8 Quality Assurance And Engineering jobs in Budapest.

Hiring now: Regulatory Safety Proj Mg @ Perrigo, Regulatory Affairs Mgr Cm @ Parexel, Safety Consultant Managed @ Veeva Syst, German Speaking Pharmacov @ Cognizant, Regulatory And Start Up S @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (4) Pharmacovigilance (4) Project Management (3) Collaboration (3) Quality Assurance (2) CMC (2) Life Sciences (2) Submission Strategies (2) Technical Documentation (2) Quality Control (2)

📍 Locations

Budapest (8)

Perrigo

Skills & Focus: Regulatory Affairs, Quality Assurance, Pharmacovigilance, Self-Care Products, Team Management, Cross-Functional Projects, Stakeholder Engagement, Budget Planning, Marketing Strategies, Licensing Activities
About the Company: Perrigo is a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula products.
Experience: Typically 7 years or more experience from within pharmaceutical/life science/selfcare, focusing on regulatory affairs and quality assurance.
Type: Hybrid Working Approach
Benefits: Competitive compensation, benefits for supporting you and your family, career development opportunities.

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.

Veeva Systems

Skills & Focus: Drug Safety, Pharmacovigilance, Consulting, Customer success, Configuration, Validation, Integration, Change management, Life Sciences, SaaS
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: Experience with configuring/supporting/implementing software solutions, ideally content management software.
Type: Full-time
Benefits: Health & wellness programs

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
Skills & Focus: Regulatory Affairs, Labelling, Artwork, Secondary Packaging, Project Management, Collaboration, Compliance, Stakeholder Liaison, Process Improvement, Training
About the Company: Parexel is a global biopharmaceutical services company that provides a range of services to clients in the pharmaceutical and biotechnology industries, special…
Experience: Few years of experience in a related pharmaceutical industry role
Type: Remote
Benefits: Flexible work arrangements, opportunities for career growth, diverse and global client exposure

Cognizant

Skills & Focus: Pharmacovigilance, Quality Control, Data entry, Adverse Event, Translation, Document Exchange, Case processing, Quality Check, Medical relevance, International Conference on Harmonization
About the Company: Cognizant is one of the world's leading professional services companies, transforming clients' business, operating, and technology models for the digital era.
Experience: Freshers to 2 years plus experience in Pharmacovigilance preferred
Type: Full-time
Benefits: Competitive salary, cafeteria benefits, All You Can Move SportPass, medical benefits, training opportunities, team even…

Parexel

Skills & Focus: Pharmacovigilance, QPPV, freelance, clinical trials, post-market, safety reporting, risk management, GVP, GCP, regulations
About the Company: Parexel is in the business of improving the world’s health. They provide a suite of biopharmaceutical services that help clients across the globe transform sci…
Experience: Minimum of at least 7 years' demonstrated experience in managing or implementing PV systems, including quality assurance experience.
Type: Freelance

Iqvia

Skills & Focus: clinical research, site activation, regulatory documents, project timelines, quality control, Hungarian language proficiency, standard operating procedures, performance metrics, GCP/ICH guidelines, contractual documents
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 years clinical research experience, including 1 year experience in a leadership capacity.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.