ZipRecruiter

Log In

1

Analytical Development Jobs in Boston, MA (NOW HIRING)

AMRI

Analytical Development Analyst II

Hopkinton, MA

$76K - $95K/yr

Analytical Development Analyst II in Hopkinton, MA Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO ...

Pacelabs

Analytical Development Scientist

Woburn, MA · On-site

$95K - $140K/yr

Analytical Development Scientist 1 Pace Life Sciences is a premier Contract Research and Development Organization located just north of Cambridge, MA providing pharmaceutical research and development ...

next page

Showing results 1-20

All JobsAnalytical Development JobsAnalytical Development Jobs in Boston, MA

Analytical Development information

See Boston, MA salary details

$40.7K

$81.5K

$121.1K

How much do analytical development jobs pay per year?

As of Jul 19, 2026, the average yearly pay for analytical development in Boston, MA is $81,465.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,600.00 and $101,000.00 per year, depending on experience, location, and employer.

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

To thrive in Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a relevant degree and experience in analytical methodologies. Familiarity with laboratory instruments such as HPLC, GC, and mass spectrometry, as well as knowledge of regulatory guidelines like ICH and GMP, is essential. Strong problem-solving skills, attention to detail, and effective communication set standout professionals apart in this role. These skills ensure the accurate development, validation, and transfer of analytical methods critical for product quality and regulatory compliance.

What is analytical development?

Analytical development is a field within pharmaceutical and biotech industries focused on creating and validating methods to analyze the quality, purity, and potency of drug substances and products. It involves developing techniques such as chromatography and spectroscopy, often requiring knowledge of regulatory standards like GMP and validation processes. Professionals in this area support drug development by ensuring analytical methods are reliable and compliant with industry regulations.

What are analytical jobs?

Analytical jobs involve examining data, processes, or systems to identify patterns, solve problems, and support decision-making. These roles often require skills in data analysis, critical thinking, and proficiency with tools like Excel, statistical software, or laboratory instruments, especially in fields like research, quality control, or product development.

What is the highest paid chemist job?

The highest paid chemist roles are typically in pharmaceutical or industrial sectors, such as senior research scientists or director-level positions in R&D, with salaries often exceeding $150,000 annually. These roles usually require advanced degrees, extensive experience, and expertise in specialized techniques or management skills.

What jobs are good for analytical people?

Analytical development roles are well-suited for individuals with strong problem-solving skills, attention to detail, and proficiency in data analysis and laboratory techniques. Common jobs include analytical chemist, data analyst, quality control analyst, and research scientist, often requiring knowledge of statistical tools and laboratory instrumentation. These positions typically involve interpreting complex data, troubleshooting, and ensuring compliance with industry standards.

What are some common challenges faced in an Analytical Development role, and how can job seekers prepare for them?

Professionals in Analytical Development often encounter challenges such as developing robust methods for complex samples, meeting tight project deadlines, and ensuring regulatory compliance. To prepare, job seekers should build strong problem-solving skills, gain familiarity with a range of analytical techniques (such as HPLC, GC, and spectroscopy), and stay current with industry regulations like ICH guidelines. Collaborating effectively with cross-functional teams, such as Quality Control and Research & Development, is also essential for success in this role.

What is the difference between Analytical Development vs Quality Control Analyst?

AspectAnalytical DevelopmentQuality Control Analyst
Primary FocusDeveloping and optimizing analytical methods for new productsPerforming routine testing to ensure product quality
Work EnvironmentLaboratories involved in method development and validationQuality control labs conducting batch testing and release
Required CredentialsBachelor's or higher in Chemistry, Biochemistry, or related fields; experience in method developmentBachelor's in Chemistry, Biology, or related fields; experience in testing procedures

Analytical Development professionals focus on creating and refining analytical methods for new products, while Quality Control Analysts perform routine testing to verify product quality. Both roles require similar educational backgrounds and work in laboratory settings, but their responsibilities differ in scope and purpose.

What are the most commonly searched types of Analytical Development jobs in Boston, MA? The most popular types of Analytical Development jobs in Boston, MA are:
What cities near Boston, MA are hiring for Analytical Development jobs? Cities near Boston, MA with the most Analytical Development job openings:
Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Boston, MA as of July 2026, with employment types broken down into 88% Full Time, 6% Part Time, and 6% Contract. Highlights an 81% In-person, 6% Hybrid, and 13% Remote job distribution, with an average salary of $81,465 per year, or $39.2 per hour.

Director, Analytical Development

Stylus Medicine

Cambridge, MA • On-site

$225K - $245K/yr

Full-time

Re-posted 25 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

Apply