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Full Time Downstream Process Development Scientist Jobs in Texas

The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure ...

The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure ...

Scientist, R&D

San Antonio, TX · On-site

$80K/yr

New Product Development - Retail Position Type: Full-Time Location: San Antonio, TX Exemption ... Work with outside applications to deliver and develop DOE of new processes and ingredient ...

The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure ...

Demonstrated experience with extrusion process development, optimization and troubleshooting ... COMPETENCIES Scientific techniques/evaluation/selection/application Scientific variable analysis ...

Senior R and D Scientist

Katy, TX · On-site

$90K - $115K/yr

SINOPEC Employee Position Overview The Senior R&D Scientist is responsible for advancing catalyst and catalytic process research at the SINOPEC-UOP Joint Research Center. This position independently ...

Principal Process Engineer

Plano, TX · On-site

$165K - $185K/yr

Principal Process Engineer Department: 46 - Process Engineering Employment Type: Full Time Location ... scientists on documentation and experimental/statistical rigor. * Leading the development and ...

... downstream processing conditions. 4. Works independently on standard projects while assistance is ... scientific technical principles in problem solving and development in order to meet the needs of a ...

FORMULATION SCIENTIST

Rosenberg, TX · On-site

$87K - $95K/yr

Design, execute, analyze, and document formulation and process development studies using scientific and risk-based approaches. * Apply Quality by Design (QbD) and Design of Experiments (DoE ...

Showing results 41-60

Full Time Downstream Process Development Scientist information

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 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.

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 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.

How much does a full time downstream process development scientist make?

In California, a full-time downstream process development scientist typically earns between $80,000 and $130,000 annually, depending on experience, education, and the specific employer. Salaries may also include benefits such as health insurance and bonuses, with higher compensation often associated with advanced skills in bioprocessing and laboratory techniques.

What is a full time downstream process development scientist?

A full-time downstream process development scientist specializes in designing, optimizing, and scaling the purification processes used in biopharmaceutical manufacturing, such as chromatography and filtration. They work to improve product yield, purity, and efficiency, often using laboratory techniques and process modeling tools, typically within a regulated environment requiring compliance with industry standards.

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 job categories do people searching Full Time Downstream Process Development Scientist jobs in Texas look for?

The top searched job categories for Full Time Downstream Process Development Scientist jobs in Texas are:

What cities in Texas are hiring for Full Time Downstream Process Development Scientist jobs?

Cities in Texas with the most Full Time Downstream Process Development Scientist job openings:

Full-time

Re-posted 28 days ago


Job description

About the company:

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical’s website or on LinkedIn.

About the role:

The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure control principles to deliver robust, optimized processes. This role provides hands-on technical leadership for tooling design, process validation (IQ, OQ, PQ), and DOE execution, while supporting NPI, sustaining engineering, and business development initiatives. The Principal Process Engineer serves as a key technical interface between Viant, customers, tool shops, and internal teams to ensure regulatory compliance and best-in-class production outcomes.

  • Work Model: Remote
  • Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana, BC, and Vega Baja, PR sites. 

What you'll do: 

  • Lead the process development cycle
  • Evaluate processes for robustness, accuracy, and optimization
  • Initiate improvement projects
  • Quality/Metrology support: Assist site QE on KPI/KPO impacting part quality and process control
  • Partner with GTS/Site Tooling Engineer on design requirements
  • Partner with Tool Engineer on design and development requirements
  • Support business development by selling tooling solutions and resolving processing issues
  • Support corrective actions, re-validations, and tool/process optimization
  • Oversee process development through I.Q. and O.Q. runs; report required
  • Complete other related projects and tasks assigned
  • Demonstrate expert knowledge and performance
  • Apply scientific molding (Decoupled 2 and Decoupled 3)
  • Expert in cavity pressure monitoring and control (RJG)
  • Join technical reviews with customers and mold shops
  • Support DFM and tool design reviews with Tool Engineers
  • Support molding cell development and execution
  • Support EOAT design and fabrication
  • Manage mold shop deliverables and expectations (SIM reports)
  • Confirm receiving-site requirements (press/shot size/tonnage/special sequence) and machine capability studies
  • Develop processes, review Moldflow data for start-up and debug
  • Travel to customer sites, tool shops, and Viant facilities as needed; trip report required
  • Prepare, track, and communicate Process DOEs, report results and recommendations
  • Manage multiple concurrent projects (minimum 20 active)

Requirements: 

Education:

  • Bachelor of Science Degree in Engineering or related plastics discipline or 4-year engineering degree or equivalent completion of a 4,000 hour or 2-year process engineering apprenticeship.
  • Certification from a school in advanced molding or RJG Master Molder 2 (or equivalent).
  • Certification in Basic Mold Flow (or equivalent) is a plus.
  • Certification in Master Molding 3 is a plus.

Years of Experience:

  • 10+ years of experience in processing and in a molding environment, process development, qualification, validation of molds, etc.

Job Knowledge :

  • Extensive knowledge and able to train in: processing and process development techniques in scientific molding principles (MM2 skill level)
  • Plastics—Injection Molding; LSR (preferred)
  • Excel, PowerPoint, Word, and general computer skills; SolidWorks (drawing); 3D printing/3D software (preferred)
  • Some knowledge in FDA, QSR, and ISO 13485 medical device regulations and standards.
  • Understanding of statistics, Cp & Cpk studies for process.  I.Q., O.Q. and P.Q. requirements
  • Strong understanding of DOE methods and implementation
  • Expert knowledge of cavity pressure technologies and advanced control principles
  • Familiarity with the various engineering grade thermoplastic resins and Mold Flow analysis."

Additional Requirements:

  • Authorized to work in the U.S.
  • Spanish proficiency
  • Ability to travel up to 75% to Viant sites (U.S., Costa Rica, Tijuana, and Vega Baja, PR)