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Documentation Specialist I
Ref No.: 18-15023
Location: Meriden, Connecticut
Job Description-
Duties may include organizing and reviewing change control and other GMP documentation.
May assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulator requirements.
Must be able to work quickly with a high degree of accuracy.
Duties will include archival and organization of GMP documents as well as review of logbooks and temperature monitoring charts to ensure adherance to SOPs and specifications.
Activation of GMP documents such as batch records and SOPs will be an additional assigned task.
Other documentation duties as assigned.

Must possess sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
Must be proficient in Microsoft Word and Excel.

Bachelor's degree in a life-sciences related field.