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Associate Scientist Analytical Development Jobs in Stoneham, MA

Biogen

Scientist II, Analytical Development

Cambridge, MA · On-site

$117K - $157K/yr

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 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 ...

Genesis10

Associate Scientist

Cambridge, MA · On-site

$30.32/hr

In this role, you will be responsible for supporting the development of analytical methods, the ... scientific/pharmaceutical experience OR Associate's degree and 4+ years of experience OR High ...

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All JobsAssociate Scientist Analytical Development JobsAssociate Scientist Analytical Development Jobs in Stoneham, MA

Associate Scientist Analytical Development information

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$20

$39

$62

How much do associate scientist analytical development jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for associate scientist analytical development in Stoneham, MA is $39.31, according to ZipRecruiter salary data. Most workers in this role earn between $30.53 and $44.71 per hour, depending on experience, location, and employer.

What does an associate scientist analytical development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What are some common challenges an associate scientist analytical development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What are the key skills and qualifications needed to thrive as an associate scientist analytical development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

What are popular job titles related to Associate Scientist Analytical Development jobs in Stoneham, MA?

For Associate Scientist Analytical Development jobs in Stoneham, MA, the most frequently searched job titles are:

What job categories do people searching Associate Scientist Analytical Development jobs in Stoneham, MA look for?

The top searched job categories for Associate Scientist Analytical Development jobs in Stoneham, MA are:

What cities near Stoneham, MA are hiring for Associate Scientist Analytical Development jobs?

Cities near Stoneham, MA with the most Associate Scientist Analytical Development job openings:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Stoneham, MA as of August 2026, with employment types broken down into 64% Full Time, 32% Contract, and 4% Nights. Highlights an 100% In-person job distribution, with an average salary of $81,772 per year, or $39.3 per hour.

Scientist II, Analytical Development

Biogen

Cambridge, MA • On-site

$117K - $157K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 19 days ago

Biogen rating

9.3

Company rating: 9.3 out of 10

Based on 20 frontline employees who took The Breakroom Quiz

3rd of 86 rated pharmaceutical

Job description

About This Role:
At Biogen, we are advancing science to deliver innovative therapies that transform patients' lives. 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 technical expertise in LC method development alongside leadership in analytical strategy across synthetics programs. Situated in Cambridge, MA, this lab-based position plays a crucial part in driving forward the development of synthetic drug substances and products, ensuring robust, stability-indicating methods. Your contributions will be vital to our mission, interfacing with various teams and shaping the analytical landscape of our drug development efforts.
What You'll Do:
  • Serve as the LC subject matter expert, leading method development, optimization, qualification, and troubleshooting (HPLC, UHPLC, LC-MS).

  • Develop robust, stability-indicating methods for synthetic drug substances and products.

  • Provide technical support to inform analytical strategy for development programs from early to late stage.

  • Collaborate cross-functionally with CMC, formulation, process development, and quality teams.

  • Provide oversight of analytical activities at CDMOs, including method validation, transfer, and lifecycle management aligned with regulatory expectations.

  • Participate in mentoring and knowledge-sharing activities to support analytical capability building within the organization.

  • Contribute to programs involving emerging modalities (e.g., oligonucleotides and peptides).

Who You Are:
You are enthusiastic about tackling complex analytical challenges to advance the development of small molecule therapeutics and oligonucleotides. You are motivated to learn new techniques and become a subject matter expert. You thrive both independently and collaboratively within a team setting, bringing a passion for scientific innovation and a commitment to excellence.
Required Skills:
  • Ph.D. with 0-3 years of relevant experience in pharmaceutical or biotech settings

  • M.S. with 4+ years of relevant experience in pharmaceutical or biotech settings.

  • BS with 6+ years of relevant experience in pharmaceutical or biotech settings

  • Deep expertise in small molecule LC method development, with strong experience in HPLC/UHPLC and familiarity with LC-MS.

  • Proven ability to lead analytical activities for drug development programs.

  • Strong knowledge of ICH guidelines and experience working within regulated (GMP/GLP) environments.

  • Excellent problem-solving, communication, and cross-functional collaboration skills.

Preferred Skills:
  • Experience with oligonucleotides and/or peptides.

  • Advanced MS techniques (e.g., LC-MS/MS, HRMS).

Job Level: Management
Additional Information
The base compensation range for this role is: $117,000.00-$157,000.00
Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
  • Medical, Dental, Vision, & Life insurances
  • Fitness & Wellness programs including a fitness reimbursement
  • Short- and Long-Term Disability insurance
  • A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
  • Up to 12 company paid holidays + 3 paid days off for Personal Significance
  • 80 hours of sick time per calendar year
  • Paid Maternity and Parental Leave benefit
  • 401(k) program participation with company matched contributions
  • Employee stock purchase plan
  • Tuition reimbursement of up to $10,000 per calendar year
  • Employee Resource Groups participation

Why Biogen?
We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.
All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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About Biogen

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At Biogen, our mission is clear - we are pioneers in neuroscience. Biogen discovers, develops, and delivers worldwide innovative therapies for people living with serious neurological and neurodegenerative diseases. Together, our employees create, commercialize, and manufacture transformative therapies for our patient population.

Industry

Scientific research and development services

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

1978

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