Process Development Scientist

Orano SA

Plano, TX(remote)

JOB DETAILS
SKILLS
Analysis Skills, Biology, Biotech and Pharmaceutical, Cancer, Career Development, Clinical Research, Clinical Trial, Communication Skills, Corporate Policies, Cross-Functional, Data Quality, Data Sets, Energy & Utilities, English Language, Establish Priorities, Facebook, GMP (Good Manufacturing Practices), Identify Issues, Intellectual Property (IP), Interpersonal Skills, LinkedIn, Manufacturing, Multitasking, Nuclear Medicine, Nuclear Power, Presentation/Verbal Skills, Problem Solving Skills, Process Development, Project/Program Management, Record Keeping, Reporting Skills, Research & Development (R&D), Strategic Planning, Team Player, Training/Teaching, Work From Home, Writing Skills
LOCATION
Plano, TX
POSTED
25 days ago

Process Development Scientist - 14316 - Orano

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Process Development Scientist

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General Information

Name Process Development Scientist Ref # 14316 Posting Date Monday, May 11, 2026 Country United States Region Texas City Plano Business Unit (BU) MED Type of Employment Permanent/Regular Desired Starting Date 01-06-2026 Work Schedule Full time Remote Work In office Job RI - R&D, INNOVATION AND INTELLECTUAL PROPERTY

Description

Description

Orano Med Theranostics

Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.

We are seeking a highly motivated Process Development Scientist with expertise in radiopharmaceutical development to join our CMC team. The successful candidate will design, execute, and analyze studies and create reports for R&D CMC to support the development of novel radiopharmaceutical compounds. This role offers an opportunity to contribute to groundbreaking therapies and collaborate with cross-functional teams to advance our pipeline toward clinical trials.

Requirements

Key Responsibilities:

  • Design, conduct and optimize R&D studies to characterize radiopharmaceutical compounds.
  • Analyze, interpret, and troubleshoot complex datasets.
  • Scale up, write reports and transfer processes from R&D to GMP manufacturing teams.
  • Review and further develop & refine existing processes.
  • Collaborate with cross-functional teams to review protocols, batch records, formulation records, deviations and other related documents.
  • Maintain accurate records of experiments and ensure data integrity in accordance with company policies.
  • Stay current with advancements in radiopharmaceutical science and contribute to the development of innovative research strategies.
  • Other duties, as needed.

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All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.

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Minimum Qualifications :

  • Ph.D. in biological sciences, or related field
  • 3+ years of demonstrated research experience in a pharmaceutical/biotech setting

Required Skills and Competencies:

  • Excellent analytical and problem solving/problem resolution skills
  • Experience working with radioisotopes
  • Experience working in a pharmaceutical/biotech setting
  • Excellent written and verbal communication skills
  • Ability to manage multiple projects and prioritize workload efficiently
  • Ability to work independently
  • Strong interpersonal skills and ability to work collaboratively in a team-oriented environment

Benefits

  • Competitive compensation
  • Health, Dental, and Vision insurance with generous employer contributions
  • 401(k) with employer matching and contribution amounts
  • Life insurance and Short- and Long-Term Disability insurance provided by the company
  • Generous Paid Time Off and holiday schedules
  • Numerous Training and Development opportunities
  • and more

Orano Group

Present in the United States for 60 years, Orano USA is a leading technology and services provider to the U.S. commercial and federal markets.

Oranos activities in the U.S. include developing uranium enrichment facility in Oak Ridge, TN ; packages and transportation of uranium & nuclear fuel assemblies ; fabricating & installing used nuclear fuel dry storage canisters and casks, conducting pool-to-pad used nuclear fuel transfers ; providing solutions to the National Labs and to the Dept of Energy ; and supplying U.S. nuclear energy utilities with uranium, conversion, and enrichment services.

In the nuclear medicine field, Orano Med is at the forefront of research in nuclear medicine and is developing a new generation of targeted therapies against cancer using the unique properties of lead-212.

In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

This position requires a pre-employment background check and drug screening.

Orano is an Equal Opportunity Employer. Orano and all subsidiaries abide by applicable legal requirements. We ensure that all personnel actions such as recruitment, compensation, career development, benefits, and company-sponsored training are administered without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, protected veteran, or other protected status.

Location Details

Plano, Texas, United States

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About the Company

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