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Q&A With Charles McRant

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Charles McRant
Senior Quality Assurance Specialist , Bachem Americas
Location: Hill, SC United States
Joined: Oct 8th, 2020

About (request update)

Education (request update)

Saint Augustines College class of 1998

Undergrad Major: Biology

Experience

I currently work with Bachem Americas as Senior Quality Assurance Specialist
I have years of experience working in the Biotechnology and Pharmaceutical industry.

Senior Quality Assurance Specialist | Bachem Americas
From September 2022 to Current • 4 year(s)
Responsible for oversight of Quality Events, SOPs interpretation, Master Control QMS utilization, and leading cross-functional teams for compliance and manufacturing support.

Compliance Investigator | Shire Pharmaceuticals
From March 2022 to August 2022 • 0 year(s)
Used technical writing skills for reports, utilized Trackwise and Veeva Vault software for cGMP tasks, and led cross-functional teams for trending investigations.

Senior Quality Assurance Specialist II | Kite Pharmaceuticals
From August 2021 to February 2022 • 1 year(s)
Reviewed and released cGMP raw materials for cancer treatment therapies and made patient/product safety decisions in real time.

Quality Manager | Plastikon Healthcare
From December 2020 to March 2021 • 1 year(s)
Served as SME for QA functions, oversaw batch review/release, and served as direct client liaison for project-related QA support.

Senior Quality Assurance Specialist | Nutramax Laboratories
From July 2014 to July 2020 • 6 year(s)
Served as direct client liaison, coordinated with project managers on manufacturing practices, and participated in internal audits and regulatory inspections.

Quality Assurance Specialist | KED PLASMA, INC
From August 2008 to July 2014 • 6 year(s)
Worked in fast cGMP environment verifying plasma donor records, wrote audit responses, and tracked procedural deviations for investigation and closure.

Assistant Chemist | Talecris Biotherapeutics Inc.
From May 2005 to August 2008 • 3 year(s)
Performed quality testing on human blood plasma medicines and recorded work on official accountable documents to cGMP standards.

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