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Internship Downstream Process Development Scientist Jobs in Rochester, NH

Lonza

MSAT Associate Principal Engineer

Portsmouth, NH · On-site

... science and technology functions, including biotech processes, process development, scale-up, tech transfer, and manufacturing. * Proven knowledge of aseptic techniques and cell culture. * Experience ...

Standex International

Process Engineer

Concord, NH · On-site

... and scientific refrigeration. We work with our customers to advance progress through innovation ... Work closely with R&D, production, and quality assurance teams to ensure seamless integration of ...

Lydall, Inc.

Development Engineer

Rochester, NH · On-site

... assist in process improvements, both within Lydall, and externally at our customers/suppliers ... science considered. • Five to seven years of industrial experience. • Normal travel ...

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$37

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

As of Jul 13, 2026, the average hourly pay for internship downstream process development scientist in Rochester, NH is $37.84, according to ZipRecruiter salary data. Most workers in this role earn between $27.74 and $45.19 per hour, depending on experience, location, and employer.

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.

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.
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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Rochester, NH as of July 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $78,708 per year, or $37.8 per hour.
Manufacturing Associate level 2 - Nights

Manufacturing Associate level 2 - Nights

Lonza

Portsmouth, NH • On-site

Full-time

Medical, Dental, Vision

Posted 14 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

23rd of 74 rated pharmaceutical

Job description

Job Title: Manufacturing Associate II (Nights)
Location: Portsmouth, NH, (On-site)
As a Manufacturing Associate II, you will support the production of therapeutic proteins in a cGMP manufacturing environment, operating equipment, performing laboratory testing, and executing production processes that help deliver life-changing therapies to patients. This hands-on role requires strong attention to detail, problem-solving skills, and a commitment to quality, safety, and continuous improvement.
This role follows a 12-hour day shift schedule from 7:00 PM to 7:00 AM on a rotating schedule of alternating days: two on, two off, three on, two off, two on, three off (repeating cycle).
What you will get
  • Competitive pay and performance-based compensation
  • Medical, dental, and vision insurance
  • A supportive and inclusive work environment
  • Opportunities for career growth and development
  • Hands-on training and skill-building
  • A dynamic and team-focused workplace

What you will do
  • Operate manufacturing equipment and execute downstream production processes in accordance with cGMP requirements
  • Set up, monitor, and support process equipment, including Clean-in-Place (CIP) and Steam-in-Place (SIP) operations
  • Perform laboratory activities, including pH testing, conductivity testing, and product sampling
  • Transfer materials and chemicals safely throughout manufacturing areas
  • Complete production documentation, batch records, and electronic records following Good Documentation Practices (GDP)
  • Support equipment troubleshooting, routine sanitization activities, and 6S initiatives
  • Participate in shift handovers, team meetings, training activities, and continuous improvement projects

What we are looking for
  • High school diploma or equivalent required; Associate's or Bachelor's degree in a science-related field preferred
  • Manufacturing experience preferred; cGMP or biopharmaceutical experience is a plus
  • Experience working in upstream and/or downstream manufacturing environments preferred
  • Strong problem-solving, critical thinking, and decision-making skills
  • Ability to follow procedures and maintain accurate documentation
  • Strong written and verbal communication skills
  • Ability to work a rotating 12-hour day shift schedule in a team-based manufacturing environment

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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