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Formulation Associate Jobs in California (NOW HIRING)

Kinetic Personnel Group

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Manufacturing Formulation Support

Tustin, CA · On-site

$20 - $21/hr

Job Summary The Formulation Support Associate provides technical and operational support for formulation development activities in a biopharmaceutical environment. This role assists in preparing ...

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Infographic showing various Formulation Associate job openings in California as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Manufacturing Formulation Associate Biopharma

Kinetic Personnel Group

Tustin, CA • On-site

$20 - $21/hr

Full-time

Medical, Dental, Vision

Posted 20 days ago

Job description

Manufacturing Formulation Associate (Entry Level)

A leading Contract Development and Manufacturing Organization (CDMO) dedicated to supporting the development and commercial manufacturing of innovative biopharmaceutical products. Committed to delivering high-quality manufacturing services while maintaining the highest standards of safety, quality, and regulatory compliance.


Position Summary

The Manufacturing Formulation Associate I is an entry-level role responsible for supporting the preparation, formulation, and manufacturing of biopharmaceutical products in a GMP-regulated environment. This position offers an excellent opportunity for recent graduates to begin a career in biopharmaceutical manufacturing and gain hands-on experience with industry-leading manufacturing processes.

Key Responsibilities

  • Prepare buffers, media, and formulation solutions according to approved batch records and standard operating procedures (SOPs).
  • Operate and monitor manufacturing equipment used in formulation and processing activities.
  • Perform equipment setup, cleaning, sanitization, and routine maintenance.
  • Accurately complete GMP documentation, batch records, and logbooks.
  • Follow current Good Manufacturing Practices (cGMP), safety procedures, and company policies.
  • Assist with material staging, inventory management, and manufacturing support activities.
  • Participate in environmental monitoring and cleaning verification activities as required.
  • Report process deviations, equipment issues, and quality concerns promptly.
  • Collaborate with Manufacturing, Quality Assurance, Quality Control, Engineering, and Warehouse teams to ensure timely production.
  • Participate in training and continuous improvement initiatives.

Minimum Qualifications

  • Bachelor's degree in Biology, Chemistry, Biochemistry, Microbiology, Biotechnology, or another Life Science discipline is required.
  • Recent graduates are encouraged to apply.
  • Strong attention to detail and organizational skills.
  • Effective written and verbal communication skills.
  • Ability to work independently and as part of a team.
  • Basic computer proficiency, including Microsoft Office applications.

Preferred Qualifications

  • Previous laboratory, manufacturing, internship, or research experience is a plus.
  • Familiarity with GMP or regulated laboratory environments is preferred but not required.
  • Knowledge of aseptic techniques and pharmaceutical manufacturing processes is beneficial.