TRABAJO QUALITY ASSURANCE REGULATORY AFFAIRS
(296 ofertas de trabajo)
Listado de trabajos de Quality assurance regulatory affairs
Regulatory affairs & quality assurance specialist
Description palex portugal, a leading company in the management and distribution of innovative hospital and research solutions, is recruiting an regulatory affairs...
Regulatory affairs and quality specialist(pharma)
Analysis and resolution of regulatory and quality issues... occasional supplier visits and international regulatory audits... minimum 5 years in quality and regulatory...
Quality and regulatory affairs specialist
quality and regulatory affairs specialistlocation: barcelona, spaincontract: permanent, full-timeat atanor productos químicos, we don’t just meet standards—we work...
Director, global regulatory affairs & clinical safety (gracs), global process lead
Lead large-scale change initiatives across global regulatory affairs and clinical safety and engage across global regulatory affairs and clinical safety leadership...
Coordinator, regulatory affairs strategy
Based in the european hq in belgium, the regulatory affairs strategy coordinator reports to the associate director, global strategy & implementation, css and assists...
Senior associate, regulatory affairs
Dossiers), and oversee compliance with regulatory materials... support the affiliate regulatory head with audits, inspections, and the implementation of the quality...
Associate director, regulatory affairs
Collaborate with global regulatory teams and the global regulatory affairs (gra) function/teams to facilitate regulatory activities... the associate director, regulatory...
Quality assurance (medical device)
Lead internal and external quality assurance audits and regulatory agency inspections... direct training programs for quality and regulatory compliance...
Medtech commercial quality manager - quality system & performance, apac
Key responsibilities: work with the director, quality systems and apac’s quality community, ensuring a proactive approach to quality assurance and quality systems...
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Support the quality assurance department in the conduct of quality risk assessments... assist the quality assurance team through any required regulatory, customer...
Director, regulatory affairs cmc
Delivers cmc regulatory strategy to support major inspections (eg pai's) or quality incidents (pircs)... creates, maintains and continually evaluates/improves cmc...
Associate director, clinical quality assurance (remote)
Job description in partnership with the quality assurance lead (qal), the quality assurance specialist (qas) will support the implementation and management of the...
Director regulatory affairs (international markets)
Oversee regulatory intelligence efforts to anticipate regulatory trends and potential impacts on business objectives... about the role:we are seeking an experienced...
Position summary as a regulatory affairs specialist, you will join a diverse team and be responsible for regulatory and compliance activities at the schaffhausen...
System & software quality assurance engineer
• raise and escalate quality alerts for major quality findings to the appropriate organizational levels... • report project’s system and software quality assurance...
Regulatory affairs specialist - johnson & johnson – located in switzerland or united states
Prepares, reviews, and submits regulatory submission to regulatory authorities... this includes the preparation of regulatory documentation for submission to regulatory...
Quality assurance manager & qualified person es_867145
Local quality management review... local gdp regulatory intelligence and quality alert monitoring... supplier quality monitoring and issues managementproduct quality...
Quality assurance officer / specialist
quality assurance specialist major accountabilities: support the the site program for ongoing inspection readiness in conjunction with the quality leadership team...
Senior regulatory affairs specialist (ees) - medtech surgery, inc.
The senior regulatory affairs specialist is responsible for regulatory activities to support new, modified and currently marketed medical devices...
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