Last updated: 2025-05-22

19 Quality Assurance And Engineering jobs in Warsaw.

Hiring now: Quality Team Mgr @ Veeva Syst, Staff Engr Supplier Quali @ Stryker, Quality Management Spec I @ Parexel, Associate Dir Patient Saf @ Astrazenec, Associate Supplier Qualit @ Baxter, Mgr Ra Labeling Prod Lead @ Johnson Jo, Prod Assessor @ Sgs, Client Quality Officer @ Primevigil, Sr Pv Auditor @ Ergomed, Sr Pharmacovigilance Phys @ Client.Explore more at at kaamvaam.com

🔥 Skills

Pharmacovigilance (4) Compliance (4) ISO 13485 (3) Medical Device (3) quality management systems (3) compliance (3) mentoring (3) training (3) Supplier Quality Controls (2) Quality Agreements (2)

📍 Locations

Warsaw (19)

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, Regulatory Compliance, Supplier Performance, Audit Support, Quality Management Systems, ISO 13485, Medical Device, Third Party Inspection, Quality Agreements
About the Company: Stryker is a global leader in medical technologies, offering innovative products and services in MedSurg, Neurotechnology, and Orthopaedics to improve patient …
Experience: 5+ years in Supply Management, Quality, or Engineering within a regulated industry
Type: Temporary Full Time

Parexel

Skills & Focus: System Validation, Validation Services, Specialist

Astrazeneca

Skills & Focus: Pharmacovigilance, Agreements, Collaboration, Compliance, Innovation, Negotiation, Partnership, Quality, Regulatory, Safety
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, committed to helping patients by delivering life-changing me…
Experience: At least 5 years relevant experience (pharmaceutical, regulatory, safety and partnership)

Stryker

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…

Baxter

Skills & Focus: Supplier Quality Management, Quality Assurance, Medical Device, Pharmaceutical, Auditing, Quality Agreements, Compliance, Supplier Audits, CAPA, Healthcare
About the Company: Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medi…
Experience: 5+ years' experience in Quality, Supplier Quality, Manufacturing, Engineering or related field
Type: Full-time
Benefits: Competitive salary, annual bonuses, recognition award program, Private medical care, Life Insurance, Multisport card, c…

Johnson & Johnson

Skills & Focus: regulatory labeling, labeling content, pharmaceutical industry, compliant labeling documents, project teams, continuously improvement, scientific concepts, regulatory guidelines, drug development, document management systems
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: Minimum of 4 years professional experience
Type: Full-time

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

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.

Stryker

Skills & Focus: Supplier Quality Controls, process improvement, medical device industry, quality management systems, supplier performance, FDA compliance, ISO 13485, regulatory requirements, inspections and audits, collaboration
About the Company: Stryker offers innovative products and services in MedSurg, Neurotechnology, and Orthopaedics that help improve patient and healthcare outcomes.
Experience: 3+ 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 i…

Johnson & Johnson

Skills & Focus: Regulatory Affairs, compliance, risk assessment, regulatory strategy, product development, labeling, submissions, audits, consultation, mentoring
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,…
Type: Full-time

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.

Primevigilance

Skills & Focus: quality management, regulatory compliance, Pharmacovigilance, training plan, audit activities, business continuity, project metrics, client management, deviation management, CAPAs

Ergomed

Skills & Focus: pharmacovigilance, audits, QA, compliance, drug safety, risk-based audit strategies, audit reports, cross-functional teams, regulatory inspections, quality management systems

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

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.

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
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…

Client

Skills & Focus: Pharmacovigilance, ICSRs, SAE, risk management, signal detection, medical review, adverse events, safety reports, training, mentoring