LAVORO LIFE CYCLE MANAGEMENT REGULATORY PARMA, EMILIA ROMAGNA

Deep understanding of quality management systems, compliance standards, and regulatory requirements within the pharmaceutical sector... experience in change management...

Align with project and portfolio management (ppm) to identify key milestones for gra to meet business objectives, from clinical trial initiation, regulatory submission...

Quality management, engineering, life sciences)... develops and implement risk management strategies and processes... in-depth knowledge of regulatory requirements...

Understands financial procedures, budget management... strong knowledge of ich-gcp, clinical trial lifecycle, regulatory requirements, and cro/vendor management...

Scopo la figura si occuperà di definire e seguire gli studi analitici a supporto della commercializzazione di nuovi prodotti e di farmaci in life cycle...

Knowledge of monitoring and management systems for utilities...   preferred skills: experience with photovoltaic plants, production monitoring, and performance management...

regulatory compliance: ensure all documents comply with the applicable regulatory guidelines and company policies, throughout the documents’ development process...

Alternatively, master’s degree/phd in scientific area relevant to pharmaceutical r&d with previous experience in quantitative evaluations of projects, finance...

Education master’s degree in life sciences, health economics / economics, management engineering... each franchise is organized by stage of development with fully...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     engage with regulatory authorities, external experts, and key...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...     collaborate with clinical program leaders, statisticians, regulatory...

Help management team to identify opportunities and threats through analytics... each franchise is organized by stage of development with fully empowered and enhanced...

Scopo il device industrial development specialist ha l’obiettivo di fungere da interfaccia tecnica tra i dipartimenti interni di chiesi e le controparti esterne...

Basic knowledge of project management    comprehensive understanding of drug development process... stay current with regulatory guidelines and industry trends...

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies...       outstanding communication skills with ability to interact with...

Participate to regulatory inspections and customer audits as required...     assist with investigations and management of the implementation and maintenance...

Stay updated with the latest industry trends and regulatory changes... it is divided into integrated functional areas focusing on pipeline projects including...

Author, review or approve pharmacometrics reports and related sections of regulatory documents; participate in meetings with clients and regulatory agencies...

To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the group researches, develops and markets...