About the Company
Pfizer Inc. is a global biopharmaceutical company committed to bringing therapies to patients that significantly improve their lives. We apply science and our global resources to deliver innovative medicines and vaccines. Our Brooklyn facility is a key part of our research and manufacturing network, focusing on advanced biopharmaceutical development.
Job Description
As a Senior QC Analyst at Pfizer, you will play a critical role in ensuring the quality and integrity of our pharmaceutical products. You will be responsible for performing complex analytical testing, reviewing data, and supporting the continuous improvement of our quality control processes. This position requires a strong understanding of cGMP regulations, analytical techniques, and a commitment to maintaining the highest standards of quality. This is an on-site position at our Brooklyn facility.
Key Responsibilities
- Perform complex analytical testing (e.g., HPLC, GC, dissolution, KF, UV/Vis) on raw materials, in-process, finished products, and stability samples.
- Accurately record, analyze, and interpret data, ensuring compliance with cGMP and company procedures.
- Investigate out-of-specification (OOS) results, deviations, and laboratory incidents, implementing corrective and preventive actions (CAPAs).
- Develop, validate, and transfer analytical methods as needed.
- Review and approve analytical data generated by other QC analysts.
- Maintain and troubleshoot laboratory equipment, ensuring calibration and qualification are current.
- Prepare and review technical documents, including test methods, reports, and SOPs.
- Provide training and mentorship to junior QC analysts.
- Contribute to continuous improvement initiatives within the QC department.
Required Skills
- Expertise in analytical techniques (HPLC, GC, spectroscopy).
- Strong understanding of cGMP, GLP, and pharmacopeial requirements (USP, EP, JP).
- Proficiency in data analysis and statistical tools.
- Excellent problem-solving and troubleshooting skills.
- Ability to work independently and as part of a team.
- Strong written and verbal communication skills.
- Proficiency with laboratory information management systems (LIMS).
Preferred Qualifications
- Master's degree in Chemistry, Biochemistry, or related scientific field.
- Experience with method development and validation.
- Certification in Lean Six Sigma or other quality improvement methodologies.
- Prior experience in a sterile manufacturing environment.
- Familiarity with regulatory submissions.
Perks & Benefits
- Competitive salary with performance-based bonuses.
- Comprehensive health, dental, and vision insurance.
- 401(k) retirement plan with company match.
- Generous paid time off and holidays.
- Relocation assistance for eligible candidates.
- Professional development and career advancement opportunities.
- On-site fitness center and wellness programs.
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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