Validation Expert
2 settimane fa
Join to apply for the Validation Expert role at Novartis Pharma Schweiz 4 days ago Be among the first 25 applicants Join to apply for the Validation Expert role at Novartis Pharma Schweiz The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and changemanagement activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.Major accountabilities:Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging.Support process validation lifecycle activities by ensuring a state of control is maintained through ongoing.Author and review process, packaging or cleaning validation protocols & reports, ongoing process and cleaning verification protocols & reports.Support execution of validation activities at the shop floor.Reviews Master Batch Records and associated change controls. Confirm revalidation need based on technical changes.Provides technical expertise (and may facilitate) pre-validation risk assessments using risk management tools.Work collaboratively and cross functionally to help ensure that process risks are analyzed, appropriately controlled and appropriately documented.Ensure that all Site validation activities are performed and are in line with the current Novartis requirements and cGMP, manage deviations associated with process validation and makes recommendations for deviation resolution as well as prevention of reoccurrence.Work in close collaboration with development organization (or sending site) for technical transfers and newproduct launches to ensure that knowledge is transferred, control strategies are appropriate, risks are analyzed and controlled and to ensure that commercial processes are validation ready.Provide technical expertise and facilitate establishment of Quality Risk Assessment (as needed).Essential requirements:Scientific Degree (CTF/Pharmacy/Biotechnology/Chemical Engineering or related field).Previous experience in a similar role within a sterile GMP environment.Knowledge of Quality and IT tools.Fluent in Italian and English. Seniority level Seniority level Entry level Employment type Employment type Full-time Job function Job function Quality Assurance Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Novartis Pharma Schweiz by 2x Sign in to set job alerts for “Validation Specialist” roles. Integration Verification, Validation and Qualification Engineer We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
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Validation Expert
1 settimana fa
Saluggia, Italia Altro A tempo pienoJoin to apply for the Validation Expert role at Novartis Pharma Schweiz4 days ago Be among the first 25 applicantsJoin to apply for the Validation Expert role at Novartis Pharma SchweizThe Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and changemanagement activities to meet cGMP...
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Validation Expert
2 settimane fa
Saluggia, Italia Altro A tempo pienoSummaryThe Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About The RoleMajor accountabilitiesSupport site validation...
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Validation Expert
2 settimane fa
Saluggia, Italia Altro A tempo pienoSummaryThe Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About The RoleMajor accountabilitiesSupport site validation...
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Validation Expert
1 settimana fa
Saluggia, Italia Altro A tempo pienoSummaryThe Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.ResponsibilitiesSupport site validation planning by writing...
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Validation Expert
2 settimane fa
Saluggia, Italia Novartis Italia A tempo pienoSummary The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About The Role Major accountabilities Support site...
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Validation Expert
1 settimana fa
Saluggia, Italia Jobs for Humanity A tempo pienoJob Description Summary The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and changemanagement activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About the Role Major accountabilities:...
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Validation Expert
1 settimana fa
Saluggia, Italia Novartis ACC A tempo pienoSummary The Validation Expert is responsible for executing and managing process, primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. Responsibilities Support site validation planning by...
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Validation Expert
6 giorni fa
Saluggia, Italia Altro A tempo pienoSummaryThe Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions.About the RoleMajor accountabilities :Support site validation...
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Validation Expert
1 settimana fa
Saluggia, Italia Novartis A tempo pieno**About the Role**: Responsible 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...
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Validation Expert
1 settimana fa
Saluggia, Italia Jobs for Humanity A tempo pienoSummary The Validation Expert is responsible for executing and managing process primary packaging and cleaning validation activities and change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory exceptions. About the Role Major accountabilities : Support site...
