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Biopharma Formulation Manufacturing Associate

Kinetic Personnel Group

Job Description

Job Description

 

We are seeking a detail-oriented Formulation Manufacturing Associate to support the preparation, formulation, and manufacturing of biopharmaceutical products in a GMP-regulated environment. The successful candidate will follow standard operating procedures (SOPs), maintain compliance with quality standards, and contribute to the production of safe and effective pharmaceutical products.

Key Responsibilities

  • Prepare and formulate biopharmaceutical products according to batch records and SOPs.
  • Operate, clean, and maintain formulation and manufacturing equipment.
  • Accurately complete manufacturing documentation and batch records.
  • Perform material preparation, weighing, mixing, and solution preparation.
  • Adhere to Good Manufacturing Practices (GMP), safety policies, and quality standards.
  • Assist with equipment setup, calibration, and troubleshooting.
  • Support investigations related to deviations and implement corrective actions as required.
  • Work collaboratively with Quality Assurance, Quality Control, and Engineering teams.
  • Maintain a clean and organized manufacturing environment.

Minimum Qualifications

  • Bachelor's degree in Life Sciences (Biology, Microbiology, Biochemistry, Biotechnology, Chemistry, or a related scientific discipline) is required.
  • 0–3 years of experience in pharmaceutical, biotechnology, or GMP manufacturing preferred.
  • Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) is preferred.
  • Strong attention to detail and organizational skills.
  • Ability to follow written procedures and work accurately in a regulated environment.
  • Strong communication and teamwork skills.
  • Basic computer proficiency, including Microsoft Office applications.

Preferred Qualifications

  • Experience with aseptic processing or formulation manufacturing.
  • Familiarity with cleanroom operations and pharmaceutical manufacturing equipment.
  • Experience working in a cGMP-regulated environment.
Vacancy posted 2 days ago
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