About the Company
Amneal Pharmaceuticals is a leading integrated global pharmaceutical company focused on the development, manufacturing, and distribution of high-quality, affordable generic and specialty pharmaceutical products. With a commitment to innovation and patient care, Amneal operates state-of-the-art facilities and fosters a culture of excellence, continuous improvement, and employee well-being. Join a team dedicated to making a difference in healthcare.
Job Description
We are seeking a highly motivated and skilled Quality Control Chemist to join our dynamic team in Las Vegas. This critical night shift position offers a substantial differential and top hourly pay for dedicated professionals committed to maintaining the highest standards of pharmaceutical quality. As a QC Chemist, you will be instrumental in ensuring the quality and integrity of our products through meticulous testing and analysis, adhering to cGMP guidelines and regulatory requirements. This role is ideal for an analytical professional who thrives in a fast-paced laboratory environment and is passionate about contributing to the safety and efficacy of life-changing medications.
Key Responsibilities
- Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, and stability samples using various analytical techniques (HPLC, GC, FTIR, UV-Vis, Karl Fischer, dissolution, etc.).
- Calibrate, maintain, and troubleshoot laboratory equipment and instrumentation to ensure accurate and reliable results.
- Document all analyses and experiments meticulously in laboratory notebooks and electronic systems, ensuring data integrity and traceability.
- Review and interpret analytical data, identify out-of-specification (OOS) results, and participate in investigations.
- Adhere strictly to current Good Manufacturing Practices (cGMP), company Standard Operating Procedures (SOPs), and safety regulations.
- Assist in the development and validation of new analytical methods as required.
- Collaborate effectively with production, R&D, and other quality departments to resolve issues and improve processes.
- Contribute to continuous improvement initiatives within the QC laboratory.
- Maintain a clean, organized, and safe working environment.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, or a related scientific field.
- Minimum of 2 years of experience in a pharmaceutical QC laboratory setting.
- Proficiency with analytical techniques such as HPLC, GC, FTIR, UV-Vis, and dissolution testing.
- Strong understanding of cGMP regulations and ICH guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Ability to work independently on the night shift and as part of a team.
- Exceptional attention to detail and strong documentation practices.
- Proficiency in Microsoft Office Suite and laboratory information management systems (LIMS).
Preferred Qualifications
- Master's degree in Chemistry or related field.
- Experience with method development and validation.
- Prior experience working on a night shift schedule.
- Familiarity with Empower 3 Chromatography Data System.
Perks & Benefits
- Highly competitive hourly wage with significant night shift differential.
- Comprehensive health, dental, and vision insurance.
- 401(k) retirement plan with company match.
- Paid time off and company holidays.
- Life insurance and disability benefits.
- Opportunities for professional development and career advancement.
- Employee assistance program.
- State-of-the-art laboratory facilities.
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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