About the Company
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $40 billion. Our mission is to enable our customers to make the world healthier, cleaner, and safer. We help our customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics and therapies, and increase laboratory productivity. Our global team of more than 100,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services.
Job Description
We are seeking a highly motivated and detail-oriented QC Chemist to join our Quality Control team in Jurupa Valley, CA. This is an immediate opening for a professional who thrives in a fast-paced pharmaceutical environment. The successful candidate will be responsible for conducting routine and non-routine analytical testing of raw materials, in-process samples, and finished products according to cGMP guidelines and established procedures. This role is crucial for ensuring the quality, safety, and efficacy of our pharmaceutical products before they reach our customers. You will utilize a variety of analytical techniques and instrumentation to perform your duties, contributing directly to our mission of making the world healthier.
Key Responsibilities
- Perform analytical testing of raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis, FTIR, Karl Fischer, dissolution, and titrations.
- Ensure all testing is conducted in compliance with cGMP, USP, and other relevant regulatory guidelines and internal standard operating procedures (SOPs).
- Document all analytical data, observations, and results accurately and contemporaneously in laboratory notebooks and LIMS.
- Calibrate, maintain, and troubleshoot laboratory equipment and instrumentation.
- Investigate out-of-specification (OOS) results and deviations, implementing corrective actions as needed.
- Participate in method validation and transfer activities.
- Prepare reagents, standards, and samples for analysis.
- Review and verify analytical data generated by peers.
- Contribute to the continuous improvement of laboratory operations and quality systems.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
- Minimum of 2 years of experience in a Quality Control laboratory within the pharmaceutical or biotechnology industry.
- Proficiency with major analytical techniques including HPLC, GC, and UV-Vis spectrometry.
- Strong understanding and practical experience with cGMP regulations.
- Experience with LIMS (Laboratory Information Management System) and other laboratory software.
- Excellent written and verbal communication skills.
- Strong problem-solving abilities and attention to detail.
- Ability to work independently and as part of a team in a regulated environment.
Preferred Qualifications
- Master's degree in Chemistry or a related field.
- Experience with Empower 3 chromatography software.
- Familiarity with microbiological testing principles.
- Knowledge of statistical analysis tools for data interpretation.
Perks & Benefits
- Comprehensive medical, dental, and vision insurance plans.
- 401(k) retirement savings plan with company match.
- Paid time off (PTO) and holidays.
- Life insurance and disability benefits.
- Employee assistance program (EAP).
- Tuition reimbursement and professional development opportunities.
- On-site fitness center (where applicable) and wellness programs.
- Employee stock purchase plan.
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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