6 Cer Jobs

Position Summary We are looking to add an experienced Clinical Writer to our team. The person in this position must be able to independently contribute to the development of initial and update(s) of CERs that support the applicable regulatory submission requirements for the medical device products. An experienced Clinical Analyst professional has relevant medical/life-science qualification and knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 4 - 6 years with a minimum of 1- 2 years of CER writing experience is essential. A minimum of 1- 2 years of medical writing/reviewing experience is needed. The experience is expected to be current or recent (preferably within the past two years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities and the therapy area. Preferred EducationMasters degree in a life science or biomedical engineering discipline preferred, or equivalent regulatory/writing experience Preferred Experience 1. The expected experience is 4- 6 years of CER writing and reviewing experience. Significant experience writing scientific, medical/clinical, and technical content. Also, a plus would be experience with writing CERs that conform to MEDDEV 2.7/1. 2. Knowledge in the therapeutic area- specifically in the field of diagnosticradiology, interventionalradiology and radiation oncology 3. Familiarity with various country specific standards and regulations for medical devices to be able to assess and provide device appropriate clinical evaluation data for registrations. Duties and Responsibilities 1. Collaborate with the project/program stakeholders for product knowledge and information to develop quality content for the CERs and within the required timelines. 2. Screen and summarize literature for relevant clinical data 3. Review literature to elucidate the clinical problem and current treatment techniques 4. Study and report device characteristics and instructions for use 5. Evaluate data for similar competitor devices 6. Summarize post-marketing surveillance and risk management data for the target device 7. Able to work in cross functional teams with strong communication, presentation & interpersonal skills 8. Analytical thinking skills with strong demonstration of scientific writing and verbal communication.

We are looking to add an experienced Clinical Writer to our team. The person in this position must be able to independently contribute to the development of initial and update(s) of CER’s that support the applicable regulatory submission requirements for the medical device products. An experienced Clinical Analyst professional has relevant medical/life-science qualification and knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 7 - 8 years with a minimum of 4-5 years of CER writing experience is essential. A minimum of 4-5 years of medical writing/reviewing experience is needed. The experience is expected to be current or recent (preferably within the past two years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities and the therapy area. Preferred EducationMasters’ degree in a life science or biomedical engineering discipline preferred, or equivalent regulatory/writing experience Preferred Experience: 1. The expected experience is 7 – 8 years with minimum 4-5 years of CER writing and reviewing experience as per EU MDR (European Union Medical Device Regulation (EU) 2017/745). Significant experience writing scientific, medical/clinical, and technical content. Also, a plus would be experience with writing CERs that conform to MEDDEV 2.7/1. 2. Knowledge in the therapeutic area – specifically in the field of diagnostic radiology, interventional radiology and radiation oncology 3. Familiarity with various country specific standards and regulations for medical devices to be able to assess and provide device appropriate clinical evaluation data for registrations.

We are looking to add an experienced Clinical Writer to our team. The person in this position must be able to independently contribute to the development of initial and update(s) of CER’s that support the applicable regulatory submission requirements for the medical device products. An experienced Clinical Analyst professional has relevant medical/life-science qualification and knowledge/direct clinical experience in the use of the device or device type in a clinical setting. The expected experience is 7 - 8 years with a minimum of 3 – 4 years of CER writing experience is essential. A minimum of 3 – 4 years of medical writing/reviewing experience is needed. The experience is expected to be current or recent (preferably within the past two years), to provide confidence in their experience considering the rapid nature of updates/changes in the regulatory landscape, the device, its functionalities and the therapy area. Preferred EducationMasters’ degree in a life science or biomedical engineering discipline preferred, or equivalent regulatory/writing experience Preferred Experience: 1. The expected experience is 7 – 8 years with minimum 3 – 4 years of CER writing and reviewing experience as per EU MDR (European Union Medical Device Regulation (EU) 2017/745). Significant experience writing scientific, medical/clinical, and technical content. Also, a plus would be experience with writing CERs that conform to MEDDEV 2.7/1. 2. Knowledge in the therapeutic area – specifically in the field of diagnostic radiology, interventional radiology and radiation oncology 3. Familiarity with various country specific standards and regulations for medical devices to be able to assess and provide device appropriate clinical evaluation data for registrations.

Role & responsibilities integrating Expressways with CUCM Voice Mail Jabber Internal & External Preferred candidate profile Cisco collaboration suite experience(CUCM, CUC, CER, IMP and expressways) Should have implementation experience with new builds, customer deployments & troubleshooting

Role & responsibilities Develop and implement detailed installation plans for signaling and telecommunication equipment to meet project schedules and quality targets. Manage the entire design and construction process of signaling and telecom systems, ensuring smooth execution and coordination across disciplines. Oversee the installation of various systems and equipment, with particular focus on signaling, telecommunication, and other critical systems at key project locations such as OCC, BCC, DCC, CER, SER, as well as civil and building works. Ensure all installations are executed strictly in line with approved design drawings, technical specifications, and safety standards , maintaining a high level of quality and compliance. Lead and coordinate the installation team , including technicians, engineers, and subcontractors, to maximize efficiency and maintain safety on site. Supervise installation execution and quality control , ensuring work progresses according to plan and meets project requirements. Facilitate troubleshooting and issue resolution on-site by acting as a liaison between technical teams, contractors, and clients. Oversee system testing and commissioning activities to ensure installed systems are fully functional and ready for operational handover. Maintain comprehensive documentation and reporting throughout the installation phase for project tracking, quality assurance, and client review. Preferred candidate profile Qualifications Bachelors degree in Electronics, Telecommunications, Electrical Engineering, or a related technical field. Minimum 7 years of experience managing installation activities in signaling, telecommunication, or related critical system projects, preferably within Metro, Railways, or High-Speed Rail sectors. Strong knowledge of signaling systems (e.g., interlocking, ATP, CBTC) and telecommunication equipment. Proven experience in managing installation teams and coordinating with multiple stakeholders on large-scale infrastructure projects. Skills & Competencies Excellent project planning, organizational, and leadership skills. Strong understanding of safety protocols, quality assurance, and compliance standards. Effective problem-solving skills and ability to manage on-site troubleshooting. Proficient in reading and interpreting technical drawings, wiring diagrams, and specifications. Strong communication skills, both verbal and written. Familiarity with project management and documentation tools. Preferred Experience with control centers such as OCC, BCC, DCC, CER, SER, and civil/building works integration. PMP or equivalent project management certification. Familiarity with industry standards and regulatory requirements applicable to signaling and telecommunication installations.

Lead and support RF, Voice/IPT, telephony, and mobile infrastructure globally. Drive innovation, reliability, and automation across network platforms, ensuring secure, scalable, and high-performance communication systems. Required Candidate profile Experienced in RF design, VOIP/IPT systems, UC tools, wireless/mobility, and SRE practices. Skilled in Tier-3 support, automation, and vendor management.