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QA Document Control Specialist

Company: Careerbuilder-US
Location: Saint Petersburg
Posted on: November 22, 2021

Job Description:

MUST HAVE GMP EXPERIENCE, LOOKING FOR SOMEONE THAT IS VERY ORGANIZED, PREVIOUS EXPERIENCE WITH BATCH RECORDS, DATA ENTRY AND PREVIOUS PHARMA. IF A CANDIDATE HAS THE DEGREE AND IS A RECENT GRADUATE, MANAGER WILL REVIEW.

--- Requires a Bachelor's degree in a relevant business discipline. A technical background in chemistry or microbiology is preferred. --- Requires a minimum of 3 to 5 years experience with documentation systems, at least 1-2 years in the pharmaceutical industry. Solid understanding of cGMPs as they apply to documentation systems. --- Direct, hands-on experience with electronic documentation systems; knowledge of Documentum is preferred. Knowledge of LIMS systems, familiarity with bar-coding systems, finished goods label generation, POMS weigh and dispense applications, and JDE is a plus. --- Proficient technical writing skills are required. --- Must be well organized, an effective communicator at multiple levels, able to grasp system concepts and communicate their applications. --- Capable of quickly learning new quality systems and associated software applications for proficient execution of tasks. --- Must be capable of managing multiple projects with time related constraints in a fast paced contract manufacturing environment. --- Must possess strong technical writing skills and be able to speak effectively before groups of internal and/or external customers or employee

Job Requirements:
--- Requires a Bachelor's degree in a relevant business discipline. A technical background in chemistry or microbiology is preferred. --- Requires a minimum of 3 to 5 years experience with documentation systems, at least 1-2 years in the pharmaceutical industry. Solid understanding of cGMPs as they apply to documentation systems. --- Direct, hands-on experience with electronic documentation systems; knowledge of Documentum is preferred. Knowledge of LIMS systems, familiarity with bar-coding systems, finished goods label generation, POMS weigh and dispense applications, and JDE is a plus. --- Proficient technical writing skills are required. --- Must be well organized, an effective communicator at multiple levels, able to grasp system concepts and communicate their applications. --- Capable of quickly learning new quality systems and associated software applications for proficient execution of tasks. --- Must be capable of managing multiple projects with time related constraints in a fast paced contract manufacturing environment. --- Must possess strong technical writing skills and be able to speak effectively before groups of internal and/or external customers or employee

Keywords: Careerbuilder-US, St. Petersburg , QA Document Control Specialist, Other , Saint Petersburg, Florida

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