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Analytical Development Jobs in Massachusetts (NOW HIRING)

Ardelyx

Director, Analytical Development

Waltham, MA · On-site

$211K - $257K/yr

The Director, Analytical Development is a leader who works as a member of an integrated team at Ardelyx overseeing small molecule analytical activities involving commercial drug substance and drug ...

Ardelyx

Director, Analytical Development

Waltham, MA · Hybrid

$211K - $257K/yr

The Director, Analytical Development is a leader who works as a member of an integrated team at Ardelyx overseeing small molecule analytical activities involving commercial drug substance and drug ...

AMRI

Analytical Development Analyst II

Hopkinton, MA · On-site

$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 ...

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Analytical Development information

See Massachusetts salary details

$41K

$81.9K

$121.8K

How much do analytical development jobs pay per year?

As of Jul 29, 2026, the average yearly pay for analytical development in Massachusetts is $81,894.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,900.00 and $101,600.00 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 Massachusetts? The most popular types of Analytical Development jobs in Massachusetts are:
What cities in Massachusetts are hiring for Analytical Development jobs? Cities in Massachusetts with the most Analytical Development job openings:
Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Massachusetts as of July 2026, with employment types broken down into 1% Internship, 85% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $81,894 per year, or $39.4 per hour.

Director, Analytical Development

Sarepta Therapeutics, Inc.

Bedford, MA • On-site

$185K - $232K/yr

Full-time

Re-posted 28 days ago

Job description

Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
  • Physical and Emotional Wellness
  • Financial Wellness
  • Support for Caregivers

For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us
The Importance of the Role
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 individual will have demonstratable expertise in managing analytical activities at external drug substance and drug product manufacturing sites, and providing chemistry expertise for RNA therapeutics. In addition, the individual will offer comprehensive experience in product characterization and comparability assessments. Additionally, the Director will lead the writing and compilation of regulatory documents to support product development and registration.
The Opportunity to Make a Difference
  • Provide leadership and mentorship to a team of scientists and analysts
  • Characterize new products to support regulatory submissions and lifecycle comparability.
  • Ensure process 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.

More about You
  • PhD in Chemistry, Chemical Engineering, Pharmaceutical Engineering, or a related field preferred.
  • Minimum of 7 years of experience in pharmaceutical/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 Module 3 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.

What Now?
We're always looking for solution-oriented, critical thinkers.
So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
#LI-Hybrid
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This position is hybrid, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $185,600 - $232,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

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