7 Quality Assurance And Engineering jobs in Zagreb.

Hiring now: Sr Pharmacovigilance Pv P @ Ergomed, Regulatory Affairs Mgr Cm @ Parexel, System Dev @ Veeva Syst.Explore more at jobswithgpt.com.

šŸ”„ Skills

risk management (2) Regulatory Affairs (2) CMC (2) Submission Strategies (2) Technical Documentation (2) Project Management (2) Collaboration (2) RTSM (2) pharmacovigilance (1) ICSRs (1)

šŸ“ Locations

Zagreb (7)

Ergomed

Skills & Focus: pharmacovigilance, ICSRs, signal detection, risk management, regulatory authority, adverse event, safety reports, medical review, mentoring, training

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: cloud-based solutions, life sciences, System Developer, RTSM, custom code, study requirements, attention to detail, full-time, exempt position, customer needs
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: flexibility to work from home or in the office

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: 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

Ergomed

EU QPPV Zagreb
Skills & Focus: adverse reactions, risk evaluation, medicinal product, safety studies, oversight, available to CAs, safety profiles, emerging safety concerns, marketing authorisations, post-authorisation

Veeva Systems

Skills & Focus: Computer Software Validation, clinical trial software, Randomization and Trial Supply Management, RTSM, technical writing, validation process, product excellence, customer implementations, fast-paced environment, ownership
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: strong technical writing capabilities and expertise in clinical trial software
Type: Full-time
Benefits: flexibility to work from home or in the office