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 manufacturing of healthcare products, including innovative medicines and vaccines. Our commitment to quality control is paramount in ensuring the integrity and efficacy of our high-volume production lines.
Job Description
We are seeking a highly motivated and detail-oriented Manufacturing Chemist specializing in Quality Control to join our dynamic team in Manhattan. This role is crucial for ensuring the highest quality standards in our high-volume production environment. The successful candidate will perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished pharmaceutical products in accordance with cGMP regulations and established procedures. This position offers an excellent opportunity to contribute to the safe and effective delivery of essential medicines to patients worldwide, coupled with a comprehensive benefits package.
Key Responsibilities
- Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various analytical techniques (HPLC, GC, UV/Vis, FTIR, Karl Fischer, titrations, etc.).
- Ensure all testing is conducted in strict compliance with cGMP, USP, and corporate quality standards.
- Document all analytical data and results accurately and meticulously in laboratory notebooks and electronic systems.
- Investigate out-of-specification (OOS) and out-of-trend (OOT) results, initiating and participating in root cause analysis and corrective/preventive actions (CAPA).
- Maintain and calibrate laboratory equipment, ensuring proper functionality and qualification.
- Develop and validate analytical methods as needed, contributing to method transfers and continuous improvement initiatives.
- Collaborate effectively with cross-functional teams including production, R&D, and quality assurance to resolve quality issues and support production schedules.
- Review and approve analytical data generated by other team members, ensuring data integrity and compliance.
- Adhere to all safety regulations and maintain a clean and organized work environment.
Required Skills
- Bachelor's degree in Chemistry, Analytical Chemistry, Biochemistry, or a related scientific field.
- Minimum of 2 years of experience in a Quality Control laboratory within a pharmaceutical, biopharmaceutical, or chemical manufacturing environment.
- Proficiency with a variety of analytical techniques, including HPLC, GC, UV/Vis, and FTIR.
- Strong understanding and practical experience with cGMP regulations, USP methodologies, and quality systems.
- Excellent data analysis, troubleshooting, and problem-solving skills.
- Demonstrated ability to work independently and as part of a team in a fast-paced, high-volume production setting.
- Meticulous attention to detail and strong written and verbal communication skills.
Preferred Qualifications
- Master's degree in a relevant scientific discipline.
- Experience with LIMS (Laboratory Information Management System) and other electronic data systems.
- Familiarity with method validation and transfer protocols.
- Knowledge of statistical process control (SPC) and lean manufacturing principles.
Perks & Benefits
- Comprehensive medical, dental, and vision insurance plans.
- Generous paid time off (PTO) and company holidays.
- 401(k) retirement plan with company match.
- Life and disability insurance.
- Professional development and continuing education opportunities.
- Employee assistance program.
- On-site fitness centers and wellness programs (at select locations).
- 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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