The final salary offered is determined based on factors like but not limited to relevant skills and experience and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and depending on the level of the role eligibility to be considered for annual equity -based eligible employees will receive a comprehensive benefits package that includes health life and disability benefits a 401(k) with company contribution and match and a variety of other addition employees are eligible for a generous time off package including vacation personal days holidays and other leaves.EEO Statement:The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment hiring training promotion or other employment practices for reasons of race color religion sex national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status.Accessibility and reasonable accommodationsThe Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If because of a medical condition or disability you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position please send an e-mail to or call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.Salary Range$103600.00 - $192400.00Skills DesiredApi (Application Programming Interface) Api (Application Programming Interface) Automation Back-End Development Business Continuity Change Control Chemistry Design Development Electronic Components General Hse Knowledge Including Gdp Java (Programming Language) Knowledge Of Capa Knowledge Of Gmp Kubernetes Managing Performance Improvement Manufacturing Production Mathematical Optimization Project Commissioning Project Engineering Project Execution Reactjs Risk Management Root Cause Analysis (RCA) Scheduler 2 moreRequired Experience:Senior IC Key Skills Python,SOC,Debugging,C/C++,FDA Regulations,Minitab,Technical Writing,GAMP,OS Kernels,Perl,cGMP,Manufacturing Employment Type : Full-Time Experience: years Vacancy: 1 Monthly Salary Salary: 103600 - 192400