QA CSV Engineer

Job Title: QA Validation Engineer - CSVWe are seeking a highly skilled QA Validation Engineer - CSV to join our team at Axepta SA. As a key member of our quality assurance team, you will be responsible for ensuring the compliance of automated and computerized systems with cGMP and applicable regulations.Key Responsibilities:Act as the main point of contact...

QA CSV EngineerFor our client, a growing biopharmaceutical company based in Vaud canton, we are currently looking for a QA Validation Engineer - CSV. This is a permanent position  YOUR RESPONSIBILITIES: • Act as the main point of contact for all quality compliance key topics regarding Automated and Computerized systems (MES,...

For our client, a growing biopharmaceutical company based in Vaud canton, we are currently looking for a QA Validation Engineer - CSV. This is a permanent position  YOUR RESPONSIBILITIES: • Act as the main point of contact for all quality compliance key topics regarding Automated and Computerized systems (MES, EBR, PLC/SCADA, EMS, LIMS, ERP...

For our client, leader in the biopharmaceutical field, is currently looking for a QA Validation Engineer - CSV - Permanent position YOUR RESPONSIBILITIES: • Act as the main point of contact for all quality compliance key topics regarding Automated and Computerized systems (MES, EBR, PLC/SCADA, EMS, LIMS, ERP systems)• Review and approve the URS and...

Job Title: QA Validation Engineer - CSVWe are seeking a highly skilled QA Validation Engineer - CSV to join our team at AXEPTA SA. As a key member of our quality assurance team, you will be responsible for ensuring the compliance of our automated and computerized systems with regulatory requirements.Key Responsibilities:Act as the primary point of contact...

For our client, a growing biopharmaceutical company based in Vaud canton, we are currently looking for a QA Validation Engineer - CSV.  This is a permanent position    YOUR RESPONSIBILITIES:   • Act as the main point of contact for all quality compliance key topics regarding Automated and Computerized systems (MES, EBR,...

JobdescriptionFor our client based in Vaud canton and specializedin biopharmaceutical area, we’re looking for a Senior QualityAssurance - CSV specialist ResponsabilityManageQuality oversight for computerized systems validation and the dataintegrity program & support QA activities for systemintroduction/upgrades, ensuring compliance with quality...

We are looking for a Senior Validation Engineer - CSV to join our team at Axepta SA. As a key member of our quality assurance department, you will be responsible for ensuring the compliance of our automated and computerized systems with cGMP and applicable regulations.Main Responsibilities:Act as the main point of contact for quality compliance key topics...

Job DescriptionWe are seeking a Senior Quality Assurance Specialist to join our team at Randstad. The ideal candidate will have a strong background in quality assurance and a deep understanding of computerized systems validation and data integrity.ResponsibilitiesAs a Senior Quality Assurance Specialist, you will be responsible for managing quality oversight...

Job DescriptionWe are seeking a Senior Quality Assurance Specialist to join our team at Randstad. As a key member of our quality assurance team, you will be responsible for managing quality oversight for computerized systems validation and data integrity programs. Your expertise will ensure compliance with quality policies, cGMP, EU/US, and Swiss...

Job Responsibilities:As a QA Validation Engineer - CSV for Axepta SA, you will be the main point of contact for all quality compliance key topics related to Automated and Computerized systems. Your responsibilities will include reviewing and approving URS and relevant design documentation, actively supporting risk assessment exercises, and reviewing and...

Job Description:As a Quality Assurance Engineer - CSV - Permanent Position at Axepta SA, you will be responsible for ensuring the quality and compliance of automated systems in the biopharmaceutical field. Your main tasks will include reviewing and approving URS and design documentation, supporting risk assessment exercises, and reviewing and approving...