LGC Axolabs
Therapeutic Production Chemist I/II/III - Weekend Shift
LGC Axolabs, Petaluma, California, United States, 94954
Job Description
The Therapeutic Production Chemist I/II/III will perform routine oligonucleotide manufacturing processes in the LGC Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophilization of oligonucleotides.
This role is for the Weekend shift: 3/12 hour shifts, Friday through Sunday, 7 a.m. to 7:30 p.m. There will be a 15% shift differential for this shift.
Responsibilities:
Perform manufacturing processes (synthesis, purification, desalting, 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.
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The Therapeutic Production Chemist I/II/III will perform routine oligonucleotide manufacturing processes in the LGC Petaluma Therapeutic GMP suite. Processes include: synthesis, cleavage and deprotection, purification, desalting, and lyophilization of oligonucleotides.
This role is for the Weekend shift: 3/12 hour shifts, Friday through Sunday, 7 a.m. to 7:30 p.m. There will be a 15% shift differential for this shift.
Responsibilities:
Perform manufacturing processes (synthesis, purification, desalting, 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.
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