Last updated 2026-08-19 · 6 listed in the past 7 days · 24 in the past 30 days
80 QA Engineering Jobs in Beijing, China
Browse 80 QA Engineering jobs in Beijing, China, including CQRA Specialist, HK, M&s, and Sr. Spclst, Quality Assurance roles from Sanofi, Fortrea, and Danaher. Listings are updated hourly.
Market data for QA Engineering jobs in Beijing, China
Professionals focused on ensuring product quality, compliance, and process improvement across various engineering and manufacturing sectors.
Companies hiring for QA Engineering jobs
| Company | Current jobs |
|---|---|
| Sanofi | 17 |
| Fortrea | 13 |
| Danaher | 9 |
| Takeda Pharmaceutical | 6 |
| MSD | 5 |
| Roche | 5 |
| MSD R&D (China) Co., Ltd. | 3 |
QA Engineering jobs by schedule
| Schedule | Current jobs | Share of current jobs |
|---|---|---|
| Full time | 80 | 100% |
QA Engineering jobs by experience level
Common QA Engineering job titles
| Title | Current jobs | Share of current jobs |
|---|---|---|
| CQRA Specialist, HK | 1 | 1% |
| M&s | 11 | 14% |
| Sr. Spclst, Quality Assurance | 1 | 1% |
| Manager, Quality Assurance | 1 | 1% |
| M&S-Quality Control Expert Microbiology IFB | 1 | 1% |
- How many QA Engineering jobs are listed in Beijing, China?
- This page currently shows 80 QA Engineering jobs in Beijing, China.
- Which companies are hiring for QA Engineering roles in Beijing, China?
- Current jobs include openings from Sanofi (17 jobs, 21%), Fortrea (13 jobs, 16%), Danaher (9 jobs, 11%), Takeda Pharmaceutical (6 jobs, 8%), and MSD (5 jobs, 6%).
- What experience levels are common for QA Engineering jobs in Beijing, China?
- Current jobs by experience level: Mid (46 jobs, 57%), Senior (24 jobs, 30%), and Entry (10 jobs, 13%).
- What work schedules are common for QA Engineering jobs in Beijing, China?
- Current jobs by schedule: Full time (80 jobs, 100%).
- What QA Engineering job titles are common in Beijing, China?
- Common titles include CQRA Specialist, HK (1 job, 1%), M&s (11 jobs, 14%), Sr. Spclst, Quality Assurance (1 job, 1%), Manager, Quality Assurance (1 job, 1%), and M&S-Quality Control Expert Microbiology IFB (1 job, 1%).
- What job data does this page include?
- Most current jobs are full-time (80 of 80). 46 of 80 current jobs are at the mid level.
Supplier Product Quality Development Engineer
Seen active yesterday
Posted Jul 30
Role highlights
- 2 YunCheng Road, Beijing, 100176, CN Copy to Clipboard Similar Jobs R&D Quality Engineer China Posted on 06/18/2026 R&D Quality…
- 1000 Required Discard Add Summary Page Supplier Product Quality Development Engineer - Mattson Careers loaded.
Global Graduate Program 2026 - Quality Assistant Engineer
Seen active today
Posted Jul 4
Role highlights
- Master's degree or above, majoring in Quality Engineering, Mechanical/Electrical Engineering, or related fields; 2.
- Support supplier quality management, including incoming material inspection and supplier audits; 6.
Dir, Project Management
Seen active today
Posted Aug 12
Role highlights
- Familiarity with regulatory-CMC topics and regulatory compendia including, but not limited to, the Chinese Pharmacopoeia Strong organizatio…
- Preferred : Large molecule method development, validation, and/or transfer experience Knowledge of deviation management and change control…
(Asso.) Manager, CMC RA
Seen active today
Posted Aug 18
Role highlights
- Manager, CMC RA Company: MSD Job Description Take CMC lead for products under clinical development and for marketed drug products.
- Coordinate various aspects of CMC regulatory activities with internal and external stakeholders.
FSP CTM
Seen active yesterday
Posted Aug 12
Role highlights
- In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
- Ensure achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical acti…
Sr. Clinical Research Lead
Seen active today
Posted Aug 4
Role highlights
- This position provides strategic guidance, oversight, and effective delivery for clinical programs in areas of focus in partnership with cr…
- Responsible for the implementation and support maintenance of the clinical trial-related policies, as well as processes and procedures rela…
M&S - IFB - USP Operation Expert
Seen active yesterday
Posted Aug 14
Role highlights
- Position Overview We are looking for 4 Operation Experts for the workstreams "Upstream" and "Downstream" for the following focus areas:…
- Partnership and collaboration with Engineering on various project topics: Creation of process-relevant and clean utilities user requirement…
M&S - Quality Assurance Expert -IFB
Seen active today
Posted Aug 12
Role highlights
- Acts as the responsible Quality Subject Matter Expert (SME) for the project in all matters of quality assurance, ensures quality…
- As an integral member of the project quality team, this role carries overall responsibility for participating in project workstreams, ensur…
M&S - IFB - Quality Manager-MES
Seen active today
Posted Aug 12
Role highlights
- Position Overview The Quality Manager MES-IFB is responsible for ensuring that all aspects of Quality Assurance activities for the project…
- Responsible Quality Subject Matter Expert (SME) for the project on all matters related to Quality assurance, developing MES IFB and…
Dir, Project Management
Seen active yesterday
Posted Aug 12
Role highlights
- Familiarity with regulatory-CMC topics and regulatory compendia including, but not limited to, the Chinese Pharmacopoeia Strong organizatio…
- Preferred: Large molecule method development, validation, and/or transfer experience Knowledge of deviation management and change control p…
(Asso.) Manager, CMC RA
Seen active yesterday
Posted Aug 18
Role highlights
- Coordinate various aspects of CMC regulatory activities with internal and external stakeholders.
