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Sanofi

Quality Control PCU manager (Incoming and Device)

Sanofi is hiring a Quality Control PCU manager (Incoming and Device). It pays €98k a year and Level rates it ; you can apply on Sanofi.

Level's read on this job

  • On Level's scale, this role is Little AI ●○○○: aI is not part of the work.
  • Sanofi has 1,000+ other open roles on Level.
  • Posted in the last few days.

AI in this role

Job Title: Quality Control PCU Manager (Incoming and Device)

  • Location: Waterford, Ireland
  • Job Type: 12-Month FTC, Full-Time
  • Working Arrangements: On-site

About the job


Quality Control (QC) is responsible for sample receipt, testing intermediate production samples, final product samples, and environmental samples to demonstrate that all products meet the standard requirements for CGMP operations. Additional functions include raw material testing, stability testing, assay transfers, and qualification of instrumentation. The Quality Control Operations group supports Laboratory Investigations, Deviation Investigations, CAPA support, Training, and Change Controls. Quality Control Validation Support consists of the Method Validation Group and the Equipment Qualification Group. Quality Control is also responsible for assisting in site wide studies and projects.


Ready to get started?


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, faster.

 

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.


Main Responsibilities

  • Overseeing daily operations of the quality control laboratory to ensure adherence to the committed scheduled plans
  • Maintaining his/her laboratory in compliance with the GMPs and quality control processes defined according to internal and external quality requirements and regulations
  • Ensuring the use of validated methods in his/her perimeter and executing any validation/transfer protocol as receiving unit
  • Managing and training laboratory staff, ensuring they follow best practices and safety guidelines
  • Ensuring his/her laboratory staff is qualified to perform the testing execution by maintaining the lab qualification matrix
  • Conducting routine shopfloor of laboratory to identify improvement opportunities
  • Ensuring accurate and timely testing of received samples according to his/her perimeter
  • Reviewing and approving laboratory test results and reports
  • Maintaining laboratory equipment by applying maintenance, qualification, and calibration plans to ensure accuracy and reliability of lab activities
  • Ensuring the follow-up and progress of the investigations, change control, and CAPAs assigned to his/her perimeter, in a timely manner
  • Investigating in a timely manner and resolving any quality control events, issues, or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs
  • Providing support during regulatory inspections and audits by answering to requests related to his/her perimeter
  • Ensuring that his/her lab/facilities, lab instruments are kept in a quality and safety status to ensure that they can be used appropriately

About you

  • Bachelor's degree in science, Engineering, Industrial Engineering, or a related discipline.
  • Significant relevant experience in manufacturing quality, including demonstrable experience in managerial or leadership role is an advantage.
  • Strong leadership, analytical, problem-solving, and communication skills.
  • Six Sigma, or equivalent quality certification is an advantage.

Why choose us?

  • Shape the future of medicine and vaccine delivery with cutting-edge technology, ensuring seamless launches and a resilient global supply.
  • Transform lives worldwide by delivering life-changing treatments anywhere, anytime.
  • Grow, thrive, and make an impact in a workplace that empowers you to bring your best self every day, with pride.
  • Help deliver 30+ new product launches by 2030, ensuring patients get treatments faster than ever.

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

The salary range for this position is :€73 200,00 - €97 600

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

How we rate this

Quality Control PCU manager (Incoming and Device) at Sanofi rates 38 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

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