Act as technical ADVISOR to BMS team; oversee BMS production runs and closely monitor high risk operations as defined by the risk assessment; observe that BMS successfully detect, identify & resolve issue/defect through in place Quality systems; communicate newly identified risks during operation or in related Quality System documents / procedure / practices; act as primary contact while on site for any troubleshooting during production; collect information and data as provided by the BMS team to facilitate communication with the rest of the team; provide periodic update on the status of the campaign; identify optimization/improvement opportunities for the future activities and escalate as needed per escalation process.
Firmenprofil
One of the world's leading biotechnology company. Deeply rooted in science and innovation.
Arbeitsort
French part of Switzerland
Arbeitsbeginn
asap
Motivation
A dynamic working environment focusing on career opportunities where multi-cultural teams from all over the world strive the best results.
Ausbildung
Master’s degree and 4 years of Engineering or Science experience
Erfahrungen
5+ years of experience in oral solid dose drug product manufacturing environment (tablets, blisters, bottling, packaging); 5+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles; 3+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products; 3+ years of project management experience leading multi-functional and multi-location team.
Sprachen
Englisch: Very good
Spezielles
If your device does not allow to include your CV, please forward it to i.vlas@universal-job.ch. This position may be offered until the end of 2021, including a strong option to get extended at a later stage.
Vakanz-Nummer
G-6-10501
One of the world's leading biotechnology company. Deeply rooted in science and innovation.
French part of Switzerland
Master’s degree and 4 years of Engineering or Science experience
5+ years of experience in oral solid dose drug product manufacturing environment (tablets, blisters, bottling, packaging); 5+ years in roles requiring knowledge of cGMP principles, FDA and other regulatory guidelines, and validation principles; 3+ years of experience working with external parties and/or leading cross-functional teams for clinical and/or commercial products; 3+ years of project management experience leading multi-functional and multi-location team.
Bau / Gewerbe / Immobilien
G-6-10501
Temporär
i.vlas@universal-job.ch