- Provide CMC expertise to support drug development at various stages including clinical trial application, NDA and post approval variations…
More roles at MSD R&D (China) Co., Ltd.
Regulatory Affairs Executive job at Abbott | Abbott Careers
Seen active yesterday
Posted Aug 17
Role highlights
- Develop and implement internal processes and system to support regulatory submissions and approvals in the most efficient way.
- Manage the regulatory and compliance systems such as DARIUS, SolTRAQs, ISOtrain etc.
Senior RA Specialist
Seen active today
Posted Aug 10
Role highlights
- As a Senior Regulatory Affairs Specialist, you'll interact with clients to provide strategic regulatory intelligence and guidance supportin…
- Assists in identifying and recognizing out of scope activities in a contract in a timely manner and liaises with other…
Associate Specialist, Product Surveillance, CT PET
Seen active today
Posted Aug 7
Role highlights
- Timely complaint handling and reporting Provide objective evidence of complaint handling process through compliant documentation Required Q…
- Excellent interpersonal, organizational, and influencing skills Familiarity with the application of medical device as it relates to patient…
More roles at GE HEALTHCARE
(Sr.) Country Study Manager - CVRM
Seen active 2 days ago
Posted Aug 7
Role highlights
- Work with other members of the organization to share knowledge, experiences and best practices Drive best practices and provide development…
- Track and manage to agreed study time lines, budget, and resource and ensure the u date of appropriate systems (e.g.…
More roles at CN50 AstraZeneca Pharmaceutical (Beijing) Co. Ltd Company
FSP CRA I (Taiyuan)
Seen active today
Posted Aug 6
Role highlights
- Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client…
- Basic knowledge of Regulatory Guidelines.
More roles at Fortrea
Regulatory Affairs Executive
Seen active 2 days ago
Posted Aug 17
Role highlights
- Manage the regulatory and compliance systems such as DARIUS, SolTRAQs, ISOtrain etc.
- Develop and implement internal processes and system to support regulatory submissions and approvals in the most efficient way.
M&S Graduate Program-Quality Lead-Beijing
Seen active today
Posted Aug 4
Role highlights
- Education : Master's Degree required in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or related technical d…
- Here is what you can expect: A structured 3-year leadership accelerator with clear milestones, defined rotations, and a guaranteed landing…
More roles at Sanofi
- M&S - IFB - USP Operation Expert
- M&S - IFB - Spare Part & Storage Engineer
- M&S - Regulatory Site Officer -IFB
- M&S - Quality Assurance Head - IFB
- M&S - Quality Assurance Expert -IFB
- M&S Graduate Program- IFB Quality Assurance Manager - Beijing
- M&S - Quality Assurance Manager-IFB
- M&S Quality Assurance Manager -IFB
- M&S - IFB - Downstream Maintenance Lead
- M&S_Quality Control Analyst - IFB
- M&S - Quality Control Expert - IFB
- M&S-Quality Control Expert Microbiology IFB
- M&S-Head of Quality Excellence & Projects-Beijing
- M&S - Quality Control Expert - IFB
Clinical Research Expert
Seen active today
Posted Jul 25
Role highlights
- Manage all phases of clinical clinical development, in strict compliance with company SOPs, policies, divisional standards, the Declaration…
- Coordinate internal cross-functional teams and external investigators (as applicable) during clinical development, optimizing both internal…
(Sr.)Manager, CMC Regulatory Affair, R&D, Shanghai/Beijing
Seen active today
Posted Jul 20
Role highlights
- With supervision, prepares CMC submission dossier, helps define CMC content requirements, ensure high quality CMC submission complying with…
- Ability to understand, apply and articulate regulatory CMC requirements for drug development and post-market support initiatives required.
Clinical Research Associate II
Seen active yesterday
Posted Jul 10
Role highlights
- Conducts site evaluation, site training, routine, and site closure monitoring activities with compliance to the protocol and monitoring pla…
- Advanced knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.
More roles at AbbVie
Manager, Clinical Research (Onco & Hema)
Seen active 2 days ago
Posted Jul 7
Role highlights
- Accountable for performance for assigned protocols in a country in compliance with ICH/GCP and country regulations, company policies and pr…
- Responsible for project management of the assigned studies: pro-actively plans, drives and tracks execution and performance of deliverables…
(Associate) Country Study Manager - Cell Therapy
Seen active 2 days ago
Posted Jul 6
Role highlights
- Qualifications and Skills Essential: Bachelors of Science degree in related discipline, preferably in medical or biological science, or equ…
- Ability to effectively lead complex non-drug projects in a world-wide environment through in depth understanding of AZ PMF, IPOM and…
More roles at CN60 AstraZeneca Global R&D (China) CO. Ltd. Company
Senior Specialist External Quality
Seen active 2 days ago
Posted Jun 30
Role highlights
- Risk mitigation actions to ensure quality compliance in responsible area Perform supplier quality management according to AZ standards/SOPs…
- This includes quality system management and supplier performance management for the following activities: QA audits, supplier risk assessme…
CQRA Specialist, HK
Seen active today
Posted Jun 29
Role highlights
- Qualifications Education: Bachelor’s degree in Quality, Engineering, Life Sciences, Regulatory Affairs, or a related discipline (required).
- Required Skills: Preferred Skills: Business Behavior, Compliance Management, Continuous Improvement, Data Analysis, Data Compilation, Detai…
More roles at Johnson & Johnson Services, Inc.
Page 1