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Manager Downstream Process Development Scientist Jobs in Texas

Orano

Process Development Scientist

Plano, TX · On-site

We are seeking a highly motivated Process Development Scientist with expertise in ... Ability to manage multiple projects and prioritize workload efficiently * Ability to work ...

Coherent

Process Development Engineer

Sherman, TX

Masters in materials science or related discipline with a minimum of 5 years of hands on experience ... Strong project management skills * Strong research analytical skills * Ability to plan, organize ...

Coherent Corp.

Process Development Engineer

Sherman, TX · On-site

Masters in materials science or related discipline with a minimum of 5 years of hands on experience ... Strong project management skills * Strong research analytical skills * Ability to plan, organize ...

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Process Development Scientist

Orano

Plano, TX • On-site

Full-time

Re-posted 10 days ago

Job 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.
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.

Requirements
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.
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

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