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Skills

  • MS Office
  • Laboratory safety protocols
  • Operational improvement
  • Environmental Health & Safety (EHS) Compliance
  • Root cause analysis
  • Medical research
  • Business operations
  • Customer service
  • MEDITECH software
  • Problem resolution

Work Experiences

  • Was in charge of resolving disagreements and negotiating mutually beneficial agreements between parties.
  • Championed the adoption of an electronic lab notebook system, improving data entry accuracy and accessibility by 61%.
  • Assisted in the validation of new production processes.
  • Championed the adoption of an electronic lab notebook system.
  • Performed EKGs, chemical analyses, urinalysis, and hematology on as many as 12 patients every day.
  • Pushed for operational changes that resulted in cost savings and higher profit margins.
  • Achieved lab-wide preparedness for unforeseen equipment failures.
  • Achieved a 50% reduction.
  • Looked for industry trends on social media and through online sources.
  • Achieved a 22% reduction in training time for new hires.

Summaries

  • Ready to contribute 6 years of relevant experience to a new and challenging role.
  • Achieved $2 monthly savings.
  • Achieved faster go-to-market timelines.
  • Action-oriented Lab Production Specialist.
  • TJC, OSHA, and FDA guidelines are all familiar to me.
  • Aided in the swift transition of Workday to full-scale production.
  • Multitasking expert with strong communication and problem-solving abilities.
  • Adept in inventory management.
  • Boosted on-time sample delivery by 74%.
  • Achieved a 33% decrease in rejected samples.

Accomplishments

  • Designed and implemented a standard resulting in a 61% increase in throughput efficiency.
  • Spearheaded contamination control procedures resulting in consistent ISO framework ratings over consecutive audits.
  • Led a cross-functional team of 10 scientists to scale-up production of Tableau from R&D to commercial scale within one year.
  • Introduced a multi-tier quality control system that reduced defective products by 63% and increased customer satisfaction.
  • Monitored and evaluated production outputs using Adobe Creative Suite, identifying trends that resulted in 29% optimization of resources.
  • Optimized usage of raw materials, reducing chemical waste by 55% through targeted waste reduction initiatives.
  • Resolved product issue through consumer testing.
  • Used Microsoft Excel to develop inventory tracking spreadsheets.
  • Compiled and reviewed production data, leading to key insights that drove a 83% increase in manufacturing yields.
  • Executed batch production reviews, achieving three years targets while ensuring complete adherence to FDA GMP regulations.

Affiliations

  • Applied Biosystems Instrumentation User Group
  • Rotary International
  • Regulatory Affairs Professionals Society (RAPS)
  • Association for Molecular Pathology (AMP)
  • American Industrial Hygiene Association (AIHA)
  • American Medical Informatics Association
  • Freemason
  • Project Management Institute
  • American Society for Quality (ASQ) – Certified Quality Engineer (CQE) Certification
  • European Federation of Clinical Chemistry and Laboratory Medicine (EFLM)

Certifications

  • Certified Public Accountant (CPA)
  • Certified Reliability Engineer (CRE) by ASQ
  • ISO 13485 Lead Auditor Certification for Medical Device Quality Management Systems
  • Salesforce
  • EPA Lab Waste Management Certification
  • Certified Biotechnology Professional (CBP) from initiative
  • Certified Lean Manufacturing Professional (LMP)
  • SHRM Senior Certified Professional (SHRM-SCP)
  • Cisco Certified Internetwork Expert (CCIE)
  • Good Manufacturing Practices (GMP) Certification

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