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Entry Level Biopharmaceutical Jobs (NOW HIRING)

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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 ...

Our teams help biopharma get their medicines to the people who need them. We help customers gain insight and access to their markets and ultimately demonstrate their product's value to payers ...

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Manufacturing Formulation Associate Biopharma

Kinetic Personnel Group

Tustin, CA • On-site

$20 - $21/hr

Full-time

Medical, Dental, Vision

Posted 21 days ago

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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.