Analytical Chemist

Pay Range- $30 - $35 per hour on W2 Position Summary

The Associate Scientist will support analytical activities within vaccine process development and GMP laboratories. This role involves hands‑on analytical testing of biological samples, chromatography-based separations, potency assays, and comprehensive electronic documentation. The position requires strong laboratory execution, attention to detail, and the ability to operate independently while collaborating cross‑functionally in a regulated environment.

• Perform analytical testing including chemical labeling of biological samples, HPLC/UPLC separations, and potency assays (e.g., ELISA)
• Prepare buffers and solutions, pack chromatography columns, set up analytical systems, and perform sterilization and sampling activities
• Execute and support chromatography techniques including IEX, SEC, HIC, and reversed‑phase chromatography
• Apply additional separation and biochemical analysis methods, including capillary electrophoresis and two‑dimensional separations
• Analyze experimental data and author internal technical reports
• Document all laboratory activities electronically and enter process data into designated databases
• Troubleshoot analytical instruments and perform minor equipment repairs as needed
• Maintain laboratory inventory, aliquot materials, and support general lab operations
• Ensure laboratory spaces remain clean, orderly, inspection‑ready, and compliant with safety and GMP standards
• Follow cGMP/cGLP practices and all company safety and quality policies

• Bachelor's degree in Biology, Chemistry, or a closely related scientific field
• Minimum of 3 years of hands‑on experience in the pharmaceutical or medical technology industry (pharma experience preferred)
• 1–2 years of wet laboratory experience
• Hands‑on experience with chromatography techniques
• Experience using Empower software
• Proficiency with Microsoft Word and Excel
• Strong computer, scientific, organizational, and documentation skills
• Excellent oral and written communication skills with strong attention to detail
• Ability to work independently and collaboratively in a team environment
• Demonstrated adaptability, self‑motivation, and positive attitude

• Experience analyzing therapeutic proteins using UPLC/HPLC techniques (IEX, SEC, HIC, RP)
• Prior experience working in cGMP or cGLP environments
• Experience using electronic laboratory notebooks (ELN)
• Demonstrated ability to author internal technical reports

• Candidate must be able to work onsite at both the West Point, PA and North Wales, PA locations (approximately 1–2 miles apart)