Pharmacist Jobs in Grand Est, France

PET radiopharmacy team at Siemens Healthineers develops and produces PET radiopharmaceuticals for medical imaging. The pharmacist will operate aseptic production, perform quality control and regulatory compliance, and lead non‑exempt team members in a high‑reliability, night‑shift environment.

Clinical Pharmacist responsible for reviewing prescriptions, checking drug interactions, dosing, and allergies to ensure patient safety. Performs medication verification, documentation of clinical activities, and communication with healthcare providers.

Senior Pharmacist at Highmark Health and Allegheny Health Network supports the Lead in developing, implementing, and maintaining prescription drug benefit strategies, formularies, and programs for the Medicare Advantage market. The role involves clinical review, regulatory navigation, claims data analysis, financial analysis, and presentation of strategic recommendations to leadership.

Quality Assurance Biotechnology team at Vetoquinol ensures product integrity throughout the industrial and logistics lifecycle. The pharmacist leads technical reviews, qualifies subcontractors, oversees analytical and production processes, and drives investigations and CAPA implementation.

Senior Pharmacist QA lead for P&G Healthcare France, overseeing quality assurance, compliance, and risk-based QA across local and global standards. Manages GMP, ISO 9001/13485, GVP, GDP, HACCP processes, vendor audits, product transfers, launches, deviations, recalls, and critical incidents.

Pfizer seeks a pharmacist process manager in Freiburg to oversee development and transfer of solid dosage forms, ensuring compliance with GMP, safety, and regulatory standards. The role involves leading projects, coordinating tech transfer, monitoring timelines and budgets, and supporting manufacturing sites.

PHOENIX OCP’s call center in Metz‑Nancy‑Lorraine supports pharmacists and hospitals with after‑sales service and back‑office tasks. The role handles phone and administrative support for short‑listing, marketplace, and hospital‑clinic activities, ensuring product availability and client satisfaction.

Pharmacien Assurance Qualité Opérationnel H/F at Cencora (Alliance Healthcare Repartition) in Pont à Mousson, France. The role supports the site’s pharmacy operations under the delegation of the company pharmacist, ensuring compliance with the Code de la Santé Publique and the guide des Bonnes Pratiques de Distribution en Gros.

BeOne Medicines Germany GmbH’s Oncology Sales team drives market penetration of immune‑oncology products across Germany. The Key Account Manager builds brand awareness, advises hospital pharmacists and oncologists, and executes commercial projects to optimize patient care.

International Medical Mediation (IMM), a French SME assembling and distributing infusion and enteral nutrition devices, seeks a Pharmacist for Regulatory Affairs and Quality. The role ensures regulatory compliance of medical devices with MDR 2017/745 and ISO 13485, leads ISO certification, oversees vigilance, supports clinical studies, and drives RSE policy while managing two mission officers.

Pharmacy Tech II on Kettering Health’s Oncology Pharmacy team in Troy, Ohio, supports oncology pharmacists and nursing staff to deliver safe, sterile IV products and manage drug inventory. The role composes chemotherapy and immunotherapy medications, maintains 340B compliance, and drives process improvements in the infusion center.

Join our mission-driven team dedicated to advancing patient care through innovative biosimilar therapies. We seek a committed Key Account Manager to expand access to high-quality treatments across Switzerland.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. The role of Pharmaberater focuses on Kardiologie, Impfstoffe and Rare Disease, engaging physicians, pharmacists and patients across Germany.

ORKYN - TECHNICIEN A&GA H/F is a fixed-term (CDD) position within Air Liquide’s Pharma Dom subsidiary, based in Atton, France. The role involves delivering and retrieving medical devices and consumables to patients’ homes or medical facilities, ensuring proper functioning and safety of equipment.

Commercial en pharmacie H/F at Cencora (Alliance Healthcare Repartition) seeks a seasoned sales professional to drive growth across the French market. Based in Pont à Mousson, the role reports to the Regional Sales Director and collaborates closely with operational teams.

Air Liquide Healthcare’s Orkyn’ team delivers home‑care medical devices and consumables to patients across France. As a Technicien A&GA, you will perform on‑site deliveries, verify equipment, explain usage and maintenance, and collect administrative data.

Pharma Dom, a subsidiary of Air Liquide, has been providing home-based respiratory, infusion, nutrition, insulin therapy, and medical equipment support for over 40 years. The Pharmacien Référent ensures compliance with BPDO (Bonnes Pratiques de Dispensation de l’Oxygène) across assigned sites, upholds professional standards, and manages pharmacovigilance and materiovigilance processes.

Air Liquide’s Pharma Dom division seeks a Délégué Médico-Technique A&GA to drive patient coverage growth in the Illkirch region. The role focuses on building a pharmacy and hospital network, promoting Orkyn products to EHPAD and other medical structures, and supporting medical‑technical teams.

Air Liquide Healthcare’s VitalAire seeks a CDD Technicien Respiratoire to support patients with chronic respiratory conditions across Alsace and Vosges. The role involves installing and maintaining respiratory medical devices at patient homes, training patients and caregivers, and ensuring compliance with quality and safety procedures.

Thermo Fisher Scientific seeks a Qualified Person / Sachkundige Person to oversee release and certification of clinical trial materials at Rheinfelden and Weil am Rhein, Germany. The role involves approving clinical trial products, managing customer projects, conducting audits, liaising with authorities, creating QP declarations, approving SOPs, handling complaints, authorizing contract labs, advising on QA, deciding on drug batch use per AMG and EU Annex 13/16, reviewing deviation statements, root cause analysis, and reviewing manufacturing and validation documents.