Manufacturing Supervisor

3 weeks ago


US Petersburg VA USA Civica Rx Full time
About Civica Rx

Civica Rx is a 501(c)(4) social welfare organization dedicated to reducing chronic generic drug shortages and related high prices in the United States. Our mission is to ensure that patients have access to affordable, high-quality medications.

Job Summary

We are seeking a highly experienced Manufacturing Supervisor to join our team at our Petersburg, VA site. As a key member of our operations team, you will be responsible for leading the Prep and Fill Operations team to execute daily and weekly production schedules, ensuring efficient, cost-effective, safe, and compliant production of quality injectable products.

Key Responsibilities
  • Lead the Prep and Fill Operations team to execute daily and weekly production schedules to meet operations objectives.
  • Conduct daily shift meetings to communicate current events and issues and solicit team feedback.
  • Monitor team productivity and resolve immediate production needs to facilitate efficiency.
  • Manage daily and weekly staffing requirements to account for absent personnel (PTO) to satisfy production needs.
  • Monitor the inventory of department supplies and report any quality issues and shortages to prevent production interruptions.
  • Conduct training and ensure staff training is documented, current, and follows cGMP requirements.
  • Review batch records, cycle reports, and other manufacturing documentation to identify and address any potential quality issues.
  • Perform and/or oversee batch accountability calculations and final batch quantity confirmations.
  • Provide immediate support in the identification and documentation of deviations and discrepancies.
  • Assist in the development and update of manufacturing procedures and training material.
  • Support cross-departmental activities, including maintenance, qualification, testing, and investigational activities.
Requirements
  • 8 years of experience in a GMP manufacturing environment, with Prep and Fill operation experience preferred.
  • 2 years of supervisory experience in GMP manufacturing.
  • Associate's degree, or 8 years of cGMP production experience and knowledge, may be considered.
  • Strong writing and documentation skills.
  • Strong interpersonal, collaboration, communication, and leadership skills.
  • Experience in a process improvement environment, including change management, optimizing process flow, and participating in Lean/Six Sigma project teams.
  • Self-directed with effective analytical and problem-solving skills.
Preferred Qualifications
  • Experience in a sterile fill-finish facility.


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