Sanofi

Sanofi

Posted via Workday

MS Quality Control Analyst IFB

Apply by Jan 20, 2027

Posted Sep 21, 2026

Role at a glance

Job function
Manufacturing & Skilled Trades Quality Assurance & Quality Control
Salary
Not Disclosed
Location
Beijing
Work arrangement
On-site
Employment
Full-time
Experience
Minimum of 2 years of pharmaceutical, food or biotechnological industry experience.
Education
Associate degree at the minimum. Preferably bachelor or above.

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Role Summary

AI-generated

This role supports the establishment and operation of the QC laboratory in IFB for insulin drug substance manufacturing. The position performs bioanalytical testing, reviews QC data, maintains laboratory documentation and equipment, and supports compliance, investigations and continuous improvement activities.

What You'll Do

  • Implement chemical and chemical-physical bioanalytical tests for drug substance release, incoming material release, in-process controls,...
  • Execute analytical testing and perform QC data review of tests completed by other analysts.
  • Document measurement results, raw data and calculations according to cGMP and data integrity requirements.
  • Support analytical method transfers, verification and validation activities, and assist in troubleshooting analytical issues.
  • Perform equipment qualification, calibration and maintenance, including associated documentation.
  • Manage reagents, reference standards, analytical columns and other testing-related consumables, including storage, records and disposal.

Generated from the employer's posting. Verify important details before applying.

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Qualifications

Degree in Chemistry/Pharmacy/Biochemistry or Equivalent; associate degree at the minimum; minimum of 2 years of pharmaceutical, food or biotechnological industry experience; experience in pharmaceutical quality control, GMP and regulatory requirements; experience with HPLC, GC, UV, IR, titration, TOC and wet chemistry analysis; familiarity with academic English/German and Mandarin across at least two modalities: reading and writing.

Required

  • Degree in Chemistry/Pharmacy/Biochemistry or Equivalent
  • Associate degree at the minimum
  • Minimum of 2 years of pharmaceutical, food or biotechnological industry experience
  • Experience in quality control within the pharmaceutical industry
  • Knowledge of Good Manufacturing Practices (GMP) and regulatory requirements
  • Professional experience in typical instrumental analysis: HPLC, GC, UV, IR, titation, TOC
  • Wet chemistry analysis
  • Familiar with academic English/German and Mandarin across at least two modalities: reading and writing

Preferred

  • Preferably bachelor or above
  • 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.

Original job description

Content provided by the employer

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!

Sanofi

About the company

Sanofi

Large Enterprise

Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.