27 Quality Engineering jobs in Warsaw.

Hiring now: Supplier Quality Controls @ Stryker, Quality Team Mgr @ Veeva Syst, Quality And Compliance Le @ Iqvia, Sr Statistical Programmer @ Astrazenec, Prod Assessor @ Sgs, Regulatory Affairs Mgr Cm @ Parexel, Mgr Immunology Regulatory @ Johnson Jo, Quality Supervisor Qc Che @ Baxter, Pv Officer @ Primevigil, Regulatory Affairs Associ @ Perrigo.Explore more at jobswithgpt.com.

🔥 Skills

Quality Assurance (5) Risk Management (5) ISO 13485 (4) Project Management (4) Regulatory Affairs (4) quality management systems (3) regulatory requirements (3) supplier performance (3) Compliance (3) GCP (3)

📍 Locations

Warsaw (27)

Stryker

Skills & Focus: quality management systems, supplier quality controls, FDA, ISO 13485, regulatory requirements, KPI tracking, third party inspection, supplier performance, corporate guidelines, manufacturing environment
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology, and Orthopaedics that help improve patient and healthcare outcomes. Alongside its …
Experience: 2+ years of experience in manufacturing environment or equivalent
Type: Full Time
Benefits: Health benefits include medical and prescription drug insurance, dental insurance, vision insurance, critical illness i…

Veeva Systems

Skills & Focus: Quality Managed Services, Consultants, Senior Consultants, Biotech, Biopharma, Production Vaults, Customer Success, Cloud Software, Service Growth, Clinical Operations
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Type: Full-time
Benefits: Work from home or in the office, flexibility to thrive in your ideal environment.

Stryker

Skills & Focus: Supplier Quality Controls, process improvement, supplier performance, KPI tracking, audit support, medical device industry, ISO 13485, quality management systems, regulatory requirements, third-party inspection
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes.
Experience: 1+ years of experience in Supply Management, Quality, or Engineering within a regulated industry (medical device industry preferred).
Type: Full Time
Benefits: Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness …

Iqvia

Skills & Focus: Quality compliance, pharmaceutical review, subject matter expert, training development, internal compliance, external regulations, quality control, audits, CAPA, risk evaluation
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3-5 years relevant experience in pharmaceutical review and/or compliance
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Astrazeneca

Skills & Focus: Statistical Programming, Clinical Drug Development, Programming Deliverables, SAS, R, CDISC, Research and Development, Technical Requirements, Quality Assurance, Regulatory Submissions
About the Company: One of the world’s most forward-thinking and connected BioPharmaceutical companies.
Type: Hybrid
Skills & Focus: Quality Management, Compliance, Clinical Development, GCP, Regulatory Standards, CAPA, Risk Management, Audit, Continuous Improvement, Project Management
About the Company: We are AstraZeneca, one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: In depth demonstrable experience in a clinical compliance or quality related position with a track record of success in managing quality and compliance activities.
Type: Hybrid
Benefits: AstraZeneca embraces diversity and equality of opportunity.

Stryker

Skills & Focus: Supplier Quality, Quality Controls, Process Improvement, Medical Device, KPI, Regulatory, ISO 13485, Procurement, Supplier Agreements, Third Party Inspection
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes. Alongside its c…
Experience: 1+ years of experience in Supply Management, Quality, or Engineering within a regulated industry (medical device industry preferred).
Type: Full Time
Benefits: Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness …
Skills & Focus: supplier quality controls, process improvement, quality management systems, medical device, FDA, ISO 13485, KPI, supplier performance, regulatory compliance, project management
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology and Orthopaedics that help improve patient and healthcare outcomes.
Experience: 0+ years of experience in manufacturing environment or equivalent.
Type: Temporary Full Time
Benefits: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness insurance, accident insur…

Sgs

Skills & Focus: Product Assessor, Cardiovascular products, Soft Tissue products, technical file reviews, European Medical Device Regulation, Medical Device Directive, UKCA, CE marking, training materials, medical device certification

Parexel

Skills & Focus: Regulatory Affairs, CMC, Life Sciences, Biopharmaceuticals, Quality Assurance, Submission Strategies, Technical Documentation, Project Management, Risk Mitigation, Collaboration
About the Company: Parexel is a global biopharmaceutical services organization that provides expertise and solutions to companies in the life sciences sector, helping them to nav…
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, and a supportive work environment.

