Petra (Rosenblad) Lindholm
Stockholm, Sweden
Medical Devices
Skills
Pharmaceutics, Chemistry, FDA GMP, SharePoint, Clinical Trials, CAPA, FDA, Quality Control, Biocompatibility, Quality System, Regulatory Affairs, Chromatography, Life Sciences, Regulatory Submissions, Cardiology, Quality Auditing, V&V, Regulatory Requirements, Clinical Research, Validation, Pharmaceutical Industry, Analytical Chemistry, Quality Systems, Molecular Biology, Six Sigma, Lifesciences, 21 CFR, ISO 14971, ISO, Quality Management, Minitab, ISO 13485, Quality Assurance, Biomaterials, Oncology, R&D, Design Control, Toxicology, CE marking, Sop, GMP, Drug Development, Change Control, HPLC, Sterilization, Design of Experiments, Medical Devices, GLP, Biotechnology, 21 CFR Part 11