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tout effacer- The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be rThe MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert. You will be r
- Location: Bergères, Switzerland Rate: Part-time 60% Duration: 4 monthsIn this 4-month contract, you will support the HR Payroll team in the following activities:ResponsibilitiesYou handle off-cycle payment runs and ensure accurate financial- and system-related processes You control and reconcile the monthly payroll run and bank transfersYou handle the withholding tax, AVS, and third-party invoices and ensure correct payments are madeYou complete disabilityLocation: Bergères, Switzerland Rate: Part-time 60% Duration: 4 monthsIn this 4-month contract, you will support the HR Payroll team in the following activities:ResponsibilitiesYou handle off-cycle payment runs and ensure accurate financial- and system-related processes You control and reconcile the monthly payroll run and bank transfersYou handle the withholding tax, AVS, and third-party invoices and ensure correct payments are madeYou complete disability
- The MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure theThe MSAT DP within the Fill & Finish Department leads and manages all the Drug Products site technical activities within our client site in Aubonne to ensure the supply of New Biologic Entities (NBEs) and the business continuity and Product-Lifecycle activities on legacy products portfolio, in compliance with specifications, registration and GMP requirements.To evolve in this environment, we are looking for our next Process Validation Expert to ensure the
- Key Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scrKey Responsibilities· Contribute to CSV strategies, plans, and protocols in accordance with regulatory As a QA IT CSV Engineer, you will be responsible for ensuring compliance for computerized systems and computerized systems validation, fulfill with regulatory requirements and operate as intended.Your primary responsibilities will include:guidelines (e.g., FDA 21 CFR Part 11, EU Annex 11, GAMP 5)· Contribute to risk assessments and participate to test scr
