Full Time 503B Compounding Pharmacist - Dayton, NJ
Soliant Health is currently seeking a highly skilled and experienced Compounding Pharmacist for a full-time opportunity at a premier 503B outsourcing facility located in Dayton, NJ. This role is ideal for a professional looking to play a critical role in sterile compounding operations and ensure compliance with federal and state regulatory requirements. If you’re passionate about compounding pharmacy, compliance, and leadership in a sterile manufacturing environment—this is the opportunity for you.
Position Overview:
As a Compounding Pharmacist, you will be responsible for supporting the Director of Operations / Pharmacist-in-Charge in the implementation and maintenance of sterile compounding policies. Your work will ensure alignment with USP 797, FDA regulations, cGMP standards, and all applicable state Board of Pharmacy rules.
You will also be an essential contributor to operational excellence, regulatory readiness, and continuous improvement initiatives within the facility.
Key Responsibilities:
Provide direct oversight of sterile compounding and production activities within a 503B facility.
Ensure ongoing compliance with USP 797, FDA CFR guidelines, DEA regulations, cGMP requirements, and state board pharmacy regulations.
Maintain current licensure in New Jersey and additional states as needed.
Monitor regulatory updates from federal and state agencies and implement necessary policy changes.
Contribute to new 503B product development, including protocols, labeling, Master Batch Records, and product specifications.
Collaborate closely with Supply Chain to manage Beyond-Use-Date stock and production planning.
Coach, mentor, and foster a culture of continuous improvement and aseptic excellence.
Execute and oversee investigations, CAPAs, and change controls.
Assist in regulatory audits and prepare formal responses.
Support site-wide GMP and quality systems training initiatives.
Required Qualifications:
Bachelor of Pharmacy or PharmD.
Active New Jersey Pharmacist license.
Eligibility and willingness to obtain licensure in multiple states (including AL, AR, ID, KS, MI, MS, NV, NY, OH, OK, KY, VA).
Proven experience in a 503B compounding environment.
Deep working knowledge of USP 797 and sterile compounding operations.
Strong familiarity with cGMP, aseptic techniques, and quality systems in a production or clinical setting.
Experience with IV infusion compounding, hospital, clinical, or long-term care pharmacy environments.
Excellent communication, documentation, and organizational skills.
Demonstrated ability to manage multiple priorities and regulatory standards in a fast-paced setting.
Additional Skills:
Strong leadership and mentoring capabilities.
A high level of accuracy, attention to detail, and a continuous improvement mindset.
Ability to adapt quickly to regulatory changes and internal process improvements.
Experience in regulatory correspondence and audit readiness is highly preferred.
This is a contract or contract-to-hire opportunity with day shift hours. These opportunities tend to move fast—don’t miss your chance to step into a high-impact role within a dynamic and compliant sterile manufacturing operation.
Apply today or contact me directly:
Farhan Mohammad, Pharmacy Recruiter
281-848-7415
[email protected]
Job ID: 8671183
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