... upstream processes. The successful candidate will bring deep expertise in microbial genetics ... Partner with process development, analytical development, downstream purification, informatics ...
... upstream processes. The successful candidate will bring deep expertise in microbial genetics ... Partner with process development, analytical development, downstream purification, informatics ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
... upstream processes. The successful candidate will bring deep expertise in microbial genetics ... Partner with process development, analytical development, downstream purification, informatics ...
... upstream processes. The successful candidate will bring deep expertise in microbial genetics ... Partner with process development, analytical development, downstream purification, informatics ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
You will gain valuable experience in applied research, process optimization, and customer-focused innovation, contributing to the development of innovative upstream processes. *Onsite role based at ...
Process Development Scientist New England
Burlington, MA · On-site
$77K - $116K/yr
The Process Development Scientist is part of a worldwide team of engineers and scientists reporting ... Sound understanding of upstream and/or downstream biomanufacturing process requirements, best ...
New
Process Development Scientist New England
Burlington, MA · On-site
$77K - $116K/yr
The Process Development Scientist is part of a worldwide team of engineers and scientists reporting ... Sound understanding of upstream and/or downstream biomanufacturing process requirements, best ...
New
Collaborate with process development scientists to translate laboratory findings into scalable ... Demonstrate expertise in upstream process operations at all scales. * Lead root cause analysis (RCA ...
New
Collaborate with process development scientists to translate laboratory findings into scalable ... Demonstrate expertise in upstream process operations at all scales. * Lead root cause analysis (RCA ...
New
Engineer, Biologics Purification, Upstream/Downstream/Tech Transfer - Remote (JP15407)
Cambridge, MA · On-site +1
$34 - $37/hr
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at ... The Engineer will apply upstream and downstream process engineering knowledge in support of ...
Quick apply
Engineer, Biologics Purification, Upstream/Downstream/Tech Transfer - Remote (JP15407)
Cambridge, MA · On-site +1
$34 - $37/hr
Seeking a Process Development Engineer to join the Drug Substance Technology Engineering team at ... The Engineer will apply upstream and downstream process engineering knowledge in support of ...
D: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process validation or manufacturing support in bioprocessing (upstream and/or downstream) - Preferred: Prior experience scaling up ...
D: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process validation or manufacturing support in bioprocessing (upstream and/or downstream) - Preferred: Prior experience scaling up ...
D.: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process validation or manufacturing support in bioprocessing (upstream and/ or downstream) * Preferred: Prior experience scaling up ...
D.: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process validation or manufacturing support in bioprocessing (upstream and/ or downstream) * Preferred: Prior experience scaling up ...
Principal Scientist, Drug Substance Process Development & Manufacturing (mAB development focus)
Somerville, MA · Hybrid
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
Principal Scientist, Drug Substance Process Development & Manufacturing (mAB development focus)
Somerville, MA · Hybrid
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
Principal Scientist, Drug Substance Process Development & Manufacturing (mAB development focus)
Somerville, MA · On-site
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
Principal Scientist, Drug Substance Process Development & Manufacturing (mAB development focus)
Somerville, MA · On-site
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
The Vertex Process Development team offers a dynamic, fast-paced, and highly collaborative ... Familiarity with biologics upstream and downstream processes. * Strong data analysis, technical ...
The Vertex Process Development team offers a dynamic, fast-paced, and highly collaborative ... Familiarity with biologics upstream and downstream processes. * Strong data analysis, technical ...
Biologics Drug Product Process Development Scientist (Contract)
Boston, MA · On-site
$55 - $60/hr
The Vertex Process Development team offers a dynamic, fast-paced, and highly collaborative ... Familiarity with biologics upstream and downstream processes. * Strong data analysis, technical ...
Biologics Drug Product Process Development Scientist (Contract)
Boston, MA · On-site
$55 - $60/hr
The Vertex Process Development team offers a dynamic, fast-paced, and highly collaborative ... Familiarity with biologics upstream and downstream processes. * Strong data analysis, technical ...
Senior Associate Scientist (EG90 Lvl2), LNP Process Development Bristol Myers Squibb is on a ... both upstream and downstream unit operations(i.e. QbD principles, DoE) * Contribute to the ...
Senior Associate Scientist (EG90 Lvl2), LNP Process Development Bristol Myers Squibb is on a ... both upstream and downstream unit operations(i.e. QbD principles, DoE) * Contribute to the ...
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
New
The position offers broad exposure across upstream and downstream operations, CDMO management, and quality systems. Here's how you will contribute: * Support Drug Substance process development and ...
New
Senior Associate Scientist (EG90 Lvl2), LNP Process Development Bristol Myers Squibb is on a ... both upstream and downstream unit operations(i.e. QbD principles, DoE) * Contribute to the ...
Senior Associate Scientist (EG90 Lvl2), LNP Process Development Bristol Myers Squibb is on a ... both upstream and downstream unit operations(i.e. QbD principles, DoE) * Contribute to the ...
Senior Engineer II, mRNA Process Development
$140K - $150K/yr
... processes for our gene editing mRNA therapeutics. You will bridge the gap between research ... Lead the development, optimization, and scale-up of upstream and downstream unit operations for ...
Senior Engineer II, mRNA Process Development
$140K - $150K/yr
... processes for our gene editing mRNA therapeutics. You will bridge the gap between research ... Lead the development, optimization, and scale-up of upstream and downstream unit operations for ...
Process Engineer, Pharmaceutical
Boston, MA · On-site
$120K - $130K/yr
We're hiring a Process Development Sales Engineer to work with industrial customers to support the ... Examples may include: • Upstream bioprocess modeling (cell culture, microbial fermentation ...
