Job Description

QC Analyst III

W2 Contract

Salary Range: $83,200 - $93,600 per year

Location: Fremont, CA - Onsite Role

Responsibilities:

• Provide timely analyses to support manufacturing and stability. Primary responsibilities include but are not limited to physical testing of components and raw materials, in-process, and release of commercial product or clinical supplies.
• Independently perform assays under GMP, maintaining data integrity and ensuring compliance with company SOPs and specifications.
• Provide accurate, written documentation of all work, including detailed observations and conclusions.
• Under general guidance, participate in laboratory investigations.
• Operate, maintain, and troubleshoot laboratory instrumentation and equipment in a safe working environment.

Required Skills:

• Well-organized, capable of multi-tasking, and able to collaborate with individuals in a matrix environment.
• Extensive hands-on experience performing relevant analytical techniques (HPLC, GC, FTIR)
• Must have experience with EMPOWER.
• Must have excellent data analysis skills with attention to detail and interpretation of results, focusing on continuous improvement.

Education and Experience:

• Bachelor\'s degree in science or related field
• 5-8 years relevant experience in a cGMP pharmaceutical QC environment, or at least 2-5 years with a Master\'s degree.

Physical Requirements:

• Prolonged periods of sitting at a desk and working on a computer
• Potentially prolonged periods of standing.
• Must be able to lift up to 15 pounds at times.
• Must be willing to travel.

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Bayside Solutions