Top 57 Scientist process development Jobs in New Haven, Ct

Scientist II, LC Development, Biologics Analytical Development
AstraZeneca —New Haven, CT
- Bachelor of Science
- Mid-level
- Analysis skills
Scientist Technical Performance Insights Sensory Testing
Henkel —Trumbull, CT
- $75,000 - $85,000 a year
- Full-time
- Hybrid work
- Bachelor's degree
- Home Health
- Older adults
- Paid holidays
- Health insurance
Quick Apply
Scientist II, LC Development, Biologics Analytical Development
Alexion Pharmaceuticals,Inc. —New Haven, CT
- Bachelor of Science
- Mid-level
- Analysis skills
Staff Scientist, Research Core
Yale University —New Haven, CT
- $68,000 - $120,500 a year
- Full-time
- Background check
- Mid-level
- Windows
Scientist III, Injectable Drug Product Development
Alexion Pharmaceuticals,Inc. —New Haven, CT
- Microsoft Word
- 5 years
- Bachelor of Science
10d
Staff Scientist, Cleanroom
Yale University —New Haven, CT
- $92,000 - $146,750 a year
- Full-time
- Hybrid work
- Background check
- 5 years
- Master's degree
Scientist III, Injectable Drug Product Development
AstraZeneca —New Haven, CT
- Microsoft Word
- 5 years
- Bachelor of Science
10d
Staff Scientist II
Yale University —New Haven, CT
- $68,000 - $120,500 a year
- Full-time
- Background check
- Bachelor of Science
- Bachelor's degree
Development Scientist III, Analytical Development and Clinical Quality Control
Alexion Pharmaceuticals,Inc. —New Haven, CT
- $138,392 - $207,590 a year
- Overtime
- Microsoft Outlook
- Management
- Master's degree
- Paid holidays
- Health insurance
DMPK Scientist
Arvinas, Inc. —New Haven, CT
- Office
- Analysis skills
- Doctor of Philosophy
- Health insurance
- Dental insurance
Associate Director, R&D Product Development, Wellbeing Collective
Unilever —Trumbull, CT
- $146,200 - $219,400 a year
- Full-time
- Background check
- 7 years
- Bachelor of Science
- Paid holidays
- Disability insurance
Product Support Scientist
Bio-Techne —Wallingford, CT
- $81,900 - $134,550 a year
- Full-time
- 5 years
- Master's degree
- Continuous improvement
- Paid parental leave
- Health savings account
Computational Social Scientist
Yale University —New Haven, CT
- $92,000 - $146,750 a year
- Full-time
- Hybrid work
- Background check
- Azure
- Mid-level
Research Associate 1, MS
Yale University —New Haven, CT
- $61,500 - $91,875 a year
- Weekends as needed
- Background check
- Current TB test
- Internal Medicine
Research Assoicate 2
Yale University —New Haven, CT
- $68,000 - $120,500 a year
- Full-time
- Background check
- Mid-level
- 3 years
Project Manager, Clinical Trials
Cogstate —New Haven, CT
- $105,000 - $120,000 a year
- Full-time
- Remote
- Computer Science
- Master's degree
- Psychology
- Paid holidays
- Disability insurance
Quick Apply
Applications Specialist
Elements Solutions Inc —Shelton, CT
- $95,406 - $143,108 a year
- Master's degree
- Continuous improvement
- Doctor of Philosophy
- Wellness program
- Paid parental leave
Design & Technology Manager
Unilever —Trumbull, CT
- $103,000 - $154,400 a year
- Full-time
- Background check
- Pass drug screening
- 8 years
- Paid holidays
- Disability insurance
Instructional Lab Support Specialist - Physics
Yale University —New Haven, CT
- $68,000 - $120,500 a year
- Weekends as needed
- Background check
- Laboratory
- Word processing
Associate Director, Analytical Development and Clinical QC
AstraZeneca —New Haven, CT
- 8 years
- Doctor of Philosophy
- Mentoring

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scientist process development jobs near new haven, ct

Scientist II, LC Development, Biologics Analytical Development

AstraZeneca -
New Haven, CT

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Job Details

Qualifications

Instrumentation troubleshooting
Records maintenance
Content creation for technical audiences
Personal protective equipment (PPE) use
Technical documentation
High-performance liquid chromatographs
Protein analysis (analytical chemistry specialty)
Technical report writing
Data integrity and documentation
Laboratory reports
Biochemical laboratory techniques
Pharmaceutical analysis
Hazardous material handling
Mass spectrometers (MS)
Regulatory submission editing and review
Technical troubleshooting support
GMP for research safety and compliance
Laboratory compliance and regulatory documentation
Research compliance quality assurance records management
Scientific reports

Full Job Description

Location New Haven, Connecticut, United States Job ID R-252034 Date posted 22/06/2026

Are you ready to elevate chromatographic science to accelerate life-changing biologics for people with the greatest unmet need? In this role, you will develop and optimize robust LC methods that define product quality for complex therapeutic proteins, enabling confident decisions from early development through commercialization.