Quick apply
Process Engineer, Pharmaceutical
Boston, MA · On-site
$120K - $130K/yr
We're hiring a Process Development Sales Engineer to work with industrial customers to support the ... Examples may include: • Upstream bioprocess modeling (cell culture, microbial fermentation ...
Senior Engineer II, mRNA Process Development
South Boston, MA · On-site
$140K - $150K/yr
... processes for our gene editing mRNA therapeutics. You will bridge the gap between research ... Lead the development, optimization, and scale-up of upstream and downstream unit operations for ...
Senior Engineer II, mRNA Process Development
South Boston, MA · On-site
$140K - $150K/yr
... processes for our gene editing mRNA therapeutics. You will bridge the gap between research ... Lead the development, optimization, and scale-up of upstream and downstream unit operations for ...
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?
- Senior Associate Scientist
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- Senior Principal Research Scientist
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- Principal Scientist Immunology
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- Cell Culture Process Development
- Associate Scientist Algae Research
- Seasonal Senior Scientist Virology

Principal Scientist, Process Development (Expression Systems)
Norwood, MA • On-site
Full-time
Medical, PTO
Re-posted 24 days ago
Moderna rating
8.9
Based on 9 frontline employees who took The Breakroom Quiz
7th of 74 rated pharmaceutical
Job description
The Role
Moderna is seeking an Individual to lead host strain, vector, and expression system strategy for E. coli-based production of recombinant enzymes, plasmids, and related biological materials supporting Moderna's technology platforms and pipeline programs.
This role owns the front end of microbial production: designing, building, screening, and selecting host/vector/expression systems that enable high-performing, scalable, and robust upstream processes.
The successful candidate will bring deep expertise in microbial genetics, molecular biology, expression-system design, screening workflows, data-driven construct selection, and translation of small-scale screening outputs into process-development-ready leads.
Here's What You'll Do
- Own the strategy for E. coli host strain, vector, and expression-system for recombinant enzymes, plasmids, and related biological materials.
- Design and execute screening cascades that identify production candidates with strong titer, yield, quality, genetic stability, robustness, and process-development potential.
- Define stage-appropriate decision criteria for host/vector selection, expression tuning, induction strategy, plasmid stability, growth, product quality, and manufacturability.
- Develop and optimize small-scale and high-throughput screening workflows, including shake flask, deep-well plate, ambr, or other scale-down systems where appropriate.
- Evaluate host strains, promoters, ribosome binding sites, copy number, plasmid architecture, induction systems, codon/design strategies, secretion or localization strategies where relevant, and expression timing.
- Use DOE and data-driven approaches to improve screening throughput, predictiveness, reproducibility, and translation to bioreactor performance.
- Lead or support strain and vector engineering to improve expression performance, stability, productivity, robustness, and manufacturability.
- Apply molecular biology, microbial physiology, and synthetic biology principles to troubleshoot poor expression, instability, toxicity, metabolic burden, inclusion body formation, degradation, or inconsistent performance.
- Define fit-for-purpose characterization and handoff packages for candidate strains and constructs, including strain/vector history, design rationale, screening data, stability observations, known risks, and recommended development paths.
- Partner with process development, analytical development, downstream purification, informatics, automation, and data science teams to ensure screening outputs are actionable and linked to relevant quality and process attributes.
- Develop platform approaches and standardized documentation, data capture, decision criteria, and knowledge-management practices for recurring enzyme, plasmid, or microbial production needs.
- Support cross-functional troubleshooting, technical reports, development summaries, CMC-supporting documentation, and regulatory responses as needed.
- Serve as a technical leader and mentor in microbial genetics, molecular biology, expression-system design, screening strategy, and data interpretation.
Here's What You'll Need (Basic Qualifications)
- PhD in Molecular Biology, Microbiology, Chemical/Biochemical Engineering, Biotechnology, Synthetic Biology, or a related discipline with 5+ years of relevant industry experience; or MS with 10+ years; or BS with 12+ years of relevant industry experience.
- Substantial industry experience with E. coli strain engineering, vector design, expression-system development, or microbial production screening.
- Hands-on expertise developing and executing microbial expression-screening workflows for recombinant proteins, enzymes, plasmids, or related biological products.
- Strong understanding of E. coli genetics, physiology, metabolism, plasmid biology, expression regulation, and genetic stability.
- Experience designing and interpreting experiments that connect host/vector/expression choices to titer, yield, quality, robustness, and manufacturability.
- Experience with small-scale or high-throughput screening systems and translation of screening data into process-development decisions.
- Demonstrated ability to lead complex technical projects, influence stakeholders across functions, and communicate clearly through technical writing, data analysis, and presentations.
Here's What You'll Bring to the Table (Preferred Qualifications)
- Direct experience developing E. coli expression systems for recombinant enzymes and/or plasmid production.
- Experience with strain engineering, promoter/RBS libraries, plasmid copy-number optimization, induction-system tuning, codon/design strategies, secretion/localization approaches, or protein solubility optimization.
- Experience building screening cascades that balance speed, throughput, biological relevance, and scale translation.
- Working knowledge of fermentation process development, downstream interfaces, and analytical methods used to assess expression, identity, purity, activity, plasmid quality, host-cell impurities, nucleic acid burden, or product-related impurities.
- Experience supporting CMC-facing documentation, technical reports, regulatory questions, and operation as either a senior technical individual contributor or manager of a small technical team.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.
Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
Family planning benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investment opportunities to help you plan for the future
Location-specific perks and extras
About Moderna
Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.
Our Working Model
As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.
Moderna is a smoke-free, alcohol-free, and drug-free work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!
Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.
Accommodations
We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com.
Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-TR2-
About Moderna
Sourced by ZipRecruiter
In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.
Industry
Manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Cambridge, MA, US
Year founded
2010