1. Robert Zeider
1556 Calle La Cumbre, Camarillo, CA 93010 · 805.204.7166 · robert.zeider940@gmail.com · linkedin.com/in/robertzeider
WORK EXPERIENCE
Shire Plc, Thousand Oaks, CA Jun. 2014 – Present
Quality Analyst I – Formulation, Filling and Finishing
 Experienced at making real-time Quality/GMP decisions during manufacturing operations.
 Experienced at reviewing QA Documentation and revising SOPs, Runsheets, and Forms.
 Qualified in Packaging Batch Record Review and the Inspection of Filled Unlabeled Vials.
 Qualified trainer in all quality roles overseeing aseptic filling, capping and packaging operations.
 QA subject matter expert streamlined aseptic filling operations as QA subject matter expert.
 Received an “Exceeds Expectations” review for strong work ethics and diligence to quality.
 Knowledge of good aseptic practices including: cGMP, ISO Class 5-9 gowning, and Federal
Regulations 21 CFR – parts 210 & 211.
 Managed issuance, segregation and destruction of QA controlled product, material and labels.
 Experienced at navigating in J.D. Edwards EnterpriseOne, SQL LIMS, PLMS.
R.L. Zeider Incorporated, Camarillo, CA Jan. 2011 – Present
Operations Specialist /CNC Mill and Wire EDM Operator
 Oversaw manufacturing operations of precision medical-grade titanium implants utilizing Computer
Numerical Control Mills (CNCs) and Wire Electric Discharge Machines (EDMs).
 Increased production nearly two-fold by developing a streamlined manufacturing schedule that
staggered all automated process to ensure maximum productivity over a 24-hour cycle.
 Inspected for and maintained a high degree of accuracy and precision required for medical implants.
 Responsible for troubleshooting production issues, deviations, NCRs/CAPAs.
 Oversaw customer audits, and implemented revisions to documents, training and/or Preventative
Maintenance scheduling to meet/exceed requirements.
 Created SOPs, Runsheets and inspection forms for the manufacturing and segregation of multiple
medical devices with varying material lot identifications at different stages of manufacturing process.
 Created training programs for Manufacturing, Inspection and Preventative Maintenance.
 Reviewed raw material stores and purchase orders to ensure on hand quantities met demand.
 Created system for organization of Invoices, Material Certifications, Material Safety Data Sheets
(MSDS), Quality Assurance/Inspection forms, and equipment Preventative Maintenance forms.
SKILLS
 Quality/Manufacturing: cGMP, cGDP, ISO Class 5-9 Gowning, 21 CFR – parts 210 & 211,
Packaging Batch Record Review, FUV Inspection, Document Review/Revision
 PC Software: Microsoft Windows and Office Suite (Excel, Word, PowerPoint), JD Edwards
EnterpriseOne, Kaye LabWatch, SQL*LIMS, IBM SPSS Statistical Analysis Software
EDUCATION
 Bachelor of Science in Biology, California State University Channel Islands Fall 2013
Minor in Chemistry
o Biology: Cell Biology, Molecular Biology, Genetics, Biostatistics, Animal Physiology
o Chemistry: General Chemistry, Organic Chemistry, Quantitative Chemical Analysis