Oligonucleotide Manufacturing Process Engineer (Contract)

Hydrogen UK Ltd; San Diego (CA); On-site; USD 51,000 - 56,000; Full time

Job summary

Hydrogen UK Ltd in San Diego, CA is seeking a Manufacturing Process Engineer – Oligonucleotides on a 9-month contract to help manufacture and process oligonucleotides, support process sustainment, optimization, and continuous improvement, and contribute to design, development, and quality testing activities.

The role requires collaboration with R&D, Manufacturing and Quality, strong documentation, and experience in biotech/pharma, chemical processes (organic chemistry), and statistics with SPC

Qualifications

• Experience in biotechnology or pharmaceutical industry is desirable.
• Experience with chemical processes, preferably organic chemistry processes.
• Experience with statistics, SPC, and DOE techniques is a plus.
• Experience with high-volume production in a high-tech or high-volume consumables environment is a plus.
• Experience with product development processes and project management is a plus.
• Strong interdepartmental communication and documentation skills are required.

Responsibilities

• Participate in the manufacture and processing of oligonucleotides.
• Support process sustainment, definition, optimization, and continuous improvement activities.
• Participate in design, development, and quality testing activities related to oligonucleotide manufacturing.
• Collaborate cross-functionally with R&D, Manufacturing, and Quality teams.
• Develop manufacturing processes for new products and improve processes supporting existing products.
• Maintain clear documentation and communicate effectively across departments.

Skills

Interdepartmental communication

Statistics, SPC & DOE

Project management

High-volume production experience

Job description

Hydrogen UK Ltd in San Diego, CA is seeking a Manufacturing Process Engineer – Oligonucleotides on a 9-month contract to help manufacture and process oligonucleotides, support process sustainment, optimization, and continuous improvement, and contribute to design, development, and quality testing activities.

The role requires collaboration with R&D, Manufacturing and Quality, strong documentation, and experience in biotech/pharma, chemical processes (organic chemistry), and statistics with SPC