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Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Quality Lab Associate 3 - QC Compliance Analyst

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeBloomington, IN, USANo salary listed

About the Job

Requirements

  • A bachelor's degree in a physical science is required.
  • A minimum of 5 years of experience in Quality is required.
  • Computer proficiency in Microsoft Word, Excel, and Outlook is required, along with the ability to use enterprise software such as JDE, BPLM, Pilgrim, or Trackwise.
  • The position sometimes requires extended periods of sitting.
  • Duties may require overtime work, including nights and weekends.
  • Use of hands and fingers to manipulate office equipment is required.

Responsibilities

  • Act as the QC Compliance lead.
  • Provide guidance, support, direction, and leadership for quality compliance risks affecting the QC group.
  • Prioritize workloads and assign duties based on compliance risk.
  • Assist with client responses and corrective improvements based on client findings.
  • Participate in client and regulatory audits.
  • Author standard operating procedure revisions and technical writing documents needed to complete corrective improvements.
  • Review regulatory changes and shifts in regulatory agency focus.
  • Communicate with QC groups to determine plans for regulatory and client compliance.

Desired Qualifications

  • Previous client or regulatory audit experience is preferred.

About the Company

Simtra BioPharma Solutions

Sterile injectable drug manufacturing

Simtra BioPharma Solutions is a contract development and manufacturing organization specializing in sterile injectable medicines. It supports pharmaceutical and biotechnology companies with formulation, process development, clinical and commercial manufacturing, filling, packaging and related technical services. Facilities and teams operate under regulated quality systems suited to complex parenteral products. Simtra is a business-to-business manufacturing partner rather than a consumer drug brand, helping sponsors move therapies from development into reliable supply through dedicated production expertise and capacity.

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