Responsibilities:
• Under general direction, supports quality assurance with compliance to GMP regulatory guidelines
• Works with quality assurance staff to ensure inspection procedures are maintained
• Coordinates and maintains documentation of manufacturing procedures, deviations, etc.
• Prepares foreign and domestic protocols and QA release checklists
• Ensures samples are sent according to schedule, processing rejections and maintaining rejection database
• May provide additional administrative support to QA management
Qualifications:
• Associate's degree or equivalent vocational or technical education
• 5+ years' related pharmaceutical experience including 2 years' experience in a regulated environment • Proficiency in MS Office and other relevant software programs
Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.