Career Opportunities

Position

Documentation Specialist III/Sr.

Description

Incumbent will be responsible for controlled GMP documentation along with playing a key role in the implementation, validation, and oversight of an electronic document management system. Develop and implement documentation practices to ensure accuracy and completeness of data input. Includes maintaining GMP filing and documentation in a state of compliance and control, maintain and coordinate archiving activities, ensure consistency of standard operating procedures with regulatory and procedural requirements, and generate summary reports as required.

Requirements
Word Processing, spreadsheet and database management proficiency are required. Excellent organizational skills, experience with complex filing systems, familiarity with pharmaceutical or medical terminology, and attention to detail are required. Prior experience with an electronic document management system would be beneficial.

Minimum--Bachelors Degree in a relevant field or Associates Degree with 3 to 5 years documentation experience required, preferably in a Quality/Compliance department.

 

The position level will be commensurate with experience.

Reference

DocSpec09_23_07

Interested?

All positions require dedicated team players with excellent communication and interpersonal skills. Dow offers excellent benefits and competitive wages. We are an Equal Opportunity Employer.

Please email résumés (in Word format), cover letters, AND salary history to HR@dowpharmsci.com.

Please indicate the job number of the position you are applying for.

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