| Job alert | Jobs 61 - 70 of 199 |
Validation Supervisor
GlaxoSmithKline
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King of Prussia, PA, 19406
... 3 years of experience utilizing current GMP's, NIH Guidelines and FDA or European validation practices for biopharmaceutical processes and supporting regulatory audits as SME; 2 years of experience in the validation of large-scale bulk ... - May 20
Histotechnologist in Reading, Pennsylvania
KA Recruiting Inc.
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Reading, PA, 19601
... enzymes for complex diagnosis and prognostic markers Contribute to corporate strategy for additional regulatory approvals (CAP, FDA, ) relating to GHI Histopathology Assess the quality of slide preparations and troubleshoot procedures if necessary ... - May 17
Quality Analyst - Global Ship Hold Center (GSHC)
Olympus Corporation of the Americas
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Upper Saucon Township, PA, 18034
... Additionally, this role entails ensuring that GSHC complies with required quality standards, such as the FDA Quality System Regulation and ISO 13485. In this role, you will report to the Director of Global Ship Hold Center, and will work closely ... - Apr 30
Mammography Technologist - Per Diem - Paoli, PA BONUS
Onsite Women's Health
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Paoli, PA
... Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate! Experience: Mammography: 2 years (Required) License: ... - Apr 22
Residential RN Coras Wellness and Behavioral Health Women's
Supportive Concepts for Families
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Wyomissing, PA, 19610
... for safekeeping of all medication stocks and records required by Company protocol, Federal and State Regulations (DEA, FDA, and ADP) * Responsible for drug screen specimen collection and processing, reading test results as ordered by Program ... - May 01
Principal Programmer
TechData Service Company
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King of Prussia, PA, 19406
... Incorporate CDISC standards in creation of SDTM datasets and derivation of AdaM datasets, adhering to FDA ICH GCP guidelines. Define analysis dataset specification, and generate tables, listings and graphs and per statistical analysis plan. Develop ... - May 16
Copy Editor, Marketing Services
Deerfield – Agency of Brand®
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Conshohocken, PA, 19429
... attitude toward acquiring knowledge and honing skills Knowledge of AMA editorial style guidelines preferred Understanding of FDA regulations as it impacts the MLR submission process Using applications: Microsoft Office At Deerfield, we are dedicated ... - May 18
Quality Control Analyst
Ecolab
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King of Prussia, PA
... Maintain compliance with all legal regulations including GMP/ FDA/ISO standards. Main Responsibilities: Performs analytical testing of in-process and final product materials in a GMP laboratory. Experienced in Quality System and SOP procedures as ... - May 17
Manager/ Sr. Manager Medical and Scientific Writer
Ocugen, Inc.
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Malvern, PA, 19355
. Target Bonus and Equity
... Collaborate with regulatory partners to prepare Orphan Drug Designation (ODD) requests based on pre-clinical efficacy data and disease prevalence, submitting them to FDA. Conduct quality control and editorial review of documents prepared by team ... - May 16
Associate Director, QA Operations
Gene Therapy Program | University of Pennsylvania
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King of Prussia, PA, 19406
... Knowledge of GxP regulations (GMP/GLP/FDA Guidelines/21 CFR Parts 210 & 211/ICH). Prior experience/knowledge in DMAIC and Lean Six Sigma (preferred). Prior experience with generation of metrics, monitoring key quality systems/KPIs, data analysis, ... - Apr 28