Experience

Emergent BioSolutions

• United States
• Biotechnology Research
• 700 & Above Employee

• Document Control Specialist

  • Dec 2013 - Present



Planned Parenthood of Maryland, Inc.

• United States
• Hospitals and Health Care
• 1 - 100 Employee

• Health Center Trainer/ Clinical Support Associate

  • Jul 2010 - May 2013

  Provided skills training for non-licensed health center staff. Conducted team meetings to review forms, communicated document changes & maintained forms database. Conducted quality audits of annual lab competency requirements and performed staff skills assessments. Collaborated with Clinical Services Management team regarding projects, center operations & patient services. Conducted, evaluated & reported results of patient satisfaction surveys for the purposes of recommending health center performance improvement activities as necessary. Show less



People Encouraging People, Inc.

• Baltimore, Maryland Area

• Evaluator/ Quality Assurance Specialist

  • Nov 2005 - Apr 2010

  Audited client charts for documentation compliance and collect client outcomes. Assisted programs in preparation of DHMH audits. Conducted consumer satisfaction surveys. Trained new staff and worked with program manager to coordinate daily duties. Created grant-related summary reports. Tracked program expenditures and client loans. Audited client charts for documentation compliance and collect client outcomes. Assisted programs in preparation of DHMH audits. Conducted consumer satisfaction surveys. Trained new staff and worked with program manager to coordinate daily duties. Created grant-related summary reports. Tracked program expenditures and client loans.



Kaztronix LLC

• United States
• Staffing and Recruiting
• 1 - 100 Employee

• Quality Assurance Specialist II

  • Apr 2005 - Nov 2005

  Audited the pharmaceutical manufacturing operations for cGMP compliance. Reviewed batch records in real time and upon completion. Released raw material for production. Audited manufacturing facility for compliance and released clean rooms. Logbook inspections. Audited the pharmaceutical manufacturing operations for cGMP compliance. Reviewed batch records in real time and upon completion. Released raw material for production. Audited manufacturing facility for compliance and released clean rooms. Logbook inspections.



Shire US Manufacturing Inc.

• Owings Mills, MD

• Change Control Coordinator/ Quality Assurance Technician

  • Oct 1998 - Oct 2004

  Audited manufacturing process, facility and logbooks for cGMP compliance. Batch record review. Disposition raw materials and finished product. Trained new staff on QA duties and SOPS. Entered inventory transactions in MRP database. Wrote QA-related SOPs, Deviations and Investigations. Analyzed changes to documents to ensure pure, safe and effective finished product. Audited manufacturing process, facility and logbooks for cGMP compliance. Batch record review. Disposition raw materials and finished product. Trained new staff on QA duties and SOPS. Entered inventory transactions in MRP database. Wrote QA-related SOPs, Deviations and Investigations. Analyzed changes to documents to ensure pure, safe and effective finished product.