1

Associate Downstream Process Development Scientist Jobs in Texas

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 ...

Scientist II, Downstream Location: This is an on-site position located in Pearland, TX. The purpose ... The ideal candidate will be responsible for leading new process development and improving existing ...

Scientist II, Downstream Location: This is an on-site position located in Pearland, TX. The purpose ... The ideal candidate will be responsible for leading new process development and improving existing ...

Operate and maintain crystal growth equipment for R&D and process development purposes * Assist in ... Masters in materials science or related discipline with a minimum of 5 years of hands on experience ...

Operate and maintain crystal growth equipment for R&D and process development purposes * Assist in ... Masters in materials science or related discipline with a minimum of 5 years of hands on experience ...

R&D Senior Scientist

Houston, TX · On-site

$90K - $115K/yr

... processes for the efficient production of antigens and antibodies. With its main manufacturing ... Lead downstream purification strategies using modern chromatography platforms (affinity, IEX, SEC ...

next page

Showing results 1-20

Associate Downstream Process Development Scientist information

What is an Associate Downstream Process Development Scientist?

An Associate Downstream Process Development Scientist is a professional who works in the biotechnology or pharmaceutical industry, focusing on developing and optimizing processes that purify biological products, such as proteins or antibodies, after they have been produced by cells. Their work is crucial for ensuring the final product meets quality and safety standards before it is used in research or clinical applications. They typically perform laboratory experiments, analyze data, and collaborate with other scientists and engineers to improve yield and efficiency. This role is often entry-level or early-career, providing hands-on experience in process development and technical troubleshooting.

What are the key skills and qualifications needed to thrive as an Associate Downstream Process Development Scientist, and why are they important?

To excel as an Associate Downstream Process Development Scientist, you need a solid understanding of biochemistry, chemical engineering, and downstream purification techniques, often supported by a bachelor's or master's degree in a life science or engineering discipline. Familiarity with chromatographic systems (such as AKTA), filtration equipment, and analytical tools, as well as knowledge of GMP/GLP regulations, is typically required. Strong problem-solving, attention to detail, and effective teamwork and communication skills help you navigate complex experiments and collaborate with cross-functional teams. These skills ensure efficient process optimization, compliance with regulatory standards, and successful development of biopharmaceutical products.

What is the difference between Associate Downstream Process Development Scientist vs Associate Upstream Process Development Scientist?

AspectAssociate Downstream Process Development ScientistAssociate Upstream Process Development Scientist
Primary FocusPurification and recovery of bioproductsCell culture and fermentation processes
Required SkillsProtein purification, chromatography, filtrationCell culture, bioreactor operation, media preparation
Work EnvironmentLaboratories, manufacturing facilitiesLaboratories, bioreactor labs
Common CertificationsBiotech or bioprocessing certificationsBiotech or bioprocessing certifications

Both roles are essential in biopharmaceutical development, focusing on different stages of the production process. The Associate Downstream Process Development Scientist specializes in purification techniques, while the Associate Upstream Process Development Scientist concentrates on cell growth and fermentation. Understanding these distinctions helps candidates target their skills and career paths effectively.

What are some typical challenges faced by an Associate Downstream Process Development Scientist, and how can they be addressed?

Associate Downstream Process Development Scientists often encounter challenges such as optimizing purification processes, troubleshooting equipment performance, and ensuring batch-to-batch consistency. These challenges can be addressed by maintaining meticulous documentation, collaborating closely with upstream and analytical teams, and staying current with best practices in chromatography and filtration. Proactively seeking feedback from experienced colleagues and participating in cross-functional meetings can also help in identifying solutions and improving process efficiency.
What are the most commonly searched types of Downstream Process Development Scientist jobs in Texas? The most popular types of Downstream Process Development Scientist jobs in Texas are:
What cities in Texas are hiring for Associate Downstream Process Development Scientist jobs? Cities in Texas with the most Associate Downstream Process Development Scientist job openings:

Process Development Scientist

Orano

Plano, TX • On-site

Full-time

Posted 19 days ago


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.


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