QC Chemist

Mindlance; Overland Park (KS); On-site; USD 60,000 - 90,000; Full time

Job summary

A leading analytical lab company in Overland Park, Kansas seeks a laboratory professional to perform testing on routine and non-routine lab samples. The role involves ensuring compliance with GMP guidelines, performing analytical and physical testing, and maintaining methods in a state of validation. Candidates should demonstrate strong documentation skills, excellent communication abilities, and a solid understanding of cGMP principles. This position offers an engaging work environment with opportunities for problem-solving and team collaboration.

Qualifications

• Fundamental knowledge of cGMP compliance requirements.
• Ability to author and/or review standards, guidelines, and SOPs.
• Willingness to interact with laboratory personnel and management.
• 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.

Responsibilities

• Perform analytical and physical testing on various samples.
• Ensure compliance with all procedures and regulatory commitments.
• Review and approve 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.

Skills

Good documentation skills

Excellent general computer skills (MS Excel, Word)

Excellent communication skills

Ability to troubleshoot problems

Knowledge of cGMP compliance

troubleshooting

root cause analysis

Tools

MS Excel

MS Word

Data presentation

Job description

Job Description

Job Description:
Perform accurate and timely testing of routine and some non-routine lab samples in accordance with appropriate GMP and safety guidelines. Completes second person verification of test results. Participates in laboratory root cause investigations and quality system improvement initiates by executing well defined protocols and procedures. Shares technical information and best practice within the group. Design and evaluation of experiments, methods development and characterization, support of process development/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 conducted and documented in accordance with the appropriate Quality System. Act as a resource for insuring adherence to quality systems.

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.

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.

Qualifications

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.

Additional Information

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