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Full Time Downstream Process Development Scientist Jobs in Dallas, TX

Orano

Process Development Scientist

Plano, TX · On-site

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 ...

Qorvo, Inc.

Process Development Engineer

Richardson, TX · On-site

QUALIFICATIONS: * BS in Engineering, Materials, Statistics or physical sciences or equivalent. MS ... process development, process control, DOE execution, yield improvement, and root-cause analysis. 3 ...

Qorvo, Inc.

Process Development Engineer

Richardson, TX · On-site

QUALIFICATIONS: * BS in Engineering, Materials, Statistics or physical sciences or equivalent. MS ... process development, process control, DOE execution, yield improvement, and root-cause analysis. 3 ...

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All JobsDownstream Process Development Scientist JobsFull Time Downstream Process Development Scientist JobsFull Time Downstream Process Development Scientist Jobs in Dallas, TX

Full Time Downstream Process Development Scientist information

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How much do full time downstream process development scientist jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for full time downstream process development scientist in Dallas, TX is $38.25, according to ZipRecruiter salary data. Most workers in this role earn between $28.08 and $45.67 per hour, depending on experience, location, and employer.

What does a full time downstream process development scientist do?

A Full Time Downstream Process Development Scientist is responsible for designing, optimizing, and scaling up processes that purify biological products such as proteins, antibodies, or vaccines after they are produced in cells or microbes. This role involves developing and improving techniques like filtration, chromatography, and centrifugation to ensure high purity and yield of the final product. The scientist also conducts experiments, analyzes data, and collaborates with cross-functional teams to transfer processes from the lab to manufacturing. Their work is critical for producing safe and effective biopharmaceuticals on a large scale.

What is the difference between Full Time Downstream Process Development Scientist vs Downstream Process Engineer?

AspectFull Time Downstream Process Development Scientist
Primary FocusDesigning, optimizing, and developing downstream purification processes for biopharmaceuticals
Required CredentialsBachelor's or Master's in Biotechnology, Biochemistry, or related field; experience in process development
Work EnvironmentLaboratories, R&D settings, collaborative teams in biotech or pharma companies
Typical ResponsibilitiesProcess scale-up, method validation, troubleshooting, documentation

While both roles involve downstream bioprocessing, the Full Time Downstream Process Development Scientist focuses on process development and optimization, whereas the Downstream Process Engineer typically handles process implementation and manufacturing support. The scientist role emphasizes research and development, while the engineer role is more operational. Candidates often hold similar degrees and certifications, but their daily tasks and focus areas differ.

What are some typical challenges faced by a full time downstream process development scientist, and how can they be addressed?

Downstream Process Development Scientists often encounter challenges such as optimizing protein purification processes to achieve high yield and purity, troubleshooting unexpected impurities, and scaling up processes from laboratory to manufacturing scale. These tasks require strong problem-solving skills, meticulous attention to detail, and effective collaboration with upstream teams, analytical scientists, and manufacturing staff. Addressing these challenges involves staying current with new purification technologies, maintaining robust documentation, and participating in cross-functional meetings to ensure seamless process integration and regulatory compliance.

What are the key skills and qualifications needed to thrive as a full time downstream process development scientist, and why are they important?

To thrive as a Full Time Downstream Process Development Scientist, you need a strong background in biochemical engineering, protein purification, and analytical techniques, typically supported by a degree in biochemistry, biotechnology, or a related field. Proficiency with chromatography systems (e.g., HPLC, FPLC), filtration technologies, and knowledge of regulatory and quality systems like GMP is essential. Strong problem-solving abilities, teamwork, and effective communication skills help you collaborate with cross-functional teams and troubleshoot process challenges. These skills are crucial for developing robust purification processes that ensure product quality, regulatory compliance, and efficient production in biopharmaceutical environments.
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Full Time Downstream Process Development Scientist jobs near you
Infographic showing various Full Time Downstream Process Development Scientist job openings in Dallas, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $79,554 per year, or $38.2 per hour.

Process Development Scientist

Orano

Plano, TX • On-site

Full-time

Re-posted 2 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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