25.04.24 | Vollzeit | Bern | Randstad Schweiz AGAnd regulatory requirements. Responsibilities - Lead CSV activities for assigned projects, ensuring validation phases are performed according to company procedures and regulatory standards. - Plan, coordinate, and execute all phases of computer system validation for production and QC Lab systems. - Perform CSV
Später ansehen22.04.24 | Vollzeit | Bern | Randstad Schweiz AGIntended for use in GMP processes - Ensure materials compliance with user requirements - Understanding biotechnology processes to ensure materials comply with GMP production user requirements - Change Control owner for Material Qualification - Coordinate and lead the introduction and changes of non-GxP
Später ansehen10.04.24 | Vollzeit | Bern | Randstad Schweiz AGBased viral- and bacterial vaccines and bacterial based therapeutic products. The aim of the position is to support the bacterial vaccine Launch project for a first GMP commercial production with focus on Downstream process step on large scale of 200L. Main Responsibilities - Writing GMP process
Später ansehen10.04.24 | Vollzeit | Bern | Randstad Schweiz AGBased viral- and bacterial vaccines and bacterial based therapeutic products. Main Responsibilities - Ensure the GMP-compliant production of active ingredients and drugs for clinical trials and market launch by organizing, coordinating, and tracking personnel training and qualification - Define
Später ansehen06.03.24 | Vollzeit | Bern | Randstad Schweiz AGLead by this position. - Hands on Plan, coordinate and execute all phases for computer system validation of production and QC Lab systems including but not limited to, Validation plans, FMEA, RTM, DQ, IQ, OQ, Validation Reports. - Perform CSV periodic review of equipment and systems. - Prepare, review
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