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Associate Scientist Analytical Development Jobs in Rhode Island

Aspen Enterprises LTD

Senior Scientist, R&D

Lincoln, RI · On-site

$89K - $114K/yr

Senior Research and Development Scientist DEPARTMENT: Research and Development REPORTS TO: Director ... Testing : Conduct shelf-life stability trials to document changes in sensory and analytical ...

Pharmaron

Senior Scientist I, QC

Coventry, RI · On-site

$100K - $140K/yr

Will also solve moderate complexity analytical and quality control issues for assigned projects and ... Pharmaron has an excellent track record in delivering R&D solutions to its partners in North ...

Pharmaron

Senior Scientist I, QC

Coventry, RI

$100K - $130K/yr

Will also solve moderate complexity analytical and quality control issues for assigned projects and ... Pharmaron has an excellent track record in delivering R&D solutions to its partners in North ...

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Associate Scientist Analytical Development information

What are the key skills and qualifications needed to thrive as an Associate Scientist Analytical Development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What are some common challenges an Associate Scientist in Analytical Development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What does an Associate Scientist in Analytical Development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

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

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

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What job categories do people searching Associate Scientist Analytical Development jobs in Rhode Island look for? The top searched job categories for Associate Scientist Analytical Development jobs in Rhode Island are:
What cities in Rhode Island are hiring for Associate Scientist Analytical Development jobs? Cities in Rhode Island with the most Associate Scientist Analytical Development job openings:
Associate Scientist Analytical Development jobs near you
Senior Scientist, Analytical Chemistry

Senior Scientist, Analytical Chemistry

Pharmaron

Coventry, RI • On-site

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Position: Senior Scientist, Analytical Chemistry
Salary Range: $90k - $130k
Location: Coventry, RI
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.
We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programmes, and 1,000+ clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,000 global customers. To learn more, visit .
Job Overview
The Senior Scientist - Analytical Chemistry will serve as a key technical resource within the Quality Control laboratory supporting API manufacturing and development programs at Pharmaron's Coventry, RI facility.
This role is responsible for supporting analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP-regulated laboratory environment. The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations.
Key Responsibilities
  • Support analytical method validation, verification, and transfer activities within the QC laboratory.
  • Troubleshoot complex analytical challenges related to API characterization and GMP testing.
  • Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.
  • Lead or support laboratory investigations, deviations, and root cause analyses.
  • Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.
  • Provide technical mentorship and scientific guidance to QC scientists and laboratory personnel.
  • Prepare and revise standard operating procedures (SOPs), analytical methods, and technical documentation.
  • Support internal and external regulatory inspections and client audits as an analytical subject matter expert.
  • Collaborate with cross-functional teams including Manufacturing, Process Chemistry, Quality Assurance, and Regulatory Affairs.
  • Contribute to continuous improvement initiatives that enhance QC laboratory efficiency and analytical capabilities.
  • Perform other related assignments and duties, as required and assigned.

What We're Looking For
  • Ph.D. in Chemistry or a related field with 1-4 years of postdoctoral or industry experience.
  • MS with 5-8 years of pharmaceutical industry experience, BS with 7-10 years of relevant pharmaceutical industry experience
  • 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.
  • Demonstrated experience applying analytical techniques to solve complex scientific problems related to method validation, troubleshooting, and implementation
  • Strong hands-on expertise with analytical instrumentation including:
    • HPLC / UPLC
    • GC
    • FTIR
    • UV
    • Mass Spectrometry
  • Experience supporting API manufacturing or pharmaceutical QC laboratories
  • Proven ability to troubleshoot analytical instrumentation and laboratory methods
  • Working knowledge of cGLP / cGMP and applicable FDA, EMA, and ICH regulatory guidelines
  • Experience contributing to multidisciplinary scientific teams and cross-functional projects
  • Experience mentoring or supervising laboratory personnel preferred
  • Strong analytical thinking, scientific judgment, and problem-solving skills
  • Excellent written and verbal communication skills

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Insurance including Medical, Dental & Vision with significant employer contributions
  • Employer-funded Health Reimbursement Account
  • Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
  • 401k plan with generous employer match
  • Access to an Employee Assistance Program

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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