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Internship Downstream Process Development Scientist Jobs in Pelham, NH

Vrtx

Process Dev Engineering Scientist

Boston, MA

$104K - $156K/yr

Vertex is seeking a talented individual to join our Process Development team as a Scientist. The primary focus of this role is to lead and manage the execution of development studies for a cell-based ...

Integrated Resources INC

Biprocess Engineer

Devens, MA · On-site

Process Engineer Scientific: * MS&T organization is seeking to fill a Process Engineer position for ... Prior experience (Ph.D.: 0 - 2 years; BS/MS: 2 - 6 years) in process development, process ...

AT Process Technologies

Process Chemist

Waltham, MA · On-site

$130K - $200K/yr

Summary We are seeking a process development chemist to own and execute the research, development ... Develop and optimize core synthesis and downstream processing, evaluating competing technical ...

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

As of Aug 23, 2026, the average hourly pay for internship downstream process development scientist in Pelham, NH is $40.20, according to ZipRecruiter salary data. Most workers in this role earn between $29.47 and $47.98 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
Infographic showing various Internship Downstream Process Development Scientist job openings in Pelham, NH as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $83,616 per year, or $40.2 per hour.

Senior Process Development Scientist

Sun Pharmaceutical Industries

Billerica, MA

$97K - $132K/yr

Full-time

Posted 13 days ago

Job description

Job Summary

Lead new product formulation, process development, transfers into manufacturing, and continuous improvement of existing processes.

Area Of Responsibility

  • Manage tasks at independent level and contribute to cross-functional project management teams
  • Design experiments using Quality by Design principles, execute and author reports in support of:
  • Formulation, aseptic filling and lyophilization development of new products
  • Continuous improvement, troubleshooting and investigations of existing processes and products
  • Process transfers into manufacturing
  • Perform analytical testing in support of product development studies
  • Prepare cGMP documents such as SOPs, batch records and protocols
  • Design, execute and write technical reports to support FDA filings
  • May direct the work of junior Process Development staff
  • Other duties as assigned

Work Conditions:

  • Office
  • Lab
  • Warehouse
  • Exposure to noise, hazardous and non-hazardous chemicals, syringes and needles, toxic metals

Physical Requirements:

  • Stand, sit, walk, use hands and fingers to handle or feel, reach with arms and hands
  • Talk or hear
  • Close, and color vision; depth perception, ability to adjust focus
  • Use of repetitive motion
  • Operates Lyophilizer, HPLC, pH meter, analytical balance, compressed gas cylinders, fume hoods, heating mantles, stirring equipment, temperature controllers, and computer/office equipment
  • Requires wearing protective clothing in lab areas - lab coat, safety glasses, and gloves
  • Lift up to 50 lbs.

Travel Estimate

Up to 5%

Education and Job Qualification

  • Minimum  B.S. in related scientific field required

Experience

  • Minimum 7-10 years related experience preferred
  • Able to work with external contractors to find new technology, equipment or solutions to process issues
  • Experience with parenteral formulation, lyophilization and sterilization techniques preferred
  • Process validation experience
  • Cleaning validation experience
  • Analytical hands-on experience with techniques such as HPLC, Karl Fischer, DSC, and spectroscopic techniques
  • Experience with aseptic techniques in a clean room environment is highly beneficial
  • Experience working in a cGMP environment
  • Understanding of Quality by Design principles and statistics is preferable
  • Process development experience and manufacturing process investigation skills
  • Strong technical writing skills and resourceful problem solving skills
  • Ability to work independently and as a member of a cross functional team
  • Excellent verbal, written and interpersonal communications skills
  • Strong attention to detail and ability to manage multiple assignments concurrently
  • Able to lead cross functional teams to design experiments and address process issues

 

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