Production Chemist I - Reagent Manufacturing
hace 1 día
Pomona
Job Description Production Chemist I – Reagent Manufacturing Location: Pomona, CA 91767 (Onsite) Job Type: Contract | Full-Time Industry: Diagnostics / Medical Devices / Biotechnology Experience Level: Entry-Level (0–2 Years) Anticipated Start Date: November 16, 2026 About the Opportunity Viltis is seeking a motivated, detail-oriented Production Chemist I to support our client's Toxicology Diagnostics manufacturing operations in Pomona, California. This entry-level opportunity is ideal for recent graduates with a bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific discipline who are interested in gaining hands-on experience in reagent manufacturing, immunoassay testing, and Good Manufacturing Practice (GMP) environments. The Production Chemist I will support bulk reagent formulation, antibody testing, and the manufacturing of critical components used in diagnostic testing products. Working closely with senior scientists, manufacturing personnel, and Quality Control and Quality Assurance teams, the selected candidate will help ensure products are manufactured accurately, safely, and in accordance with established quality standards. Key Responsibilities Reagent Manufacturing & Formulation • Prepare and manufacture bulk reagents used in ELISA, HEIA, and other enzyme immunoassay applications., • Formulate antibody solutions, enzyme conjugates, drug-positive solutions, calibrators, controls, and other diagnostic reagents., • Support antibody purification, antigen testing, and reagent preparation., • Perform analytical in-process testing to verify reagent quality and performance., • Follow approved batch manufacturing records, Standard Operating Procedures (SOPs), and GMP requirements., • Assist with material evaluations, reagent formulations, and production troubleshooting. Laboratory Operations & Quality Compliance • Operate, calibrate, clean, and maintain laboratory equipment according to established procedures., • Perform routine equipment maintenance and daily temperature monitoring., • Maintain accurate laboratory notebooks, batch records, equipment logs, and manufacturing documentation., • Record manufacturing and testing results in appropriate tracking systems., • Collaborate with Quality Control (QC) and Quality Assurance (QA) teams to resolve manufacturing and quality issues., • Assist with documentation updates, deviations, nonconforming material reports (NCMRs), and Bills of Materials (BOMs)., • Ensure laboratory materials are properly labeled, approved, and available for production. Manufacturing Support & Continuous Improvement • Support daily manufacturing schedules and production objectives., • Participate in Lean manufacturing and continuous improvement initiatives., • Maintain a clean, safe, and organized laboratory environment., • Identify potential quality concerns and communicate findings to senior staff., • Follow all applicable laboratory safety policies and quality system requirements., • Work collaboratively with cross-functional teams to meet manufacturing goals. Required Qualifications • Bachelor's degree (BS/BA) in Chemistry, Biology, Biochemistry, Biological Sciences, or a closely related scientific field., • 0–2 years of laboratory experience; relevant academic laboratory experience is acceptable., • Familiarity with basic laboratory techniques, equipment, and scientific procedures., • Ability to follow detailed SOPs and written manufacturing instructions., • Strong attention to detail and accurate documentation skills., • Good written and verbal communication skills., • Ability to work effectively in a team-oriented laboratory environment., • Strong organizational skills and commitment to laboratory safety., • Willingness to learn GMP manufacturing processes and quality systems. Recent college graduates are encouraged to apply. Previous industry experience is not required. Preferred Qualifications • 1–2 years of laboratory experience in biotechnology, diagnostics, pharmaceutical, or medical device manufacturing., • Familiarity with Good Manufacturing Practices (GMP)., • Hands-on experience with reagent preparation, solution formulation, or buffer preparation., • Exposure to ELISA, enzyme immunoassays, antibody purification, or antigen-antibody testing., • Experience completing batch manufacturing records and following SOPs., • Familiarity with Quality Control (QC) and Quality Assurance (QA) procedures., • Experience using Microsoft Office or laboratory/manufacturing documentation systems., • Strong analytical, troubleshooting, and problem-solving skills., • Demonstrated leadership, teamwork, or initiative in an academic or professional laboratory setting. Work Environment & Schedule • Location: 829 Towne Center Drive, Pomona, CA 91767, • Work Arrangement: 100% onsite, • Schedule: Full-time; occasional overtime or weekend work may be required., • Environment: Laboratory-based diagnostic reagent manufacturing., • Contract Duration: Anticipated through November 15, 2027, subject to business needs. Why Join Us? This position offers an excellent opportunity to launch your career in the biotechnology and medical diagnostics industry while gaining practical experience in: • GMP-regulated manufacturing operations, • Diagnostic reagent formulation and production, • ELISA and immunoassay technologies, • Antibody purification and testing, • Quality systems and manufacturing documentation, • Collaboration with experienced scientists and quality professionals Apply Today If you are a recent science graduate or early-career laboratory professional looking to build your experience in diagnostic manufacturing, we encourage you to apply. Viltis is an equal opportunity employer. We are committed to providing equal employment opportunities to qualified applicants without regard to legally protected characteristics.