Chemist

Pay Rate Low: 28 | Pay Rate High: 38

About The Role

We are seeking a detail-oriented and motivated Chemist to join a pharmaceutical manufacturing team responsible for producing active pharmaceutical ingredients (APIs) in a cGMP-regulated environment. This is a hands-on role combining technical chemistry skills with rigorous documentation and quality compliance. The successful candidate will play a key role in day-to-day manufacturing operations, in-process testing, and continuous process improvement.

Type: 2-month contract (Possibility for extension) | Hours: M-F 8am-4:30pm | Location: Onsite in Torrance, CA

Key Responsibilities

• Execute solid-phase and liquid-phase synthesis and purification processes, including chromatography and crystallization, following approved manufacturing directions.
• Follow and maintain GMP documentation systems including Master Batch Records, SOPs, and Standard Test Procedures. Investigate deviations, author reports, initiate document change requests, and support equipment calibration programs.
• Support project planning and raw material procurement. Coordinate with QA/QC and materials management teams to facilitate material release and maintain inventory levels.
• Maintain clean and organized work areas in compliance with GMP and safety standards. Handle hazardous chemicals per approved procedures, including proper disposal of chemical waste and upkeep of equipment cleaning logs.
  
  

Required Qualifications

• Bachelor's degree in chemistry or a related discipline, or 10 years of relevant hands-on experience in lieu of a degree.
• Proficiency with standard laboratory instrumentation including HPLC and UV spectrometry.
• Strong written and oral communication skills with a collaborative, team-oriented mindset.
• Ability to work independently, manage competing priorities in a fast-paced environment, and communicate proactively with supervisors.
• Comfortable working with hazardous materials and chemicals under appropriate safety protocols.
  
  

Preferred qualifications

• Prior experience in a GMP manufacturing environment with working knowledge of cGMP standards and FDA regulations.
• Background in the manufacture of peptides, oligonucleotides, or similar complex molecules.
  
  

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

#INDBH