Develop, evaluate, and optimize the QC method transfer program for both analytical and microbiological assays.
Assess incoming client methods and compendial test methods for raw materials, container / closures, APIs, in-process samples, and finished products, determining suitability with existing laboratory capabilities and identifying any additional instrumentation or reagents required.
Collaborate with clients and internal teams to plan, review, approve, and execute method transfers into the laboratory.
Work closely with the Quality team to maintain and enhance laboratory safety programs and promote a quality-driven culture.
Maintain rigorous scientific and quality standards, ensuring accuracy, reproducibility, and compliance in all laboratory activities.
Coordinate resources, scheduling, and logistics to support client testing needs, including microbiological sampling, laboratory instruments, and personnel availability.
Ensure laboratory readiness for inspections, audits, and regulatory compliance by applying knowledge of cGMP, cGLP, and other regulatory standards.
Lead and support investigations for out-of-specification (OOS), out-of-trend (OOT), and other non-conformance events using troubleshooting and corrective action processes.
Manage laboratory documentation and technical records throughout their lifecycle, including authoring, reviewing, approving, and retiring procedures and reports, utilizing both manual and automated systems.
Qualifications :
Bachelors degree in Biology, Microbiology, Biochemistry, or related field.
5+ years of experience in microbiology or related roles within GMP manufacturing or QC laboratory testing.
Practical experience implementing FDA, EMA, and other regulatory authority expectations for QC, particularly regarding method development and method transfer.
Proficiency with laboratory instrumentation and automated data management systems (e.g., LIMS, JMP, Minitab).
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Quality Control • Indianapolis, IN, US
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