Last updated 2026-08-07
40 QA Engineering Jobs in Warsaw, Poland
Browse 40 QA Engineering jobs in Warsaw, Poland, including Manager Global QMS, Computer System Validation Coordinator, and Quality Manager roles from AstraZeneca, PL10 AstraZeneca Pharma Poland Company, and MSD. Listings are updated hourly.
Market data for QA Engineering jobs in Warsaw, Poland
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 |
|---|---|
| AstraZeneca | 9 |
| PL10 AstraZeneca Pharma Poland Company | 5 |
| MSD | 3 |
| Perrigo | 3 |
| Roche | 3 |
| Alexion | 2 |
| BR2718 GE Vernova Hitachi Nuclear Energy International LLC (Sp. z o.o) oddzial w Polsce | 2 |
QA Engineering jobs by schedule
| Schedule | Current jobs | Share of current jobs |
|---|---|---|
| Full time | 40 | 100% |
QA Engineering jobs by experience level
Common QA Engineering job titles
| Title | Current jobs | Share of current jobs |
|---|---|---|
| Manager Global QMS | 1 | 3% |
| Computer System Validation Coordinator | 1 | 3% |
| Quality Manager | 1 | 3% |
| Director, Training & Documentation | 1 | 3% |
| (Senior) Clinical Quality Associate Director | 1 | 3% |
- How many QA Engineering jobs are listed in Warsaw, Poland?
- This page currently shows 40 QA Engineering jobs in Warsaw, Poland.
- Which companies are hiring for QA Engineering roles in Warsaw, Poland?
- Current jobs include openings from AstraZeneca (9 jobs, 20%), PL10 AstraZeneca Pharma Poland Company (5 jobs, 11%), MSD (3 jobs, 7%), Perrigo (3 jobs, 7%), and Roche (3 jobs, 7%).
- What experience levels are common for QA Engineering jobs in Warsaw, Poland?
- Current jobs by experience level: Mid (19 jobs, 48%), Senior (16 jobs, 40%), and Entry (5 jobs, 13%).
- What work schedules are common for QA Engineering jobs in Warsaw, Poland?
- Current jobs by schedule: Full time (40 jobs, 100%).
- What QA Engineering job titles are common in Warsaw, Poland?
- Common titles include Manager Global QMS (1 job, 3%), Computer System Validation Coordinator (1 job, 3%), Quality Manager (1 job, 3%), Director, Training & Documentation (1 job, 3%), and (Senior) Clinical Quality Associate Director (1 job, 3%).
- What job data does this page include?
- Most current jobs are full-time (40 of 40). 19 of 40 current jobs are at the mid level.
Related jobs
AstraZeneca
Aug 7- Identify regulatory risks, opportunities and proactively develop mitigation strategies for operational regulatory activities, e.g. planned…
- Be a core member of strategy teams, e.g. GRST (Global Regulatory Strategy Team) and RSST (Regulatory Submission Strategy Team), successfull…
More roles at AstraZeneca
Clinical Research Associate
- Trains, supports and advises Investigators and site staff in study related matters, including Risk Based Quality Management (RbQM) principl…
- Follows quality issue processes by raising systematic or serious quality issues, data privacy breaches, CSP or ICH-GCP compliance issues to…
More roles at PL10 AstraZeneca Pharma Poland Company
Worldline
Aug 4- Senior Quality Control Analyst Job Details | worldline We use cookies to offer you the best possible website experience.
- Day-to-day responsibilities Quality Control: Perform quality checks according to internal procedures to ensure they are compliant with regu…
Haleon
Aug 4- Inspection Readiness and Audit Manager # ## ## About the role The purpose of this role is to coordinate external…
- Ability to deliver key process improvement initiatives. *.
Haleon Poland Sp. z o.o.
Aug 4- Inspection Readiness and Audit Manager About the role The purpose of this role is to coordinate external Competent Authorities Pharmacovigi…
- Ability to deliver key process improvement initiatives.
Zimmer Biomet Polska Sp.
Aug 3- You will work closely with manufacturing sites and cross-functional teams to resolve process-related issues, build strong stakeholder relat…
- Experience within an industrial, manufacturing, medical device, or healthcare environment is an advantage.
More roles at Zimmer Biomet Polska Sp.
