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Associate Scientist Analytical Development Jobs in Boston, MA

Genesis10

Associate Scientist

Cambridge, MA · On-site

$30.32/hr

In this role, you will be responsible for supporting the development of analytical methods, the ... scientific/pharmaceutical experience OR Associate's degree and 4+ years of experience OR High ...

New

Pacelabs

Associate Scientist I

Woburn, MA

$28/hr

Associate Scientist I Pace Analytical Life Sciences, LLC is a premier Contract Research and Development Organization located in Woburn, MA providing pharmaceutical development services for biologics ...

Pace

Associate Scientist I

Woburn, MA · On-site

$28/hr

Associate Scientist I Pace Analytical Life Sciences, LLC is a premier Contract Research and Development Organization located in Woburn, MA providing pharmaceutical development services for biologics ...

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All JobsAssociate Scientist Analytical Development JobsAssociate Scientist Analytical Development Jobs in Boston, MA

Associate Scientist Analytical Development information

See Boston, MA salary details

$20

$39

$62

How much do associate scientist analytical development jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for associate scientist analytical development in Boston, MA is $39.03, according to ZipRecruiter salary data. Most workers in this role earn between $30.29 and $44.38 per hour, depending on experience, location, and employer.

What does an associate scientist 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 are some common challenges an associate scientist 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 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 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.

What are popular job titles related to Associate Scientist Analytical Development jobs in Boston, MA?

For Associate Scientist Analytical Development jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Associate Scientist Analytical Development jobs in Boston, MA look for?

The top searched job categories for Associate Scientist Analytical Development jobs in Boston, MA are:

What cities near Boston, MA are hiring for Associate Scientist Analytical Development jobs?

Cities near Boston, MA with the most Associate Scientist Analytical Development job openings:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Boston, MA as of August 2026, with employment types broken down into 64% Full Time, 32% Contract, and 4% Nights. Highlights an 100% In-person job distribution, with an average salary of $81,179 per year, or $39 per hour.

Director, Analytical Development

Stylus Medicine

Cambridge, MA • On-site

$225K - $245K/yr

Full-time

Re-posted 24 days ago

Job description

About Stylus Medicine:
Stylus Medicine is developing transformative in vivo genetic medicines to unlock cures. Stylus combines engineered recombinases with non-viral delivery to specifically encode therapeutics. The company's approach is versatile and modular, with potential therapeutic application across oncology, autoimmune, genetic diseases, and beyond.
About the Role:
Stylus Medicine is seeking a Director of Analytical Development to provide strategic and technical leadership for analytical development within our portfolio. This individual will guide oversight of analytical method development, phase-appropriate qualification/validation of analytical methods for drug substance (DS) and drug product (DP), method transfer to CMOs, and support of regulatory filings, including investigational new drugs (INDs) and investigational medicinal product dossiers (IMPDs).
Key Responsibilities & Accountabilities:
  • Lead a high performing team of scientists and associates in setting and executing the analytical development and quality control strategy across portfolio programs
  • Define and implement phase-appropriate analytical methods and control strategies to support DS and DP development
  • Interpret and apply global regulatory guidelines (e.g., ICH, FDA) to assay development and lifecycle activities
  • Define and drive potency assay strategy, aligning with product mechanism of action, CQA frameworks, and regulatory expectations
  • Act as a company liaison with contract laboratories, coordinating method transfers and overseeing method qualification and validation activities
  • Advise and oversee CDMOs' analytical method development, validation and transfer
  • Ensure analytical methods and specifications are scientifically justified, phase appropriate, and compliant with applicable compendial standards and regulatory guidelines
  • Review and approve analytical methods, validation protocols, analytical reports, and stability protocols and test reports
  • Oversee the reference standard program, including establishing and maintaining reference standards, approving qualification protocols and reports, and coordinating release testing at external laboratories
  • Drive resolution of investigations, deviations, and comparability assessments
  • Collaborate with Quality Assurance to review and manage change controls and quality event documentation
  • Establish best practices internally and externally for analytical lifecycle management, data integrity, documentation, and knowledge transfer
  • Partner cross-functionally to support data-driven decision-making and operational excellence
  • Provide analytical CMC leadership for regulatory filings, including INDs and IMPDs with direct responsibility for authoring and reviewing analytical sections
  • Travel may be required

Qualifications & Skills:
  • PhD in Biochemistry, Molecular Biology (or) Chemical / Biological Engineering with 10+ years of progressive industry experience in leading analytical method development, validation, regulatory submissions and lifecycle management
  • Proven experience as a functional leader, including team leadership and accountability for analytical strategy execution
  • Demonstrated expertise in compendial methods, high-throughput sequencing (e.g., NGS, RNA-seq) bioanalytical methods (e.g., ddPCR, RT-PCR, ELISA, DLS) and chromatographic techniques (e.g., LC), employing detectors such as UV/vis, CAD, MS, fluorescence
  • Experience managing stability studies, protocol development and performing trending analysis, OOS/OOT investigations, root cause analysis, etc.
  • Demonstrated track record of successful method transfers to CROs/CDMOs
  • Attention to detail and accuracy in developing and reviewing SOPs, batch records and technology transfer documents
  • Strong knowledge of global regulatory requirements and ICH guidelines applicable to analytical development and control strategies
  • Experience in authoring/contributing to Module 3 for analytical methods and stability studies
  • Excellent writing, organization, communication and people management skills with the ability to work effectively with a diverse group of internal and external stakeholders in a fast-paced, integrated multidisciplinary team environment
  • Commitment to technical excellence with a strong ability to embrace an entrepreneurial spirit
  • Experience with IND filing and answering queries from health authorities preferred
  • Experience with bioassay development for RNA and/or LNP-related products preferred
  • Demonstrated expertise in cell-based potency assays for immunology/oncology applications including development, qualification, validation, and lifecycle management preferred

Pay Range; $225,000 - $245,000

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