QC Lab Analyst VI-VII at Zoetis

Portage, Michigan, United States

Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Animal HealthIndustries

AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred
5 years minimum related experience in Quality Control
Preferred experience: GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, use of Empower3
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
Willingness and ability to learn
Ability to work in a team environment
Job duties involve occasional lifting (less than 35 lbs)
Must not be Cephalosporin/Penicillin sensitive
Authorization to work in the US

Performs, documents, and record checks qualitative and quantitative assays on samples
Works with primary technologies: HPLC, Dissolution, and KF
Interprets and evaluates data for accuracy, precision, trends, and potential GMP impact
Recommends and executes process improvements to improve laboratory performance
Demonstrates efficient work practices (Level VI-VII)
May train others
Troubleshoots instrumentation
Reviews documentation of other analysts
Participates in laboratory investigations as required
Contributes to process and method improvements, training (Level VI-VII)
May participate in manufacturing QC support such as cleaning verification
Works SHIFT HOURS: 8:00pm-4:30pm (some flexibility; overtime may be required)