Pharmacist in Charge (PIC)

Pharmacist in Charge (PIC)Ledgewood, NJHarrow is a leading provider of ophthalmic disease management solutions in North America. Harrow is an entrepreneurial company where we celebrate the ability of every member of the Harrow Family to be the CEO of their job. Harrow's values have driven interest over the past decade in attracting high-performing professionals in a variety of disciplines. Members of our Harrow Family often express their pride in being a part of our commitment to innovation, patient access to affordable medicines, and our track record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the gift of sight to those most in need.Harrow's ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including:An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZ™, and OPUVIZ™A broad Dry Eye Disease product line, led by VEVYE® and bolstered by well-known adjacent ocular surface disease products such as FLAREX® and FRESHKOTE®A peri-operative Surgical product line, led by TRIESENCE® and BYQLOVI™A Rare and Specialty product line, which includes various high-need and utility products such as ILEVRO®, NATACYN®, and VERKAZIA®A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01Job SummaryUnder the Head of Quality's leadership, the PIC will provide leadership and support for the development and implementation of strategic quality and operational initiatives for the company's 503B outsourcing facility in Ledgewood, NJ, to deliver business results focused on quality and compliance. The PIC position requires a high level of knowledge across aseptic manufacturing, good manufacturing practices, quality, and regulatory compliance. The PIC must maintain pharmacist licensure in good standing in specific states and is expected to provide clinical expertise on matters with the potential to impact product safety.Core ResponsibilitiesNOTE: Core responsibilities will be finalized based on the incumbent's expertise and the organizational needs of the company.QA Oversight of ProductionComplete training and remain qualified to perform all operations that the PIC oversees, including sterile garbing and gowning, compounding, aseptic filling, visual inspection, and labelingPerform production review of executed batch production recordsParticipate in investigations related to potential or actual deviations, out-of-specification results, or other incidents related to the drug productRespond to internal audit findingsPIC Licensure ResponsibilityServe as a designated Pharmacist-in-Charge, assuming state pharmacist licensure responsibility.Ensure operations conducted under PIC responsibility meet all applicable legal, regulatory, and professional standards.Support policies, procedures, and operational practices required to maintain facility and pharmacist licensure and good standing.Clinical & Regulatory ComplianceOversight and management of Adverse Drug Event (ADE) reporting, investigation, trending, and corrective action processes.Ensure ADEs are handled and reported in alignment with federal, state, accrediting body, and organizational requirements.Assist with compliance & regulatory evaluation of and (as requested) provide clinical input on new product development opportunities.Regulatory Communication & SupportAssist with regulatory communications, including drafting responses, gathering documentation, and participating in inspections or audits as assigned.Support regulatory inquiries, deficiency responses, and follow-up actions within the defined scope of responsibility.Serve as a clinical liaison during regulatory interactions when delegated.Qualifications & RequirementsDoctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy (BSPharm).Active, unrestricted pharmacist license in good standing (state(s) as required by the organization as listed below and ability to obtain licensure in additional states as requested:Minimum 5–7 years of pharmacy experience, including GMP and regulatory or compliance-related responsibilities.Demonstrated knowledge of sterile compounding, ADE & complaint management, and controlled substance regulations.Experience participating in regulatory inspections, audits, or compliance investigations.Strong written and verbal communication skills, including regulatory correspondence.Familiarity with DEA, State Board of Pharmacy, accrediting organizations, and patient safety standards.Demonstrates sound regulatory and clinical judgment when interpreting pharmacy laws, regulations, and accreditation standards within assigned scope.Appropriately balances patient safety, operational realities, and compliance obligations when making recommendations or decisions.Understands when to escalate issues and when to act independently under delegated authority.Pharmacist License RequiredAlaska, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Nebraska, Nevada, Ohio, Oklahoma, Oregon, Texas, Virginia, and West VirginiaPharmacist License PreferredAlabama, Arkansas, Mississippi, Tennessee, California, and IllinoisPosition TypeOn-SiteTravelUp to 20% as an Imprimis NJOF representative