Target PR Range:

19-27/hr DOE The ideal candidate will have a bachelors degree in a scientific discipline and prior academic or industry laboratory experience. They should be familiar with basic lab techniques including pipetting, weighing, calculations and dilutions, and be comfortable working in a GMP-regulated environment. Experience with multichannel pipetting and ELISA experience is a plus, but not required, as full training will be provided. Strong attention to detail, good documentation practices (GDocP), and comfort with lab notebooks and electrronic systems are essential.

Job Details:

Under general supervision, this position will perform routine procedures and testing in support of the lab. This position will be responsible for one or more of the following activities:

• Performing routine laboratory procedures
• Routine analytical testing
• Documenting, computing, compiling, interpreting, and entering data
• Maintaining and operating specialized equipment
• Initiating and / or implementing changes in controlled documents.

Must learn and comply with safety guidelines and cGMPs/CFRs which includes, but is not limited to, the maintenance of training records, laboratory documentation, written procedures, building monitoring systems and laboratory logbooks. Preferred Qualifications Ability to adhere to regulatory requirements, written procedures and safety guidelines. Ability to evaluate documentation/data according to company and regulatory guidelines Ability to organize work, handle multiple priorities and meet deadlines. Strong written and oral communication skills. Must be detail orientated. Must be flexible and adaptable to changing priorities and requirements. Demonstrate understanding of regulatory requirements, safety guidelines and factors impacting compliance. Demonstrates understanding of when and how to appropriately escalate. May identify, recommend and implement improvements related to routine job functions. Must learn and comply with safety guideline and cGMPs.