QC Lab Analyst I – III (Second Shift) at Zoetis

Portage, Michigan, United States

Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

PharmaceuticalsIndustries

AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science
Minimum of 2 years related experience in Quality Operations (preferred)
Demonstrated proficiency in at least one high complexity technology (e.g., HPLC, uHPLC, GC, advanced spectroscopy) or at least 2 or more low to medium complexity technologies (e.g., TLC, titrations, wet chemistry/physical testing, water testing)
Ability to work effectively in a fast-paced, customer-oriented, team laboratory 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 comprehend and perform routine and non-routine analyses from compendial and internal sources
Ability to quickly learn new skills/techniques
Not sensitive to Cephalosporin/Penicillin
Physical ability for occasional lifting (less than 35 lbs), reaching, and sitting at a computer terminal
Authorization to work in the US

Analyze raw materials, packaging materials, in-process materials, APIs, utilities, and/or finished product samples in support of the company's quality program
Perform, document, record checks, and troubleshoot qualitative or quantitative assays using standard laboratory equipment to highly modern and automated instrumentation
Participate in manufacturing QC support such as cleaning verification
Interpret and evaluate data for accuracy, precision, trends, and potential GMP impact; recommend corrective action as necessary
Train others as skills and knowledge allow
Participate in laboratory investigations as required
Write routine assay protocols or conduct assay, process, or instrument qualifications