QC Chemist II​/III

QC Chemist II & III for Release Team

We are hiring for (2) positions in the release team. This role is located in North Augusta, South Carolina, relocation is REQUIRED. Relocation assistance is available, apply now to learn more!

• Use basic understanding and knowledge of techniques, instrumentation, and lab functions to identify problems and support the completion of work assignments.
• Hands on experience with HPLC, GC, IC, KF and other routine analytical equipment such as pH meter and balance.
• Perform quality control routine testing for raw material/ Intermediate/ Release / Stability testing.
• Perform Method development and method validation execution, including writing protocols and reports. Must be proficient.
• Responsible for reviewing analytical laboratory raw data and electronic records.
• Participate in out of specification (OOS) investigations, as well as other deviations and writing investigation reports.
• Perform and review QC stability and release testing.
• Maintain the QC lab by ordering supplies routinely used for testing.
• Assist the QC/QA group with writing and editing of SOPs and STPs.
• Other duties as assigned.

• Master’s Degree in Chemistry or life sciences with 1-2 years of experience in a GMP environment, or Bachelor’s degree in Chemistry or life sciences with 2-5 years of experience in a GMP environment.
• Hands-on experience with HPLC/UPLC, GC, GC-MS/LC-MS, KF, IC.
• Hands-on experience with Empower and/or Chemstation. Experience with Mass Lynx is desirable.
• Familiarity with both CFR 21 and ICH guidelines regarding GMP.
• Computer skills in MS Word, EXCEL, and Access.
• Effective communication skills (oral and written).
• Flexibility in working hours is required.
• Supervisory experience is preferred.

• The successful candidate must be able to work on multiple projects with a minimum of supervision and meet established timelines.
• Master’s Degree in Chemistry or life sciences with 2-3 years of experience in a GMP environment, or Bachelor’s Degree in Chemistry or life sciences with 2-5 years of experience in a GMP environment.
• Be familiar with both CFR 21 and ICH guidelines in regards to GMPs’. Computer skills in MS Word, EXCEL, and Access are desirable.
• Must possess strong interpersonal and communication (written and oral) skills.

• Must be able to push, pull, squat, stand and walk through-out the day
• Must be able to lift up to 50lbs
• Must be able to wear safety shoes & glasses through-out the day while in designated areas. (provided by the company)
• You must be cleared by a physician to wear a respirator throughout the day while in designated areas.
• Must be able work in a chemical environment.