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Job Title: Chemist
Job ID : LLYJP00006309
Duration: 6+ Months (Possible Of Extension)
Location: Overland Park, KS

Job Details:
QC Chemist position, they will be doing HPLC Analyses with possible dissolution testing. They will be working in a lab environment using GMP skills with a GC headspace, potentially could be running it. They will be an influx of testing required for the lab move which is requiring them to do comparative testing between the two spaces. There is a potential for hormone exposure so there is a respirator testing required.

Perform accurate and timely testing of routine and some non-routine lab samples in accordance withappropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executingwell defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of processdevelopment/optimization and the analysis and interpretation of data. Conduct studies to validate methods, develop methods, evaluate new technologies. Sample Analysis. Sample preparation, instrument set-up and operation, data entry, primary data review. Coordination of method transfers and co-validations. Qualifying, calibrating, and maintaining analytical instrumentation. All laboratory work will be conductedand documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems

Requirements / have to haves not listed elsewhere
Bachelor of Science in Chemistry or related field

Request preferences / nice to haves
• Fundamental knowledge of cGMP compliance requirements, instrument qualification procedures and computer system validation principles. • Good documentation skills and ability to author and/or review standards, guidelines, SOPs, templates, protocols, and other GMP documentation. • Excellent general computer skills (MS Excel, Word, etc.) and the ability to compile summarize and present information to a diverse group. • Excellent communication skills and willingness to interact with laboratory personnel, contractors and management. • Ability to troubleshoot problems and identify solutions. • Ability to influence and partner with individuals both within and outside of a formal reporting relationship towards realization of team goals. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination

Primary Position Responsibilities (major or daily tasks)
• Perform analytical and physical testing on in-process, finished product and stability samples. • Assist laboratory leader in ensuring compliance with all procedures, safety and regulatory commitments in Quality Control. • Perform review and approval of analytical data. • Maintain analytical methods in the laboratory in a state of validation. • Assist in addressing laboratory investigations within specified timeframe. Promote elimination of problems by identifying and addressing root cause.

Requirements / have to haves not listed elsewhere
Bachelor of Science in Chemistry or related field

Request preferences / nice to haves

• Fundamental knowledge of cGMP compliance requirements, instrument
qualification procedures and computer system validation principles. •
Good documentation skills and ability to author and/or review standards,
guidelines, SOPs, templates, protocols, and other GMP documentation. •
Excellent general computer skills (MS Excel, Word, etc.) and the ability
to compile summarize and present information to a diverse group. •
Excellent communication skills and willingness to interact with
laboratory personnel, contractors and management. • Ability to
troubleshoot problems and identify solutions. • Ability to influence and
partner with individuals both within and outside of a formal reporting
relationship towards realization of team goals. • Assist in addressing
laboratory investigations within specified timeframe. Promote
elimination

Primary Position Responsibilities (major or daily tasks)

• Perform analytical and physical testing on in-process, finished
product and stability samples. • Assist laboratory leader in ensuring
compliance with all procedures, safety and regulatory commitments in
Quality Control. • Perform review and approval of analytical data. •
Maintain analytical methods in the laboratory in a state of validation. •
Assist in addressing laboratory investigations within specified
timeframe. Promote elimination of problems by identifying and addressing
root cause.

All your information will be kept confidential according to EEO guidelines.