Meds.com

Quality Control Analyst, HPLC

Meds.com Greater Chicago Area

Direct message the job poster from Meds.com

Rubina Gul

Rubina Gul

Senior HR Leader - Employee Relations, People Operations, Talent Acquisition

Quality Control Analyst, HPLC


Overview


We are a fast-growing healthcare technology company seeking a Quality Control Analyst to join our dynamic team. Meds.com is a rapidly expanding compounding pharmacy based in Elmhurst, IL, specializing in technology-driven processes to customize compounded medications for individual patients.


We are searching for a qualified and motivated Quality Control Analyst to join our team to carry out Quality Control activities.


Responsibilities and Duties

  • Perform GMP release testing in Quality Control including, but not limited to, raw materials and finished product assay and identification by HPLC
  • Participate in analytical method transfer and method qualification
  • Perform drug product testing to support formulation and process development
  • Maintain accurate records of laboratory studies
  • Work simultaneously on multiple projects
  • Manage and operate QC Laboratory equipment in a cGMP-compliant manner
  • Perform maintenance and calibration of laboratory equipment
  • Perform related duties, as assigned


Qualifications

  • BS in Chemistry, Pharmaceutics or Chemical Engineering
  • A minimum of 1-3 years of HPLC experiment
  • Working knowledge of laboratory instrumentation like HPLC, UV, Dissolution etc.
  • Knowledge of chromatography data systems, such as Waters Empower, HP Chem Station or other laboratory software.
  • Computer literacy in Windows applications and MS Office.
  • Demonstrated excellent technical writing and verbal communication skills.
  • Maintain a safe working environment, ensuring compliance to all local, state and federal regulations.
  • Excellent attention to detail, compliance and quality
  • Self-motivated individual with the ability to learn, lead and contribute to the team.


The ideal candidate will be familiar with USP, US FDA 21 CFR guidelines, US FDA guidance and, ICH guidelines for prescription pharmaceutical small molecules.

The candidate must have excellent time management, organization and planning skills. The individual must be able to multi-task, prioritize and manage timelines in a fast-paced environment. The ideal candidate will have the ability to maintain a high level of accuracy and attention to detail, while meeting deadlines for assigned projects

  • Seniority level

    Mid-Senior level
  • Employment type

    Full-time
  • Job function

    Quality Assurance
  • Industries

    Health and Human Services and Pharmaceutical Manufacturing

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