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Analytical Development Scientist Jobs (NOW HIRING)

Serán is seeking a Scientist II who will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase ...

Role Summary We are looking for a talented analytical scientist to lead analytical development and product characterization for monoclonal antibodies and other biologics produced using Neion Bio ...

Role Summary We are looking for a talented analytical scientist to lead analytical development and product characterization for monoclonal antibodies and other biologics produced using Neion Bio ...

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Analytical Development Scientist information

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How much do analytical development scientist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for analytical development scientist in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What does an analytical development scientist do?

An Analytical Development Scientist is responsible for developing, validating, and implementing analytical methods used to test and characterize pharmaceutical products, raw materials, or biological samples. They ensure the accuracy and reliability of laboratory data by designing experiments, optimizing protocols, and troubleshooting analytical instruments like HPLC, GC, or mass spectrometry. Their work is essential for quality control, regulatory submissions, and supporting product development in pharmaceutical or biotechnology industries.

How does an analytical development scientist typically collaborate with cross-functional teams during the drug development process?

Analytical Development Scientists frequently work alongside formulation scientists, process engineers, quality assurance, and regulatory teams to ensure the integrity and compliance of analytical methods. They contribute expertise in developing and validating analytical assays, interpreting data, and troubleshooting method-related issues. Regular meetings, data reviews, and joint problem-solving sessions are common, fostering a collaborative environment that supports successful product development and regulatory submissions.

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

To thrive as an Analytical Development Scientist, you need a solid background in chemistry or a related field, supported by at least a bachelor's or master's degree and experience in analytical method development. Familiarity with laboratory instrumentation such as HPLC, GC, mass spectrometry, and software like Empower or ChemStation is typically required, along with knowledge of regulatory standards (e.g., ICH, GMP). Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities are highly valued in this role. These skills and qualities are essential for ensuring reliable analytical results, maintaining regulatory compliance, and supporting the development of safe and effective pharmaceutical products.

What is the difference between Analytical Development Scientist vs Analytical Chemist?

AspectAnalytical Development ScientistAnalytical Chemist
CredentialsBachelor’s/Master’s in Chemistry or related field; experience in method developmentBachelor’s/Master’s in Chemistry; often entry-level or specialized in analysis
Work EnvironmentResearch labs, pharmaceutical or biotech companies, focus on method developmentLaboratories, quality control, manufacturing settings, focus on sample analysis
Industry UsageUsed in R&D for developing analytical methodsUsed in quality control and routine analysis

While both roles involve chemistry and analysis, Analytical Development Scientists focus on creating and optimizing analytical methods, often in R&D settings. Analytical Chemists typically perform routine sample testing and quality control. The roles are complementary but differ mainly in scope and focus.

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Infographic showing various Analytical Development Scientist job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 81% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 3% Hybrid, and 12% Remote job distribution, with an average salary of $80,420 per year, or $38.7 per hour.

Analytical Development Scientist II

Charles City, IA • On-site

Cambrex
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

Full-time

Medical, Life, Retirement

Re-posted 28 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

The Scientist II will provide analytical support for multiple project teams. This individual will collect and analyze data to support the development, validation and transfer of analytical methods for APIs, API intermediates and raw materials. Strict compliance with cGMP guidelines is required to perform most job tasks.

Responsibilities:
  • Safely and effectively collect analytical data to help develop, establish, and validate analytical
  • testing methodologies used to control raw materials, production intermediates, and final products
  • Perform analytical chemistry assays based on new and existing methodologies
  • Operate analytical instrumentation such as HPLC, GC, GC/MS, LC/MS, FTIR, Titrator, Particle
  • Size Analyzer
  • Maintain laboratory notebooks documenting work
  • Maintain compliance with GMP SOPs and DEA regulations
  • Transfer documented analytical methods to the QC and Process Support Group departments
  • Set up new or existing analytical methods for compound identification, purity and potency testing.
  • Coordinate off-site testing as necessary
  • Conduct testing of analytical samples for the Chemical Development Department as needed.
  • Collect analytical data to help qualify reference materials.
  • May also perform other duties as required
Qualifications / Skills:
  • Analytical Chemistry Knowledge: Basic understanding of the principles of Analytical Chemistry, some practical laboratory experience
  • Cross Discipline Knowledge: Basic understanding of the principles of cross-functional departments, including organic chemistry.
  • GMP/Regulatory Knowledge: Basic understanding of GMP; with manager assistance can help to answer client inquiries related to SOP or regulatory guidance.
  • Instrumentation: Good fundamental understanding and ability to use/investigate issues with HPLC,GC.
  • Communication: Good written and oral communication skills, demonstration of successful interdepartmental communication.
  • Problem Solving: Ability to support laboratory investigations with manager support.
  • Time Management: Reasonable ability to handle one or more tasks or projects, often with supervision.
  • Leadership: Shares ideas with peers.
  • Technical Documentation and Review: Ability to write technical documents with assistance.
  • External Influence: Occasionally participates in internal project team meetings, as needed; demonstrated ability to work within a team matrix.
  • Industry Credibility and Rapport: Known as a solid scientific contributor within the department/group.
  • Operational Excellence: Demonstrated interest in improvements of operational aspects of the group/team.
  • Change Orientation: Provides constructive feedback for Cambrex initiatives
Education, Experience, and Licensing Requirements: (Text Only)- M.S. in Chemistry or related field with minimum 2 years of experience or B.S. degree in Chemistry or related field with 6 years of experience in lab environment, pharmaceutical experience preferred. - Excellent verbal and written communication/interpersonal skills, organizational skills, and the ability to work in a diverse team environment are essential.  Employment Type: FULL_TIME

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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