Job Description

Target PR Range: 38-48/hr
*Depending on experience

Upon assignment given by the team, independently plans and conduct analytical chemistry analyses in a timely and efficient manner. Prompt and accurate documentation of experiments, results, and conclusions to ensure data integrity and accuracy.

Additional responsibilities include proper maintenance of laboratory equipment and instrumentation to ensure laboratory operational capability and procuring necessary chemical reagents, reference standards, and other components from appropriate sources.
The candidate independently complies, evaluates, and/or statistically analyzes technical data.

With some guidance, design, plan, and perform a variety of project-oriented analytical assignments( e.g.: maintain the integrity of the stability testing program and respective stability data, analyze samples, perform method Feasibility/ Qualification/Validation, and analyze/record/ report results and conclusion of experiments ).

Candidates that are energetic, proactive, collaborative and have cross functional communication skills, and are willing to work with various team members/ groups, learn new techniques.

Participate, collaborate, and contribute at group and projects meetings as required, by presenting data, and discussing data and future outcomes.

A working knowledge of phase appropriate analytical development (methods, validation, and stability program) is preferred. The candidate must conduct their work activities in compliance with all company internal requirements and with applicable regulatory requirements. Company internal requirements include compliance with ethics, environmental health and safety, financial, human resources and general business policies, requirements, and objectives.

MINIMUM REQUIREMENTS FOR EDUCATION AND EXPERIENCE:

-Strong technical writing and communication skills. Must be proficient using Word, Excel, and statistical programs for analytical data evaluation. Ability to review and understand new and innovative analytical methods and provide critical feedback. In addition, the following career elements are required.

-M.S. in Analytical Chemistry or related discipline with minimum 2 years of experience or B.S. in Analytical Chemistry or related discipline with minimum 3-5 years of experience in analysis of pharmaceutical products or pharmaceutical method development and validation.

-Minimum 3 years of experience in the analysis of data and writing of technical protocols, reports, and submission of ready documents.

Job Tags

Contract work,

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