QC Lab Analyst IV at Zoetis

Portage, Michigan, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

PharmaceuticalsIndustries

Requirements

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

Responsibilities

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

Skills

Key technologies and capabilities for this role

HPLCDissolutionGMP documentationSAPLIMSEmpower3Laboratory assaysData interpretationTroubleshooting instrumentation

Questions & Answers

Common questions about this position

What are the shift hours for this QC Lab Analyst IV position?

The shift hours are 2:00pm-10:30pm, nominally, with some flexibility allowed, and overtime may occasionally be required.

What education and experience are preferred for this role?

AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science is preferred, along with related experience in Quality Control. Preferred experience includes GMP documentation, drug product formulation, in-plant laboratory, Incoming Inspection, SAP, LIMS, HPLC, Dissolution, and use of Empower3.

What key characteristics make a successful candidate for this position?

Key characteristics include willingness and ability to learn, ability to work in a team environment, and attention to detail.

What is the work environment like for this QC Lab Analyst role?

This is a fast-paced, customer-oriented, team laboratory environment within a dynamic, growing lab at a growing manufacturing site, with opportunities to learn new skills and work cross-functionally.

What is the salary or compensation for this position?

This information is not specified in the job description.