LAVORO DEVELOPMENT QUALITY REGULATORY SPECIALIST PARMA, EMILIA ROMAGNA

The collaborator will be specialized in:  - carrying out gxp/iso audits of gmd contractors in full authonomy, - drafting quality agreements, - ensuring supplier...

Previous activity as supplier quality assurance... therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the...

Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and to collective...

Proponiamo un’interessante opportunità come: master batch record specialist – sede: monza l’azienda nostra cliente è un’azienda globale leader nella produzione di...

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

Experience required 5 years in regulatory with good knowledge of drug development and regulatory procedures education at least bachelor’s degree in life sciences...

quality management, engineering, life sciences)... in-depth knowledge of regulatory requirements and industry standards related to product quality and complaints...

Participate to regulatory inspections and customer audits as required...       develop and review quality documentation and procedures as requested...

Therefore, we strive to continuously promote and satisfy development needs, paying particular attention to the quality of our working environment and collective...

Engage with regulatory authorities, external experts, and key stakeholders to shape development plans and ensure compliance with global regulatory requirements...

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

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

Strong understanding of gcp, regulatory requirements, and clinical trial methodologies... they ensure scientific and medical integrity in the development and...

Conduct regular 1:1 meetings, performance appraisals, and career development discussions...    ensure cpms maintain compliance with internal sops, gcp, and regulatory...

We strive to enhance patients’ well-being and quality of life through the continuous development of effective treatments...      basic knowledge of project management...