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Associate Scientist Analytical Development Jobs in Massachusetts

Sr. Scientist, Analytical Development

Lexington, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Supervise and train AD Associates and AD Technicians and work closely with other departments ... scientific excellence, staying current with industry developments, making data-driven decisions ...

Senior Associate Scientist, Analytical R&D

Andover, MA · On-site

$68K - $114K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

As a Senior Associate Scientist, you will be at the forefront of this mission, working within our ... Within Analytical R&D the candidate will join the Characterization and Analytical Sciences (CAS ...

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Associate Scientist Analytical Development information

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 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 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 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 Massachusetts?

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

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

The top searched job categories for Associate Scientist Analytical Development jobs in Massachusetts are:

What cities in Massachusetts are hiring for Associate Scientist Analytical Development jobs?

Cities in Massachusetts with the most Associate Scientist Analytical Development job openings:

Infographic showing various Associate Scientist Analytical Development job openings in Massachusetts as of August 2026, with employment types broken down into 66% Full Time, 30% Contract, and 4% Nights. Highlights an 100% In-person job distribution.

Associate Scientist, Analytical Development

Celldex Therapeutics

Fall River, MA • On-site

$66K - $86K/yr

Full-time

Medical, Retirement, PTO

Re-posted 14 days ago


Job description

Celldex is pioneering new horizons in immunology to deliver life-changing therapies. We are relentless in our pursuit of novel antibody-based treatments that engage the human immune system and directly affect critical pathways to improve the lives of patients with allergic, inflammatory and autoimmune disorders. We have built a culture where innovative and talented people thrive—focusing a significant effort on attracting and retaining passionate and motivated employees who want to play a role in helping people with serious health conditions and who see this effort as personally rewarding. In our highly entrepreneurial environment, employees are empowered and the opportunity for professional development occurs every day.


The Associate Scientist, Analytical Development (AD) is a key contributor responsible for supporting the development and qualification of robust, fit-for-purpose analytical methods for Quality Control (QC). The Associate Scientist will provide analytical support and document all activities in laboratory notebooks and technical reports following Good Documentation Practices (GDP).

Additional responsibilities include solution preparation, inventory tracking and ordering, and maintaining a clean and orderly laboratory environment.


  • Method Development & Optimization (30%):
    • Under the guidance of AD management and scientists, execute experimental protocols for developing and optimizing novel analytical methods (e.g., HPLC, UPLC, CE-SDS, cIEF, UV/Vis, ELISA) for testing drug substances and drug products.
  • Method Qualification (30%)
    • Under the guidance of AD management and scientists, perform hands-on execution of qualification studies, including accuracy, precision, linearity, range, specificity, detection limit, and quantitation limit assessments.
  • Documentation & Compliance (20%)
    • Assist in authoring GxP-compliant technical reports and Standard Operating Procedures (SOPs).
    • Maintain meticulous laboratory notebooks and electronic records and submit for review in a timely manner.
  • Additional (20%)
    • Order and receive reagents and labware, as needed.
    • Maintain general and assay-specific inventory.
    • Log and store all received samples and items.
    • Track tasks, meetings, events, etc. in AD team weekly schedule and keep up to date.
    • Fully operate all laboratory equipment necessary to complete responsibilities.
    • Log all equipment usage in necessary locations.
    • Coordinate with other groups for testing/equipment needs.
    • Assist with the day-to-day maintenance of an orderly analytical laboratory.
    • Perform a weekly laboratory walk-through:
      • Update inventory list(s).
      • Dispose of hazardous waste (bench tops, large bins, HPLC waste).
      • Dispose of expired materials (wet and dry reagents).
      • Wash/put away glassware.
      • Clean/organize bench tops.
      • Discard/create waste streams.
    • Seek opportunities for personal and professional growth (conferences, webinars, trainings, etc.).

  • BS/BA degree in science or similar area with 2-4 years of lab experience.
  • MS degree in science or similar area with 0-2 years of lab experience
  • 0-4 years’ experience in the Biotechnology/Pharmaceutical industry working with biological products.
  • Experience with HPLC, ELISA, CE-SDS (CGE), cIEF, and standard analytical techniques is preferred but not required. 
  • The ability to think and solve problems creatively from a critical and analytical perspective.
  • Meticulous documentation and strong writing skills.
  • Strong interpersonal skills.
  • Exceptional self-management skills, including taking initiative and time management.
  • Strong attention to detail and thorough cleanliness/organization.
  • Excellent written and oral communication skills.
  • Ability to work both independently and as part of a team.
  • Confidence to ask questions and take calculated risks.

Compensation

The expected base salary range for this position is $66,413 - $86,250.

We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.


Compensation for this role includes base salary, annual discretionary bonus, long term incentive, 401(K) plan with employer contribution, health care and other insurance benefits (for employee and family), paid holidays, vacation, and sick days. A summary of our benefits can be found on our careers page.

Celldex is proud to be an equal opportunity employer that strives to foster a culture of diversity, equity, and inclusion. We are committed to promoting a diverse environment through development, recruiting and community outreach.