Shelli L. Connelly

Senior Drug Product Consultant


Ms. Connelly is a pharmaceutical professional with over 20 years of long- term success in the pharmaceutical/medical device manufacturing industry. She has expertise in pharmaceutical/medical device transfer/process validation (product, cleaning, and equipment), business development activities, strategic planning, process improvements/project management activities, risk assessment, quality assurance, quality audits, cGMP (Current Good Manufacturing Practices)/manufacturing support, regulatory submission support and technical writing.

She’s well versed in parental process equipment: tanks, single use mixers, microfluidizer, milling equipment, ophthalmic fillers, syringe fillers, vial fillers, , and isolator filling lines,. She is able to effectively handle multiple projects simultaneously, and understands customers needs and how best to meet them.

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Core Competencies

  • Sterile Fill/Finish
  • Product Scale-Up
  • Filter Validation
  • Liquids
  • Tech Transfer
  • Parenterals
  • Single Use Technology
  • Suspensions
  • Process/Cleaning Validation
  • Containment