| Distance: | Resume alert | Resumes 251 - 260 of 25478 |
Customer Service, Problem Solving, Organizational skills, Financial/Ta
Itasca, TX
... Assisted with FDA submissions, updated clinical trials data spreadsheets, updated procedures manuals, and assisted with delivery of PMA Module submission. Highland Homes Exec Admin Asst to President & CFO July 2014 - February 2016 Liaison for staff ... - 2025 Oct 13
... Assisted with FDA submissions, updated clinical trials data spreadsheets, updated procedures manuals, and assisted with delivery of PMA Module submission. Highland Homes Exec Admin Asst to President & CFO July 2014 - February 2016 Liaison for staff ... - 2025 Oct 13
Human Resources Resource
Middletown, DE
... BRYANT Tasha.bryant@ fda.hhs.gov *******@*****.*** *** ********** ****. ******, ** 19711 302-***-**** OVERVIEW Forward thinking, flexible individual with advanced knowledge of human resource principles and ability to professionally handle any human ... - 2025 Oct 13
... BRYANT Tasha.bryant@ fda.hhs.gov *******@*****.*** *** ********** ****. ******, ** 19711 302-***-**** OVERVIEW Forward thinking, flexible individual with advanced knowledge of human resource principles and ability to professionally handle any human ... - 2025 Oct 13
Supply Chain Procurement Specialist
Palmdale, CA
... equipment and service agreement for internal use •Collaborate with internal Customers (A/P, Quality, Receiving/Shipping, Engineers) and external customers (Vendors, subcontractors and consultants) •Adhere to regulatory requirements (FDA, TUV,etc. ... - 2025 Oct 11
... equipment and service agreement for internal use •Collaborate with internal Customers (A/P, Quality, Receiving/Shipping, Engineers) and external customers (Vendors, subcontractors and consultants) •Adhere to regulatory requirements (FDA, TUV,etc. ... - 2025 Oct 11
Quality Control, AMV All Activities & Development
Pune, Maharashtra, India
... FDA Query Analysis related to methods. Method verification of new pharmacopeial methods. Analysis of Routine Formulation Batches of Tablets, Capsules, Powders for oral suspensions Oral solutions and Oral suspensions received from F&D for regulated ... - 2025 Oct 11
... FDA Query Analysis related to methods. Method verification of new pharmacopeial methods. Analysis of Routine Formulation Batches of Tablets, Capsules, Powders for oral suspensions Oral solutions and Oral suspensions received from F&D for regulated ... - 2025 Oct 11
Technical Assistant Pharmaceutical Manufacturing
Visakhapatnam, Andhra Pradesh, India
... Audits FDA, MHRA, WHO, TGA, Customer audits (TEVA, LUPIN, SUN PHARMA, Breckenridge) Internal audit and GMP audit. Qualification S.S.C 2005 From Board Secondary Education AP. Diploma(Mechanical) 2008 From A.I.I.T. Intermediate 2021 from open school ... - 2025 Oct 11
... Audits FDA, MHRA, WHO, TGA, Customer audits (TEVA, LUPIN, SUN PHARMA, Breckenridge) Internal audit and GMP audit. Qualification S.S.C 2005 From Board Secondary Education AP. Diploma(Mechanical) 2008 From A.I.I.T. Intermediate 2021 from open school ... - 2025 Oct 11
Regulatory Affairs Operations
Garner, NC, 27529
... Proven track record in preparing, compiling, and submitting eCTD-compliant regulatory dossiers, including INDs, NDAs, BLAs, ANDAs, and IMPDs across multiple regions (FDA, EMA, Health Canada, and MHRA) in alignment with ICH, FDA, and regional ... - 2025 Oct 10
... Proven track record in preparing, compiling, and submitting eCTD-compliant regulatory dossiers, including INDs, NDAs, BLAs, ANDAs, and IMPDs across multiple regions (FDA, EMA, Health Canada, and MHRA) in alignment with ICH, FDA, and regional ... - 2025 Oct 10
Quality Assurance in Pharmaceuticals, Medical Device, & Planning.
Raleigh, NC
... • Partnered with global teams to ensure FDA/QSR/GMP compliance and drive continuous improvement. • Developed vendor qualification and review processes to align external partnerships with regulatory expectations. • Facilitated internal and external ... - 2025 Oct 10
... • Partnered with global teams to ensure FDA/QSR/GMP compliance and drive continuous improvement. • Developed vendor qualification and review processes to align external partnerships with regulatory expectations. • Facilitated internal and external ... - 2025 Oct 10
Quality Assurance Continuous Improvement
Edgemere, MD, 21219
... Skilled in regulatory compliance (CLIA, FDA, OSHA, AGES, EMA, PPTA), supplier quality management, CAPA and risk management. Adept in cross functional collaboration, team leadership and inspection readiness. Committed to maintaining high product ... - 2025 Oct 10
... Skilled in regulatory compliance (CLIA, FDA, OSHA, AGES, EMA, PPTA), supplier quality management, CAPA and risk management. Adept in cross functional collaboration, team leadership and inspection readiness. Committed to maintaining high product ... - 2025 Oct 10
Pharmacy Intern Clinical Research
Pune, Maharashtra, India
... "Completed PG Diploma in Clinical Research with knowledge of drug development, clinical trial design, regulatory guidelines (ICH-GCP, FDA, CDSCO), pharmacovigilance, and data management." "Trained in clinical pharmacology, rational drug therapy, ... - 2025 Oct 10
... "Completed PG Diploma in Clinical Research with knowledge of drug development, clinical trial design, regulatory guidelines (ICH-GCP, FDA, CDSCO), pharmacovigilance, and data management." "Trained in clinical pharmacology, rational drug therapy, ... - 2025 Oct 10
Business Analyst Process
Dallas, GA
... Ensured compliance with regulatory requirements, including FDA regulations, ICH guidelines, and institutional policies. Developed and implemented study plans, timelines, and budgets. Identified, screened, and recruited potential study participants, ... - 2025 Oct 09
... Ensured compliance with regulatory requirements, including FDA regulations, ICH guidelines, and institutional policies. Developed and implemented study plans, timelines, and budgets. Identified, screened, and recruited potential study participants, ... - 2025 Oct 09