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Internship Downstream Process Development Scientist Jobs in Concord, NH

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Internship Downstream Process Development Scientist information

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

As of Aug 29, 2026, the average hourly pay for internship downstream process development scientist in Concord, NH is $38.92, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $46.44 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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For Internship Downstream Process Development Scientist jobs in Concord, NH, the most frequently searched job titles are:

What job categories do people searching Internship Downstream Process Development Scientist jobs in Concord, NH look for?

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What cities near Concord, NH are hiring for Internship Downstream Process Development Scientist jobs?

Cities near Concord, NH with the most Internship Downstream Process Development Scientist job openings:

Infographic showing various Internship Downstream Process Development Scientist job openings in Concord, NH as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 11% Part Time, 7% Temporary, and 3% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $80,949 per year, or $38.9 per hour.

Scientist II PharmDev Analytical

Bedford, NH • On-site

$90 - $120/hr

Other

Posted 13 days ago


Job description

## Scientist II PharmDev AnalyticalApplylocations: Bedford, NH, USAtime type: Full timeposted on: Posted Todayjob requisition id: JR116482Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.**We are PCI.**Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.**Summary of Objective:**The Scientist II position is a key collaborator of the Analytical Development team in Pharmaceutical Development department within a fast-paced, expanding CDMO. This job will require both support and leadership in hands-on experimentation, testing, and strategic project management to support clients.**Essential Duties and Responsibilities:*** Leads Analytical Development activities to support projects for various modalities, serving as the technical lead and SME for analytical methods development and testing.* Supports more complex formulation and process development projects as an Analytical Development SME, working with a senior scientist to achieve project milestones.* Executes method development and transfer to achieve project milestones without supervision.* Develops and implements phase-appropriate analytical method development strategies aligned with program objectives and regulatory expectations.* Acts as an Analytical Development representative on internal and client-facing project calls, providing technical updates and strategic input.* Demonstrates proficiency in method development for both small molecules and biologics, analytical data interpretation and trending.* Develops and optimizes analytical methods to support formulations development for high-potency compounds, including antibody-drug conjugates (ADCs) and other complex modalities.* Drives analytical methods transfer activities to QC and provides supports in scale-up or manufacturing process transitions as an analytical development SME.* Performs analytical testing within Pharmaceutical Development laboratory to support formulation and process development, such as HPLC/UPLC, Capillary Electrophoresis, UV-Vis spectroscopy, FlowCam, Karl Fischer titration, DSC/FDM, and other related assays to confirm acceptance criteria as part of formulation development activities.* Provides training on analytical methods execution for formulation and process development scientists.* Troubleshoots analytical methods challenges and proposes scientifically sound corrective actions.* Responsible for proper maintenance, calibration, and cleanliness of laboratory instruments and equipment.* Performs or assists in routine facilities cleaning and equipment upkeep as required.* Authors and reviews Analytical Development records, protocols, and reports to ensure technical accuracy and compliance with quality standards and client demand.* Reviews executed documentation for accuracy and completeness prior to submission to management.* Drafts and maintains Standard Operating Procedures (SOPs) and related controlled documents for Pharmaceutical Development operations.* Provides technical guidance and mentorship to junior scientists and laboratory staff.* Drives analytical methods transfer activities to QC and provides supports in scale-up or manufacturing process transitions as an analytical development SME.## **Qualifications:** **EDUCATION/EXPERIENCE:*** Advanced Degree in (PhD) in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, Biochemistry, or other related fields with 0-3 years’ experience in pharmaceutical development or CDMO industry.* MS/BS in Pharmaceutical Sciences, Chemistry, Analytical Chemistry, Biochemistry, or other related fields with 3/5+ years’ experience in pharmaceutical development or CDMO industry.* A strong foundation in clinical-phase development and analytical characterization of drug products, including biologics and other complex modalities.* In-depth knowledge of biopharmaceutical and/or medical product regulation, analytical methods development for small and large molecules.* Experience with MS Office (Word/Excel/Teams/PowerPoint/SharePoint), SmartSheets, LabX, and Empower. **QUALITIES:*** Detail oriented and a results-driven team player* Ability to work in a dynamic, fast-paced work environment* Honesty, integrity, respect and courtesy with all colleagues* Creative with the ability to work with minimal supervision and balance with independent thinking* Resilient through operational and organizational change#LI-AK2Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future #J-18808-Ljbffr