assigned portfolio of products: Assisting with internal product queries from relevant departments Assisting regulatory authorities Work in collaboration with internal and external stakeholders to assess regulator's Guidelines pertaining to the pharmaceutical industry. Internal training and mentoring Establish and maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate or implement maintained or enhanced. Support activities such as internal audits or regulatory agency inspections Ensure
equipment is looking for a dynamic Scientific Internal Sales Officer to join their team. Duties will driven: hunting/closing opportunity skills •Support internal staff members with their sales initiatives •Be equipment and reagents supported/driven with an internal learning program and continued self-learning actions requirements should apply Please quote “ Scientific Internal Sales Officer (G861) ” in the subject line Only
of deep learning models when considering their internal structure. While our theoretical work is very collaborating researchers. We invite South African and international fellows with an interest in machine learning that conducts machine learning research of international standing. You will develop your research skills skills, collaborate and publish internationally, and grow your own research profile. You will work in collaboration Assistance in this regard can be provided by the International office. A short motivation of why you are interested
of deep learning models when considering their internal structure. While our theoretical work is very collaborating researchers. We invite South African and international fellows with an interest in machine learning that conducts machine learning research of international standing. You will develop your research skills skills, collaborate and publish internationally, and grow your own research profile. You will work in collaboration Assistance in this regard can be provided by the International office. A short motivation of why you are interested
customer complaints and develop report Investigate internal and external quality issues Team member training alert. Conduct Internal Process & systems audit and Issue report. Monthly report – Internal (Scrap rate)
in order to obtain a qualification. Successful interns will be expected to enter into a 12-month contract Successful interns will be expected to enter into a 12-month contract. Prospective interns must submit
that only quality products are released into the market. Ensure that at least one executed batch record the timely release of quality products into the market. Ensure that retention and release samples are are kept of all product batches released to market. Quality Management Processes: Manage all final product Management meetings. Manage all Deviations (both internal and from external suppliers) as per approved processes etc. to all appropriate individuals (QA, RA, Marketing, Supply Chain, EXCO etc.). Support the Responsible
that only quality products are released into the market. Ensure that at least one executed batch record the timely release of quality products into the market. Ensure that retention and release samples are are kept of all product batches released to market. Quality Management Processes: Manage all final product Management meetings. Manage all Deviations (both internal and from external suppliers) as per approved processes etc. to all appropriate individuals (QA, RA, Marketing, Supply Chain, EXCO etc.). Support the Responsible
information collected from pre-clinical through to post-marketing, including medical review of individual case safety information collected from pre-clinical through to post-marketing, including medical review of individual case safety diseases/biologics preferred. Understanding of international PV requirements and drug development and approval
information collected from pre-clinical through to post-marketing, including medical review of individual case safety information collected from pre-clinical through to post-marketing, including medical review of individual case safety diseases/biologics preferred. Understanding of international PV requirements and drug development and approval