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Specialist, Quality Compliance US-GQC-CA&SQ C
Apotex
Plainfield, IN
Category
Data Analyst
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Job Description
ApoPharma, a member of the Apotex group, is seeking a Specialist, Quality Compliance - US at their Indianapolis Distribution Center to develop and analyze quality metrics data, generate reports, and provide technical leadership. The role involves overseeing cGMP and DEA-related activities, contributing to CAPA, and supporting quality program development. The ideal candidate will ensure adherence to regulations, manage systems, and prioritize compliance.
Requirements
Bachelor’s degree in science
In-depth knowledge of cGMP and DEA regulations
Experience in pharmaceutical industry (at least 5 years)
Experience in quality assurance (at least 2-5 years)
Experience with pharmaceutical manufacturing and quality systems (preferred)
Excellent communication and organizational skills
Competency in computer systems and software platforms
Benefits
Flexible work arrangements
Supportive and inclusive work environment
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