About the Company
Abbott Laboratories is a global healthcare leader committed to helping people live fuller lives through health. With a diverse portfolio spanning diagnostics, medical devices, nutritionals, and branded generic pharmaceuticals, Abbott has been creating innovative solutions for over 130 years. We are dedicated to groundbreaking science and technology, improving health outcomes, and fostering a collaborative, inclusive environment. Our mission is to advance health and well-being worldwide.
Job Description
We are seeking a highly motivated and detail-oriented Finished Products Chemist to join our quality control team in Temecula. This high-demand role is critical to ensuring the integrity, quality, and compliance of our pharmaceutical products before release. The ideal candidate will perform a variety of analytical tests on finished products, raw materials, and in-process samples, contributing significantly to our commitment to patient safety and product excellence. This position offers weekly pay and a dynamic work environment within a leading global healthcare company.
Key Responsibilities
- Perform chemical and physical testing on finished pharmaceutical products, raw materials, and in-process samples according to established SOPs and compendial methods (USP, EP, JP).
- Operate and maintain analytical instrumentation including HPLC, GC, UV-Vis, FTIR, Karl Fischer titrators, and dissolution apparatus.
- Accurately record, analyze, and interpret experimental data, ensuring compliance with cGMP, FDA regulations, and internal quality standards.
- Investigate out-of-specification (OOS) results, out-of-trend (OOT) data, and deviations, documenting findings and participating in root cause analysis.
- Develop, validate, and transfer analytical methods as needed to support new product development or improvements.
- Calibrate and qualify laboratory equipment, maintaining proper documentation and calibration schedules.
- Prepare and standardize reagents and solutions required for testing.
- Collaborate with production, R&D, and quality assurance teams to resolve quality issues and support continuous improvement initiatives.
- Adhere to all safety protocols and maintain a clean and organized laboratory workspace.
- Review and approve analytical data, laboratory notebooks, and technical reports.
Required Skills
- Strong knowledge of analytical chemistry principles and laboratory techniques.
- Proficiency in operating and troubleshooting analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
- Familiarity with cGMP, GLP, USP, and FDA regulations.
- Experience with data analysis and statistical process control.
- Excellent problem-solving and critical thinking abilities.
- Strong written and verbal communication skills.
- Ability to work independently and as part of a team.
- Meticulous attention to detail and accuracy in all work.
Preferred Qualifications
- Master's degree in Chemistry, Analytical Chemistry, or a related scientific field.
- Experience with LIMS (Laboratory Information Management System).
- Previous experience in a pharmaceutical or medical device manufacturing environment.
- Knowledge of method development and validation guidelines (ICH).
- Familiarity with Lean Six Sigma principles.
Perks & Benefits
- Competitive weekly pay structure.
- Comprehensive medical, dental, and vision insurance.
- 401(k) retirement plan with company match.
- Paid time off and company holidays.
- Life and disability insurance.
- Employee assistance program.
- Opportunities for professional development and career advancement.
- On-site fitness center and wellness programs (where applicable).
- Tuition reimbursement 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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