CMC Specialist
- CMC Specialist Location: Warsaw - Poland Employment type: Full-time Hybrid work: yes Role Overview The CMC Specialist is responsible for…
- The CMC specialist contributes to the regulatory submissions, post‑approval activities (variations, renewals) by providing high‑quality CMC…
Perrigo
Jul 30- Acts as a senior Regulatory Operations professional, supporting governance, continuous improvement and consistent ways of working.
- Support execution of regulatory commitments and operational deliverables, escalating risks where required.
More roles at Perrigo
MSD
Jul 28- Key Responsibilities Strategic Leadership & Operational Excellence Lead global Safety Data Management processes, governance, and documentat…
- Provide strategic direction for safety case management, medical coding, and operational performance across geographies.
Fortrea
Jul 27- Regulatory Submissions Manager - EMEA Job Overview: Collaborate with peers across the organization to achieve client-centric delivery in a…
- Provide the highest quality advice on regulatory issues to members of project teams and its clients by maintaining awareness of…
Sonova AG
Jul 24- Drive consistent execution of core QMS processes, including CAPA, non-conformities, document control, change control, audits, training and…
- Strong knowledge of international quality and regulatory standards, including ISO 13485, MDR/IVDR, FDA 21 CFR Part 820, GMP/GDP and MDSAP.
Mars
Jul 24- Deliver technical expertise on SAP Quality Management modules, including Quality Planning, Quality Inspection (incoming materials, in-proce…
- Experience with SAP PP / MM experience Experience with SAP global template development / deployment Strong knowledge of manufacturing and…
Alexion
Jul 23- The Senior Medical Reviewer will work closely with the study team (including but not limited to the following roles: Global…
- Work with study physicians and/or clinical/project scientists to support standardized high-level data review and medical evaluation across…
More roles at Alexion
Labcorp
Jul 20- Minimum Qualifications Bachelor’s degree in a life science 6 or more years of experience working in the clinical research industry…
- Coordinate internal processes and communications related to study design (including but not limited to internal feasibility requests, mater…
Getinge
Jul 16- Required Knowledge, Skills and Abilities Expert on Computer System Validation lifecycle and System Periodic Reviews.
- Solid understanding of global Computer System Validation regulatory expectations , including applicable international standards and guideli…
Medical Device Product Support Engineer
- What you will do: Provide technical support expertise for medical devices and software products, including troubleshooting, root cause anal…
- Participate in cross-functional product development, technical review boards, and lifecycle management teams, providing customer support in…
Reckitt
Jun 22- This role drives business value by building purpose fit MES capabilities, cultivating strategic vendor relationships, and overseeing the fu…
- The experience we're looking for Lead MES strategy, architecture, and deployment within a regulated manufacturing environment.
Abbott Laboratories
Jun 9- Ensure compliance with Abbott’s Quality System, ISO 13485, MDR/IVDR, and local regulations.
- What You’ll Do Lead and manage regulatory activities for new product launches and rollouts across EMEAP Prepare, review, and maintain…
GRIFOLS, S.A.
Jun 4- Quality Manager Role: Responsible person according international and local laws for maintaining a Quality System based on applicable Good D…
- Professional Experience: 5 years’ experience managing a Quality System in a similar position, Experience in GDP.
GE Vernova
Jun 2- Proven ability to lead complex technical projects independently and provide regulatory guidance to cross-functional stakeholders, including…
- Process skills related to coordinating and documenting complex technical documents.
More roles at GE Vernova
Polish Technical Leader
- Proven ability to lead complex technical projects independently and provide regulatory guidance to cross-functional stakeholders, including…
- Process skills related to coordinating and documenting complex technical documents.
More roles at BR2718 GE Vernova Hitachi Nuclear Energy International LLC (Sp. z o.o) oddzial w Polsce
Roche
May 25- The Opportunity: You are accountable for handling complex medical software complaints, safety issues, and product inquiries for software pr…
- The Position As a Senior Software Engineer in Post Market Quality (PMQ), you will be at the forefront of ensuring…
More roles at Roche
QbD Group
Mar 2- Looking for a role where you can think critically, take initiative, and contribute to innovation 🫵 Who you are Our…
- Collaborate with stakeholders such as regulatory, quality, IT, production and marketing to implement our solutions successfully.
Veeva
Feb 27- Senior Technical Consultant - Quality Systems - Careers at Veeva Veeva.com Regions United States Canada Europe Asia Pacific China Japan…
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