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How much do analytical development scientist jobs pay per hour?

As of May 30, 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 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.

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 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.

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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Analytical Development Scientist jobs near you
Development Scientist II, Analytical Development and Clinical QC (ADQC)

Development Scientist II, Analytical Development and Clinical QC (ADQC)

Alexion Pharmaceuticals

New Haven, CT • On-site

Full-time

Posted 18 days ago

Job description

This is what you will do:
This Development Scientist II will be a key team member in Alexion's External Analytical Development and Quality Control group. This position is responsible for maintaining the highest standard of quality and compliance of external quality control testing (GMP) laboratories. This candidate will be responsible for initiation and ownership of laboratory investigations (LIRs) through strong liaison with external contract laboratories and change controls relevant to ADQC biologic programs. The candidate will ensure timely, compliant, and high-quality delivery for LIR closure to enable the generation of final release CoAs. The role will work closely with internal Quality Assurance, Compliance, Analytical Development and Stability teams to ensure product to patients.
You will be responsible for:
  • Responsible for generating and/or mirroring, reviewing, providing assessments, and driving ownership of LIRs to close out Out-of-Specification (OOS), Out-of-Trend (OOT), and atypical results with structured root cause analysis, impact assessment, and/or corrective/preventive actions (CAPAs).

  • Design investigational testing plans ensuring compliant closure of all testing related investigations within the quality system.

  • Lead and/or facilitate cross-functional meetings with quality assurance to ensure structured investigation alignment.

  • Create plans, track, and present timelines to meet established targets, goals, and objectives.

  • Perform review of analytical data to ensure expected assay performance.

  • Identify opportunities for improvement in systems and make recommendations for effective changes to ensure compliance with cGMP.

  • Strong presentation skills

You will need to have:
  • A successful candidate will have strong mental acuity with high attention to detail and ability to maintain accuracy in documentation and processes.

  • Excellent analytical and problem-solving skills with the ability to conduct risk assessments and root cause analysis.

  • A broad knowledge of Pharmaceutical Quality Assurance, regulatory compliance, and/or quality control inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations.

  • Strong proficiency in quality management systems and effective communication skills for interacting with cross-functional teams.

  • Strong proficiency with MS Word, Excel, PowerPoint.

  • Ability to bend, reach and stand, with lifting to 15 pounds and carrying over short distances.

  • Ability to travel up to 10%, if needed.

  • Advanced (M.S. or Ph.D.) degree in Biochemistry, Chemistry or related discipline with 2-5 years (Ph.D.) or 10+ (M.S.) hands on biological analytical development experience in pharmaceutical industry.

We would prefer you to have:
  • Working knowledge in validated documentation systems: Veeva Vault (EQV), LIMS, ValGenesis, Kneat, etc.

  • Knowledge of pharmaceutical/biotechnology manufacturing process

  • Database management /statistical analysis (e.g., JMP, Tableau, SAS) with proficiency in Microsoft SharePoint and/or BOX.

Date Posted
12-May-2026
Closing Date
28-May-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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