24 Quality Assurance And Engineering jobs in Bucharest.

Bucharest

• Skills: Pharmacovigilance, medical writing, PSURs/PBRERs, aggregate reports, RMPs, QC, training, compliance, audits, risk management
• Level: mid
• Type: full_time

Bucharest

• Skills: Oncology, Rare Disease, Study Start Up, Regulatory, Project Management, FDA, EMA, ICH GCP, Documentation, Interpersonal Skills
• Level: mid
• Type: full_time

Bucharest

• Skills: pharmacovigilance, medical writing, aggregate reports, DSURs, PSURs, RMPs, team management, regulatory documents, communication skills, CRO
• Level: mid
• Type: full_time

Bucharest

• Skills: Site Management, CRA, Late Phase studies, Good Clinical Practice, Clinical Trial Management, Regulatory Compliance, Data Collection, Patient Recruitment, Remote Monitoring, Project Management
• Level: mid
• Type: other

Bucharest

• Skills: Clinical Research, Good Clinical Practice, Regulatory requirements, Site practices, Subject recruitment, Monitoring visits, Data integrity, Pharmaceutical industry, Problem-solving, Organizational skills
• Level: entry
• Type: full_time

Bucharest

• Skills: medical devices, certification, audit, regulations, QMS, ISO13485, final reviewer, compliance, decision maker, European notified body
• Level: mid
• Type: full_time

Bucharest

• Skills: regulatory affairs, clinical trials, biopharmaceutical, compliance, documentation, project management, stakeholder engagement, labeling, submission, artwork review
• Level: mid
• Type: full_time

Bucharest

• Skills: medical writing, clinical study protocols, regulatory standards, ICH E3 guidelines, biopharmaceutical, statistical analysis, clinical trials, FDA regulations, collaborative skills, peer reviewer
• Level: mid
• Type: other

Bucharest

• Skills: Medical Device, QMS Auditors, regulatory compliance, MDR, IVDR, auditing, training programs, technical guidance, quality management system, stakeholder engagement
• Level: senior
• Type: full_time

Bucharest

• Skills: Quality Management, Compliance, ISO 13485, Risk Management, Process Improvement, CAPA, Medical Devices, Product Quality, Regulatory Requirements, Communication Skills
• Level: mid
• Type: temporary

Bucharest

• Skills: medical writing, clinical study reports, FDA regulations, ICH guidelines, clinical protocols, patient narratives, IND submissions, team leadership, clinical research, data interpretation
• Level: mid
• Type: full_time

Bucharest

• Skills: Pharmacovigilance, Medical Information, Clinical Development, Safety Evaluations, Regulatory Affairs, Quality Assurance, Signal Detection, Risk Management, Medical Training, Aggregate Reports
• Level: senior
• Type: full_time

Bucharest

• Skills: Regulatory Affairs, OTC products, Compliance, Labeling, Market Authorization, Documentation, Stakeholder Engagement, Regulatory Strategy, Commercialization, Consumer Safety
• Level: mid
• Type: full_time

Bucharest

• Skills: clinical trial submission, regulatory affairs, communication, clinical research, EU CT Regulation, regulatory training, safety reporting, ethics submissions, project documentation, team collaboration
• Level: mid
• Type: other

Bucharest

• Skills: regulatory strategy, drug development, health authorities, communication skills, negotiation skills, clinical trials, project management, quality standards, medical affairs, regulatory compliance
• Level: mid
• Type: full_time

Bucharest

• Skills: pharmacovigilance, quality management system, GxP environment, regulatory compliance, SOPs, project management, auditing, training development, process improvement, risk assessment
• Level: mid
• Type: full_time