Process Development Chemist

16h16 hours ago

LGC Group

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

About this role

LGC Biosearch Technologies delivers mission critical genomics to diverse customers in molecular diagnostics, pharma/biotech and agrigenomics. The Process Development Chemist supports oligonucleotide manufacturing process development, transfer, continuous improvement, and troubleshooting production issues. This role operates in a high-growth, purpose-driven organization advancing Science for a Safer World.

Optimize, improve, and scale up/down solid-phase oligonucleotide synthesis, purification, concentration, conjugation, and downstream processing methods for routine manufacturing. Provide technical support for developing manufacturing procedures and root cause failure analysis of production and quality incidents. Maintain detailed records of activities, procedures, and analytical data while ensuring experimental space complies with safety regulations.

Onsite work at Petaluma and Novato sites supports collaboration with project managers on technical customer updates for internal and external stakeholders. Function in a GxP environment adhering to GMP, ISO, and FDA rules. Contribute to an integrated portfolio enabling research into life-altering disease treatments worldwide.

Grow within expanding manufacturing sites across the US, UK, Germany, and Denmark. Tackle challenges in a dynamic team focused on process capability and stakeholder progress. Advance expertise in oligonucleotide production for global impact.

Requirements

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

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
Perform onsite work 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- 8, 10 and 12 hour shifts available with option of day, swing and night shifts
Pet Insurance for our furry friends
Enhanced Parental leave of 8 additional weeks
PTO that begins immediately