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Manager Analytical Development Jobs in Boston, MA

Pace

Analytical Development Scientist

Woburn, MA · On-site

$95K - $140K/yr

Analytical Development Scientist 1 Pace Life Sciences is a premier Contract Research and ... Ability to manage people and projects PHYSICAL/MENTAL REQUIREMENTS: The physical demands described ...

Pacelabs

Analytical Development Scientist

Woburn, MA

$95K - $140K/yr

Analytical Development Scientist 1 Pace Life Sciences is a premier Contract Research and ... Ability to manage people and projects PHYSICAL/MENTAL REQUIREMENTS: The physical demands described ...

Takeda

Head of Process Analytics Development

Boston, MA · On-site

... analytical development, automation, and PAT, while driving cross-functional collaboration and stakeholder alignment. * Provide multi-site leadership, establish standards/governance, manage external ...

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Showing results 1-20

All JobsManager Analytical Development JobsManager Analytical Development Jobs in Boston, MA

Manager Analytical Development information

See Boston, MA salary details

$35.9K

$84.1K

$144.5K

How much do manager analytical development jobs pay per year?

As of Jul 3, 2026, the average yearly pay for manager analytical development in Boston, MA is $84,129.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,600.00 and $98,300.00 per year, depending on experience, location, and employer.

What are the typical day-to-day responsibilities for a Manager Analytical Development?

As a Manager Analytical Development, your typical day involves overseeing laboratory teams, managing analytical method development and validation projects, and ensuring compliance with relevant quality standards. You’ll often collaborate with R&D, quality assurance, and production departments to support product development timelines and troubleshoot analytical challenges. Additionally, you may conduct data reviews, prepare regulatory documentation, and participate in meetings to drive project progress. Your role also includes mentoring team members and optimizing lab workflows for productivity and accuracy.

What does an analytical development manager do?

An analytical development manager oversees the design, validation, and implementation of analytical methods used to test and analyze products, often in pharmaceutical or biotech industries. They lead teams, ensure compliance with regulatory standards, and utilize laboratory instruments and software to support product development and quality control.

What is a Manager Analytical Development job?

A Manager Analytical Development oversees the development, validation, and implementation of analytical methods to support product development and manufacturing. They ensure compliance with regulatory standards, manage a team of scientists, and collaborate with cross-functional departments to drive innovation and efficiency. Their role is critical in ensuring product quality, consistency, and regulatory approval.

What kind of jobs in media bring in $150,000 a year?

High-paying media jobs that can reach $150,000 annually include roles such as media director, senior producer, or executive producer, often requiring extensive experience, leadership skills, and industry knowledge. These positions typically involve managing large teams, overseeing major projects, and possessing advanced skills in content strategy, digital platforms, or broadcast technology.

Is BD manager a stressful job?

A BD (Business Development) manager role can be stressful due to targets, client negotiations, and project deadlines. Managing multiple priorities and maintaining relationships often requires strong organizational and communication skills, which can contribute to work pressure.

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

To excel as a Manager Analytical Development, you typically need an advanced degree in chemistry, biochemistry, or a related field, along with experience in analytical method development and leadership. Familiarity with laboratory information management systems (LIMS), chromatographic software (HPLC/UPLC), and regulatory standards such as ICH and FDA guidelines is common. Outstanding project management, team leadership, and communication skills help you effectively coordinate cross-functional projects and mentor staff. These competencies enable delivery of high-quality analytical solutions, ensure regulatory compliance, and drive successful product development.

How much do R&D managers make in the US?

R&D managers in the US typically earn a median annual salary of around $130,000 to $150,000, with variations based on industry, experience, and location. They often hold advanced degrees and oversee research teams, requiring strong leadership and technical skills.
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:
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Manager Analytical Development jobs near you
Infographic showing various Manager Analytical Development job openings in Boston, MA as of June 2026, with employment types broken down into 58% Full Time, 29% Part Time, 1% Temporary, 11% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $84,129 per year, or $40.4 per hour.
Director, Analytical Development

Director, Analytical Development

Sarepta Therapeutics

Bedford, MA • Hybrid

$185K - $232K/yr

Full-time

Posted 20 hours 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 crossfunctional 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-HybridBlankThis 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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