Descrizione dell'offerta
Experteer Overview
As a Manufacturing Process Expert, you will serve as a senior root cause analysis resource within a cross‑functional problem‑solving team. You’ll lead investigations, manage deviations, and guide CAPA definition to drive quality excellence and prevent errors in manufacturing. You will apply advanced analytical methods to resolve complex technical issues and support continuous improvement across the Technical Unit. You’ll work closely with Quality, operations, and external partners to reduce risk and improve process reliability. This role offers a chance to shape corrective actions, share lessons learned, and contribute to critical quality and delivery objectives. Retribuzione / Benefits
Lead and conduct advanced root cause analyses for deviations and investigations Coordinate cross‑functional investigation teams across the Technical Unit Define investigation plans and guide CAPA development with cross‑functional input Support implementation of CAPA in collaboration with Quality Apply technical process knowledge to identify and mitigate manufacturing issues Participate in audits (internal/external) to address deviations Contribute to zero past due objectives and improve RFT and OTIF metrics Share lessons learned during Technical Unit huddles Responsabilità
Degree in Chemistry/ CTF/ Biological Sciences or similar fields Strong GMP knowledge and regulatory literacy (cGMP) Fluency in English and Italian Experience in quality assurance operations with deviation management Proficiency in writing and reviewing GMP documentation (Deviations, CAPAs) Experience with root cause analysis tools; TapRoot preferred Good interpersonal and communication skills; capable of facilitating meetings
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As a Manufacturing Process Expert, you will serve as a senior root cause analysis resource within a cross‑functional problem‑solving team. You’ll lead investigations, manage deviations, and guide CAPA definition to drive quality excellence and prevent errors in manufacturing. You will apply advanced analytical methods to resolve complex technical issues and support continuous improvement across the Technical Unit. You’ll work closely with Quality, operations, and external partners to reduce risk and improve process reliability. This role offers a chance to shape corrective actions, share lessons learned, and contribute to critical quality and delivery objectives. Retribuzione / Benefits
Lead and conduct advanced root cause analyses for deviations and investigations Coordinate cross‑functional investigation teams across the Technical Unit Define investigation plans and guide CAPA development with cross‑functional input Support implementation of CAPA in collaboration with Quality Apply technical process knowledge to identify and mitigate manufacturing issues Participate in audits (internal/external) to address deviations Contribute to zero past due objectives and improve RFT and OTIF metrics Share lessons learned during Technical Unit huddles Responsabilità
Degree in Chemistry/ CTF/ Biological Sciences or similar fields Strong GMP knowledge and regulatory literacy (cGMP) Fluency in English and Italian Experience in quality assurance operations with deviation management Proficiency in writing and reviewing GMP documentation (Deviations, CAPAs) Experience with root cause analysis tools; TapRoot preferred Good interpersonal and communication skills; capable of facilitating meetings
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Candidatura e Ritorno (in fondo)
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