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Biotech Process Development Jobs in Connecticut (NOW HIRING)

Beeline Medicines

Director, Accounting

Stamford, CT · Hybrid

Own the monthly, quarterly, and annual financial close processes, including journal entry review ... encountered in clinical-stage biotechnology such as clinical trial accruals, R&D cost ...

Beeline Medicines

Director, Accounting

Stamford, CT · On-site

Own the monthly, quarterly, and annual financial close processes, including journal entry review ... encountered in clinical-stage biotechnology such as clinical trial accruals, R&D cost ...

LanceSoft Inc

Quality Engineer III

North Haven, CT · On-site

We provide staffing solutions specializing in all areas of the clinical development process for the Pharmaceutical, Biotechnology, and Medical Device industries. We understand the clinical trial ...

Premier Research

$122K/yr

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and ... Assists in Business Development activities, including proposal development and leading proposal ...

System One Holdings, LLC

Scientist II

Ridgefield, CT · On-site

$40.04/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

System One

Scientist II

Ridgefield, CT · On-site

$30 - $40/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

System One

Scientist II

Ridgefield, CT · On-site

$30 - $40/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

System One

Scientist II

Ridgefield, CT · On-site

$30 - $40/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

System One

Scientist II

Ridgefield, CT · On-site

$30 - $40/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

System One

Scientist II

Ridgefield, CT · On-site

$30 - $40/hr

... and development process. * Independently operates and maintains laboratory equipment and ... biotechnology or CRO experience is highly desirable; non-PhD applicant required. * Understanding of ...

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Biotech Process Development information

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How much do biotech process development jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for biotech process development in Connecticut is $30.61, according to ZipRecruiter salary data. Most workers in this role earn between $26.68 and $33.80 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Connecticut? For Biotech Process Development jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Connecticut look for? The top searched job categories for Biotech Process Development jobs in Connecticut are:
What cities in Connecticut are hiring for Biotech Process Development jobs? Cities in Connecticut with the most Biotech Process Development job openings:
Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Connecticut as of July 2026, with employment types broken down into 1% As Needed, 87% Full Time, 5% Part Time, 1% Temporary, 4% Contract, and 2% Summer. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution, with an average salary of $63,675 per year, or $30.6 per hour.
Scientist II, LC Development, Biologics Analytical Development

Scientist II, LC Development, Biologics Analytical Development

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Re-posted yesterday

Job description

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.

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