Software Placement Group
Senior Quality Control Chemist
Software Placement Group, Lancaster, South Carolina, us, 29721
Senior Quality Control Chemist
Join our dynamic team as a Senior Quality Control Chemist and contribute to our mission of delivering high-quality chemical products in the pharmaceutical industry. In this role, you will leverage your extensive experience in analytical chemistry and regulatory compliance to ensure our products meet and exceed quality standards. This position offers the chance to work with cutting-edge laboratory technologies and collaborate with industry experts in a supportive and growth-oriented environment.
Salary:
DOE per year Essential Duties and Responsibilities: Perform precise analysis of raw materials, in-process, and finished products using various analytical methods to ensure quality compliance. Regularly maintain and calibrate analytical instruments and laboratory equipment to ensure operational accuracy. Develop, validate, and document technical protocols including SOPs and test methods. Conduct thorough investigations into any quality non-conformances, drafting reports and implementing necessary corrective and preventative actions. Work collaboratively with R&D, production, and regulatory teams to drive product development and process optimizations. Uphold strict adherence to regulatory standards including GMP and GLP across all quality control processes. Minimum Position Qualifications: Bachelor’s degree in Chemistry, Biochemistry, or closely related field. At least 5 years of professional experience in quality control within the pharmaceutical or chemical manufacturing sectors. Demonstrated proficiency in utilizing analytical equipment like HPLC, GC, FTIR, and UV-Vis spectrometry. Solid understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Strong analytical, problem-solving skills, and a keen eye for detail. Excellent oral and written communication skills, comfortable in a team-oriented environment. Preferred Qualifications: Master’s degree in Chemistry or related field. Experience in leading quality control projects, including setting timelines and coordinating team efforts. Advanced certification or training in analytical techniques or quality management systems. Prior role in auditing and compliance within regulatory frameworks relevant to the pharmaceutical industry. Proven track record of implementing process improvement initiatives in a QC environment. Skills: Expert handling of analytical instrumentation, particularly HPLC and GC. Strong organizational skills for handling documentation and workflow management. Effective interpersonal skills to engage and collaborate with various internal departments. Critical thinking and decision-making abilities to solve complex problems. Proficiency in computer applications, including laboratory information management systems (LIMS). Benefits: Competitive salary package, including comprehensive health benefits. Generous paid time off and opportunities for professional development. Supportive team environment that fosters professional growth. Access to state-of-the-art laboratory facilities and equipment.
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DOE per year Essential Duties and Responsibilities: Perform precise analysis of raw materials, in-process, and finished products using various analytical methods to ensure quality compliance. Regularly maintain and calibrate analytical instruments and laboratory equipment to ensure operational accuracy. Develop, validate, and document technical protocols including SOPs and test methods. Conduct thorough investigations into any quality non-conformances, drafting reports and implementing necessary corrective and preventative actions. Work collaboratively with R&D, production, and regulatory teams to drive product development and process optimizations. Uphold strict adherence to regulatory standards including GMP and GLP across all quality control processes. Minimum Position Qualifications: Bachelor’s degree in Chemistry, Biochemistry, or closely related field. At least 5 years of professional experience in quality control within the pharmaceutical or chemical manufacturing sectors. Demonstrated proficiency in utilizing analytical equipment like HPLC, GC, FTIR, and UV-Vis spectrometry. Solid understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Strong analytical, problem-solving skills, and a keen eye for detail. Excellent oral and written communication skills, comfortable in a team-oriented environment. Preferred Qualifications: Master’s degree in Chemistry or related field. Experience in leading quality control projects, including setting timelines and coordinating team efforts. Advanced certification or training in analytical techniques or quality management systems. Prior role in auditing and compliance within regulatory frameworks relevant to the pharmaceutical industry. Proven track record of implementing process improvement initiatives in a QC environment. Skills: Expert handling of analytical instrumentation, particularly HPLC and GC. Strong organizational skills for handling documentation and workflow management. Effective interpersonal skills to engage and collaborate with various internal departments. Critical thinking and decision-making abilities to solve complex problems. Proficiency in computer applications, including laboratory information management systems (LIMS). Benefits: Competitive salary package, including comprehensive health benefits. Generous paid time off and opportunities for professional development. Supportive team environment that fosters professional growth. Access to state-of-the-art laboratory facilities and equipment.
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