×
Register Here to Apply for Jobs or Post Jobs. X

Quality Control Inspector

Job in Irving, Dallas County, Texas, 75084, USA
Listing for: Carie Boyd Pharmaceuticals
Full Time position
Listed on 2026-01-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
    Data Scientist
Job Description & How to Apply Below

Company Overview

Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a variety of office use products including but not limited to injectables, pellets, and topicals. Being a member of the Carie Boyd team means prioritizing patient needs, dedication to quality, and the drive to continue to scale our innovative business in new and diverse ways.

Job Description

Quality Control Inspector

Responsibilities
  • Perform routine tasks including sampling: personnel monitoring (PM) and environmental monitoring (EM)
  • Incubate and read sample plates (TSA and SDA) per standard operating procedures
  • Send off PM & EM samples to contract laboratory for identification
  • Confirm growth promotion test results
  • Document actions
  • Start-Up and In-Process Checks
  • Label Verification
  • Assist production to verify steps critical to quality of final product
  • Perform visual inspections
  • Enforce good hygiene practices and aseptic techniques in GMP areas
  • Successfully pass garbing qualification to enter clean rooms
  • Perform aseptic processing media fill simulations for personnel certifications and garb qualifications for personnel monitoring
  • Clearly communicate and enforce the company’s quality expectations outlined in standard operating procedures in a productive manner
  • Prepare product to be shipped to contract testing laboratories, select appropriate testing on portals, and correspond with laboratories as needed
  • Perform GDP review of documents as needed
  • Assist production with reconciliation as needed
  • Assist Quality Management with other Quality Control duties as needed
  • Has the decision‑making authority for the start‑up and shut down of compounding suites
Qualifications
  • Minimum 3 years combined GMP experience in any of the following: contract manufacturing, food packaging or manufacturing, medical device, and/or 503B outsourcing facility.
  • Strong documentation skills
  • Cleanroom experience preferred, but not required
  • Aseptic Processing and Aseptic Technique skills preferred
Confidentiality
  • The employee must maintain the confidentiality of company information and, pursuant to State and Federal Law (including the Health Insurance Portability and Accountability (HIPAA) Act of 1996), protected health information.
EOE/ADA
  • Carie Boyd Pharmaceuticals is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, Carie Boyd Pharmaceuticals will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer.

Referrals increase your chances of interviewing at Carie Boyd Pharmaceuticals by 2x.

#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary