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Qc Associate Jobs In Spain - 25 Job Positions Available

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Fortrea jobs

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of

Fortrea  9 days ago
Fortrea jobs

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of

Fortrea  9 days ago
Skydance jobs

Skydance offers a dynamic, inclusive, and ever-evolving culture where innovative ideas are welcomed, and growth fostered. The partnership between unique creativity and technological advancements are demonstrated within each pillar of the company. At the heart of

Skydance  11 days ago
CTI jobs

Please submit your application in English What Youll Do: Support of Regulatory Affairs Study Start-Up (RASSU) department: Informs the RASSU department about any change of Drug Law/guidelines and updated requirements for submission on the country level

CTI  10 days ago

Associate Electrical Design Engineer (Data Centres) - Madrid, Spain RED are an expanding international M&E consultancy, with a proven track record in low energy design, focused on providing excellent design solutions to clients Through our market leading

RED Engineering Design  4 hours ago

RED are an expanding international M&E consultancy, with a proven track record in low energy design, focused on providing excellent design solutions to clients Through our market leading technical expertise, we enable the world’s digital infrastructure

TRACTEBEL  4 hours ago
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BeiGene jobs

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. ¿Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a continuación y pulse en solicitar para ser considerado. When

BeiGene  2 hours ago
Worldwide Clinical Trials jobs

Who We Are Were a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it safe. It

Worldwide Clinical Trials  4 days ago

RED are an expanding international M&E consultancy, with a proven track record in low energy design, focused on providing excellent design solutions to clients Through our market leading technical expertise, we enable the world’s digital infrastructure

TRACTEBEL  4 hours ago

Associate Mechanical Design Engineer (Data Centres) - Madrid, Spain RED are an expanding international M&E consultancy, with a proven track record in low energy design, focused on providing excellent design solutions to clients Through our market leading

RED Engineering Design  4 hours ago

The Global Study Associate Director (GSAD) is a business-critical role within Study Management, BioPharmaceuticals Clinical Operations, whose main accountability is the delivery of clinical studies. The GSAD is responsible for leading a cross-functional study team and for

IQVIA Argentina  3 hours ago
Novartis jobs

Summary La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación. In this role you will lead, support and report independent GMP audits

Novartis  22 days ago
Confidential jobs

Overview La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto. Sign-on Bonus Available! Relocation bonus available for 1yr+ experience and 50mi To perform routine and specialized examinations in Ultrasound;

Confidential  3 days ago
CTI Clinical Trial and Consulting Services jobs

What You’ll Do Assist/Advise project teams on all regulatory requirements for clinical studies Perform compliance assessments according to country requirements and document any activity discovered; notify Project Managers of any findings Review and adapt study specific

CTI Clinical Trial And Consulting Services  4 hours ago
Novartis jobs

Job Description SummaryIn this role you will lead, support and report independent GMP audits according to the Novartis Quality System and the current GMP regulations to assess compliance with applicable regulations, standards, and guidance documents. ¿Tiene

Novartis  2 hours ago

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