Project Manager
sites. Support US and LATAM sales teams, with occasional collaboration with EU and Asia regions. Provide weekly project...
sites. Support US and LATAM sales teams, with occasional collaboration with EU and Asia regions. Provide weekly project...
sites. Support US and LATAM sales teams, with occasional collaboration with EU and Asia regions. Provide weekly project...
: Strong knowledge of FDA and EU cGMP requirements. Proficiency in root cause analysis techniques. Experience in writing, reviewing... regulations, including FDA, EU, and other regulatory bodies. Collaborate with manufacturing management to provide quality...
timelines. Develop and review validation protocols, reports, and supporting documentation in compliance with FDA, EU standards... in validation within the pharmaceutical or biotech industry. Strong knowledge of cGMP, FDA, ICH, and EU regulations. Proven...
, EU MDR, and MDSAP requirements Communicates product compliance and process expectations to the manufacturing floor...
14971, and CMDR. Key Responsibilities: Manage and maintain international product registrations (EU, China, ROW...). Support preparation and submission of US FDA 510(k)s, EU Technical Files, and other global filings. Update Technical Files...
, ISO, and EU-MDR standards, leading risk management activities, and executing design and process validations. This position.... 3–5+ years of experience in Quality or Engineering roles. Detailed knowledge of FDA 21 CFR 820, GMP, MDD, EU-MDR, ISO...
, MDSAP, EU MDR/IVDR) as it relates to the design and continued support of Client products. Applied knowledge of Corporate...
supports EU MDR and manufacturing-related testing activities. This role assists with preparing, staging, labeling, and tracking...
, Philippines, UK, India, Netherlands, and the EU. IntelliPro, a global leader connecting individuals with rewarding employment...