Provide regulatory input for product lifecycle planning to ensure compliance & approval process; perform lab & QC tasks, including analysis, data management & equipment maintenance, etc; similar.
Req: MS or foreign equivalent in Regulatory Affairs/Microbiology/Lab Science/Pharma or related + 1 yr exp in QC & QA & regulatory requirements for pharma lab. Pre-MS exp accepted. Full-time/trial/relocation.
Mail resume: HR, Sparklife Solutions Inc, 101 East Park Blvd. #600, Plano TX 75074
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