You will join a high-energy analytical development team that partners closely with Research & Development, Manufacturing, Quality Assurance and Quality Control. Your methods will drive release and stability strategies, resolve investigations, and strengthen regulatory submissions—turning scientific rigor into meaningful progress for patients. Could your next method power a pivotal study or unlock a critical root cause?

Accountabilities:

Chromatography Method Development:

Build, optimize, and phase-appropriately qualify custom (U)HPLC methods (SEC, RP, ion exchange, HIC) to monitor critical quality attributes for therapeutic proteins with a focus on fitness for purpose and lifecycle readiness.

Instrumentation Ownership:

Independently operate, maintain, and troubleshoot UPLC/HPLC systems and detectors (UV, FL, ELSD, CD) to increase reliability, throughput, and data integrity in a cGMP setting.

Method Qualification, Transfer, and Troubleshooting:

Plan and implement method qualification, validation, and transfer to internal and external laboratories; diagnose and resolve performance issues to ensure successful adoption and sustainable performance.

Analytical Testing and Investigations:

Perform phase-appropriate testing to support release and stability, contribute to characterizations and investigations, and translate findings into clear, actionable recommendations.

Technology Innovation:

Evaluate and implement new instruments, methods, and platforms to improve analytical capability and efficiency; introduce fit-for-purpose technologies that improve speed and insight.

Regulatory and Documentation Excellence:

Author SOPs, study plans, protocols, development reports, and draft content that supports regulatory submissions, ensuring clarity, traceability, and compliance.

Cross-Functional Collaboration:

Partner with R&D, Manufacturing, QA and QC to align analytical deliverables with program needs, enable process understanding, and support decision-making across development stages.

Scientific Leadership:

Stay current with evolving scientific principles and regulatory expectations; apply emerging knowledge to solve analytical problems and mentor standard methodologies within the team.

Essential Skills/Experience:

M.S. degree in Chemistry, Biochemistry, or a related biological science with 3+ years of relevant industry experience (or B.S. degree with 5+ years of experience)
Hands-on experience with (U)HPLC and practical knowledge of method development and optimization for protein therapeutics
Ability to take initiative in problem solving and apply an independent, scientific approach to method development and troubleshooting.
Ability to contribute technical content to regulatory submissions related to analytical sections.
Hands-on experience with LC systems from multiple vendors (e.g., Waters, Thermo Fisher), with strong proficiency in chromatography data systems (CDS) such as Empower and Chromeleon.
Experience developing and optimizing chromatographic methods for protein heterogeneity, aggregation, and degradation pathways.
Ability to organize and complete work independently with minimal direction.
Travel may be required on an as‑needed basis to support training and troubleshooting.
Ability to work in a laboratory environment, including performing tasks with or without accommodation such as lifting/carrying materials, working with biological and hazardous materials, gowning/degowning PPE, and maintaining accurate laboratory documentation.
Compliance with cGXPs and maintenance of clear, accurate, and complete laboratory records with strong attention to detail

Desirable Skills/Experience:

Ph.D. with 1-3 years industry experience (particularly in CMC within pharmaceutical or biotech settings)
Experience with LC‑MS–based protein characterization, including intact mass and peptide mapping using high‑resolution MS platforms (e.g., Orbitrap, Q‑TOF).
Experience independently generating procedures, protocols, and reports related to analytical test methods.
Strong working knowledge of current regulatory guidelines (e.g., ICH Q2 and Q14) and cGMP requirements
Strong analytical thinking skills, including problem solving and data interpretation.
High emotional intelligence with clear, professional communication skills
Ability to recognize aberrant test or sample conditions and propose scientifically sound corrective actions.

When we put unexpected teams in the same room, we spark ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace and challenge perceptions. That's why we work, on average, a minimum of four days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and bold world!

Why AstraZeneca:

Join a science-led, mission-driven organization where advanced analytics and chromatography translate directly into patient impact. You will work at the intersection of cutting-edge platforms, rigorous quality standards, and real-world needs—combining the agility of a biotech with the reach of a global biopharma. We bring diverse experts together to tackle the hardest problems in biologics, equip teams with modern LC, LC‑MS and digital tools, and value kindness alongside ambition so ideas become medicines faster and smarter. Your craft will scale beyond the bench to help people with severe, underserved conditions live fuller lives.

If you are ready to shape high-performance LC methods that accelerate transformative biologics to patients, step forward and make your impact with us today.

Date Posted

23-Jun-2026

Closing Date

20-Jul-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.

Apply Now

Refine Your Search

scientist process development jobs in new haven, ct

Scientist II, LC Development, Biologics Analytical Development

Scientist Technical Performance Insights Sensory Testing

Scientist II, LC Development, Biologics Analytical Development

Staff Scientist, Research Core

Scientist III, Injectable Drug Product Development

Staff Scientist, Cleanroom

Scientist III, Injectable Drug Product Development

Staff Scientist II

Development Scientist III, Analytical Development and Clinical Quality Control

DMPK Scientist

Associate Director, R&D Product Development, Wellbeing Collective

Product Support Scientist

Computational Social Scientist

Research Associate 1, MS

Research Assoicate 2

Project Manager, Clinical Trials

Applications Specialist

Design & Technology Manager

Instructional Lab Support Specialist - Physics

Associate Director, Analytical Development and Clinical QC

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