On-Floor QA Specialist – Sterile Pharma Manufacturing

Civica Rx

Petersburg (VA)

On-site

USD 85,000 - 115,000

Full time

14 days+

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Job summary

Civica Rx in Petersburg, VA is seeking a Quality Assurance Operations Shop Floor Associate to ensure ongoing cGMP compliance on the manufacturing floor. The role collaborates with operators and supervisors to review batch records and uphold SOP adherence in a new fill-finish facility.

The position requires a scientific degree and 2+ years in pharma manufacturing, with experience in sterile isolator tech and training on cGMP regulations. Strong communication and teamwork are essential.

Qualifications

  • Bachelor's degree in a scientific discipline.
  • Minimum 2+ years of experience in a pharma cGMP manufacturing environment.
  • Experience in sterile pharmaceutical isolator technology, combination products, or medical devices.
  • Demonstrated experience delivering training on cGMP regulations, SOPs, and quality systems.
  • Excellent written and verbal skills and ability to present technical data effectively.
  • Ability to work in a fast-paced team and lead peers through changing priorities.
  • Detail-oriented and task-focused with ability to meet deadlines.

Responsibilities

  • Provide QA oversight on the manufacturing floor during operations.
  • On-the-floor review of batch records to ensure compliance and resolve discrepancies.
  • Familiarity with electronic management systems (Veeva, Deacom, Blue Mountain RAM).
  • Facilitate QA oversight through walkthroughs and process observations.
  • Identify and implement procedural improvements as part of CI initiatives.

Skills

Quality Assurance
cGMP
Sterile isolator tech
Training delivery
Technical presentation
Team leadership
Detail oriented

Education

Bachelor's degree in a scientific discipline

Tools

Veeva
Deacom
Blue Mountain RAM

Job description

Civica Rx in Petersburg, VA is seeking a Quality Assurance Operations Shop Floor Associate to ensure ongoing cGMP compliance on the manufacturing floor. The role collaborates with operators and supervisors to review batch records and uphold SOP adherence in a new fill-finish facility.

The position requires a scientific degree and 2+ years in pharma manufacturing, with experience in sterile isolator tech and training on cGMP regulations. Strong communication and teamwork are essential.

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