Temporary QC Associate (20-17442)
Job Description
Job Description: This position will perform routine testing in support of the Biologics Manufacturing and Global Stability programs. Primary testing responsibilities include HPLC, SDS-Page, CE-SDS, iCIEF as well as performing routine lab duties, reagent ordering and preparation, and instrument maintenance. Other analytical support required as needed.
Ideal candidate will have 2-3 years of relevant laboratory experience in a GMP commercial QC Laboratory, with demonstrated ability using pipettes, pH meter, analytical balances,
• Prior experience with LIMS, Empower, and electronic lab notebooks is preferred.
• Candidate will also have proficiency in common computer software applications such as Microsoft Office and Outlook email.
• Candidate must be able to communicate effectively with co-workers and management.
• Candidate must have strong general laboratory and organizational skills, attention to detail, flexibility, and the ability to work as part of a team.
Position will be onsite.
Additional Job Requirements:
Position Handles Hazardous Materials
How to Apply
Please send your updated resume to iris.chen@axelon.com350 total views, 0 today