Johnson & Johnson

Skills & Focus: Immunology, Regulatory, Medical Writing, Clinical Documents, Project Management, Cross-Functional, Team Leadership, Process Improvement, Pharmaceutical, Communications
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: At least 8 years of relevant pharmaceutical/scientific experience; at least 6 years of relevant medical writing experience.
Type: Full-time

Baxter

Skills & Focus: quality, microbiology, quality management system, healthcare, innovation, manufacturing, patient care, medical devices, chemistry, compliance
About the Company: Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare…
Type: Full time
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Johnson & Johnson

Skills & Focus: Regulatory Affairs, healthcare, submissions, clinical trials, compliance, lifecycles, regulatory strategy, product strategy, pharmaceuticals, health authorities
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: 6+ years overall experience required, with 5+ years relevant industry experience preferred.
Type: Hybrid

Astrazeneca

Skills & Focus: Clinical Supply Planning, Supply Chain, Inventory Management, Team Leadership, Risk Identification, Process Improvement, Training, GMP Standards, Collaboration, Problem-Solving
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, committed to delivering life-changing medicines.
Experience: Experience in a supply chain planning environment

Primevigilance

Skills & Focus: case processing, individual case safety reports, pharmacovigilance, SAE/SUSAR management, PBRER, DSUR, PADER, mentoring, training, workflow cycle
About the Company: PrimeVigilance is a company focused on providing case processing services, including pharmacovigilance activities for clinical trials and post-marketing produc…
Experience: Demonstrated experience in case processing
Type: Full-time

Astrazeneca

Skills & Focus: Quality Culture, GCP risk based quality management, regulatory inspections, Risk assessment, CAPA management, clinical compliance, inspection readiness, stakeholder management, cross-functional collaboration, continuous improvement
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies.
Experience: Minimum of 8+ years of experience in clinical research area
Type: Full-time

Veeva Systems

Skills & Focus: Post-Implementation services, Quality Consultant, life sciences, Vault Quality solution, business processes, customer success, configuration, regulations, training, communication skills
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: Experience in configuring, supporting, or implementing software solutions; exposure to Quality Management is highly valued.
Benefits: Flexibility to work from home or in the office, extensive training, mentoring, and intensive learning opportunities.

Parexel

Skills & Focus: Quality Assurance, Auditor, GCP, GXP, Clinical Research, Regulatory Compliance, Biologics, Documentation, Risk Management, Data Integrity
Skills & Focus: Quality Assurance, Auditor, GCP, GXP, Clinical Research, Regulatory Compliance, Biologics, Documentation, Risk Management, Data Integrity

Perrigo

Skills & Focus: Regulatory Affairs, compliance, life cycle maintenance, submissions, legislation, Medicines Directive, Quality, documentation preparation, authorisations, regulatory systems
About the Company: At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 pl…
Experience: Minimum one year experience in a Regulatory environment
Benefits: Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career dev…

Baxter

Skills & Focus: Medical Devices, Adverse Events, Safety Reviews, Clinical Investigation, Risk Management, Regulatory Authorities, Medical Interpretation, Data Entry, Pharmacovigilance, Quality Control
About the Company: Baxter's Research and Development teams work cross functionally to innovate, develop and introduce creative solutions for patients needs globally.
Experience: At least 5 years of medical professional experience, including 2 years related clinical, safety, pharmacovigilance or regulatory experience in the medical device industry.
Benefits: Fixed-term contract for 3 months and then for an indefinite period. Competitive salary, annual bonuses, recognition awa…

Parexel

Skills & Focus: Regulatory Affairs, CMC, Biologics, Pharmaceuticals, Submission Strategies, Quality Control, Risk Management, Project Management, Technical Documentation, Collaboration
About the Company: Parexel is a global biopharmaceutical services company that helps clients navigate the complex and ever-changing regulatory landscape.
Experience: Previous experience in regulatory affairs, particularly related to technical/CMC/quality, within the pharmaceutical industry.
Type: Remote/Office-based

Sgs

Skills & Focus: Final Reviewer, Certification, Medical Device, Compliance, Audit, QMS, Technical Documentation, ISO13485, Regulations, Decision Making
About the Company: SGS is a global leader in inspection, verification, testing and certification services.

Veeva Systems

Skills & Focus: Drug Safety, Pharmacovigilance, consultant, customer requirements, solution design, implementation, SaaS, configuration, change management, life sciences
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Type: Full-time
Benefits: Health & wellness programs, options for working from home, annual giving program.

Baxter

Skills & Focus: Healthcare, Medical Devices, Sales, Quality, Finance, Engineering, Operations, Supply Chain, Information Technology, Compliance
About the Company: Baxter is dedicated to saving and sustaining lives through innovative medical products and services.
Type: Full-time
Benefits: Comprehensive benefits options

Perrigo

Skills & Focus: Patient Safety, adverse events, case handling, MedDRA coding, regulatory requirements, data entry, electronic complaints management, Good Pharmacovigilance Practices, medical devices, complaints databases
About the Company: Perrigo is a top player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula, committed t…
Experience: Life Science degree, adverse event handling, knowledge of medical terminology, fluent in English, proficient computer skills
Type: Hybrid
Benefits: Competitive compensation, career development opportunities

Baxter

Skills & Focus: Research and Development, Medical Devices, Adverse Events, Healthcare, Innovation, Product Development, Clinical Research, Patient Safety, Quality Assurance, Therapies
About the Company: Baxter is a global healthcare company dedicated to saving and sustaining lives through innovative medical devices and therapies.
Type: Full time
Benefits: Comprehensive benefits options reflect the value placed on employees.