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Analytical Development Jobs in Lowell, MA (NOW HIRING)

Vrtx

Analytical Development Senior Scientist

Boston, MA · On-site

$122K - $183K/yr

General Summary Vertex is seeking a Senior Research Scientist to join Analytical Development in Boston, MA . This role supports the advancement of transformative medicines by leading analytical ...

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Analytical Development information

See Lowell, MA salary details

$37.2K

$74.4K

$110.6K

How much do analytical development jobs pay per year?

As of Sep 1, 2026, the average yearly pay for analytical development in Lowell, MA is $74,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,600.00 and $92,200.00 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 popular job titles related to Analytical Development jobs in Lowell, MA?

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

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

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

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

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

Analytical Development jobs near you
Infographic showing various Analytical Development job openings in Lowell, MA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 18% Part Time, 2% Temporary, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $74,369 per year, or $35.8 per hour.

Sr. Advisor - Analytical Development

Eli Lilly and Company

Boston, MA • On-site

$148K - $148K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 5 days ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Position Summary
We are seeking an accomplished Senior Advisor, Analytical Sciences to provide scientific leadership for analytical development supporting our gene therapy pipeline, with a particular focus on late-stage lentiviral vector (LVV) bioassay and potency assay development. This individual will serve as the technical subject matter expert for assay development, characterization, qualification, validation, and lifecycle management - driving phase-appropriate analytical strategies from early development through late-stage, licensure, and commercial readiness.
The successful candidate will combine scientific excellence and strategic leadership, partnering closely with CMC, Research, Quality, Manufacturing, and external partners while mentoring scientists and strengthening analytical capabilities across the organization.
Responsibilities
Analytical Strategy & LVV Bioassay/Potency Leadership
  • Define and execute analytical development and control strategies across the product lifecycle, serving as technical lead for development, clinical-stage, and late-stage/commercialization programs.
  • Lead end-to-end development, optimization, qualification, and validation of LVV bioassays and potency assays (e.g., cell-based transduction/infectivity assays, functional reporter assays, titer methods), including matrix or multi-method potency strategies, assay orthogonality, and surrogate potency justification.
  • Drive potency assay comparability and bridging across process changes, manufacturing site transfers, and reference standard updates, applying strong statistical design (e.g., DOE) to reduce variability and improve robustness.
  • Provide scientific guidance on product characterization, comparability, and control strategy, and partner with Regulatory and Quality to align potency strategy with evolving FDA/EMA expectations for advanced therapies.

Method Lifecycle, Characterization & Technology
  • Lead development, optimization, and troubleshooting of methods across the broader LVV/gene therapy analytical panel (identity, purity, safety, process-related impurities), and define qualification, validation, and lifecycle strategies with emphasis on bioassay/potency methods.
  • Partner with Operations and Quality on successful method transfer, including complex cell-based bioassays, to internal and external testing laboratories, and provide technical oversight for specification development.
  • Drive implementation of novel analytical technologies, including next-generation potency and bioassay platforms, and provide scientific oversight for data interpretation and technical investigations.

Leadership, Mentorship & Regulatory Engagement
  • Mentor and develop scientists across the analytical organization, building bench strength in bioassay and potency assay science, and serve as the primary analytical SME in cross-functional and technical review settings.
  • Author and review analytical/potency sections of regulatory submissions and technical reports, and support health authority interactions and inspections as an analytical SME.
  • Provide scientific oversight of external analytical development activities and technology transfers, and maintain awareness of emerging technologies and regulatory expectations.

Basic Requirements
  • PhD in analytical chemistry, biochemistry, molecular biology, pharmaceutical sciences, or a related discipline with 5+ years of industry experience; or MS with 12+ years of industry experience.
  • Extensive, hands-on experience developing, optimizing, qualifying, and validating late-stage lentiviral vector bioassays and cell-based potency assays.
  • Demonstrated expertise in analytical development within cell and gene therapy, biologics, viral vectors, or related advanced modalities, including method transfer to internal/external labs and CMC support from early through late-stage development.

Additional Preferences
  • Recognized expertise in LVV bioassay/potency science (surrogate potency, matrix approaches, multi-attribute methods) and demonstrated success leading complex technical programs.
  • Experience supporting regulatory filings and health authority interactions, including potency-related BLA/MAA sections and inspection readiness.
  • Strong leadership, mentoring, and communication skills, with the ability to influence scientific direction across stakeholders and a commitment to scientific excellence and talent development.

Additional Details
  • Position Location: Boston MA
  • This role is a lab based position.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$141,000 - $228,800
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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