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Pharmacist

Tailstorm Health Inc
Posted 18 days ago, valid for 17 days
Location

Phoenix, AZ 85001, US

Salary

$80,000 - $96,000 per year

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Contract type

Full Time

Health Insurance
Paid Time Off

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Sonic Summary

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  • The Full-Time Pharmacist position at Medivant involves supporting sterile injectable manufacturing operations while ensuring compliance with FDA regulations and internal SOPs.
  • Candidates must have an active Pharmacist License in Arizona and a minimum of 2-3 years of experience in sterile compounding or a related field.
  • Key responsibilities include overseeing compounding operations, verifying batch records, and ensuring quality assurance compliance.
  • The position offers a competitive base salary, health benefits, paid time off, and opportunities for career growth and advancement.
  • This role is set in a highly regulated cGMP manufacturing environment, providing stability and long-term employment.

Position Summary

The Full-Time Pharmacist supports Medivant’s sterile injectable manufacturing operations by ensuring all compounding, labeling, and documentation processes comply with FDA regulations, USP <797>/<800>, and internal SOPs.

This role involves verifying batch records, supervising compounding operations, ensuring quality assurance compliance, and overseeing controlled substance handling as required.

This is a full-time position offering long-term career growth, stability, and the opportunity to work in a highly regulated cGMP manufacturing environment.

Key Responsibilities

  • Review and approve batch production records, labels, and associated documentation
  • Supervise sterile compounding and aseptic filling operations to ensure compliance with USP <797>/<800> standards
  • Verify and document calculations for compounding and formulation accuracy
  • Monitor cleanroom operations, gowning compliance, and aseptic techniques
  • Support internal and regulatory audits, CAPA investigations, and validation activities
  • Ensure compliance with DEA, FDA, and state pharmacy board regulations
  • Collaborate with Quality Assurance and Production teams to maintain continuous compliance
  • Provide guidance to technicians and operators on cGMP and pharmacy standards
  • Participate in review of deviations, investigations, and process improvements

Qualifications

Required:

  • Active Pharmacist License in the state of Arizona (in good standing)
  • Minimum 2–3 years of experience in sterile compounding, manufacturing pharmacy, or 503B facility
  • Strong understanding of USP <797>, USP <800>, cGMP, and FDA manufacturing guidelines
  • Strong documentation, verification, and analytical skills
  • Excellent communication and teamwork abilities

Preferred:

  • Experience in sterile injectable production or pharmaceutical quality assurance
  • Familiarity with LIMS, ERP, or electronic batch record systems
  • Prior experience in a 503B outsourcing facility or hospital cleanroom setting

Compensation & Benefits

  • Competitive base salary (based on experience)
  • Health, dental, and vision insurance
  • Paid time off (PTO) and holidays
  • Opportunities for career growth and advancement
  • Stable, long-term employment with a growing organization
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