Analytical Development Scientist II (Contract)

R&D Partners; San Carlos (CA); On-site; USD 146,000 - 158,000; Full time

Benefits offered by this job

Medical insurance

401k plan

Employee Assistance Program

Long-term disability

Weekly payroll

Online timecard approval

Job summary

R&D Partners in San Carlos, CA is seeking an energetic analytical development scientist to support ongoing laboratory activities in a 12-month contract. The role focuses on method development, optimization, and qualification/validation readiness.

Responsibilities include designing experiments to test method parameters, troubleshooting instrument performance, overseeing method transfer, maintaining inventory and cGMP/SOP documentation, and coordinating with cross‑functional teams to meet project

Qualifications

• PhD, MS or Bachelor’s degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or related field.
• PhD with 2–5 years; MS with 7+ years; BS with 10+ years of relevant industry experience in analytical development, QC, or related field.
• Strong hands‑on experience with multiple analytical techniques, such as UV-Vis, HPLC, CE, SDS-PAGE, icIEF, liquid chromatography, enzyme kinetics, colorimetric and fluorescent plate‑based assays, ELISA, Western Blot, and PCR.
• Experience independently driving method development or optimization activities preferred.
• Strong knowledge of analytical chemistry/biochemistry principles with demonstrated application to assay development and control strategies.
• Proven ability to independently troubleshoot non‑routine assay and instrument issues using structured root-cause analysis and data-driven decision making.
• Proficient with analytical software, data processing workflows, and statistical tools.
• Strong scientific judgment and attention to detail; consistently produces high‑quality, inspection‑ready documentation.
• Ability to independently plan and prioritize work, manage multiple projects, and meet timelines with minimal supervision.

Responsibilities

• Contribute to method development, optimization, and qualification/validation readiness activities.
• Design and execute experiments to evaluate critical method parameters and define appropriate system suitability and control strategies.
• Troubleshoot assay and instrument performance issues using a structured approach; interpret data to identify likely root causes, implement corrective actions, and document outcomes and recommendations.
• Support and/or execute method transfer activities, including protocol preparation, training support, execution at receiving labs, and resolution of transfer issues.
• Support lab management and operations, including sample and inventory tracking.
• Author and revise analytical methods, SOPs, protocols, and technical reports; ensure clear documentation of experimental rationale, results, and conclusions for internal review and stakeholder communication.
• Coordinate routine instrument maintenance and service activities; interface with vendors and lab management team as needed and support timely issue resolution.
• Ensure laboratory organization, cleanliness, and compliant material labeling/storage practices.
• Manage inventory of reagents, standards, and consumables; initiate procurement, track critical supplies, and support forecasting to avoid stockouts.
• Partner effectively with cross-functional teams to define analytical plans, meet project timelines, and deliver high-quality outputs.
• Communicate experimental progress, data interpretation, and emerging risks clearly; propose mitigation plans and align next steps with stakeholders.
• Contribute to a compliant, safety-focused, and scientifically rigorous lab culture; model good documentation practices and data integrity expectations.
• Train and mentor junior staff/new team members on analytical assays, workflows, and troubleshooting; provide day-to-day technical guidance and feedback.
• Perform routine and non-routine analytical testing using modern analytical methods (e.g., HPLC/UPLC, SEC, CE, UV-Vis, ELISA, electrophoresis, plate-based assays, and other biochemical/biophysical techniques).
• Execute assays in accordance with approved methods, SOPs, and applicable quality standards (GLP/GMP as applicable); identify and troubleshoot common issues.
• Perform data processing and interpretation; summarize results, trends, and potential risks, and elevate complex findings for review and decision-making.
• Maintain accurate, timely documentation in laboratory notebooks or electronic systems; contribute to clear technical communications to project and cross-functional stakeholders.
• Follow all Environmental Health & Safety (EHS) policies and laboratory safety practices.
• Handle chemicals and biological materials safely and in compliance with regulatory requirements.
• Ensure proper waste disposal and adherence to hazardous material handling procedures.
• Support audit and inspection readiness activities where applicable.

Skills

HPLC

CE

UV-Vis

SDS-PAGE

ELISA

PCR

Data processing

Root-cause analysis

Statistical tools

Lab safety

Education

PhD

MS

Bachelor's degree

Tools

HPLC instruments

LC-MS

icIEF

Job description

R&D Partners in San Carlos, CA is seeking an energetic analytical development scientist to support ongoing laboratory activities in a 12-month contract. The role focuses on method development, optimization, and qualification/validation readiness.

Responsibilities include designing experiments to test method parameters, troubleshooting instrument performance, overseeing method transfer, maintaining inventory and cGMP/SOP documentation, and coordinating with cross‑functional teams to meet project