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Internship Downstream Process Development Scientist Jobs in Randolph, MA

Eurofins

mRNA Process Development Scientist

Boston, MA · On-site

$32 - $41/hr

We are seeking a process development scientist to join the messenger-RNA (mRNA) process development team. The successful candidate will be contributing to early and operational tech development. In ...

CEDENT

Senior Scientist, Process Development

Watertown, MA

$99K - $135K/yr

We are seeking a Senior Scientist, Process Development, responsible for executing cell culture experiments, downstream processing, analyzing data, and contributing to process development projects.

Managed Staffing

Purification Scientist

Boston, MA · On-site

$44 - $46/hr

Monday-Friday | 8:00 AM-5:00 PM (40 hrs/week Position Summary Seeking an early-career Biologist / Purification Scientist to join the Downstream Process Development team in Boston, MA. This role will ...

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How much do internship downstream process development scientist jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for internship downstream process development scientist in Randolph, MA is $39.42, according to ZipRecruiter salary data. Most workers in this role earn between $28.94 and $47.07 per hour, depending on experience, location, and employer.

What does an internship downstream process development scientist do?

An Internship Downstream Process Development Scientist works in the biopharmaceutical industry, assisting with the development and optimization of processes that purify biological products such as proteins, antibodies, or vaccines after they are produced by cells. Their role often involves supporting laboratory experiments, analyzing samples, and documenting results to improve the efficiency and scalability of downstream processes like filtration and chromatography. Interns in this position gain hands-on experience with cutting-edge technologies and learn about regulatory requirements and industry standards. This role helps prepare students or recent graduates for a career in process development or biomanufacturing.

What types of projects and responsibilities can an internship downstream process development scientist expect to work on?

As an Internship Downstream Process Development Scientist, you can expect to be involved in hands-on laboratory work focusing on the purification and characterization of biopharmaceutical products. Typical responsibilities include preparing buffer solutions, operating chromatography and filtration systems, analyzing samples using various analytical techniques, and documenting experimental results. Interns often collaborate with experienced scientists and engineers, contributing to process optimization and troubleshooting. The role provides valuable exposure to industry-standard procedures and the opportunity to develop technical skills in a team-oriented environment.

What are the key skills and qualifications needed to thrive as an internship downstream process development scientist, and why are they important?

To thrive as an Internship Downstream Process Development Scientist, you need foundational knowledge in biochemistry, molecular biology, or chemical engineering, often supported by ongoing or recent enrollment in a relevant degree program. Familiarity with laboratory techniques such as chromatography, filtration, and analytical instruments, as well as experience with lab management software, is typically expected. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills in this role. These skills and qualifications are crucial for conducting reliable experiments, analyzing data, and contributing to the optimization of bioprocesses in a collaborative research environment.

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Internship Downstream Process Development Scientist jobs near you

Head of Downstream BioProcess Development (Sr. Director)

Takeda Pharmaceutical Company Limited

Lexington, MA • On-site

Full-time

Re-posted 10 days ago

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical

Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
About the role:
You will lead the Biotherapeutics Downstream Process Development function, directing a multidisciplinary team of scientists and engineers who develop and characterize purification processes for biotherapeutics across early- and late-stage assets. You will oversee internal development work and external partners, including contract development and manufacturing organizations, to ensure project deliverables, timelines, and quality expectations are met. You will manage preparation and approval of CMC sections for global regulatory submissions and lead responses to regulatory questions. You will drive rapid, phase-appropriate early-stage development toward Investigational New Drug (IND) applications using platform strategies, maintain a strong external presence to bring scientific advances and efficiency into the organization, and contribute to Pharmaceutical Sciences-wide initiatives that shape development strategy and long-term technical priorities.
How you will contribute:
  • Lead and develop a multidisciplinary team responsible for purification process development and characterization for monoclonal antibodies, fusion proteins, and related biologic modalities across discovery, preclinical, clinical, and commercial phases.
  • Serve on the biotherapeutics process development leadership team to set technical strategy, coordinate priorities across programs, and support decisions that advance the portfolio.
  • Work closely with upstream, analytical, and drug product development organizations to align activities, reduce handoffs, and streamline process development to accelerate time to market.
  • Contribute to Pharmaceutical Sciences-wide initiatives, collaborating with peers across development, manufacturing, quality, and regulatory groups to drive standardization, platform improvements, and capability building.
  • Oversee downstream development activities conducted internally and at contract development and manufacturing organizations to ensure project deliverables, timelines, and transfer readiness.
  • Manage preparation, review, and approval of chemistry, manufacturing, and controls sections for global regulatory submissions and coordinate timely responses to agency questions.
  • Drive rapid, phase-appropriate development to Investigational New Drug applications using platform process strategies and risk-based decision making.
  • Lead technology transfer, scale-up, process characterization, and validation efforts to enable reliable manufacture at scale.
  • Ensure adherence to Good Manufacturing Practices and quality systems across internal teams and external partners.
  • Cultivate and leverage external scientific and industry networks, partnerships, and vendors to introduce new approaches, efficiencies, and best practices.
  • Mentor and develop leaders and scientists within the team and influence partners and senior leadership on downstream strategy.

Skills and qualifications:
  • Ten or more years of industry experience in biologics downstream process development with progressive leadership responsibility; advanced degree in biochemical engineering, chemical engineering, biochemistry, chemistry, or a related discipline required; doctoral degree preferred.
  • Demonstrated experience collaborating with partner organizations to streamline development activities and shorten time to market.
  • Demonstrated experience preparing and approving chemistry, manufacturing, and controls sections for global regulatory submissions and responding to regulatory agency queries.
  • Proven track record managing external development and manufacturing partners, including contract development and manufacturing organizations, and overseeing technology transfer and scale-up.
  • Deep technical expertise in downstream purification platform technologies, including chromatography and filtration, process characterization, viral clearance strategy, and product quality attributes.
  • Experience driving early-stage development to IND applications using phase-appropriate, platform-based approaches and risk-based development strategies.
  • Experience serving on process development or biotherapeutics leadership teams and contributing to organization-wide Pharmaceutical Sciences initiatives that enable standardization and capability growth.
  • Strong leadership skills with experience building, mentoring, and retaining high-performing, diverse teams and influencing cross-functional partners and senior leadership.
  • Established external scientific presence and professional network used to source new approaches, collaborations, and efficiency gains.
  • Working knowledge of Good Manufacturing Practices, quality systems, process validation, and regulatory requirements for clinical and commercial biologics manufacturing.
  • Experience using AI-enabled tools (for example, for experiment planning, data analysis, or knowledge search) alongside automation and digital tools to improve process consistency and reproducibility.
  • Clear written and verbal communication skills with experience drafting technical sections of regulatory filings and presenting technical strategy to senior leadership and external audiences.

As a strategic leader overseeing multiple functional areas, divisions, or product groups through directors and managers, with global or multi-country-level responsibility. You will shape corporate policies, provide guidance to directors and senior managers, and hold a recognized influential position. Your decisions impact the success of the division, group, company, or corporation, and you may sit on a leadership team, directly influencing the overall business strategy of your area.
This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.
Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Lexington, MA
U.S. Base Salary Range:
$212,000.00 - $333,190.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
For information about our benefits, please click here.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Lexington, MA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

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Headquarters location

San Diego, CA, US

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