9 Quality Engineering jobs in Budapest.

Hiring now: Regulatory Affairs Mgr Cm @ Parexel, Ssu Regulatory Spec Ii Sp @ Syneos Hea, Labelling Operative Spec @ Cognizant, Safety Sr Consultant @ Veeva Syst, Regulatory And Start Up S @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

Regulatory Affairs (4) Project Management (3) Collaboration (3) Pharmacovigilance (3) CMC (2) Submission Strategies (2) Technical Documentation (2) Quality Control (2) GCP (2) communication skills (2)

đź“Ť Locations

Budapest (9)
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Parexel

Regulatory Affairs Manager - CMC biologics Budapest
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.
Regulatory Affairs Manager - CMC biologics Budapest
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

Syneos Health

SSU & Regulatory Specialist II - Sponsor dedicated Budapest
Skills & Focus: SSU Specialist, Clinical Trials, Health Authority Submissions, Ethics Committees, Regulatory Requirements, Clinical Trial Management, Study Start Up, Document Management, GCP, ICH Guidelines
About the Company: Syneos Health is a leading integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical and …
Experience: Min of 3 years experience as a SSU Specialist, including handling of trial start-up activities coordination of trial start-up activities and Health Authority / Ethic Committee submissions
Type: Full-time
Benefits: Competitive remuneration package with excellent benefits, commitment to your development and training, and opportunitie…

Cognizant

Labelling Operative Specialist Budapest
Skills & Focus: Microsoft Word, regulatory program, quality mindset, Docuvera, training, Regulatory Affairs, Pharmacovigilance, data handling, product life cycle management, communication skills
About the Company: Cognizant is a global leader in technology and consulting services, dedicated to helping businesses transform and innovate. We are committed to fostering a div…
Experience: Relevant experience in Regulatory Affairs / Pharmacovigilance
Type: Full-time
Benefits: Competitive salary and benefits, Opportunities for professional growth and development, Collaborative and innovative wo…

Parexel

Senior Regulatory Affairs Associate - Labelling & Artwork Budapest
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

German speaking Pharmacovigilance QC Associate Budapest
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

Local Qualified Person for Pharmacovigilance (QPPV) Freelancer Budapest
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

Veeva Systems

Safety Senior Consultant Budapest
Skills & Focus: Drug Safety, Pharmacovigilance Operations, life sciences, software solutions, customer support, business processes, collaboration, product management, communication skills, project delivery
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.
Type: Full-time
Benefits: Work Anywhere company policy, flexibility to work from home or in the office.

Iqvia

Regulatory and Start Up Specialist 2 Budapest
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.