AAS, BA/BS, or MS in Chemistry, Biochemistry, or related science preferred
Related experience in Quality Control preferred (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
Willingness and ability to learn
Ability to work in a team environment
Good laboratory technique to avoid cross-contamination or misidentification of samples
Ability to follow written procedures
Flexibility/agility and engagement in a changing environment
Occasional lifting (less than 35 lbs)
Must not be Cephalosporin/Penicillin sensitive
Authorization to work in the US (sponsorship at company's discretion)
Availability for 2:00pm-10:30pm shift (overtime may be required)
Responsibilities
Work effectively in a fast-paced, customer-oriented, team laboratory environment
Analyze finished product samples prior to commercial release
Perform, document, and record checks for qualitative and quantitative assays on samples (primary technologies: HPLC and dissolution)
Interpret and evaluate data for accuracy, precision, trends, and potential GMP impact
Recommend and execute process improvements to improve laboratory performance
Demonstrate flexibility/agility in a changing environment
May train others as skills and knowledge allow
Troubleshoot instrumentation as skills and knowledge allow
Participate in laboratory investigations as required
May participate in manufacturing QC support such as cleaning verification