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Manager Analytical Development Jobs in Boston, MA

We are seeking a Scientist II to join our Analytical Development team as a Liquid Chromatography ... Management Additional Information The base compensation range for this role is: $117,000.00-$157 ...

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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 Aug 16, 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 is a manager analytical development?

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 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.

What does a Manager Analytical Development do?

A Manager of Analytical Development oversees the design, validation, and implementation of analytical methods used to test and ensure the quality of pharmaceutical or biotech products. They lead teams of scientists, coordinate method development projects, and ensure compliance with regulatory standards such as GMP and FDA guidelines. The role often requires expertise in analytical techniques, laboratory management, and relevant certifications.

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 Manager Analytical Development jobs in Boston, MA?

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

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

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

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

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

Infographic showing various Manager Analytical Development job openings in Boston, MA as of July 2026, with employment types broken down into 1% Internship, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $84,129 per year, or $40.4 per hour.

Senior Manager, Analytical Development & Quality Control

Alpha-9 Oncology

Boston, MA

Full-time

Medical, Retirement, PTO

Posted 16 days ago


Job description

Your Impact

Alpha-9 Oncology is seeking a highly motivated Senior Manager, Analytical Development & Quality Control, to provide technical and operational leadership for quality control and analytical lifecycle activities across clinical-stage radiopharmaceutical programs. This role will serve as a primary analytical and QC representative supporting development programs through data trending, statistical analysis, batch release support, investigation management, CDMO oversight, analytical readiness activities, and clinical supply support.

The successful candidate will lead interactions with multiple external manufacturing and testing partners to ensure effective analytical control strategies, successful technology transfers, timely issue resolution, and reliable clinical supply support. The role will partner closely with Quality, Regulatory, Technical Operations, and Program Leadership teams to proactively identify analytical risks and support program progression. This role is based in our Boston office.

This role is based in our Boston office.

How You'll Contribute

  • Lead QC data review, trending, and lifecycle monitoring to support product quality and program progression.
  • Manage technical relationships with external CDMOs, contract laboratories, and suppliers to ensure timely execution of testing, investigations, and program deliverables.
  • Partner with Quality Assurance and CDMO partners to drive the resolution of deviations, non-conformances, OOS/OOT investigations, CAPAs, and other quality events.
  • Review and provide technical oversight for analytical development, method qualification/validation, reference standard programs, stability studies, and technology transfer activities conducted by external partners.
  • Collect, organize, trend, and interpret analytical, manufacturing, and stability data to identify variability, emerging risks, and opportunities for process improvement.
  • Utilize JMP, Excel, and other statistical tools to evaluate assay performance, process performance, and product quality trends.
  • Support analytical method lifecycle management, including method transfer, qualification, validation, and continuous improvement activities.
  • Manage the review and approval of analytical and process qualification, validation, and stability protocols and reports, collaborating with CDMOs and internal stakeholders to ensure phase-appropriate development, control strategies, and regulatory readiness.
  • Provide technical oversight and support for critical raw material, precursor, API, and drug product development activities conducted by external partners.
  • Author, review, and approve technical reports, specifications, protocols, trend reports, and other CMC documentation.
  • Collaborate with cross-functional teams and external partners to support clinical supply readiness, analytical control strategies, reference standard programs, and technology transfer activities.


The Skills You Bring

  • Ph.D. in Analytical Chemistry, Chemistry, Radiochemistry, Pharmaceutical Sciences, or a related scientific discipline with 6+ years of relevant industry experience, or M.S. with 8+ years of relevant industry experience.
  • Strong background in analytical development, quality control, and GMP pharmaceutical development.
  • Experience supporting external CDMOs, contract testing laboratories, and technology transfer activities.
  • Demonstrated ability to interpret analytical, manufacturing, and quality data to inform technical decision-making.
  • Solid understanding of analytical method qualification, validation, transfer, and lifecycle management.
  • Experience with statistical analysis and data trending tools (e.g., JMP, Excel).
  • Working knowledge of cGMP, ICH, and pharmaceutical regulatory requirements.
  • Strong communication, organizational, and stakeholder management skills.
  • Ability to manage multiple priorities in a fast-paced development environment.
  • Ability to travel up to 25% (domestic and international).

What's in it for you

At Alpha-9 Oncology, we offer a competitive and comprehensive benefits package designed to support all employees. Our benefits include a competitive salary, bonus, equity, 20 vacation days, 5 sick days, a technology allowance, and commuter reimbursement. We also provide generous retirement savings plans with employer matching, extended health benefits, and paid holidays, tailored to local standards in each region. While specific offerings may vary by location, our commitment to fostering a supportive and rewarding work environment is consistent across the company.