... 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 strategic guidance to R&D teams on GxP expectations to support downstream GMP manufacturing and regulatory requirements for gene therapy BLAs. * Oversee process development, scale-up ...
Provide strategic guidance to R&D teams on GxP expectations to support downstream GMP manufacturing and regulatory requirements for gene therapy BLAs. * Oversee process development, scale-up ...
Provide strategic guidance to R&D teams on GxP expectations to support downstream GMP manufacturing and regulatory requirements for gene therapy BLAs. * Oversee process development, scale-up ...
Provide strategic guidance to R&D teams on GxP expectations to support downstream GMP manufacturing and regulatory requirements for gene therapy BLAs. * Oversee process development, scale-up ...
... 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 ...
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 ...
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 ...
Strong understanding of biologics workflows, including upstream process development and/or downstream analytics. * Demonstrated ability to engage credibly with scientists, engineers, and operational ...
Strong understanding of biologics workflows, including upstream process development and/or downstream analytics. * Demonstrated ability to engage credibly with scientists, engineers, and operational ...
... downstream processing, and related analytical techniques. * Strong business acumen paired with ... and development prospects. We offer an exciting company culture that stands for integrity ...
... downstream processing, and related analytical techniques. * Strong business acumen paired with ... and development prospects. We offer an exciting company culture that stands for integrity ...
Senior Scientist - Cell Culture & Upstream Process Development
Philadelphia, PA · On-site
$92.30K - $126.10K/yr
Senior Scientist - Cell Culture & Upstream Process Development The success of a company depends on ... with Downstream, Analytical, and Quality teams to align upstream processes with overall CMC ...
Senior Scientist - Cell Culture & Upstream Process Development
Philadelphia, PA · On-site
$92.30K - $126.10K/yr
Senior Scientist - Cell Culture & Upstream Process Development The success of a company depends on ... with Downstream, Analytical, and Quality teams to align upstream processes with overall CMC ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Our department is responsible for the process development and clinical manufacturing of drug ... Extensive DS experience in upstream, downstream, and analytical development for vaccines/biologics ...
Analytical Scientist
Audubon, PA · On-site
Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...
Analytical Scientist
Audubon, PA · On-site
Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...
Analytical Scientist
Audubon, PA · On-site
Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...
Analytical Scientist
Audubon, PA · On-site
Collaborate cross-functionally with upstream/downstream process development, formulation, and quality teams to support CMC development. * Analyze and interpret complex data, provide scientific ...
Design and execute fit-for-purpose early process development studies to generate the foundational data packages required for process lock, comparability assessments, and downstream regulatory filings ...
Design and execute fit-for-purpose early process development studies to generate the foundational data packages required for process lock, comparability assessments, and downstream regulatory filings ...
Design and execute fit-for-purpose early process development studies to generate the foundational data packages required for process lock, comparability assessments, and downstream regulatory filings ...
Design and execute fit-for-purpose early process development studies to generate the foundational data packages required for process lock, comparability assessments, and downstream regulatory filings ...
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 ...
Process Engineer
Lyndora, PA · On-site
Collaborate with other departments to stay up-to-date on the latest technical developments to ... downstream finishing, stamping, tooling, and tubing. We offer an excellent total compensation ...
Process Engineer
Lyndora, PA · On-site
Collaborate with other departments to stay up-to-date on the latest technical developments to ... downstream finishing, stamping, tooling, and tubing. We offer an excellent total compensation ...
Vice President, ESIS Customer Experience (CX) Operations
$139.80K - $179.10K/yr
... with downstream processes. * Manage multiple initiatives and projects concurrently, ensuring ... Familiarity with the system development lifecycle and experience in providing business support for ...
Vice President, ESIS Customer Experience (CX) Operations
$139.80K - $179.10K/yr
... with downstream processes. * Manage multiple initiatives and projects concurrently, ensuring ... Familiarity with the system development lifecycle and experience in providing business support for ...
Downstream Process Development information
What is a Downstream Process Development job?
A Downstream Process Development job involves optimizing and scaling purification processes for biologics, such as proteins, antibodies, or gene therapies. Scientists and engineers in this role develop efficient methods for isolation, purification, and formulation of therapeutic products while ensuring quality and regulatory compliance. Key activities include chromatography, filtration, and process analytics to improve yield, purity, and consistency. This role is critical in biotech and pharmaceutical industries to ensure safe and effective drug production for clinical and commercial use.
What are the key skills and qualifications needed to thrive in the Downstream Process Development position, and why are they important?
To excel in Downstream Process Development, you generally need a strong background in biochemistry, chemical engineering, or a related life sciences field, often with experience in bioprocessing or purification technologies. Familiarity with chromatography systems, filtration equipment, process analytical technology (PAT), and relevant software such as DeltaV or Unicorn is frequently required, along with knowledge of GMP and regulatory standards. Excellent problem-solving, project management, and cross-functional communication skills help professionals succeed in dynamic team environments. These competencies are crucial for developing efficient, scalable purification processes that ensure high product quality and support organizational goals.
What are typical daily responsibilities for someone in Downstream Process Development?
Professionals in Downstream Process Development are typically responsible for designing, optimizing, and scaling up purification processes for biopharmaceutical products. Their day-to-day work may involve conducting laboratory experiments, analyzing data, troubleshooting technical issues, and documenting process changes in accordance with regulatory standards. They also frequently collaborate with upstream processing, analytical, and quality teams to ensure seamless transfer and integration of processes. The role often includes participating in project meetings, contributing to process validation efforts, and supporting technology transfer to manufacturing teams, making it both technically challenging and collaborative.
More about Downstream Process Development jobs
What are the most commonly searched types of Downstream Process Development jobs in Pennsylvania? The most popular types of Downstream Process Development jobs in Pennsylvania are:
What are popular job titles related to Downstream Process Development jobs in Pennsylvania? For Downstream Process Development jobs in Pennsylvania, the most frequently searched job titles are:
- Organic Chemistry Master Degree
- Remote Biologics Manufacturing
- Pharmacokinetic Scientist
- Cell Culture Scientist
- Contract Protein Engineering Scientist
- Work From Home Formulation Scientist
- Director Protein Purification Scientist
- Pharmaceutical Scientist
- Full Time Senior Scientist Virology
- Biochemical Engineering
What job categories do people searching Downstream Process Development jobs in Pennsylvania look for? The top searched job categories for Downstream Process Development jobs in Pennsylvania are:
What cities in Pennsylvania are hiring for Downstream Process Development jobs? Cities in Pennsylvania with the most Downstream Process Development job openings:
Job description
Title: Process Scientist
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
Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.
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