Pharmacist in Charge in Athens, OH

Athens, OH
Soliant Pharmacy-Pharmacist in Charge Temp-To-Hire 1 day ago Apply

An established compounding pharmacy is seeking an experienced Pharmacist-in-Charge (PIC) to lead regulatory, compliance, and quality operations at its facility in Ohio. This onsite position offers long-term stability, leadership exposure, and growth potential within a nationally recognized organization. Candidates willing to relocate may receive relocation assistance, and a temp-to-perm traveler option can be considered for the right fit.

Schedule:

  • Monday through Friday
  • Onsite in Albany, Ohio
  • Key Responsibilities:

  • Serve as Pharmacist-in-Charge for Ohio and additional non-resident state licenses as needed
  • Ensure compliance with FDA, DEA, State Boards of Pharmacy, and Section 503B regulations
  • Maintain pharmacist and facility licensure across multiple states
  • Lead inspections and represent the facility during regulatory meetings with the Board of Pharmacy, FDA, and DEA
  • Develop, review, and maintain SOPs and training programs
  • Oversee regulatory reporting, recalls, complaints, and quality investigations
  • Provide regulatory guidance to cross-functional teams
  • Manage QA/QC functions including batch record review, deviations, investigations, and environmental monitoring
  • Lead validation activities related to equipment, systems, and processes
  • Implement and maintain the Quality Management System (QMS)
  • Review and approve change controls, product labeling, and annual product reviews
  • Oversee incoming materials, vendor qualification, and reserve sampling
  • Develop environmental monitoring programs, trending, and root cause analysis
  • Present quality metrics to site and corporate leadership
  • Qualifications:

  • Active Ohio Pharmacist license in good standing
  • Experience with licensure in multiple states preferred
  • Bachelor’s Degree in Pharmacy (BS) or Doctor of Pharmacy (PharmD)
  • Minimum 5 years of leadership experience managing teams
  • Strong knowledge of cGMP, FDA and DEA regulations, sterile injectable manufacturing, and non-sterile compounding
  • Proven experience leading inspections and regulatory audits
  • Proficient in Microsoft Office; strong communication skills for presenting complex information Preferred:
  • 10+ years in pharmaceutical, biotech, or medical device industries
  • 7+ years in quality or compliance roles with increasing responsibility
  • Benefits:

  • Competitive salary
  • Relocation assistance
  • Comprehensive health, dental, and flexible spending accounts
  • 401(k) with company contribution
  • Company-paid life and disability insurance
  • Generous paid time off with accrual increasing over time
  • Tuition reimbursement
  • Opportunities for long-term growth and advancement
  • This position is a direct hire opportunity with a temp-to-perm option available. Qualified candidates interested in shaping regulatory and quality operations in a dynamic compounding environment are encouraged to apply.

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