Solomon Page
Our client is looking to fill the role of Senior Quality Control Chemist. The Senior Chemist will conduct laboratory testing and analysis of intermediate and finished products to support quality assurance operations and production requirements.
Responsibilities
Provide hands-on instruction and mentorship to new laboratory analysts Review, revise, and maintain current training materials and modules Serve as a technical resource and subject matter expert for the department Organize and schedule training sessions for new team members Manage training records and documentation within the Veeva system Collaborate with training administrators across departments to maintain site-wide training compliance Assist with onboarding new employees and cross-training existing staff on laboratory procedures Identify training gaps, resolve learning challenges, and guide professional development of analysts Adhere to good manufacturing practices (GMP) and good documentation practices (GDP) Ensure all documentation remains current and accurate; communicate updates as necessary Maintain confidentiality while providing performance feedback to the department manager Demonstrate strong communication abilities when collaborating across facility departments Diagnose and resolve issues with quality control equipment Apply advanced technical expertise in analytical testing methods Complete additional tasks as assigned Required Qualifications
Bachelor’s degree in chemistry, biology, or related natural science; minimum 5 years of pharmaceutical industry experience or equivalent background Hands-on expertise with HPLC, GC, IC, Karl Fischer titration, IR spectroscopy, UV spectroscopy, dissolution testing, microscopy, sampling procedures, and production gowning procedures Thorough understanding of current good manufacturing practices (cGMP) Proficient in Microsoft Office Suite applications Foundational pharmaceutical industry knowledge combined with effective verbal communication skills Strong documentation practices (GDP) with clear, legible handwriting Experience with intermediate and finished product sampling (preferred) Background working with controlled substances (preferred) Experience collecting cleaning validation samples using swab and rinse methods (preferred) Experience conducting trace analysis (preferred)
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Provide hands-on instruction and mentorship to new laboratory analysts Review, revise, and maintain current training materials and modules Serve as a technical resource and subject matter expert for the department Organize and schedule training sessions for new team members Manage training records and documentation within the Veeva system Collaborate with training administrators across departments to maintain site-wide training compliance Assist with onboarding new employees and cross-training existing staff on laboratory procedures Identify training gaps, resolve learning challenges, and guide professional development of analysts Adhere to good manufacturing practices (GMP) and good documentation practices (GDP) Ensure all documentation remains current and accurate; communicate updates as necessary Maintain confidentiality while providing performance feedback to the department manager Demonstrate strong communication abilities when collaborating across facility departments Diagnose and resolve issues with quality control equipment Apply advanced technical expertise in analytical testing methods Complete additional tasks as assigned Required Qualifications
Bachelor’s degree in chemistry, biology, or related natural science; minimum 5 years of pharmaceutical industry experience or equivalent background Hands-on expertise with HPLC, GC, IC, Karl Fischer titration, IR spectroscopy, UV spectroscopy, dissolution testing, microscopy, sampling procedures, and production gowning procedures Thorough understanding of current good manufacturing practices (cGMP) Proficient in Microsoft Office Suite applications Foundational pharmaceutical industry knowledge combined with effective verbal communication skills Strong documentation practices (GDP) with clear, legible handwriting Experience with intermediate and finished product sampling (preferred) Background working with controlled substances (preferred) Experience collecting cleaning validation samples using swab and rinse methods (preferred) Experience conducting trace analysis (preferred)
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