About Company
AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines, primarily for the treatment of diseases in three main therapy areas – Oncology, Cardiovascular, Renal & Metabolism, and Respiratory & Immunology. Headquartered in Cambridge, UK, AstraZeneca operates in over 100 countries, and its innovative medicines are used by millions of patients worldwide. We are driven by a commitment to delivering life-changing medicines and making a meaningful difference to patient health.
Job Description
Are you a meticulous and dedicated Quality Control Analyst ready to make an immediate impact? AstraZeneca in Downtown Pompano Beach is urgently seeking a highly skilled and motivated Quality Control Analyst to join our dynamic team. This is a critical role that directly contributes to the integrity and safety of our groundbreaking pharmaceutical products. As a Quality Control Analyst, you will be instrumental in performing a variety of analytical tests on raw materials, in-process samples, and finished products, ensuring strict adherence to Good Manufacturing Practices (GMP) and regulatory standards. Your work will directly support the release of products that help improve the lives of patients globally.
We are looking for an individual with a keen eye for detail, strong analytical capabilities, and a proactive approach to problem-solving. In this fast-paced environment, you will operate and maintain state-of-the-art laboratory equipment, meticulously document all testing procedures and results, and contribute to the continuous improvement of our quality systems. This urgent hiring signifies a significant opportunity for someone who thrives in a challenging yet rewarding atmosphere, where their contributions are valued and directly linked to our mission of delivering life-changing medicines. If you are passionate about quality assurance in the pharmaceutical industry and eager to join a world-class organization that fosters innovation and professional growth, we encourage you to apply immediately.
Key Responsibilities
- Perform routine and non-routine analytical testing on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV/Vis, KF, dissolution, spectroscopy).
- Ensure all testing is conducted in strict compliance with current Good Manufacturing Practices (cGMP), company policies, and regulatory requirements.
- Accurately record, analyze, interpret, and report all laboratory data, ensuring data integrity and timely delivery of results.
- Operate, calibrate, and maintain laboratory instrumentation, troubleshooting minor equipment issues and coordinating with external service providers for complex repairs.
- Assist in the development, validation, and transfer of analytical methods, as well as the preparation of standard operating procedures (SOPs) and other quality documents.
- Participate in laboratory investigations for out-of-specification (OOS) results, out-of-trend (OOT) data, and other quality events, proposing and implementing corrective actions.
- Contribute to a culture of continuous improvement, safety, and operational excellence within the QC laboratory.
Required Skills
- Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 2 years of experience in a Quality Control laboratory within the pharmaceutical or biotechnology industry.
- Demonstrated expertise in analytical techniques such as HPLC, GC, UV/Vis spectrophotometry, and Karl Fischer titration.
- Thorough understanding and practical application of cGMP principles and FDA regulations.
- Proficiency in laboratory information management systems (LIMS) and electronic laboratory notebooks.
- Excellent written and verbal communication skills, with strong attention to detail and ability to meticulously document work.
- Proven ability to work independently and as part of a team in a fast-paced, regulated environment.
Preferred Qualifications
- Master's degree in a relevant scientific field.
- Experience with method validation and transfer activities.
- Familiarity with statistical analysis tools for data interpretation.
- Experience with advanced analytical techniques such as mass spectrometry (LC-MS/GC-MS).
- Prior experience in an urgent hiring or rapid-response laboratory setting.
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement savings plan with company match.
- Generous paid time off (PTO) and company holidays.
- Life and disability insurance.
- Opportunities for continuous learning, professional development, and career advancement.
- Employee assistance program.
- Wellness programs and resources.
- Access to innovative research and development facilities.
How to Apply
To apply for this urgent and impactful role, please click on the application link below. Ensure your resume and cover letter clearly highlight your relevant experience and qualifications for a Quality Control Analyst position in a cGMP environment. We look forward to reviewing your application and potentially welcoming you to the AstraZeneca team.