Qureos Mentor

Orano

<div><div><ul><li>Regular/Permanent</li>
<li>USA / Texas</li>
</ul></div><div><ul><li>Remote Options</li></ul></div></div>
<br><div><div><h2 class="jobSectionHeader"><b>Welcome to Orano</b></h2>
<div><div>Helping to meet current and future challenges to preserve our world and build the world of tomorrow while taking care of everyone's health is stimulating for you. For us too. By joining the Orano Group, a leading international player in the nuclear industry, you are in the right place.<br>
<br>
Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.<br>
<br>
Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.</div></div><p></p><div><p><br>
</p></div></div><div><h2 class="jobSectionHeader"><b>Job description</b></h2>
<div><p><b>Orano Med Theranostics</b></p><p>
Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a <b>fast-paced, detail-oriented environment</b> where your work directly impacts clinical trial success?</p><p>
Join our team as a <b>Senior Synthetic Chemist</b> and play a vital role in safeguarding the integrity of raw materials and sterile drug products. Are you seeking your next challenge as a Senior Synthetic Chemist? If so, this is your chance to grow within a dynamic, mission-driven organization that&rsquo;s transforming oncology from the inside out.</p><p>
The Synthetic Chemist is responsible for manufacturing products inside a traditional chemistry lab. These products support the business catalog, custom synthesis business, as well as the GMP business. Key responsibilities include developing methods to synthesize compounds, providing internal technical guidance, proposing solutions to complex chemistry problems, and acting as a backup for chemists, as needed.</p><p><b>
Key Responsibilities</b></p><p><b>
Synthetic Knowledge:</b></p><ul><li>
Research and design multi-step synthetic routes for targeted compounds</li><li><br>
Fundamental familiarity with classic reactions mechanisms and principles</li><li><br>
Optimize reaction conditions and troubleshooting synthetic challenges</li><li><br>
Characterize products and identify impurities using NMR, LC-MS, LC-QTOF, and related techniques</li></ul><p><b><br>
Laboratory Skills:</b></p><ul><li>
Perform extractions, crystallizations, and chromatographic separations (normal and reverse phase)</li><li><br>
Operate and maintain standard chemistry equipment (rotary evaporators, hydrogenation apparatus, chromatography systems, high-vacuum systems, overhead stirrers, etc.)</li><li><br>
Maintain accurate laboratory notebooks, records, and reports in compliance with company standards</li></ul><p><b><br>
Team Integration:</b></p><ul><li>
Provides technical guidance to Macrocyclics team for problem solving</li><li><br>
Generates ideas for new compounds for radio imaging, radiotherapy, and fluorescent applications</li><li><br>
Collaborate with colleagues across project teams to ensure timely completion of deliverables</li><li><br>
Mentors and develop other chemists</li></ul><br>
<p></p>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Our Full-Time </b><b>Benefits</b></h2>
<ul><li>Competitive compensation</li>
<li>Health, Dental, and Vision insurance &ndash; with generous employer contributions</li>
<li>401(k) with employer matching and contribution amounts</li>
</ul><ul><li>Life insurance and Short- and Long-Term Disability insurance provided by the company</li>
<li>Generous Paid Time Off and holiday schedules</li>
<li>Numerous Training and Development opportunities</li>
</ul><ul><li>and more&hellip;</li>
</ul></div></div><div><h2 class="jobSectionHeader"><b>Ideal qualifications</b></h2>
<div><p><b>Education &amp; Experience</b></p><p><b>
Minimum Qualifications:</b></p><ul><li>
Ph.D. Organic or Synthetic Chemistry, or other discipline with relevant industry experience</li><li>
M.S. in Organic or Synthetic Chemistry with 15+ years of relevant industry experience</li></ul><p><b>
Required Skills &amp; Competencies:</b></p><ul><li>
Strong synthetic chemistry skills with demonstrated understanding of reaction mechanisms.</li><li>
Hands-on experience with chromatographic separations and purification strategies.</li><li>
Familiarity with solvent solubility principles, extraction, and crystallization techniques.</li><li>
Exceptional analytical skills.</li><li>
Familiarity with the principles of coordination chemistry (preferred)
</li><li>Demonstrated ability to troubleshoot experiments and adapt to project needs.</li></ul><p><b>
Preferred Skills &amp; Competencies:</b></p><ul><li>
Familiarity with the principles of coordination chemistry, metal-ligand design, and complexation kinetics.</li><li>
Familiarity with quality systems and GMP protocols for clinical phase drug substances</li><li>
Experience handling and working with radionuclides/radiopharmaceuticals</li></ul></div>
<div>Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.</div></div></div>

