Overview

Performs any basic to complex Analytical assay(s) according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Completes Test Methods and other required documentation and performs laboratory maintenance duties according to GLP, cGMP, CFR and/or PTC guidelines and SOPs. Performs daily work activities with minimal supervision. Sufficiently competent in science to initiate and carry out scientific development projects related to the development of new assays, initiation of new programs, assay validations and associated projects. Performs and thoroughly documents Research & Development activities as required.

Responsibilities

• Conducts any basic to complex Analytical assays and lab procedures according to and in compliance with GLP, cGMP, CFR and/or PTC guidelines and SOPs.

• Accurately completes Test Methods and other required documentation according to and in compliance with GLP, cGMP, CFR and/or PTC guidelines and SOPs

• Follows all general and laboratory SOPs

• Maintains a laboratory notebook for Research & Development activities as required

• Conducts critical review of results and reports data to Technical Reviewer or supervisor

• Communicates with supervisor and other colleagues re: daily lab activities

• Prepares reagents and completes reagent batch records

• Checks reagents for expired chemicals and disposes of any expired reagents

• Performs laboratory maintenance (i.e. decontaminates and disposes of medical and other waste as appropriate, maintains laboratory supply inventories, keeps work surfaces clean and neat) and keeps records of maintenance according to guidelines and SOPs

• Performs routine equipment monitoring and cleaning (i.e. centrifuges, biosafety and chemical hoods, refrigerators, incubators and freezers) and keeps records according to guidelines and SOPs

• Orders reagents and consumables as required and uses commodity specification procedure as assigned

• Contributes to the preparation of Protocols, Testing Records and Final Reports, as needed and with supervision. Revise existing SOPs as assigned by Management

• Author investigations and deviations with minimal supervision

• Demonstrates proficiency in scientific theory and applies scientific rigor in the laboratory

• Correctly analyzes scientific data with accuracy and precision

Qualifications

• 3-4 years of relevant experience or equivalent

• Bachelor’s or Master’s degree with major in Biological Sciences or other science-related major

• Strong Technical and Scientific knowledge of protein based assays (i.e. ELISA, electrophoresis, etc).

• Ability to use proficiently advanced laboratory equipment, such as, but not limited to; Plate Readers, HPLC, Gel scanners, etc.

Our Values:

Integrity & Dedication, Working Together & Sharing Success; Do the Right Thing & Do it Right.

Our greatest asset is our people, WuXi is dedicated to providing opportunities for internal growth with direct access to a dedicated and accessible Human Resources team.

WuXi AppTec provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.

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Job Locations US-PA-Philadelphia

Job ID 2023-12291