About the Company
Bristol Myers Squibb is a leading global biopharmaceutical company whose mission is to discover, develop, and deliver innovative medicines that help patients prevail over serious diseases. With a diverse portfolio spanning oncology, immunology, cardiovascular, and fibrotic diseases, we are committed to making a meaningful impact on global health. Join our team in Wesley Chapel, FL, and contribute to our legacy of scientific excellence and patient-focused innovation.
Job Description
We are seeking a highly motivated and experienced Senior QC Analyst to join our Quality Control team in Wesley Chapel, FL. In this pivotal role, you will be responsible for performing complex analytical testing of raw materials, in-process samples, and finished products to ensure compliance with cGMP regulations and internal specifications. You will play a key role in method development, validation, and troubleshooting, contributing directly to the quality and integrity of our life-saving products. This position offers an excellent opportunity for professional growth within a dynamic and collaborative environment, complete with performance bonuses and relocation assistance for qualified candidates.
Key Responsibilities
- Perform complex analytical testing using techniques such as HPLC, GC, FTIR, UV/Vis, and dissolution.
- Analyze raw materials, in-process samples, and finished pharmaceutical products according to cGMP guidelines.
- Review and interpret data, identify trends, and troubleshoot analytical issues.
- Develop, optimize, and validate analytical methods in accordance with ICH guidelines.
- Prepare and review technical documents, including test methods, specifications, and validation protocols.
- Participate in OOS/OOT investigations and support root cause analysis.
- Ensure all laboratory equipment is calibrated and maintained according to schedule.
- Train and mentor junior QC analysts.
- Contribute to continuous improvement initiatives within the QC department.
Required Skills
- Extensive experience with HPLC, GC, FTIR, and UV/Vis spectroscopy.
- Strong understanding of cGMP, ICH guidelines, and pharmaceutical quality systems.
- Proficiency in data analysis and statistical tools.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team.
- Detail-oriented with strong problem-solving abilities.
- LIMS experience.
Preferred Qualifications
- Master's degree in Chemistry, Biochemistry, or a related scientific field.
- Experience with method development and validation.
- Knowledge of microbiology testing.
- Familiarity with regulatory submissions.
- Experience in a sterile manufacturing environment.
Perks & Benefits
- Competitive annual salary with performance 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.
- Tuition reimbursement program.
- On-site fitness center and wellness programs.
- Opportunities for professional development and career advancement.
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.
⚠️ Important Disclaimer
Welcome to Westford Trust. We publish job opportunities aggregated from public sources, employers, and job portals. We never charge any fees to access or use our website; all information is provided entirely for free.
Westford Trust does not directly offer or manage these positions, nor are we directly involved in the hiring process for the vacancies published on https://career.westfordtrust.com.
If you suspect a fraudulent listing or have any questions, please contact us at techturna@gmail.com.