QC Analyst II

Job description

**Sunday- Wednesday 6am-4:30pm- Flexible with start/end time**

Key Responsibilities may differ among employees with same job title and may change over time in accordance with business needs.

This position is responsible for performing routine and complex testing of in-process samples and final products in accordance with SOPs for product release and validation.

Responsibilities include:

• Performing UV-Vis spectrophotometry assays for in-process and final product samples

• Performing Gel Electrophoresis assays for in-process and final product samples

• Performing HPLC methods for final bulk material/finished goods • Performing maintenance on complex laboratory equipment including HPLC and GC systems

• Review of QC Data for compliance to procedures and specifications

• Calculation and evaluation of results

• Participation in training of less experienced staff

• Transferring methods from support groups to the QC laboratory

• Authors protocols and technical reports related to the implementation of QC equipment

Effectively demonstrates an understanding of CGMP's and how it applies to specific responsibilities:

• Following accurate oral and written procedures for testing of in-process and final product samples

• Communicates inter-departmentally and with outside contacts to solve technical issues

• Exercises sound judgment and decision making when problem solving

• Revises standard operating procedures as needed

• Works independently under general supervision and direction

• Work in compliance with CGMP's

• Practices safe work habits and adheres to Genzyme's safety procedures and guidelines

Basic Requirements:

Bachelor's Degree in Life Sciences discipline and 2 years experience in CGMP lab environment Or • Master's Degree in Life Sciences discipline and 1 year experience in CGMP lab Environment

• Proficient in Outlook and Microsoft Word and Excel and lab based data management systems

Preferred Qualifications:

• Exp with UV Vis Spectroscopy and wet Chemistry

• Scientific technical writing ability

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.

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At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.