TRABAJO REGULATORY AFFAIRS SPECIALIST MANAGER BARCELONA, BARCELONA

Overview are you interested in a career in r&d in pepsico? then now is the time to explore the opportunities of pepsico: join us as the next regulatory affairs specialist...

At least 3 years of experience in regulatory affairs with good knowledge of flavor, food or chemical regulations, safety data sheets and database systems...

Parets del vallès (barcelona)empresa: grifolsjornada: completacontrato: indefinido...

As regulatory professionals working on oncology products, we work in areas of unmet need and take innovative regulatory approaches to bring life-changing treatments...

Support the study team in the implementation of audits and regulatory inspections...   the global study manager is responsible for supporting the delivery of clinical...

• direct the study team in the implementation of audits and regulatory inspections... location: barcelona, spain (on-site) role description the senior global study...

• extensive knowledge of clinical research regulatory requirements (incl ich-gcp) and demonstrated abilities in clinical study management processes and clinical/drug...

We have ambitious plans to expand our specialist fulfilment centres and delivery stations across the uk and europe... key job responsibilities - create roadmaps...

Partner with our internal it team to manage corporate affairs content publishing requests for nucleus... you will be expected to contribute to a positive, collaborative...

The manufacturing project manager contributes to the execution of the regional manufacturing strategy by managing a broad variety of projects within and across the...

Actively seek and promote creative and innovative ideas to drive performance and bring new solutions to customers   establish a global mind-set to systematically...

The metabolics medical advisor will report to the medical affairs manager, metabolics... ensure that internal and external legal and regulatory guidelines are...

• ensure medical insights are provided to cross functional groups, including, but not restricted to: pharmacovigilance, regulatory affairs, market access, qa, commercial...

Job description: about the role dow jones risk & compliance is a global provider of third-party risk management and regulatory compliance solutions...

The associate director study leader, early oncology clinical is responsible for the delivery of clinical studies including quality, timelines, budgets, resources...

You will ensure reports are timely, complete and accurate summarize complex information from another language into english compile and summarize information from...

Seguimiento interno de nuevos productos en desarrollo, en comunicación y colaboración con i+d, regulatory affairs, marketing, etc... dependencia de la business development...