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LGC Group

Process Development Chemist

16h

LGC Group

Petaluma, US · Full-time · $64,480 – $97,760

About this role

LGC Biosearch Technologies delivers mission critical genomics to customers in molecular diagnostics, pharma/biotech and agrigenomics. With manufacturing sites across the US, UK, Germany and Denmark, the company supports Science for a Safer World. The Process Development Chemist supports oligonucleotide manufacturing process development, transfer, continuous improvement, and trouble-shooting production issues.

Optimize, improve, and scale up/down solid-phase oligonucleotide synthesis, purification, concentration, conjugation, and downstream processing methods in routine manufacturing. Provide technical support in developing manufacturing processes and drafting procedures. Conduct root cause failure analysis for production and quality incidents.

Maintain good records of production activities, experimental procedures and analytical data. Ensure the experimental space complies with safety regulations. Deliver technical customer support and progress updates to stakeholders alongside project managers.

Onsite work at Petaluma and Novato sites is required in this high-growth, purpose-driven organization. Join a team enabling research into life-altering treatments for disease worldwide. Operate in an environment focused on continuous improvement and regulatory compliance.

Requirements

  • Bachelors in Science in Chemistry, Biochemistry or related field
  • 1-3 years industry experience in this or related field strongly preferred
  • Knowledge of DNA/RNA synthesis and/or liquid chromatography purification at small or medium scale preferred
  • Experience with Instrumentation software including MassLynx, Empower, Chromeleon or Unicorn and/or data analysis software including Minitab, R, MATLAB or StatView strongly preferred
  • Working knowledge of GMP, ISO, and FDA rules and regulatory requirements
  • Proficiency with Lean manufacturing philosophy and techniques preferred
  • Experience in a GxP environment preferred

Responsibilities

  • Optimize, improve, and scale up/down solid-phase oligonucleotide synthesis, purification, concentration, conjugation, and downstream processing methods in routine manufacturing
  • Provide technical support in the development of manufacturing process and capability, including developing and drafting of manufacturing procedures
  • Provide technical support in root cause failure analysis for production and quality incidents
  • Keep good records of production activities, experimental procedures and analytical data
  • Maintain the experimental space in compliance with safety regulations
  • Provide technical customer support and routine progress updates to internal/external stakeholders in conjunction with project manager
  • Work onsite at both Petaluma and Novato sites

Benefits

  • Comprehensive medical, dental, and vision benefits for employees and dependents
  • FSA/HSA Pre-tax savings plans for health care, childcare, and elder care
  • 401(k) retirement plan with matching employer contribution
  • Company-paid short- and long-term disability, life insurance, and employee assistance program
  • Flexible work options with 8, 10 and 12 hour shifts available including day, swing and night shifts
  • Enhanced Parental leave of 8 additional weeks
  • PTO that begins immediately and full week paid off during the holidays