Quality Control Manager

John w. hall

** ******* ***** ******, ** ***** 603-***-**** *************@*******.***

Professional Summary

Eighteen years of Analytical/Quality Control experience in the pharmaceutical industry. Proficiency in usage,

maintenance, and validation of HPLC, GC, Karl Fischer instrumentation. Proven ability to manage highly

efficient and productive Quality Control support teams under cGMP guidelines. Attributes include strong

organization skills, ability to overcome barriers and obstacles, exceptional time management skills, and the

ability to multitask to consistently achieve multiple objectives in a timely manner. Computer experience

includes Microsoft Word and Excel.

Areas of Expertise

Quality Control Management Staff Scheduling & Management Method Development/Validation

Productivity Improvement Problem Solving In-process Testing Support

Staff Coaching & Mentoring Efficiency Improvement Quality Data Review

Proactive Management FDA/cGMP Compliance SOP Writing/Revision

Professional Experience

Johnson Matthey Pharma Services, N. Andover and Devens, MA 2001 to 2011

ANALYTICAL/QC ASSISTANT MANAGER, 2005 to 2011

ANALYTICAL/QC SUPERVISOR, 2003 to 2005

SENIOR ANALYTICAL CHEMIST, 2001 to 2003

• Developed and managed a highly efficient and productive Quality Control support team that

supported 24-hour/7-day API manufacturing at the N. Andover facility.

• Improved the efficiency and quality of the Quality Control support team that supported 24-hour/7-

day API manufacturing at the Devens facility.

• Increased accuracy and cGMP compliance of Quality Control support team through mentoring and

training of team members.

• Initiated and implemented improvements in Quality Systems through revisions to SOP’s.

• Continued to contribute to analytical projects through developing test methods, writing validation

protocols, executing validations, and writing validation reports.

Diatide, Inc., Londonderry, NH 2000 to 2001

SCIENTIST II

• Performed release testing on radiopharmaceutical products.

• Transferred and validated analytical test methods.

• Lead initiative to upgrade Karl Fischer instrumentation, included the writing of the instrument

qualification protocol.

Oread Inc., Lawrence, KS 1999

SCIENTIST II

• Performed release testing on formulated products.

• Developed and transferred analytical test methods.

Pharm-Eco Laboratories, Lexington and N. Andover, MA 1993 to 1999

STAFF CHEMIST

• Setup and managed Quality Control laboratory at the N. Andover site.

• Performed in-process and release testing on API’s.

• Performed analytical testing to support stability study programs

• Performed instrument calibration, maintenance, and troubleshooting procedures.

• Developed, transferred, and validated analytical test methods.

Education

Oral Roberts University, Tulsa, OK 1993

BS IN CHEMISTRY (MINOR IN MATHEMATICS)

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