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Analytical Development Jobs in Boston, MA (NOW HIRING)

Vrtx

Analytical Development Principal Scientist

Boston, MA · On-site

$140K - $211K/yr

As a member of the Drug Substance Control Strategy team in Analytical Development, this role will support synthetic drug development programs at Vertex with a focus on small molecule drug substance ...

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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 Aug 7, 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?

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 is the job description of analytical development?

Analytical development involves designing, optimizing, and validating analytical methods to measure the quality and stability of pharmaceutical products. Professionals in this field use techniques such as chromatography and spectroscopy, often working in laboratories under Good Laboratory Practice (GLP) standards. The role requires strong attention to detail, scientific knowledge, and proficiency with laboratory instruments and regulatory guidelines.

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 are popular job titles related to Analytical Development jobs in Boston, MA? For Analytical Development jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Analytical Development jobs in Boston, MA look for? The top searched job categories for 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 August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $81,465 per year, or $39.2 per hour.

Director, Analytical Development

Sarepta Therapeutics

Bedford, MA • On-site

$185.60 - $232/hr

Other

Re-posted 5 days ago

Job description

Role Overview

The Director of Analytical Development will spearhead the advancement of analytical methods and control strategies critical to our siRNA and antisense oligonucleotides portfolio. The role will represent Analytical Development on CMC teams and provide leadership that will be crucial from R&D transition to commercialization, ensuring robust support throughout the product lifecycle. The director will have demonstrable expertise in managing analytical activities at external drug substance and drug product manufacturing sites, and providing chemistry expertise for RNA therapeutics. The incumbent will also offer comprehensive experience in product characterization and comparability assessments, and will lead the writing and compilation of regulatory documents to support product development and registration.

Responsibilities
  • Provide leadership and mentorship to a team of scientists and analysts.
  • Characterize new products to support regulatory submissions and lifecycle comparability.
  • Ensure processes for documenting and transferring analytical methods to Quality Control and external facilities are in place.
  • Drive innovation in analytical method development for oligonucleotide therapeutics.
  • Collaborate with cross‑functional teams including process development, MS&T, QC, QA and regulatory affairs.
  • Manage relationships with CDMOs, CTLs, and other external partners.
  • Oversee critical sections of IND and NDA submissions and respond to health‑authority inquiries.
Qualifications
  • PhD in Chemistry, Chemical Engineering, Pharmaceutical Engineering, or a related field preferred.
  • Minimum of 7 years of experience in pharmaceutical or biopharmaceutical analytical development.
  • Minimum of 5 years of experience in a managerial capacity.
  • Extensive expertise in analytical method development and control strategy for RNA‑based therapeutics.
  • In‑depth knowledge of analytical techniques and regulatory requirements.
  • Strong analytical and problem‑solving abilities.
  • Proven track record in preparing Module3 sections for regulatory submissions.
  • Demonstrated ability in leading cross‑functional teams and projects.
  • Strong collaboration and teamwork skills, with the ability to support cross‑functional peers and maintain a safe, efficient, and compliant laboratory environment.
  • Capability to foster innovation and integrate new technologies into analytical development practices.
  • Experience working with contract laboratories and external vendors (CROs/CMOs) is highly desirable.
Benefits
  • Physical and emotional wellness resources.
  • Financial wellness programs.
  • Support for caregivers.
Compensation

Hybrid: The position is hybrid and will require on‑site work at one of Sarepta’s facilities in the United States and/or attendance at company‑sponsored in‑person events from time to time. The targeted salary range for this position is $185,600–$232,000 per year. Candidates must be authorized to work in the U.S.

EEO Statement

Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e‑Verify.

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