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Manufacturing Formulation Support

Kinetic Personnel Group

Job Description

Job Description

Job Summary
The Formulation Support Associate provides technical and operational support for formulation development activities in a biopharmaceutical environment. This role assists in preparing formulations, maintaining laboratory equipment, documenting experiments, and ensuring compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and company quality standards.

Key Responsibilities

  • Prepare buffers, media, and formulation solutions according to approved procedures.
  • Support formulation scientists in the development and optimization of biologic drug products.
  • Perform weighing, mixing, filtration, pH adjustment, and sample preparation.
  • Operate and maintain laboratory equipment such as balances, pH meters, mixers, and filtration systems.
  • Record experimental data accurately in laboratory notebooks and electronic systems.
  • Assist with stability studies by preparing, labeling, storing, and monitoring samples.
  • Maintain laboratory inventory, order supplies, and ensure adequate stock levels.
  • Follow SOPs, GLP, GMP, and safety regulations at all times.
  • Participate in equipment calibration, cleaning, and preventive maintenance.
  • Support investigations related to laboratory deviations and documentation.
  • Collaborate with analytical, manufacturing, quality assurance, and process development teams.

Qualifications

  • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Biology, Chemical Engineering, or a related scientific discipline.
  • 0–3 years of laboratory experience in the pharmaceutical or biopharmaceutical industry (internship experience may be considered).
  • Knowledge of formulation principles and laboratory techniques.
  • Familiarity with GMP, GLP, and FDA regulations is preferred.
  • Experience with laboratory documentation and electronic data systems is an advantage.

Required Skills

  • Strong laboratory and analytical skills.
  • Attention to detail and accuracy in documentation.
  • Ability to follow written procedures and SOPs.
  • Good organizational and time management skills.
  • Strong communication and teamwork abilities.
  • Basic proficiency in Microsoft Office (Excel, Word, Outlook).

Preferred Qualifications

  • Experience with protein or biologics formulations.
  • Knowledge of aseptic techniques and sterile processing.
  • Experience working in a regulated pharmaceutical or biotechnology environment.
Vacancy posted 14 days ago
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