Associate Specialist Quality Control

Imsapharma Com Ar

Base: $65,100.00 - $102,500.00; bonus/equity: elig...
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Manufacturing and packaging documentation
Raw material and finished goods retention
Sample information into trackwise system
** The Associate Specialist Quality Control position at Imsapharma Com Ar involves maintaining manufacturing and packaging documentation, coordinating sample shipments, and supporting quality control processes in a pharmaceutical setting. The ideal candidate should have 0-3 years of experience in the pharmaceutical industry and possess a high school diploma or equivalent. **

Job Summary

  • Maintains final retention of all manufacturing and packaging documentation and samples, coordinating and preparing documentation for shipment of raw material and finished goods retention sample shipment.
  • Completes annual inspections of retained samples, tracks sample levels, and coordinates the archival and retrieval of batch record documentation.
  • The salary range for this role is $65,100.00 - $102,500.00, with eligibility for annual bonus and long-term incentive, and a comprehensive package of benefits including medical, dental, vision, and retirement benefits.

Matching Summary

Match Score: 75

** The Associate Specialist Quality Control position at Imsapharma Com Ar involves maintaining manufacturing and packaging documentation, coordinating sample shipments, and supporting quality control processes in a pharmaceutical setting. The ideal candidate should have 0-3 years of experience in the pharmaceutical industry and possess a high school diploma or equivalent. **

Salary

Base: $65,100.00 - $102,500.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, compassionate and sick days

Skills & Requirements

Must-have

  • manufacturing and packaging documentation
  • raw material and finished goods retention
  • sample information into Trackwise system
  • Quality Policies and Guidelines
  • GMP, NDA, and related regulations
  • pharmaceutical operations systems

Nice-to-have

  • respect and appreciation for diverse perspectives
  • customer needs, requirements, and expectations
  • new ways to improve services
  • expresses views and ideas
  • develop new skills and abilities
  • incorporates feedback into future performance

Key Requirements

  • 0-3 years pharmaceutical industry experience
  • High School Diploma or equivalent

Work Rights

Not specified

Tailored Resume

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