Senior Synthetic Chemist

<div><div><ul><li>Regular/Permanent</li>
<li>USA / Texas</li>
</ul></div><div><ul><li>Remote Options</li></ul></div></div>
<br><div><div><h2 class="jobSectionHeader"><b>Welcome to Orano</b></h2>
<div><div>Helping to meet current and future challenges to preserve our world and build the world of tomorrow while taking care of everyone's health is stimulating for you. For us too. By joining the Orano Group, a leading international player in the nuclear industry, you are in the right place.<br>
<br>
Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.<br>
<br>
Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.</div></div><p></p><div><p><br>
</p></div></div><div><h2 class="jobSectionHeader"><b>Job description</b></h2>
<div><p><b>Orano Med Theranostics</b></p><p>
Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a <b>fast-paced, detail-oriented environment</b> where your work directly impacts clinical trial success?</p><p>
Join our Clinical Supply Chain team as <b>Senior Manager, Clinical Supply Chain</b> and play a vital role in safeguarding the integrity of raw materials and sterile drug products. Are you seeking your next challenge as Senior Manager, Clinical Supply Chain? If so, this is your chance to grow within a dynamic, mission-driven organization that&rsquo;s transforming oncology from the inside out.</p><p>
The Senior Manager, Clinical Supply supports day-to-day drug supply operations for Orano Med clinical trials, reporting to the Director of Clinical Supply. Key responsibilities include coordinating production schedules, tracking shipments, and resolving site-level supply issues to ensure timely drug delivery and dosing.</p><p><b>
Key Responsibilities</b></p><p><b>
Production and Delivery Coordination:</b></p><ul><li>
Assist the Director of Clinical Supply with coordinating radiopharmaceutical production schedules to align with site-specific dosing timelines</li><li>
Manage logistics planning for dose deliveries from manufacturing sites to clinical sites, considering half-life constraints, time zones, and customs clearance</li><li>
Communicate regularly with manufacturing partners and courier vendors to confirm production status, pickup timing, and delivery confirmations</li></ul><p><b>
Order and Shipment Tracking:</b></p><ul><li>
Maintain and update internal tracking tools with real-time shipment status, from production through confirmed site receipt, including delivery confirmations and any delays</li><li>
Proactively follow up with depots, clinical sites, courier vendors, and internal logistics stakeholders to ensure timely deliveries and address any in-transit issues or exceptions</li></ul><p><b>
Site and Vendor Communication Support:</b></p><ul><li>
Support the Director of Clinical Supply by assisting with site-facing logistics, including shipment tracking, drug availability, and receipt follow-up</li><li>
Work closely with Clinical Operations, manufacturing, and vendor teams to help monitor schedule changes, resupply needs, and enrollment forecasts</li><li>
Identify and document any shipment delays, temperature excursions, or discrepancies, and escalate to the Director for resolution</li></ul><p><b>
Cross-Functional Support:</b></p><ul><li>
Collaborate with cross-functional teams to align on enrollment projections, production scheduling, and logistics activities.</li><li>
Join recurring supply calls to keep internal teams informed of upcoming shipments and constraints.</li><li>
Support the Director in coordinating day-of dosing communications with manufacturers, couriers, and clinical sites</li></ul><br>
<p></p>
</div></div><div></div><div><div><h2 class="jobSectionHeader"><b>Our Full-Time </b><b>Benefits</b></h2>
<ul><li>Competitive compensation</li>
<li>Health, Dental, and Vision insurance &ndash; with generous employer contributions</li>
<li>401(k) with employer matching and contribution amounts</li>
</ul><ul><li>Life insurance and Short- and Long-Term Disability insurance provided by the company</li>
<li>Generous Paid Time Off and holiday schedules</li>
<li>Numerous Training and Development opportunities</li>
</ul><ul><li>and more&hellip;</li>
</ul></div></div><div><h2 class="jobSectionHeader"><b>Ideal qualifications</b></h2>
<div><p><b>Education &amp; Experience</b></p><p><b>
Minimum Qualifications:</b></p><ul><li>
Bachelor&rsquo;s degree in a relevant field (e.g., Supply Chain Management, Life Sciences, Pharmacy, or related discipline)</li><li>
Minimum of 5 years of experience in clinical supply chain operations within the pharmaceutical or biotechnology industry</li><li>
Experience coordinating day-to-day drug supply logistics in support of global or regional clinical trials</li><li>
Prior experience supporting production and delivery timelines in partnership with third-party manufacturers and courier vendors</li></ul><p><b>
Required Skills &amp; Competencies:</b></p><ul><li>
Strong operational understanding of clinical supply logistics, including production coordination, shipment tracking, and clinical site support</li><li>
Familiarity with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical
</li><li>Practice (GCP) and regulatory expectations for investigational products</li><li>
Excellent organizational skills, with the ability to manage multiple time-sensitive priorities across sites, vendors, and manufacturing facilities</li><li>
Strong communication and interpersonal skills, with the ability to work effectively across cross-functional teams and with external partners</li><li>
Proactive problem-solving mindset with attention to detail and a focus on execution and issue escalation</li><li>
Proficiency in Excel and supply tracking tools; working knowledge of IRT systems is preferred</li></ul><p><b>
Preferred Skills &amp; Competencies:</b></p><ul><li>
Experience with radiopharmaceutical trials or time-sensitive drug products</li></ul></div>
<div>Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.</div></div></div>

Senior Manager, Clinical Supply Chain

Join Orano and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Orano

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Senior Synthetic Chemist

Senior Manager, Clinical Supply Chain