About the Company
Gilead Sciences is a biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet medical need. We are committed to advancing treatments for life-threatening diseases worldwide. Our mission drives us to create a healthier world, and we achieve this through cutting-edge science, collaboration, and a deep commitment to patient care.
Job Description
Join Gilead Sciences as a QC Chemist in Fontana, CA. This role is critical for ensuring the quality and integrity of our pharmaceutical products. You will perform analytical testing on raw materials, in-process samples, and finished products, playing a vital part in our mission to improve patient lives. We are looking for a dedicated individual ready to contribute to a dynamic and fast-paced environment with immediate openings and excellent pharmaceutical benefits. This is an on-site position requiring hands-on laboratory work.
Key Responsibilities
- Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished products using various laboratory techniques (HPLC, GC, UV-Vis, FTIR, Karl Fischer, Titration).
- Accurately document all experimental data, observations, and results in laboratory notebooks and LIMS systems, ensuring data integrity.
- Adhere to cGMP, GLP, SOPs, and safety guidelines at all times to maintain a compliant and safe working environment.
- Calibrate and maintain laboratory equipment according to schedules and procedures, troubleshoot minor equipment issues.
- Investigate OOS (Out-of-Specification) and OOT (Out-of-Trend) results, assisting in root cause analysis and implementing corrective actions.
- Participate in laboratory audits, inspections, and continuous improvement initiatives to enhance quality systems and processes.
- Prepare reagents, solutions, and standards according to established procedures and maintain proper inventory.
- Review and approve analytical data generated by peers for accuracy and compliance.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
- Minimum 2 years of experience in a pharmaceutical QC laboratory.
- Proficiency with analytical techniques such as HPLC, GC, UV-Vis, FTIR, and Karl Fischer.
- Strong understanding of cGMP and GLP regulations.
- Excellent data analysis, documentation, and technical writing skills.
- Ability to work independently and as part of a team in a fast-paced, regulated environment.
- Strong problem-solving abilities and attention to detail.
Preferred Qualifications
- Master's degree in Chemistry or a closely related scientific field.
- Experience with LIMS (Laboratory Information Management System) and electronic laboratory notebooks.
- Knowledge of statistical process control (SPC) and its application in a QC setting.
- Familiarity with compendial testing (USP, EP, JP) and pharmacopeial guidelines.
- Experience in method validation, verification, and transfer activities.
- Certifications in relevant analytical techniques or quality systems.
Perks & Benefits
- Comprehensive medical, dental, and vision insurance for employees and their families.
- 401(k) retirement plan with generous company match.
- Generous paid time off, including vacation, sick leave, and company holidays.
- Life and disability insurance programs.
- Employee assistance program offering counseling and support services.
- Tuition reimbursement for approved educational development.
- Opportunities for professional development and career growth within a leading biopharmaceutical company.
- On-site wellness programs and facilities (at select locations).
- Commuter benefits program.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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