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Sanofi

MS Quality Control Analyst IFB

Sanofi is hiring an MS Quality Control Analyst IFB in Beijing, China. Level rates it ; you can apply on Sanofi.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • Level classifies it as a mid-level role.
  • Level lists 1,200+ other open roles at Sanofi.

AI in this role

Main responsibilities:


• Participation in the establishment, qualification and commissioning of the QC laboratory in IFB.

• Implementation of chemical and chemical-physical bioanalytical tests as part of the DS release, incoming material release, in-process controls, clean utility monitoring and cleaning validation of insulin drug substance manufacturing.

• Supporting analytical method transfers and verification/validation activities.

• Executing analytical testing in a timely manner, ensuring adherence to the committed scheduled plans

• Performing the QC data review of executed tests by other analysts in a timely manner, ensuring adherence to the committed scheduled plans

• Conscientious documentation of all measurement results, raw data and calculations according to cGMP and data integrity requirements.

Participation in the preparation and review of laboratory specifications, methods, procedures, templates, protocols and reports.

• Implementation of device (re-)qualifications under supervision.

• Calibration and maintenance of the assigned equipment or coordination of it, e.g. by external service providers, including the associated documentation.

• Ensuring that he/she is trained and qualified to the assigned analytical testing that requires to be qualified

• Assist in troubleshooting and investigating analytical issues.

• Receiving, storing, documenting, handling and disposing of reagents and reference standards. Managing reagents, column, reference standards and other testing relates consumables stocks to ensure proper amounts can be used. Manage archives of analytical columns.

• Maintenance of documents, e.g. form sheets, test instructions, SOPs, SOP attachments, Logbooks

Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records, related to these tasks

• Informing his/her manager of any quality or HSE event (deviations, OOx,…) in a timely manner to ensure investigation and impact assessment are performed appropriately

• Executing assigned CAPAs related to remediation plans, continuous improvements

• Execute other works which is assigned by the line manager.

About you


Experience

• Degree in Chemistry/Pharmacy/Biochemistry or Equivalent.

• Associate degree at the minimum. Preferably bachelor or above.

• Minimum of 2 years of pharmaceutical, food or biotechnological industry experience.

• Experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements

• Experience or wiliness in in-process control analysis of active ingredients is an advantage.

• Experience in carrying out equipment qualification or method validation/verification/transfer is an advantage.

Soft Skills:

• Precise, independent and structured way of working

• Proactive Problem-Solving and communication

• Resilience

Technical Skills:

• Professional experience in the field of typical instrumental analysis (HPLC, GC, UV,IR, titration, TOC) and wet chemistry analysis.

• 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

• Proficiency in identifying issues and implementing effective solutions to resolve quality control problems

Languages:

• Familiar with academic English/German and Mandarin across at least two modalities: reading and writing.

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!

How we rate this

MS Quality Control Analyst IFB at Sanofi rates 39 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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