42 specialist English-speaking jobs in Canton of Aargau

  • Lonza
  • Frick
  • May 22
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.
  • Lonza
  • Stein
  • May 22
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.
  • Lonza
  • Hornussen
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Villmergen
  • May 22
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.
  • Lonza
  • Ehrendingen
  • May 22
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.
  • Lonza
  • Gipf-Oberfrick
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Densbüren
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Wölflinswil
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Gränichen
  • May 22
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.
  • Lonza
  • Oberhofen bei Etzgen
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Möhlin
  • May 22
Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.
  • Lonza
  • Möhlin
  • May 22
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.
  • solvias
  • Kaiseraugst
  • May 29
LogoThe 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
  • solvias
  • Kaiseraugst
  • May 29
LogoThe Quality Assurance Specialist plays a central role in ensuring quality, compliance, and regulatory
  • CTC Resourcing Solutions
  • aargau
  • May 11
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
  • solvias
  • Kaiseraugst
  • May 29
LogoThe 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.
  • Hitachi Rail
  • Baden
  • April 9
Description The opportunity We are looking for a passionate and proficient industrial specialist with
  • Hitachi Rail
  • Aargau
  • April 9
Description The opportunity We are looking for a passionate and proficient industrial specialist with
  • Kuehne+Nagel
  • Möhlin
  • May 25
LogoJoin our National Information Systems Expert Team in Switzerland as a Blue Yonder WMS Specialist (m/w
  • RM Staffing B.V.
  • Lupfig
  • April 24
As DCT Recruitment Specialist for the Asia-Pacific — covering India, Southeast Asia, East Asia, and Oceania
Email me future jobs like these:
next page