QC Analyst

Sanofi • Swiftwater, PA

7d • $24 - $32 • Onsite

About The Position

Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, fast About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.

Requirements

• Bachelor of Arts or Bachelor of Science in life sciences.
• Experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements
• Ability to analyze complex data and laboratory results to make informed decisions and identify areas for improvement
• Keen attention to detail to ensure accuracy in testing, reporting, and compliance with regulatory requirements
• Expertise in analyzing and interpreting complex analytical data to support product quality and compliance
• Skilled in diagnosing and resolving technical issues related to analytical methods and laboratory equipment.
• Language: English is a must.
• Quality Control candidate must be able to be receive influenza vaccine which is required for laboratory access.
• T his position is considered Site-Essential: candidate must be able to work onsite during inclement weather as directed by their manager.
• Must be able to lift up to 40 lbs., and bend/lift/move objects as part of the job.

Responsibilities

• Execute analytical testing on products (e.g., pH, Volume Check, UV, IR, etc.) in a timely manner, in compliance with Good Manufacturing Practices, ensuring adherence to the committed scheduled plans.
• Perform tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks
• Record all expected raw data, calculations, information, related to tasks, to comply with cGMP and data integrity requirements
• Support the need to revalidate, optimize, or replace analytical methods
• Ensure that laboratory/facilities, laboratory instruments are kept in a quality and safety status to ensure they can be used appropriately
• Support Quality Control teams during internal and external audits and inspections
• Analysis on technical issues and troubleshooting strategies
• Identify priorities and propose remediation plan on ALCM strategy
• Propose remediation actions from findings and CAPAs related to analytical methods

Benefits

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
• Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level