QC Lab Analyst IV at Zoetis

Portage, Michigan, United States

Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

PharmaceuticalsIndustries

AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred
Related experience in Quality Control preferred but not required
Preferred experience with GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, or Empower3
Willingness and ability to learn
Ability to work in a team environment
High productivity, ability to multi-task, low error rate, and attention to detail
Flexibility/agility and engagement in a changing environment
Good laboratory technique to avoid cross-contamination or misidentification of samples
Ability to follow written procedures
Job duties involve occasional lifting (less than 35 lbs)
Must not be Cephalosporin/Penicillin sensitive
Authorization to work in the US
Availability for 2:00pm-10:30pm shift (some flexibility), with occasional overtime

Performs, documents, and record checks qualitative and quantitative assays on samples, primarily using HPLC and dissolution
Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact
Recommends and executes process improvements to improve laboratory performance
Demonstrates flexibility and engagement in a changing environment
May train others as skills and knowledge allow
Troubleshoots instrumentation as skills and knowledge allow
Participates in laboratory investigations as required
May participate in manufacturing QC support such as cleaning verification
Works effectively in a fast-paced, customer-oriented, team laboratory environment to analyze finished product samples prior to commercial release