About the Company
Pfizer Inc. is one of the world’s premier biopharmaceutical companies, dedicated to applying science and our global resources to improve health and well-being at every stage of life. We strive to set the standard for quality, safety, and value in the discovery, development, and manufacture of health care products, including innovative medicines and vaccines. Join our team in Stamford, CT, and contribute to our mission of bringing therapies to people that significantly improve their lives.
Job Description
We are seeking a highly motivated and detail-oriented Finished Products Chemist to join our Quality Control team. In this high-demand role, you will be instrumental in ensuring the quality and integrity of our pharmaceutical products before they reach our patients. You will perform critical analytical testing on finished goods, ensuring compliance with strict regulatory standards and internal specifications. This position requires a strong understanding of analytical chemistry principles, meticulous execution, and a commitment to upholding the highest standards of quality and safety in a fast-paced environment. Weekly pay ensures a consistent and rewarding compensation structure for your dedication.
Key Responsibilities
- Perform routine and non-routine analytical testing on finished pharmaceutical products using various techniques (e.g., HPLC, GC, UV/Vis, KF, dissolution).
- Interpret and analyze data, ensuring accuracy and adherence to established specifications and cGMP guidelines.
- Troubleshoot and maintain laboratory instrumentation to ensure optimal performance and calibration.
- Document all analytical procedures, results, and observations meticulously and in compliance with regulatory requirements.
- Participate in Out-of-Specification (OOS) investigations and laboratory investigations, contributing to root cause analysis and corrective actions.
- Collaborate with manufacturing, quality assurance, and R&D teams to support product release and investigations.
- Maintain a clean, organized, and safe laboratory environment, following all safety protocols.
- Stay current with industry trends, regulatory changes, and new analytical methodologies.
Required Skills
- Proficiency in analytical chemistry techniques (HPLC, GC, UV/Vis spectroscopy, Karl Fischer titration).
- Strong understanding of cGMP (current Good Manufacturing Practices) and GLP (Good Laboratory Practices).
- Excellent data analysis, interpretation, and problem-solving skills.
- Ability to work independently and as part of a team in a fast-paced, regulated environment.
- Exceptional attention to detail and strong organizational skills.
- Proficient in using laboratory information management systems (LIMS) and other relevant software.
Preferred Qualifications
- Master's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
- Prior experience in the pharmaceutical or biotechnology industry.
- Experience with method validation and transfer.
- Knowledge of statistical process control (SPC) and quality by design (QbD) principles.
Perks & Benefits
- Competitive weekly pay structure.
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Generous paid time off (vacation, sick leave, holidays).
- Opportunities for professional development and career advancement.
- On-site fitness centers and wellness programs.
- Employee assistance program and work-life balance initiatives.
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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