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Analytical Development Jobs in Massachusetts (NOW HIRING)

Alkermes

Supervisor, Analytical Development

Waltham, MA · On-site

$131K - $142K/yr

The Analytical Development Supervisor provides technical and operational leadership for small molecule analytical activities within a growing, dynamic Pharmaceutical Development organization. This ...

Alkermes

Supervisor, Analytical Development

Waltham, MA · On-site

$131K - $142K/yr

The Analytical Development Supervisor provides technical and operational leadership for small molecule analytical activities within a growing, dynamic Pharmaceutical Development organization. This ...

Genezen

Sr. Scientist, Analytical Development

Lexington, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

JOB SUMMARY Lead the establishment of methods in the Analytical Development (AD) and Quality Control lab from the bench. This individual will be accountable for development and validation of ...

Biogen

Scientist II, Analytical Development

Cambridge, MA

$117K - $157K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a Scientist II to join our Analytical Development team as a Liquid Chromatography (LC) Subject Matter Expert (SME) and Analytical Project Lead. This role is pivotal,leveragingdeep ...

Biogen

Scientist II, Analytical Development

Cambridge, MA · On-site

$117K - $157K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We are seeking a Scientist II to join our Analytical Development team as a Liquid Chromatography (LC) Subject Matter Expert (SME) and Analytical Project Lead. This role is pivotal, leveraging deep ...

Vrtx

Analytical Development Principal Scientist

Boston, MA

$140K - $211K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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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All JobsAnalytical Development JobsAnalytical Development Jobs in Massachusetts

Analytical Development information

See Massachusetts salary details

$41K

$81.9K

$121.8K

How much do analytical development jobs pay per year?

As of Aug 18, 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?

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 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 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 stability of drug substances and products. It involves developing techniques such as chromatography and spectroscopy, often requiring knowledge of regulatory standards and laboratory skills. 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 or chemical products. Professionals in this field use techniques such as chromatography, spectroscopy, and other laboratory tools, often working in regulated environments that require compliance with industry standards and documentation practices.

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 are popular job titles related to Analytical Development jobs in Massachusetts?

For Analytical Development jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Analytical Development jobs in Massachusetts look for?

The top searched job categories for 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 August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $81,894 per year, or $39.4 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

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