Job Description The position The incumbent is accountable for all activities at the External Entity (EE) site associated with the manufacturing of Company products which includes quality oversight over manufacturing, testing, packaging, storage, and distribution of
Are you an experienced Regulatory Affairs professional who enjoys taking ownership, challenging existing ways of working and turning regulatory expertise into practical improvements? Would you like to work across Southern European markets while helping colleagues and
Location: Spain (Madrid or Barcelona based) Who we are? Optimapharm is a mid-sized, global Contract Research Organisation turning science into hope through agile, patient-focused clinical development. At Optimapharm, youll have the opportunity to work on diverse
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
The position The incumbent is accountable for all activities at the External Entity (EE) site associated with the manufacturing of Company products which includes quality oversight over manufacturing, testing, packaging, storage, and distribution of the products
Medicine moves forward here. So willyou. At PrimeVigilance, patient safety is not one part of the job. It is why we exist. We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while
Responsibilities Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management Prepare and proofread packaging materials, artwork files, mock-ups, item lists, and regulatory documentation Communicate with competent authorities and stakeholders across assigned markets
Job Description The incumbent is accountable for all activities at the External Entity (EE) site associated with the manufacturing of Company products which includes quality oversight over manufacturing, testing, packaging, storage, and distribution of the products
Are you an experienced Regulatory Affairs professional who enjoys taking ownership, challenging existing ways of working and turning regulatory expertise into practical improvements? Would you like to work across Southern European markets while helping colleagues and
Responsibilities Asegúrese de leer detenidamente la información sobre esta oportunidad antes de presentar su candidatura. Acquire and maintain parallel trading licenses, including dossier preparation, submissions, and lifecycle management Prepare and proofread packaging materials, artwork files, mock-ups,
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
TakeTalent joins PharmaMar i n the search for a Clinical Pharmacology Scientist to support the development of innovative oncology therapies through cutting-edge clinical pharmacology and model-informed drug development strategies . At PharmaMar , they are committed
Crovelis Madrid, Community of Madrid, SpainSr Clinical Project ManagerCrovelis Madrid, Community of Madrid, Spain3 days ago Be among the first 25 applicants Join Crovelis as a Senior Clinical Project ManagerCrovelis, a pioneering AI-powered CRO, is a
What You’ll Do Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required deliverable as appropriate Update Clinical Project Manager / Director
Job TitleClinical Specialist Iberia Surgery (Field)LocationBD in San Agustín de Guadalix, MD, ESFull time on site position offers great opportunities for career growth.Now We are the people who give possibilities purpose BD is one of the
Product Development / Quality Technician Nutris Madrid, Community of Madrid, Spain Nutris is a highly motivated company, whose steps are based on a constant innovating activity and following the most exigent quality procedures in both Food