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Online Resumes with "Auditing Batch Records"
Quality Assurance Associate
Quality Bio-Pharmaceutical professional with ISO/GMP/TQM experience and strong data management in inventory control & distribution. Ability to design, develop and improve process systems. Bi-lingual in Spanish and English. Additional skills and knowledge include: Package & Labeling Design; Documentation Editing; Contract Facility Audits; Statistical Analysis; Return Destruction Processing; Charting Trending; Contract Vende...
Ideal Companies: Open to all Medical device and bio pharmaceutical companies
Tags for this Online Resume: Quality Assurance, Documentation Specialist, Inspector, Audits, Calibration, GMP, ISO, CAPA, Change Control
Sr QA Analyst - 10 years experience, Statistical trend analysis, Quality metrics, CAPA, Audits, Batch Record Reveiw
As a Quality Assurance Analyst, I have acquired vast knowledge in product quality from both Pharmaceutical and Medial Device industries. I am eager to apply my knowledge to further expand industry experience.
Tags for this Online Resume: Quality Auditor, Quality Engineer, Complaint Specialist, QA Auditor, Supervisor, Quality Control, Sr QA Analyst
Bio Production Technician - 4 years Experience - Durham, NC - Fortune 500 Experience - GMP
I am a a four year experienced Merck biopharmaceutical technician and exceptional assistant floor lead who has 4 years experience in the pharmaceutical field and GMP environment. Knowledgable in Operations Reviews, cGMP production, Auditing Batch Records, MMD Sigma Yellow Belt Certified,
Tags for this Online Resume: Durham, NC, SAP, GMP, Operations Reviews, Auditing Batch Records, Experienced
Quality Coordinator - 20 Years of Experience - Near 18353
Areas of Expertise & Technical Skills * Regulation Compliance * Agile (Scrum Master) * Internal/External Audits * Batch Record Reviews * CAPA / Risk Management * QA System Management & Implementations * Project Life Cycle * Technical Writing * Process Improvements * Six Sigma (Green Belt) * Document Controls * Software Implementation * CFR 210/211/820/803/58/11 * Team Training & Development
Tags for this Online Resume: Audit, Business Contingency Planning, Compliance, Documentation, Good Manufacturing Practices, Manufacturing, MDR, Packaging
General
SUMMARY Pharmaceutical Professional 20 years' experience, Quality Assurance, auditor batch review /release, Clinical Supplies, OTC and Governance meeting manager, worked in a Consent Decree environment with special projects, audit, and review and approve label change controls folders, Bill of Materials setup, master batch records, validation documentations. label inspection/review, quality notifications, produce/update sour...
Tags for this Online Resume: Manufacturing, Proofreading, Management, Packaging, Project Management, Audit, Distribution, Documentation, Inventory, Process Improvement
Director of Quality - 24 Years of Experience - Near 11801
Professional Summary Highly effective professional offering 30 years of US global quality leadership experience developing strategies, improvement action plan and solutions. Dedicated leader to bring organizations together, focusing on hi performance culture leading to improvement and efficiency. Built fully engaged team that is motivated to achieve metrics and deliver ROI. Lead and empowered cross functional teams to impro...
Ideal Companies: end of the year 449.00 + 4 months of our service. resume rewtire and cover letter.
Tags for this Online Resume: TQM (Total Quality Management), Manufacturing, Assessments, Audit, Quality, Quality Management System, HACCP, Continuous Improvement, PCQI, Supplier site and internal audits, USDA, FDA, ISO 9001, SQF, BRC, ISO 22000, ERP, OOS, Investigation, CAPA, NCR
