Search the 37 jobs at Ergomed

The Senior Quality Audits Manager leads the design, implementation, and management of internal and vendor audits while fostering a culture of quality within PrimeVigilance. Responsibilities include managing audit programs, ensuring compliance with regulations, mentoring team members, and documenting findings for process improvement.

The Senior Manager of Quality Management leads teams to ensure compliance with Pharmacovigilance and Medical Information regulations. Responsibilities include oversight of quality assurance activities, management of controlled procedures, training compliance, and supporting audits and inspections as a subject matter expert. They will manage quality management systems and ensure effective communication and organizational skills within the team.

The Senior Manager of Quality Management leads teams to ensure compliance with GVP regulations and quality standards in pharmacovigilance and medical information. They oversee quality management system activities, manage deviations and improvements, and provide training while supporting audits and inspections as a subject matter expert.

The Senior Manager of Quality Management leads teams to ensure compliance with regulations in Pharmacovigilance and Medical Information activities. Responsibilities include managing Quality Management System operations, supporting compliance issues, overseeing training, and participating in audits and inspections. The role demands effective communication, project management, and a solid understanding of GVP-related processes.

The Senior Manager of Quality Management leads teams within Quality Management, ensuring compliance with regulations and company policies in Pharmacovigilance and Medical Information. The role involves oversight of quality systems, managing deviations, training compliance, and supporting audits, while fostering skill development among team members.

The Principal Safety Technology Support Specialist leads the technology support for safety systems and databases. Responsibilities include gathering user requirements, optimizing safety systems, developing training materials, participating in audits, maintaining SOPs, administering databases, and mentoring junior staff.

The Senior Digital Marketing Manager will develop and execute digital marketing strategies to enhance brand visibility and generate leads. This role involves managing the digital marketing budget, overseeing website functionality, and integrating Salesforce for automation. The manager will analyze performance metrics and lead cross-functional initiatives to drive commercial growth.

The Senior Manager of Digital Marketing at Ergomed Group leads the development and execution of digital marketing strategies across various channels to enhance brand awareness and generate leads. They oversee website management, utilize Salesforce for marketing automation, and manage SEO/SEM initiatives, while analyzing performance metrics to optimize campaigns and improve ROI.

The PV Project Manager acts as the primary contact for project matters, manages client expectations, prepares project scopes, plans activities, and reports for clients and management. They ensure services exceed client satisfaction in pharmacovigilance activities.

The Office Administrator supports the Office Manager in organizing the office, participating in events, onboarding new hires, implementing office procedures, and maintaining relationships with suppliers and clients. Additionally, they will handle health and safety duties, assist with tasks related to mobile phones and car pool, and provide ad-hoc support across departments.

The PV Associate will assist in literature monitoring and screening for pharmacovigilance activities. Responsibilities include developing search strategies, reviewing literature for safety information, maintaining records of screened articles, and supporting regulatory audits. Requires strong communication skills and a life science background, with opportunity for professional growth.

The PV Associate - Japanese speaker will process Individual Case Safety Reports, performing pharmacovigilance activities under supervision. Responsibilities include data entry, quality review, and submissions workflow in compliance with regulations. This role is ideal for recent graduates in life sciences or healthcare fields eager to contribute to patient safety and grow in their careers.

The Data Engineer will construct and optimize data integration pipelines essential for enterprise data management and analytics. They will work closely with various stakeholders to ensure data solutions meet organizational needs and assist in problem-solving through curated insights.

The Data Engineer will build and operationalize enterprise data management and analytics pipelines. They will manage and optimize data integration processes for organizational data consumption, focusing on BI development and data architecture.

As a Data Engineer, you will build and optimize data integration pipelines, manage data architectures, and support analytics initiatives. Your role will involve designing data solutions and utilizing technologies for data movement and ingestion, ensuring efficient data access for stakeholders.

The Senior Proposal Associate/Manager will lead the development of proposals, collaborating with various stakeholders to create high-quality client-focused documents. Responsibilities include training staff, ensuring compliance with internal procedures, and supporting contract negotiations. The role emphasizes process improvement and development of junior staff.

The PV Associate/Literature role involves supporting literature monitoring activities, assisting with literature search strategies, participating in peer review QC of abstracts, and managing literature screening processes in compliance with safety regulations. The position requires effective communication and organization skills to contribute to patient safety.

The Associate, Quality Projects and Metrics will support the team by compiling, analyzing, and reporting compliance metrics, ensuring that data is gathered from departments, and tracking actions through completion. They will manage report templates and assist with administration and training responsibilities.

The PV Associate/Literature role involves managing literature screening in pharmacovigilance, assisting with literature search strategies, maintaining records, and ensuring compliance with regulations. Responsibilities include tracking literature searches, reviewing documents, and contributing to the company’s objectives related to patient safety.

The Associate, Quality Projects and Metrics supports the compilation, analysis, and reporting of Quality and Compliance Metrics following global regulations. Responsibilities include gathering metrics, compiling reports, tracking actions, and assisting in quality management tasks.