LAVORO PRINCIPAL SCIENTIST DRUG PRODUCT

The principal scientist in the drug product development & delivery will be a lab-based role with expertise in protein science and support formulation development...

Position summary the principal clinical research scientist for the surgical vision platform is an expert in ophthalmic and medical device research who is a core...

The role we’re looking for a principal applied scientist to lead our machine learning research and advance the state of the art of artificial intelligence applied...

B principal scientist – functional immunophenotyping and flow cytometry core facility irbm, oncology unit irbm is a scientific contract research organization...

Johnson & johnson recruiting for a principal scientist, animal welfare scientific manager, located in spring house, pa... experience and skills: required: minimum...

R, python, matlab, … proven ability to transform drug delivery challenges into innovative ideas and practical solutions... we are seeking a talented postdoctoral...

Support to formulation and process development studies of drug products... support to scale up for drug products and active ingredients process...

The manager sas will have in-depth product knowledge, will serve as product point of contact, and will provide mentoring to, and oversight of deliverables prepared...

Dpem is responsible for the commercialization of drug products (dps) at selected contract manufacturers (cms) located globally, but also is responsible for technology...

This position regularly works cross functionally with manufacturing, quality, logistics, facilities, drug product development and vendors...

Generates documents for orphan drug designation, if applicable...  thorough knowledge of drug development process is required... key responsibilities: list major...

Your responsibilities will include: be the expert: act as a process analytics and modelling expert in drug product development teams, sharing your engineering and...

· supervision of the preparation of the annual product review (apqr) and guarantees its execution within the due date... · review and release of purchased materials...

It is divided into integrated functional areas focusing on pipeline projects including discovery and preclinical research, global technical development, drug delivery...

The senior director/executive director, global regulatory affairs (gra)-emea regional regulatory scientist performs regulatory evaluations of external business opportunities...

O execute safety monitoring and assessment as one of core members of j-smt o he or she can be also regarded as study responsible scientist (srs) of assigned local/regional...

​ overall purpose:    the associate director/director, global regulatory affairs (gra)-emea regional regulatory scientist is accountable for the below;     to establish...

The demand for high quality real-world evidence (rwe) and health outcomes (ho) research to support drug development, /access decisions, product differentiation,...