42 specialist English-speaking jobs in Canton of Aargau

Senior GMP Quality Assurance Specialist will oversee raw material quality processes, including review and approval of documentation and support QC/QA activities. Experience in QA within a GMP environment and material management is preferred. Fluency in English is required.

Senior QA Validation Specialist will oversee raw material quality processes, including review and approval of documentation. Responsibilities include supporting QC/QA activities, driving qualification and validation activities, and contributing to warehouse and logistics quality oversight. Requires solid QA experience in a GMP environment and fluency in English. German language skills are an advantage.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Senior QA Validation Specialist will oversee raw material quality processes, including review and approval of documentation. Responsibilities include supporting QC/QA activities, driving qualification and validation activities, and contributing to warehouse and logistics quality oversight. Requires solid QA experience in a GMP environment and fluency in English. German language skills are an advantage.

Senior GMP Quality Assurance Specialist will oversee raw material quality processes, including review and approval of documentation and support QC/QA activities. Experience in QA within a GMP environment and material management is preferred. Fluency in English is required.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Senior GMP Quality Assurance Specialist will oversee raw material quality processes, including review and approval of documentation and support QC/QA activities. Experience in QA within a GMP environment and material management is preferred. Fluency in English is required.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Senior QA Validation Specialist will oversee raw material quality processes, including review and approval of documentation. Responsibilities include supporting QC/QA activities, driving qualification and validation activities, and contributing to warehouse and logistics quality oversight. Requires solid QA experience in a GMP environment and fluency in English. German language skills are an advantage.

The LIMS Master Data Specialist is responsible for the creation, modification, maintenance, and verification ... Working within the governance framework defined by the master data governance council, the Specialist

The Quality Assurance Specialist plays a central role in ensuring quality, compliance, and regulatory

Analytical Compliance Record Specialist Our client is a pioneer in Drug Discovery and Development and ... We are currently looking for an Analytical Compliance Record Specialist for a 12-month contract based

The CSV Manager supports quality operations for testing services in a GMP laboratory environment. Ensures compliance with regulatory requirements related to computerized systems, including validation, maintenance, and lifecycle management. Reviews and approves CSV deliverables and procedures. Provides compliance oversight for the validation and maintenance of electronic systems. Collaborates with IT and other teams to ensure regulatory compliance. Requires a Bachelor's degree and a minimum of 7 years of experience in a pharmaceutical, biotechnology, or related environment with a minimum of 3 years of experience in GxP Computer System validation. Up to 20% travel required.

Description The opportunity We are looking for a passionate and proficient industrial specialist with

Description The opportunity We are looking for a passionate and proficient industrial specialist with

Join our National Information Systems Expert Team in Switzerland as a Blue Yonder WMS Specialist (m/w

As DCT Recruitment Specialist for the Asia-Pacific — covering India, Southeast Asia, East Asia, and Oceania