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Associate Scientist Product Development Jobs in Connecticut

AllSTEM Connections

Associate Scientist

Trumbull, CT · On-site

$49K - $52K/yr

The Associate Scientist works closely with team of scientists and senior scientists to plan and perform laboratory assignments in the development of product formulations, measurement of physical ...

Coherent

Product Development Engineer

Monroe, CT · On-site

... military, life sciences, semiconductor equipment, and consumer markets. Coherent provides a ... development platform within an environment that challenges employees to perform at their best ...

Eurofins

Associate Materials Scientist

Groton, CT · On-site

... products they supply are safe, their ingredients are authentic and labelling is accurate. The ... Contribute to the development of new scientific approaches and knowledge within the Materials ...

Coherent Corp.

Product Development Engineer

Monroe, CT · On-site

... military, life sciences, semiconductor equipment, and consumer markets. Coherent provides a ... development platform within an environment that challenges employees to perform at their best ...

Waterworks

Product Development Manager, Plumbing

Danbury, CT · On-site

$117K - $146K/yr

We empower our associates with extensive training, career growth opportunities, competitive ... The Role The Product Manager - Fittings Development is responsible for the end-to-end execution and ...

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Associate Scientist Product Development information

What are some common challenges faced by an associate scientist in product development, and how can they be addressed?

Associate Scientists in Product Development often encounter challenges such as balancing tight project timelines with the need for thorough experimental design and data analysis. They may also need to quickly adapt to changing project priorities or troubleshoot unexpected results in the lab. Collaborating effectively with cross-functional teams, such as quality assurance, manufacturing, and regulatory affairs, is essential to overcome these hurdles. Proactively communicating progress, seeking feedback, and staying organized can help Associate Scientists navigate these challenges and contribute successfully to product advancement.

What does an associate scientist in product development do?

An Associate Scientist in Product Development plays a crucial role in researching, designing, and testing new products or formulations in industries like pharmaceuticals, biotechnology, or consumer goods. They conduct laboratory experiments, analyze data, and collaborate with cross-functional teams to improve product performance and ensure regulatory compliance. Their work helps bring innovative and safe products to market efficiently.

What is the difference between Associate Scientist Product Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Product DevelopmentAssociate Scientist Quality Control
CredentialsBachelor's or Master's in Life Sciences, Chemistry, or related fieldBachelor's or Master's in Life Sciences, Chemistry, or related field
Work EnvironmentResearch labs focused on product formulation and innovationLaboratories conducting testing and quality assurance of products
Industry UsageUsed in pharmaceutical, biotech, and consumer goods companiesCommon in manufacturing and quality assurance departments
Search IntentComparing roles in product development and formulationLooking into quality testing and compliance roles

Associate Scientist Product Development and Associate Scientist Quality Control are both entry-level roles in the life sciences industry. While they share similar educational backgrounds, the former focuses on creating and improving products, whereas the latter emphasizes testing and ensuring product quality. Both roles are essential in bringing safe, effective products to market, but they differ in daily tasks and objectives.

What are the key skills and qualifications needed to thrive as an associate scientist in product development?

To thrive as an Associate Scientist in Product Development, you typically need a degree in chemistry, biology, or a related field along with strong laboratory and analytical skills. Familiarity with laboratory information management systems (LIMS), analytical instrumentation (such as HPLC or GC), and relevant regulatory guidelines is often required. Attention to detail, teamwork, and effective problem-solving are vital soft skills for success in collaborative and fast-paced environments. These abilities ensure the accurate development, testing, and optimization of products while maintaining compliance and fostering innovation.
What are popular job titles related to Associate Scientist Product Development jobs in Connecticut? For Associate Scientist Product Development jobs in Connecticut, the most frequently searched job titles are:
What job categories do people searching Associate Scientist Product Development jobs in Connecticut look for? The top searched job categories for Associate Scientist Product Development jobs in Connecticut are:
What cities in Connecticut are hiring for Associate Scientist Product Development jobs? Cities in Connecticut with the most Associate Scientist Product Development job openings:
Associate Scientist Product Development jobs near you
Infographic showing various Associate Scientist Product Development job openings in Connecticut as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution.

Associate Scientist II, Injectable Drug Product Development

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Posted 18 days ago

Job description

This is what you will do:

The Associate Scientist II candidate will be a part of the Injectable Drug Product Development (IDPD) team within the Pharmaceutical Development and Clinical Supply (PDCS) department at Alexion-AstraZeneca Rare Disease. The job entails experimental work on various aspects of drug product formulation and process development activities in support of drug product manufacturing, characterization, including analytical and biophysical comparability testing. The ability to work with minimal supervision as well as being part of a collaborative team is essential. The position entails study design, execution, and preparation of development reports and other required documentation.

You will be responsible for:

  • With some supervision, design and execute formulation and process development studies for clinical biologic candidates.
  • Execute drug development studies including physico-chemical characterization and stability studies for clinical and commercial drug products.
  • Characterize conformational and colloidal stability using industry standard methodology (e.g., circular dichroism, differential scanning fluorimetry, analytical ultracentrifugation, size-exclusion chromatography with multi-angle light scattering detection, etc.)
  • Maintain organized records and use team tools to keep multiple assignments on track.
  • Assist in the preparation of internal technical reports on executed studies with minimal supervision.
  • Participate in cross-functional development teams.

You will need to have:

  • BS or MS degree in Biochemistry, Pharmaceutical Science, Chemical Engineering, or relevant field with 2 to 4 years relevant work experience with a pharmaceutical or biotechnology company
  • Scientific and practical knowledge of protein/peptide biochemistry, protein formulation, and stability is essential.
  • Experience of working with imaged capillary electrophoresis (iCE/Maurice), H/UPLC's (IEX, SEC), DLS, CD, DSC, AUC, and NanoTemper
  • Ability to execute experiments with minimal supervision is required.
  • The individual must be able to work in a collaborative setting and has ability to adhere to timelines is essential.
  • Excellent interpersonal, collaborative and communication skills
  • Ability to take initiative in problem solving and finding solutions to scientific challenges.
  • Experience with various software packages like MS Office programs, including Word, Excel, Outlook, and PowerPoint
  • The duties of this role are generally conducted in a lab environment. As is typical of a lab-based role, employees must be able, with or without an accommodation to: lift/carry 15/30 pounds unassisted/assisted; work comfortably in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video and electronic messaging; engage in problem solving and non-linear thought, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer you to have:

  • Hands-on experience with process development, scale up, tech transfer, and manufacturing.
  • Experience working with sub-visible particle testing and characterization.
  • Experience of working with biophysical and analytical testing
  • Familiarity with regulatory guidelines.
  • High level proficiency in MS Office software including Word, Excel, Outlook, and PowerPoint.
  • Experience with electronic record keeping software, like ELN, EndNote, e-logbooks; maintenance of laboratory instrumentation (organizing PMs, data backup, SW upgrade, etc.) will be a plus.

Date Posted

23-Jul-2026

Closing Date

05-Aug-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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