The Therapeutic Production Chemist I will perform routine processes associated with oligonucleotide manufacturing in the LGC Petaluma Therapeutic GMP suite. Processes include: synthesis cleavage and deprotection purification desalting and lyophilization of oligonucleotides.
Swing Shift: 12:30 pm to 11:00 pm Monday to Thursday 4 10s with a 10% differential
What youll do
- Perform manufacturing processes (synthesis purification desalt freeze drying etc) in accordance with the production schedule and maintain a high quality of work that aligns with internal standard operating procedures and cGMP protocols.
- Work with an array of equipment (synthesizers HPLC purifiers HPLC columns TFF skids lyophilizers etc) for production at various scales
- Maintain batch records logs and other production records as directed per company procedures and cGMP protocols.
- Maintain a safe and orderly laboratory environment through regular cleanings and organization that is in alignment with internal GMP SOPs
- Develop best practices to facilitate execution of manufacturing operations in accordance with SOPs.
Qualifications :
- Bachelor of Science in a relevant STEM field is required.
- Proficient Microsoft Office Outlook Word and Excel.
- cGMP experience is required.
- Experience with oligonucleotide production is a huge plus.
- Experience with instrumentation software maintenance and trouble shooting.
- Professional presence and strong attention to detail is required.
- Technical proficiency that enables effective execution of documented procedures.
- Critical analysis and understanding of oligonucleotide manufacturing activities.
- Proficient writing
Remote Work :
No
Employment Type :
Fulltime