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Internship Downstream Process Development Scientist Jobs in Watertown, CT

PTA Plastics

Sr. Process Engineer

Oxford, CT · On-site

$120K - $135K/yr

Develop and optimize injection molding processes for new and existing molds using scientific molding principles. * Lead mold sampling, process development, validation activities, and production ...

PTA Plastics

Sr. Process Engineer

Oxford, CT · On-site

$120 - $135/hr

Develop and optimize injection molding processes for new and existing molds using scientific molding principles. * Lead mold sampling, process development, validation activities, and production ...

IDEX

Director of Process Engineering

Farmington, CT · On-site

$158.60 - $237.80/hr

The Director of Process Engineering leads the development, optimization, and scale‑up of ... sciences and industrial applications. Total Rewards The compensation range for this position is ...

Danaher

R&D Internships

Danbury, CT

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Danaher

R&D Internships

Waterbury, CT · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Danaher

R&D Internships

Waterbury, CT

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Danaher

R&D Internships

Hamden, CT · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

Danaher

R&D Internships

Danbury, CT · On-site

By submitting your interest, you'll be among the first to know when internship opportunities open ... You'll work in a collaborative environment alongside experienced scientists and contribute to real ...

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Internship Downstream Process Development Scientist information

See Watertown, CT salary details

$20

$37

$59

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 Watertown, CT is $37.57, according to ZipRecruiter salary data. Most workers in this role earn between $27.55 and $44.86 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.

What are popular job titles related to Internship Downstream Process Development Scientist jobs in Watertown, CT?

For Internship Downstream Process Development Scientist jobs in Watertown, CT, the most frequently searched job titles are:

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

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Internship Downstream Process Development Scientist jobs near you
Infographic showing various Internship Downstream Process Development Scientist job openings in Watertown, CT as of July 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $78,155 per year, or $37.6 per hour.

Development Scientist II, Analytical Development and Clinical QC (ADQC)

AstraZeneca

New Haven, CT • On-site

Full-time

Re-posted 5 days ago

AstraZeneca rating

8.4

Company rating: 8.4 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

23rd of 86 rated pharmaceutical

Job description

This is what you will do: This Development Scientist II will be a key team member in Alexion's External Analytical Development and Quality Control group. This position is responsible for maintaining the highest standard of quality and compliance of external quality control testing (GMP) laboratories. This candidate will be responsible for initiation and ownership of laboratory investigations (LIRs) through strong liaison with external contract laboratories and change controls relevant to ADQC biologic programs.

The candidate will ensure timely, compliant, and high-quality delivery for LIR closure to enable the generation of final release CoAs.The role will work closely with internal Quality Assurance, Compliance, Analytical Development and Stability teams to ensure product to patients. You will be responsible for: Responsible for generating and/or mirroring, reviewing, providing assessments, and driving ownership of LIRs to close out Out-of-Specification (OOS), Out-of-Trend (OOT), and atypical results with structured root cause analysis, impact assessment, and/or corrective/preventive actions (CAPAs). Design investigational testing plans ensuring compliant closure of all testing related investigations within the quality system

Lead and/or facilitate cross-functional meetings with quality assurance to ensure structured investigation alignment. Create plans, track, and present timelines to meet established targets, goals, and objectives. Perform review of analytical data to ensure expected assay performance.

Identify opportunities for improvement in systems and make recommendations for effective changes to ensure compliance with cGMP. Strong presentation skills You will need to have: A successful candidate will have strong mentalacuity with high attention to detail and ability tomaintainaccuracy in documentation and processes. Excellent analytical and problem-solving skills with the ability to conduct risk assessments and root cause analysis.

A broad knowledge of Pharmaceutical Quality Assurance, regulatorycompliance,and/or quality control inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations. Strongproficiencyin quality management systems and effective communication skills for interacting with cross-functional teams. Strong proficiency with MS Word, Excel, PowerPoint.

Ability tobend, reach and stand,withliftingto15poundsand carrying over short distances. Ability to travel up to 10%, if needed. Advanced (M.S

or Ph.D.) degree in Biochemistry, Chemistry or related discipline with 2-5 years (Ph.D.) or 10+ (M.S.) hands on biological analytical development experience in pharmaceutical industry. We would prefer you to have: Working knowledge in validated documentation systems: Veeva Vault (EQV), LIMS, ValGenesis, Kneat, etc. Knowledge of pharmaceutical/biotechnology manufacturing process Database management /statistical analysis(e.g., JMP,Tableau, SAS) with proficiency in Microsoft SharePoint and/or BOX

Date Posted 09-Aug-2026 Closing Date 03-Sep-2026 Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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About AstraZeneca

Sourced by ZipRecruiter

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious diseases. But we're more than one of the world's leading pharmaceutical companies. A place built on courage, curiosity and collaboration - we make bold decisions driven by patient outcomes. Empowered to lead at every level, free to ask questions and take smart risks that write the next chapter for our pipeline and Oncology team. Make a meaningful impact that brings real benefits to society. By applying your knowledge of data, you will help to redefine our industry and ultimately save lives. Work with experts who share a common goal: to accelerate the potential of medicines and the science of tomorrow.

Industry

Pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Cambridge, Cambridgeshire, GB

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