Manufacturing Technician - II*

The Fountain Group; San Francisco (CA); On-site; USD 39,000 - 44,000; Full time

Job summary

The Fountain Group is seeking a Manufacturing Technician for an onsite role in Oceanside, CA. The position involves executing cGMP manufacturing processes, following batch records and SOPs, and handling raw materials weighing, chromatography, and viral vector manufacturing using aseptic techniques.

Responsibilities include operating single-use systems, MES/EBS transactions, buffer prep, and GMP documentation review, with collaboration across MSAT, Facilities & Engineering, and Quality teams to

Qualifications

• GMP/ISO regulations experience required.
• Experience with downstream purification techniques.
• Experience with SOP adherence and chromatography.

Responsibilities

• Execute cGMP manufacturing processes following batch records and SOPs.
• Weigh raw materials, operate chromatography and ultrafiltration/diafiltration.
• Perform viral vector manufacturing operations using aseptic technique.
• Collaborate with MSAT, Facilities & Engineering and Quality teams; review GMP docs.

Skills

GMP/ISO compliance

SOP adherence

Chromatography techniques

Aseptic technique

Batch records

Education

High school diploma or GED

Associates or Bachelor's degree

Tools

MES/EBS systems

Job description

We are a national staffing firm and are currently seeking a Manufacturing Technician for a prominent client of ours. This position is located in Oceanside, CA, 92056. Details of the position are as follows:

Job Description:

• Pay: $28.00- 31.78/hr to start.
• 1 year contract with the possibility of extension or conversion based on budget and performance.
• Monday- Friday, standard day shift, onsite position.
• Position will mainly be responsible for executing cGMP manufacturing processes, following batch records and SOPs, performing raw material weighing, chromatography, ultrafiltration/diafiltration, and viral vector manufacturing operations using aseptic technique and proper cleanroom practices.
• Responsibilities also include operating single-use systems and MES/EBS transactions, supporting buffer preparation, filter integrity testing, viral vector filling, equipment troubleshooting, and reviewing in-process GMP documentation for accuracy and compliance.
• Position will also be responsible for collaborating with MSAT, Facilities & Engineering, and Quality teams, supporting SOP and MPR revisions, escalating process or equipment issues, and maintaining a safety-first, right-the-first-time manufacturing environment.

Qualifications:

• High school Diploma, GED, Associates, or Bachelors degree is required.
• Experience in GMP/ISO regulations is required.
• Experience with downstream purification techniques is required.
• Experience with SOP adherence is required.
• Experience with chromatography is required.