... developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical ...
... developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical ...
... developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical ...
... developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development. * Deep expertise spanning the full product lifecycle, from early development ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development. * Deep expertise spanning the full product lifecycle, from early development ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development. * Deep expertise spanning the full product lifecycle, from early development ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development. * Deep expertise spanning the full product lifecycle, from early development ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development.Deep expertise spanning the full product lifecycle, from early development ...
Provide expert consultation on upstream, downstream, analytical, and manufacturing strategies ... process development.Deep expertise spanning the full product lifecycle, from early development ...
Candidate must have hands-on experience with upstream or downstream biological processes in cGMP or ... Responsibilities include (1) execution of process development laboratory studies (fermentation ...
Candidate must have hands-on experience with upstream or downstream biological processes in cGMP or ... Responsibilities include (1) execution of process development laboratory studies (fermentation ...
Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled. * Apply QbD and traditional process validation principles to existing and new gene ...
Quick apply
Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled. * Apply QbD and traditional process validation principles to existing and new gene ...
Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled. * Apply QbD and traditional process validation principles to existing and new gene ...
Partner with Process Development and Manufacturing to ensure upstream and downstream processes are well controlled. * Apply QbD and traditional process validation principles to existing and new gene ...
Process Validation Engineer
$70 - $80/hr
Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... Join a team where your contributions matter, your development is prioritized, and your success is ...
New
Quick apply
Process Validation Engineer
$70 - $80/hr
Process Engineer -- Upstream / Downstream / Clean Utilities (Consultant) -- Contract Engagement ... Join a team where your contributions matter, your development is prioritized, and your success is ...
New
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Physical Therapist Assistant PRN
Du Bois, PA ยท On-site
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Physical Therapist Clinic Director
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Continue developing your leadership and clinical skills through Upstream's professional development ... Specific details will be provided during the hiring process. Upstream Rehabilitation is an Equal ...
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Upstream Process Development information
What jobs pay 500,000 a year in the US?
What are the key skills and qualifications needed to thrive in Upstream Process Development, and why are they important?
What are common upstream jobs?
What biology jobs pay over $100k?
What is the difference between Upstream Process Development vs Downstream Process Development?
| Aspect | Upstream Process Development | Downstream Process Development |
|---|---|---|
| Focus | Development of cell culture, fermentation, and bioreactor processes | Purification, filtration, and formulation of bioproducts |
| Skills & Credentials | Bioprocess engineering, molecular biology, biochemistry | Bioprocessing, chromatography, analytical chemistry |
| Work Environment | Laboratories, bioreactors, pilot plants | Purification facilities, labs, quality control |
| Industry Usage | Biotech, pharmaceutical manufacturing | Biotech, pharmaceutical manufacturing |
Upstream Process Development focuses on creating and optimizing cell culture and fermentation processes to produce bioproducts. In contrast, Downstream Process Development involves purifying and finishing these products. Both roles are essential in biopharmaceutical manufacturing and require similar scientific backgrounds, but they specialize in different stages of bioprocessing.
What is upstream process development?
What are some common challenges faced in upstream process development and how do teams typically address them?

Job description
Report: CTO
Location: Philadelphia, PA
Position Type : Full Time, Exempt
Travel: Occasional (0-10%)
Position Summary
This position is part of the Technology team responsible for Client technology development, process development, and assisting in transferring developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical processing that utilizes bioreactors. A Scientist is responsible for hands-on execution of experiments and technology transfer, as well as authoring experimental protocols, SOPs, and batch documents. A Scientist is expected to independently complete objectives given by supervisor, serve as a role model to junior scientists, collaborate cross-functionally, and provide support with any other technology, process development, and manufacturing needs.
Key Responsibilities
- Independently contribute to technology/process development for specific bioprocessing steps, ensuring delivery in alignment with Client strategy
- Support Senior/Principal Scientist with experimental design, execution and data analysis, effectively communicating technical results to management
- Author protocols, SOPs, and batch documents to ensure the successful transfer of technology/process development to GMP manufacturing
- Perform as a Subject Matter Expert on a cross-functional team to implement novel process.
- Work closely with suppliers and other partners to drive forward technology development initiatives
- Serve as a good financial steward to the Technology team at Client and help to implement budgetary adherence and financial governance
- Coach and train junior scientists/employees on activities and documentation related to technology development, process development.
- Other related duties as assigned.
- Minimum Bachelor's degree in Biological Engineering, Biotechnology, Biology, Biochemistry, or other related field. Master's preferred.
- 2-3 years of industry or academic experience in combination with Bachelor's or Master's degree.
- Experience with methodologies used for upstream or downstream viral vector production in either industry or academia
- Experience in experimental design, execution, and data analysis
- Excellent communication, collaboration, and technical writing skills
- Innovative and creative mindset, with problem solving capabilities
- Proficient in Microsoft Office products.
- Ability to lift and carry up to 30lbs
- Ability to sit and stand for extended periods
- Excellent manual dexterity and ability to perform repetitive movements with fingers/hands
Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.
About Cedent
Sourced by ZipRecruiter
CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Plano, TX, US
Year founded
2008