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Synthetic DNA Process Development Scientist

Job in Louisville, Jefferson County, Kentucky, 40201, USA
Listing for: Eurofins
Full Time position
Listed on 2026-07-01
Job specializations:
  • Research/Development
    Research Scientist, Biotechnology, Pharmaceutical Science/ Research
Job Description & How to Apply Below

Synthetic DNA Process Development Scientist

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services.

Job Description

Position Summary

We are seeking a highly skilled and motivated Organic Chemist with expertise in oligonucleotide synthesis and purification to support process development and manufacturing. This role focuses on developing, optimizing, and scaling chemical processes for high-throughput and high-quality oligonucleotide production.

Key Responsibilities

• Design, develop, and optimize chemical synthesis processes for nucleotides and oligonucleotides

• Process development and scale-up from R&D to manufacturing

• Develop and improve oligonucleotide purification processes (e.g., HPLC, ion-exchange, desalting)

• Troubleshoot synthesis and purification challenges to improve yield and purity

• Collaborate with manufacturing, QC, and engineering for process transfer

• Evaluate new chemistries and technologies

• Author SOPs, batch records, and technical reports

• Ensure compliance with quality systems

• Mentor lab technicians

Qualifications

• Ph.D. or Master's degree in Organic Chemistry or related field (required)

• Minimum 5 years of industrial experience in chemical synthesis

• Experience with solid-phase oligonucleotide synthesis

• Experience in oligonucleotide purification process development

• Strong analytical skills (HPLC, LC-MS)

• Experience scaling processes to manufacturing

Preferred Qualifications

• Experience in GMP or regulated environments

• Familiarity with automated DNA/RNA synthesizers

• Knowledge of modified nucleotides

• Experience in high-throughput oligo production

Work Environment

• Fast-paced, collaborative environment

• Ability to manage multiple priorities

• Occasional off-hours support as needed

Work Schedule

Location:

Louisville, KY

Schedule:

Monday–Friday, 8:00 AM – 5:00 PM

Weekend Work as needed

Additional Information

All your information will be kept confidential according to EEO guidelines.

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