Senior Validation Specialist – Process
4 settimane fa
A prominent pharmaceutical company in Piemonte is seeking a Validation Expert to oversee validation activities to ensure compliance with cGMP requirements. The role involves writing validation protocols, collaborating with cross-functional teams, and maintaining master plans for processes. Ideal candidates will have a scientific degree and previous experience in a sterile GMP environment. Fluency in both Italian and English is essential. The company promotes collaboration and innovation, aiming to improve patients' lives.#J-18808-Ljbffr
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Process & Validation Expert
6 giorni fa
Saluggia, Italia Novartis A tempo pieno**About the Role**: Responsible for developing, implementing and managing the site process validation, primary packaging validation, 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...
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Pharma Validation Specialist
4 settimane fa
Saluggia, Italia Novartis Pharma Schweiz A tempo pienoA leading pharmaceutical company in Italy is seeking a Validation Expert to manage process and cleaning validation activities. You will ensure compliance with cGMP requirements and collaborate across functions to analyze and control risks. The ideal candidate should have a scientific degree and previous experience in a sterile GMP environment, along with...
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Validation Expert
3 settimane fa
saluggia, Italia Novartis Pharma Schweiz A tempo pienoJoin 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 change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory...
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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
4 settimane fa
Saluggia, Italia Novartis Pharma Schweiz A tempo pienoJoin 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 change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory...
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Validation Expert
6 ore fa
Saluggia, Piemonte, Italia Novartis A tempo pienoBandLevel 3Job Description SummaryThe 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.Job DescriptionMajor...
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Validation Expert — GMP Process
3 settimane fa
Saluggia, Italia Jobs for Humanity A tempo pienoA prominent health organization in Saluggia, Italy seeks a Validation Expert to manage packaging and cleaning validation activities in compliance with cGMP standards. The ideal candidate holds a scientific degree and has experience in a sterile GMP environment. Key responsibilities include maintaining master validation plans, reviewing validation protocols,...
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Customer Service
6 giorni fa
Saluggia, Italia Corcym A tempo pienoThe Customer Service & Logistics Specialist is in charge of managing the order-to-cash process to overseas subsidiaries and specific International Distributors, with special focus on order management, returns, product allocation/billing, as well as supporting Whs and Logistics activities. - The Customer Service & Logistics Specialist must operate in...
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Product Steward
2 settimane fa
Saluggia, Italia Novartis A tempo pieno**Summary**: The Product Steward owns the process knowledge of the product(s) assigned throughout the commercial lifecycle, maintains the oversight on process capability, through data trending and statistical analysis of critical variables, ensuring process(es) are robust, in continued state of validation and continuously improving. Ensures seamless flow of...
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Microbiological Qc Technician
2 settimane fa
Saluggia, Italia Novartis A tempo pieno**Summary**: The Microbiological QC Technician is responsible for the execution and documentation of biologic and microbiological testing in conformity to GMP standards and SOPs in force efficiently, competently and in the planned terms. Compliance with the existing regulation on ecology and security. **About the Role**: **Major Accountabilities** - Perform...