Job Description SummaryResponsible for developing, implementing and managing the site performance qualifications and requalification of existing equipment and cycles as well any new equipment. Responsible for developing, implementing and managing the site process validation, primary packaging validation, process performance qualification, cleaning validation and revalidation strategies to meet cGMP and quality requirements on time and on budget to ensure that programs are compliant with Regulatory Authorities' expectations and related SOPs. Responsible for scale-up cold kits by developing and executing a validation strategy according to cGxP. Executing and managing equipment performance qualifications, requalification, periodic reviews and process, primary packaging, shipping and cleaning validation activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory expectations. Validation Expert -Support Product Steward in maintaining the process control strategy. Job DescriptionMajor accountabilities: Stewardship, Launches/Transfer:Support Product Steward in maintaining the process control strategy.Provide technical expertise and facilitate establishment of Quality Risk Assessment (as needed).Monitor all critical variables and key variables as appropriate using statistical analysis andconducting regular product specific data trending.Participate in transfers and launches by aligning on the product validation approach. Providetechnical expertise for pre-validation / validation strategy.Ensure equipment is in qualified state and qualified ranges are aligned to meet processparametersAssess impact of technical changes, assess their technical feasibility and determine scope / designof technical batches, challenge technical risk and business benefit of technical changes proposed.Contribute to registration strategy and support registration activities providing experimental data obtained during the validation activities, which will be used to prepare the related registrationdocumentation.Validation:Establish a qualification and requalification program (PQ) for the site and execute activitiesaccording to plan and defend to authorities.Perform equipment periodic reviews according to internal proceduresDefine and implement validation strategy (process, cleaning, ongoing verification) and defend toauthorities.Overall responsibility for establishment, prioritization, execution and tracking of Validation Master Plan for process, cleaning, packaging validation and ongoing process verification (OPV).Ensure equipment is qualified and manufacturing and cleaning processes are validated; overview on site state of validation is maintained.Establish and monitor validation KPIs. Maintain all validation activities in an inspection ready status.Author validation protocols and reports.Establish local procedures & templates for respective validation documentation.Ensure that all Site validation activities are performed and are in line with the current AAA (or applicable) Novartis requirements and cGMP, handling any deviations associated to these activitiesincluding oversight of pre-validation and validation resulting from technical changes.Support MS&T activities in ensuring that responsible departments execute and maintain the VMP activities.Partner with Engineering, IT, QC, AS&T to define the interfaces to equipment, utilities and system qualification, analytical method validation. Execute equipment qualification and requalificationProvide all necessary information to perform the validation documentation, align with stability experts and QC labs to organize the stability samples.Manufacturing Excellence:Contribute to efficiency improvement programsTraining:Own the Training Curriculum for own Profile and internal or external contributorsNovartis Manufacturing Manual:· Support implementation of Novartis Manufacturing Manual principle 3 where applicableKey Performance Indicators· Maintenance of Site Validation Master Plan, no overdue validation and qualification activities· Timely creation (and fulfilment) of Project Validation Master Plans.· Meet established validation milestones according to approved validation plans.· Validation execution according to plan, as a measure of appropriate validation readiness activities.· Audit and inspection outcomes as a measure of validation compliance with global regulatory expectations.· Transfers/launches implemented on target without preventable validation related issues.· Validation protocols executed and reports delivered according to schedule.· Validation/annual monitoring/revalidation activities scheduled in collaboration with stakeholders to ensure that site activities continue with minimal disruptionPharmaceutics.Process and Cleaning Validation.Process Control.Process Engineering.Risk Management.Root Cause Analysis (Rca).Scheduler.Six Sigma.Sop (Standard Operating Procedure).Languages :English.Skills DesiredAssembly Language, Change Control, Chemical Engineering, Chemistry, Continual Improvement Process, Cost Reduction, Data Analytics, Electronic Components, General Hse Knowledge , Including Gdp, Knowledge Of Capa, Knowledge Of Gmp, Lean Manufacturing, Manufacturing Process, Manufacturing Production, Pharmaceutics, Process and Cleaning Validation, Process Control, Process Engineering, Risk Management, Root Cause Analysis (RCA), Scheduler, Six Sigma, Sop (Standard Operating Procedure)SummaryLocation: SaluggiaType: Full time