Overview

The Scientist III will independently conduct a variety of complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in a GLP regulatory laboratory environment. The employee is responsible for the scientific excellence, project management as well as client relationship development. They may be required to supervise a team of scientists to ensure timely delivery of data and reports

This is a contingent/temp position.

Responsibilities

• Designs, plans, and caries out experiments and associated research assignments.

• May independently devise procedures or studies to search out causes and remedies for problems.

• Performs and/or oversees work to attain objectives.

• Utilizing the effective time management to complete assigned tasks on time with high accuracy

• Operates and/or oversees the operation of equipment to acquire experimental data.

• Compiles, calculates, plots, and analyzes, and with experience, interprets data; records and maintains data in accordance with accepted standards and practices.

• May act as principal investigator. Assumes complete responsibility for assigned projects, assumes a continuing responsibility for contributing ideas related to this area of investigation.

• Prepares reports, oral and written, covering work objectives, methods, and results, which may include recommendation for further experimentation.

• Thorough understanding of Good Laboratory Practices and EPA, FDA, or other regulations pertaining to the study.

• Promotes implementation and compliance with WuXi AppTec safety policies, practices, and procedures in order to maintain a safe work environment and minimize or eliminate injury.

• Maintains and enhances technical expertise, knowledge in the Bioanalytical area which include up-to-date-technology in method development and sample analysis for parent drugs and its metabolites in various biological matrices.

• Prepare draft scientific presentation in-house and in scientific meetings

• Guides and counsels employees in order to contribute to the goals of XBL for both the long and short period and to encourage personal growth.

• Identifies safety hazards and initiates corrective action. Assists in the safety training for subordinates and/or less experienced staff.

• Supervises and participates in training of Associate Scientists, Scientist I and II.

• Other duties as assigned.

Qualifications

• Bachelor’s or M.S. degree in chemistry, biology, or equivalent

• At least 8-13 years of relevant experience in animal research field or equivalent

• Any similar combination of education and/or work equivalent experience

Knowledge / Skills / Abilities:

• Knowledge of commonly used scientific concepts, practices, and procedures within pharmacology or animal science field

• Well organized, detail oriented, and adaptable to changes

• Effective oral and written communication skills

• Effective interpersonal skills

• Computer skills: knowledge of internet research, MS Word, Excel, Outlook, and PowerPoint

• Knowledge of Laboratory Information Management System (LIMS)

• Knowledge of Data Acquisitions and Operating Software as Analyst, MassLynx.

• Ability to work under pressure of multiple projects and deadlines

• Ability to effectively prioritize workload and manage changes in direction

• Ability to work in a team environment

• Familiarity with and adherence to regulatory guidelines consistent with WuXi AppTec requirements

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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Job Locations US-NJ-Plainsboro

Job ID 2024-12922