QC Analyst I

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The Opportunity
Description
We're looking for a QC Analyst I, working in Biotechnology/Medical Devices industry in Novato, California, 94949, United States.

Responsibilities:

• Performs, under direct supervision, chemical analyses of incoming raw materials under cGMP to meet specified timelines.
  
• Coordinates and track outside laboratory testing activities.
• Maintains the laboratory in an inspection ready state.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success

Education and Experience:

• BS/BA degree in Science (major in biology-biochemistry-chemistry or related field) with 1-2 years of relevant laboratory experience, OR
• AS degree in Science (major in biology-biochemistry-chemistry or related field) with atleast 2 years of relevant laboratory experience

Skills:

• Experience working in a GMP laboratory
• Experience with physical and chemical methodologies and a variety of analytical instrumentation
• Organizational skills as well as good written and verbal communication skills essential
• Experience with Microsoft Word and Excel required
• Experience with Labware LIMS, O365 a plus
• Must have a positive, team minded personality

What Do You Think?
Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible?