Validation Expert — GMP Process

Join 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...

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 change management activities to meet cGMP requirements on time and quality to ensure that site validation programs are compliant with global regulatory...

**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...

A 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...

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...

**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...

A leading pharmaceutical company in Italy is seeking a qualified professional to manage and improve analytical methods and ensure compliance with regulatory standards. The ideal candidate will have a degree in Biology, Microbiology, or Biotechnology, along with proven experience in GMP environments. Responsibilities include method validation, equipment...

A leading pharmaceutical company in Italy is seeking a qualified professional to manage and improve analytical methods and ensure compliance with regulatory standards. The ideal candidate will have a degree in Biology, Microbiology, or Biotechnology, along with proven experience in GMP environments. Responsibilities include method validation, equipment...

Major AccountabilitiesResponsible for the development / validation / verification / transfer / troubleshooting / monitoring of analytical methods.Manage the method lifecycle and periodically monitor the performance.Lead the qualification of new equipment according to Novartis and regulatory standards.Guarantee the compliance with dossiers and relevant...

Major AccountabilitiesResponsible for the development / validation / verification / transfer / troubleshooting / monitoring of analytical methods.Manage the method lifecycle and periodically monitor the performance.Lead the qualification of new equipment according to Novartis and regulatory standards.Guarantee the compliance with dossiers and relevant...