T

TransMedics

Ex-vivo organ perfusion platform

Head of Pharmacy Operations

PharmacyConfirmed live in the last 24 hours
Full-timeAndover, MA, USA

About the Job

Requirements

  • A PharmD or Bachelor of Science in Pharmacy from an ACPE-accredited program is required.
  • An active, unrestricted U.S. pharmacist license in at least one state is required, along with willingness to obtain additional state licenses within the first 12 months.
  • At least 8 years of pharmacy practice experience, including at least 3 years as Pharmacist-in-Charge or equivalent in specialty, mail-order, central-fill, wholesale distribution, 3PL, or health-system operations, is required.
  • Hands-on experience with multistate licensure, board of pharmacy inspections, and DEA compliance for Schedule II–V products is required.
  • Working knowledge of DSCSA, cold-chain and USP <659>/<1079> storage and distribution standards, and NABP drug distributor accreditation is required.
  • A track record authoring SOPs, leading audits or inspections, and managing CAPA in a regulated environment is required.
  • The role requires communicating with non-pharmacist executives and representing the company with regulators.
  • Willingness to travel approximately 25% to clinical hubs and headquarters is required.

Responsibilities

  • Serve as Pharmacist-in-Charge, Designated Representative, or Responsible Person for the company's main and clinical hub pharmacies, wholesale distributor, and 3PL licenses.
  • Own multistate licensing for resident and non-resident pharmacy, wholesale distributor, 3PL, and controlled-substance registrations for every clinical hub and ship-to state, including renewals, changes of ownership, and inspection follow-up.
  • Lead NABP, drug distributor accreditation, and state board inspection readiness, and serve as the primary company contact during inspections and audits.
  • Partner with Supply Chain to establish remote controlled pharmaceutical and solution dispensing systems across clinical hubs to maintain quality control and tracking.
  • Define and maintain SOPs for receipt, verification, storage, pick/pack, dispensing, shipping, returns, recalls, and destruction of prescription drugs at every hub.
  • Set cold-chain and environmental-monitoring standards for temperature-sensitive and specialty products, including excursion evaluation and product disposition.
  • Set controlled-substance standards to DEA requirements, covering CSOS ordering, receipt, secure storage, inventory reconciliation, suspicious-order monitoring, theft/loss reporting, and reverse distribution.
  • Drive network-wide DSCSA compliance, including serialization, transaction data, trading-partner verification, and suspect or illegitimate product investigations.
  • Assess each hub on-site on a regular cadence and address deficiencies through successful closure.
  • Build and run the pharmacy compliance program, including risk assessments, monitoring, internal audits, deviations, and CAPAs, with reporting to executive leadership and the board-level compliance committee.
  • Partner with Quality and Regulatory Affairs to align pharmacy SOPs with the company QMS, including 21 CFR Part 820 and ISO 13485 for device operations and applicable cGDP expectations for drug distribution.
  • Track evolving federal and state pharmacy, wholesale, and controlled-substance regulations and translate them into operational requirements and training.
  • Lead pharmacy-related investigations, recalls, and field actions with Quality, Legal, and manufacturers.
  • Act as pharmacy subject-matter expert for new hub openings, product development and launches (including drug-device combination products), payer and manufacturer contracting, and technology selection for pharmacy management, inventory, serialization, and temperature monitoring.
  • Build and deliver pharmacy training and competency programs for hub technicians and warehouse staff.
  • Represent the company with state boards, NABP, trade associations, manufacturers, and key customers on pharmacy practice matters.
  • Mentor pharmacists and technicians across the network and shape the future pharmacy organization as it scales.

Desired Qualifications

  • Experience in a medical device or drug-device combination product company, or within an FDA-registered QMS, is preferred.
  • Experience opening or licensing new pharmacy or distribution sites from greenfield is preferred.
  • Familiarity with 340B, specialty pharmacy accreditation (URAC, ACHC), or manufacturer limited-distribution networks is preferred.
  • Board certification (BCPS, BCSCP) or credentials in regulatory affairs or quality (RAC, CQA) are preferred.
  • Experience selecting or implementing pharmacy management, serialization, or environmental-monitoring systems is preferred.

About the Company

TransMedics

Ex-vivo organ perfusion platform

TransMedics develops the Organ Care System (OCS), a portable device that keeps donor organs alive outside the body using warm, oxygenated perfusion, allowing continuous viability monitoring and assessment. It makes money by selling the OCS consoles, selling disposable sets per transplant, and offering the National OCS Program, which provides trained procurement surgeons, clinical support, and dedicated organ transport logistics. The company stands apart by having FDA-approved preservation and assessment for hearts, lungs, and livers, including DBD and DCD indications, and by offering an integrated hardware, disposables, and logistics platform. Its goal is to increase viable transplants and donor organ utilization by improving preservation, assessment, and logistics across transplant centers.

Company size
501-1,000
Company stage
IPO
Headquarters
Andover, MA
Founded
1998

Recently Posted Jobs

Explore more opportunities at TransMedics

See more jobs