TRABAJO REGULATORY QUALITY SPECIALIST MEDICAL

Demonstrated expertise in medical device regulatory requirements and processes... experience in worldwide regulatory systems preferred... at least 3+ years of regulatory...

The senior regulatory affairs specialist is responsible for regulatory activities to support new, modified and currently marketed medical devices in the depuy joint...

Documentation preparation: prepare comprehensive regulatory documentation for medical devices, including ivds and medical device software, ensuring compliance with...

regulatory affairs, operations, product quality management, etc...   the innovative medicines regulatory compliance organization is recruiting for a senior compliance...

Importante empresa dedicada al diseño y desarrollo de software propio dirigido a los sectores salud y ensayo clínico, inmersa en ambicioso proyecto de crecimiento...

G pv, regulatory affairs activities... implement supplier quality program at spain loc according to takeda global quality requirements and regulatory expectations...

At least 2 years of experience in regulatory affairs within the medical device industry... participate in strategic planning and provide regulatory guidance...

Direct training programs for quality and regulatory compliance... lead internal and external quality assurance audits and regulatory agency inspections...

We are seeking a highly skilled quality assurance specialist (qas) to oversee and ensure the quality and compliance of government contractor performance in rota...

Your role: promote quality awareness level and fostering quality culture drive quality systems deployments and promoting continuous improvements drive achievement...

Person responsible for regulatory compliance (prrc)... the primary responsibility of the quality and regulatory manager is to oversee the implementation of quality...

Actively participate in medical writing and cross-functional meetings... maintain knowledge of industry, company, and regulatory guidelines... may lead project-level/submission/indication...

Due to our constant growth, we are looking for a regulatory affairs specialist to support our projects in our office in madrid (spain)you will be responsible for:execution...

We are currently seeking a dedicated and skilled quality specialist gdp... knowledge of quality management processes and regulatory requirements in the pharmaceutical...

Previous experience in clinical trial regulatory submissions...    job description the specialist/senior specialist, study start up and regulatory is responsible...

Acquire, maintain, and apply knowledge of the industry, company, and regulatory guidelines... johnson & johnson innovative medicine is recruiting for an analyst...

medical information and adverse event intake specialist with estonian and english language this position will put you at the forefront of patient safety...