Quality Control Analyst - Lancaster, South Carolina United States - 19278


Job #: 19278
Title: Quality Control Analyst
Job Location: Lancaster, South Carolina - United States
Employment Type:
Salary: $35,000.00 - $55,000.00 - US Dollars - Yearly
Employer Will Recruit From: Nationwide
Relocation Paid?: Negotiable


We are looking for a Quality Control Analyst to perform release and stability testing on raw materials and finished products following Standard Operating Procedures (SOPs), in-house test methods, and/or compendial methods.



  • Train in the operation of the following instrumentation: Laboratory Balances, High Performance Liquid Chromatographs (HPLCs), Gas Chromatographs (GCs), Automated Titrators, and Dissolution and Disintegration Instrumentation. The operation of additional instrumentation and/or the performance of additional test methods may also be required.
  • Follow Current Good Manufacturing Practice (cGMP) documentation guidelines to record all procedures in a timely fashion.
  • Report the results of analyses on raw material or finished product Certificates of Analysis (COAs).
  • Generate COAs to be reviewed for release by a senior analyst.
  • Review the Data Control Reports or notebook entries of other personnel, once properly trained.
  • Assist with training new laboratory personnel, when applicable. All training performed under the supervision of the QCA I will be documented in accordance with established SOPs and the Laboratories training program.
  • Provide input for the improvement, revision, or generation of QC Standard Operating Procedures (SOPs), Test Methods, Finished Product Specifications, and Raw Material Specifications, as appropriate.
  • Maintain a safe working environment and will ensure that all equipment used in the testing procedures is calibrated and properly maintained.
  • Perform other assigned duties as may be required in meeting company objectives
  • Communicate effectively with other departments within the organization and function within a team environment.



The QCA I should have a working knowledge of the cGMP environment. The analyst will preferably have laboratory experience in a cGMP facility, including experience with the proper operation of laboratory instrumentation. Effective interpersonal skills and the ability to interact with all levels of personnel are required.

A Bachelor of Sciences (B.S.) or Bachelor of Arts (B.A.) degree in a science-related field such as Chemistry, Biochemistry, Biology


University - Bachelor's Degree/3-4 Year Degree


Our recruiters are currently seeking to fill this position and hundreds like this in our network. If you are a match you'll be contacted with additional details.

We value your privacy and will never share your information with any employer without your consent.

Send your profile and resume to the recruiter who posted this job. You may include a cover letter to introduce yourself.

Cover Letter Text:

5,000 character limit