Research Scientist -Data analysis
Descrizione dell'offerta
Our client, Chiesi Farmaceutici – one of the top 50 pharmaceutical companies in the world, with more than 80 years of experience within the pharmaceutical and biotechnology industry - in order to expand their staff, entrusted to IQVIA the recruitment of a Analytical Scientist who can join an exciting working environment in a dynamic and international atmosphere.
Support analytical activities required for producing information and documentation suitable for preclinical and clinical development and registration of drug products, including excipients and intermediates, with particular focus on quality in accordance with GMP/cGMP.
Execute the development strategy of the assigned project
Preparation and revision of technical documentation in line with quality and regulatory requirements and according to relevant internal procedures
Writing/reviewing of regulatory documentation (CTD/NDA, IMPD/IND, Q&A, Briefing documents for Scientific advice)
Support Change Control Evaluation
Support quality investigations (Deviations or OOS, Complaints)
Languages:
English fluent
Permanent contract
Chemical contract
IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.
Support analytical activities required for producing information and documentation suitable for preclinical and clinical development and registration of drug products, including excipients and intermediates, with particular focus on quality in accordance with GMP/cGMP.
Execute the development strategy of the assigned project
Preparation and revision of technical documentation in line with quality and regulatory requirements and according to relevant internal procedures
Writing/reviewing of regulatory documentation (CTD/NDA, IMPD/IND, Q&A, Briefing documents for Scientific advice)
Support Change Control Evaluation
Support quality investigations (Deviations or OOS, Complaints)
Languages:
English fluent
Permanent contract
Chemical contract
IQVIA reserves the right to evaluate candidates with domicile / residence and work experience / study with requirements responding to the open request. Applications WITHOUT the requirements Will NOT be fully taken into account. Please enter the authorization for the processing of personal data (DL196/2003) - General Data Protection Regulation (13 GDPR 679/16 –) to IQVIA and to transfer those data to IQVIA’s Clients. The research is urgent and is intended for candidates of both sexes (L.