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Quality Control Analyst II, Ridgefield, NJ

date posted 06/23/2022
contract type Full time
job id R2631764
location Ridgefield, New Jersey

This position is responsible for performing routine and complex techniques associated with daily QC use. It provides an in-depth investigative and technological orientation in implementing, executing, and interpreting quality procedures. The successful candidate will substantially contribute to the process within the Quality Control laboratory. This position will be required to work a dayshift (8:00am to 4:30pm) as required by business needs.

CORE RESPONSIBILITIES

  • Perform routine analysis on complex laboratory equipment including HPLC and GC systems.

  • Practice safe work habits and adhere to Sanofi's safety procedures and guidelines.

  • Implement new quality control procedures.

  • Recommend laboratory and equipment-related improvements.

  • Work effectively with others to achieve shared goals and meet timelines.

  • Interact with internal and external personnel on technical matters requiring  coordination between sites.

  • Develops and authors complex, explicit documentation for current and new procedures, protocols, and reports.

  • Identifies potential problems and proactively suggests technical solutions.

  • Contributes to the development of project strategy in consultation with the supervisor.

  • Train new personnel on laboratory procedures

  • Work independently with some supervision and direction.

  • Work in compliance with cGMPs.

BASIC QUALIFICATIONS

  • Bachelor’s degree in Life Sciences discipline and at least 4 years of experience in CGMP lab environment, or Master’s degree in Life Sciences discipline and 0- 2 years experience in CGMP lab Environment.

PREFERRED QUALIFICATIONS

  • Experience in Microsoft Office; Empower data system and lab-based data management systems.

  • Ability to present technical data.

  • Familiarity with USP and global compendia regulations.

  • Scientific technical writing ability including authoring and revising SOPs, validation protocols, and technical reports.

  • Experience troubleshooting assay and equipment issues.

As a healthcare company and a vaccine manufacturer, Sanofi has an important responsibility to protect individual and public health. All US based roles require individuals to be fully vaccinated against COVID-19 as part of your job responsibilities.

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.

#GD-SG

#LI-GZ

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.

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