The QO Lab Analyst position works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release. This is a dynamic, growing lab within a growing manufacturing site with opportunity to learn new skills and to work cross-functionally.
*Performs, documents and record checks qualitative and quantitative assays on samples.
*The primary technologies in this lab are HPLC and dissolution.
*Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact.
*Recommends and executes process improvements to continually improve laboratory performance.
*High productivity and the ability to multi-task coupled with a low error rate and attention to detail are critical characteristics of this position.
*Demonstrates flexibility/agility and engagement in a changing environment.
*The candidate is expected to display good laboratory technique to avoid cross-contamination or misidentification of samples.
*Ability to follow written procedures.
*May train others as skills and knowledge allow.
*Troubleshoot instrumentation as skills and knowledge allow.
*Participates in laboratory investigations as required.
*May participate in manufacturing QC support such as cleaning verification.
*SHIFT HOURS: 2:00pm-10:30pm, nominally (some flexibility is allowed). Overtime may occasionally be required.
EDUCATION AND EXPERIENCE
*AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred.
*Related experience in Quality Control is preferred but not required.
*Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3
*Key characteristics of a successful candidate in this position: willingness and ability to learn, ability to work in a team environment, and attention to detail.
*Job duties involve occasional lifting (less than 35 lbs).
*Candidate must not be Cephalosporin/Penicillin sensitive.
Full time
Regular
Colleague
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