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Quality Control Analyst

Location : Rock Hill, SC
Job Type : Direct
Reference Code : CRC_QCA
Hours : Full Time
Required Years of Experience : 2+
Required Education : 4 year degree
Travel : No
Relocation : No
Industry : Pharmaceutical

Job Description :

COMPANY:



  • Reputable manufacturer of specialty health products who are industry leaders in setting and adhering to high standards in manufacturing and quality control.

  • Company focuses on researching and developing products to promote consumer health and is highly regarded in the industry for their advancements in the medical space.


 


SCOPE OF THE ROLE:



  • 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 company 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.


Required Qualifications :

BACKGROUND PROFILE:


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


·         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.






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