Associate Quality Tech – Sanofi Pasteur – Swiftwater, PA, USA
Sanofi Pasteur, the vaccines division of Sanofi, is a global company that provides more than one billion doses of vaccine each year, making it possible to immunize more than 500 million people across the globe. A world leader in the vaccine industry, Sanofi Pasteur offers the broadest range of vaccines protecting against 20 infectious diseases. The company’s heritage, to create vaccines that protect life, dates back more than a century. Every day, the company invests more than one million Euros in research and development.
Parent company; Sanofi is an integrated global healthcare leader which discovers, develops and distributes therapeutic solutions focused on patients’ needs. Sanofi has core strengths in the field of healthcare with seven growth platforms: diabetes solutions, human vaccines, innovative drugs, consumer healthcare, emerging markets, animal health and the new Genzyme.
This position will perform Quality inspections on incoming materials, such as documentation verification, statistical sample removal, and identification tagging of materials by strictly adhering to sanofi pasteur policies and procedures and cGMP. They will also be required to perform cleaning of work areas, equipment, and any other jobs as required, ensure all duties are completed on time, and complete required Safety and Compliance training and associated training modules as assigned.
Note: This is a Second Shift Position. Required hours are 12pm to 8:30pm
Perform inspection, sampling, testing and release of raw materials
Maintain laboratory in a safe and compliant state
Manage inventory of raw material sampling utensils, sample containers and safety supplies
Perform cleaning of laboratories sampling equipment
Process and inspect product samples from contract manufacturers
Ensure cold chain of custody is kept on samples and samples are distributed to the applicable testing unit
Perform identification tagging for raw materials within the Building 38 warehouse and associated off site warehouse locations
Perform status tagging for intermediates, final bulks, final containers, and finished product released by PQ Batch Release
Perform document and procedure review
Trains on departmental training modules as assigned. Pursues professional and or technical development training on/off site as assigned
Support implementation of change controls, CAPAs, and deviation corrective actions
Ability to work independently with a level of autonomy and authority within the defined scope of the job.
Excellent working knowledge of cGMPs (US, Canada, Japan, Europe). Experience in SAP, LabWare, Trackwise, Forklift Certification, and Aseptic Technique is beneficial
- People Skills
Who You Are
You are inspired and driven by Sanofi Pasteur IO mission to improve worldwide human health. You would fit in well with our sanofi values of innovation, solidarity, confidence, respect and integrity and our ways of working (Focus, Agility, Accountability and Simplicity).
Sanofi Pasteur SA is an Equal Opportunity and Affirmative Action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment regardless of their race, color, religion, sex, national origin, or any other characteristics protected by applicable law.
- Bachelors Degree in Life Sciences
- 1 – 3 years of relevant experience in a cGMP controlled/pharmaceutical industry
Job : Quality
Primary Location : United States-Pennsylvania-Swiftwater