Analytical Scientist

AL Solutions; Bristol Township (Bucks County); On-site; USD 34,000 - 41,000; Part time

Job summary

AL Solutions in Bristol, PA is seeking Analytical Scientists for a contract role to advance biologics development. You will perform hands-on chromatography-based analytical testing, manage method development and validation, and support GMP documentation and tech transfer activities.

The ideal candidate has a strong background in HPLC/UPLC, GMP environments, and problem-solving in a fast-paced CDMO setting, contributing to a diverse client portfolio.

Qualifications

• Bachelor's degree or higher in a chemical or life science field.
• 4+ years in analytical development or QC within a GMP lab.
• Hands-on experience with HPLC/UPLC including method development, qualification, validation or transfer.
• Strong GMP, GDP and data integrity knowledge.

Responsibilities

• Perform analytical testing using HPLC, UPLC and other chromatography techniques.
• Develop, qualify, validate and transfer analytical methods for biologics development and manufacturing.
• Conduct development batch testing, product release, stability and characterization.
• Troubleshoot chromatography methods, instruments and system-suitability failures.
• Review chromatograms, integrations and analytical data.
• Prepare and review GMP documentation and lab records.
• Support investigations and deviations as needed.
• Collaborate with cross-functional teams for tech transfers and manufacturing activities.

Skills

HPLC

UPLC

Analytical testing

GC/LC-MS

Chromatography troubleshooting

Education

Bachelor's degree in Chemistry/related field

Job description

Employment Type: Contract

Hourly Rate: $25-$30 per hour

Schedule: Three 12-hour shifts per week (36 hours total)

Shift Options: Friday, Saturday & Sunday OR Saturday, Sunday & Monday

Contract Duration: Initial contract through December 2026, with anticipated extension throughout 2027 and potential permanent conversion.

Company Overview

We are partnering with a leading global Contract Development and Manufacturing Organization (CDMO) specializing in biologics, bioconjugates and advanced therapeutics.

Due to continued growth and expansion of its GMP manufacturing and analytical capabilities, our client is seeking multiple experienced Analytical Scientists to join its Analytical Services team in Bristol, Pennsylvania.

This is an exciting opportunity to contribute to innovative biologics development programmes, work with advanced analytical technologies and support a diverse portfolio of pharmaceutical and biotechnology clients.

Position Overview

The Analytical Scientist will be responsible for performing hands-on laboratory activities supporting analytical development, method qualification, validation, technology transfer and GMP testing.

The successful candidate will work closely with Analytical Development, Quality Control, Quality Assurance and Manufacturing teams to ensure the accurate and timely delivery of analytical results in compliance with GMP requirements.

This position is ideal for a technically strong analytical scientist with extensive chromatography experience who enjoys laboratory-based problem-solving and working within a fast-paced CDMO environment.

Key Responsibilities

• Perform hands-on analytical testing using HPLC, UPLC and other chromatography-based techniques.
• Develop, optimize, qualify, validate and transfer analytical methods supporting biologics development and manufacturing.
• Conduct analytical testing for development batches, product release, stability studies and product characterization.
• Troubleshoot chromatography methods, instrumentation and system-suitability failures.
• Evaluate analytical method performance, including linearity, accuracy, precision, specificity, range and robustness.
• Review and interpret chromatograms, integrations, analytical results and laboratory data.
• Prepare and review GMP documentation, including laboratory notebooks, protocols, technical reports and analytical records.
• Support analytical investigations, deviations and troubleshooting activities.
• Collaborate with cross-functional teams to support technology transfers, process development and manufacturing activities.
• Ensure compliance with GMP, Good Documentation Practices (GDP), data integrity requirements and internal quality procedures.
• Contribute to continuous improvement initiatives to enhance analytical methods, laboratory efficiency and testing capabilities.

Required Qualifications & Experience

• Bachelor's degree or higher in Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences or a related scientific discipline.
• Ideally 4+ years of experience in Analytical Development or Quality Control within a GMP pharmaceutical or biotechnology laboratory.
• Strong hands‑on experience with HPLC and/or UPLC, including method development, optimization, qualification, validation or transfer.
• Demonstrated understanding of analytical method qualification and validation parameters.
• Experience troubleshooting chromatography methods and investigating system-suitability failures.
• Experience performing GMP analytical testing supporting development, release, stability or characterization activities.
• Strong understanding of GMP, GDP and laboratory data integrity requirements.
• Experience reviewing analytical data, chromatograms, integrations and technical documentation.
• Strong analytical, problem‑solving and communication skills.