Therapeutic Production Chemist I - Swing Shift
Posted on Sep 23, 2024 by LGC Axolabs
Petaluma, CA
Research
Immediate Start
Annual Salary
Full-Time
Job Description
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 you’ll 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.
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 you’ll 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.
Reference: 202205694
https://jobs.careeraddict.com/post/95515400
Therapeutic Production Chemist I - Swing Shift
Posted on Sep 23, 2024 by LGC Axolabs
Petaluma, CA
Research
Immediate Start
Annual Salary
Full-Time
Job Description
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 you’ll 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.
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 you’ll 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.
Reference: 202205694
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