Gilead Pharmaceutical Limited, is recruiting for a suitably qualified candidate to fill the position below:
Job Title: Discharge Coordinator
Location:
LagosJob Description
- As Discharge Coordinator you will be responsible for planning and facilitating patient discharge and ensuring high standards of patient care are consistently maintained.
- Reporting to the Associate Director of Nursing you will develop discharge plans that enable patients to be safely discharged into their homes and provide patient-centred interventions and enable service users and carers to optimise and maintain their independence in their homes and the local community.
- Working alongside a multidisciplinary team you will ensure patient’s needs are met before their return to home and support patients through the discharge assessment process.
Qualifications/Skills
- Be a Registered Nurse (RN/ RGN) with experience in an acute hospital (NHS or independent).
- Experience of working as a Discharge Nurse is not essential but advantageous.
- Have the ability to communicate clearly with a range of people at differing levels across the hospital, deploying a range of techniques to do this effectively.
- Possess strong organisational and planning skills, including risk management.
Remuneration
The Hospital offers an excellent benefits package including free car parking, a wide range of training and career opportunities, life assurance cover, pension scheme, private healthcare cover and 25 days holidays, rising to 30 days with service.
Job Title: Regulatory Affairs Manager
Location: Lagos
Responsibilities
- Implement regulatory strategies to forecast potential issues and flag these through clear and effective communication
- To oversee and manage the post CE approval products to guarantee an effortless integration of new products following launch
- Uphold a current knowledge of industry standards to distribute to direct reports and project teams
- To confirm submissions are of high standard and compliant with industry requirements
Experience Required
- Must have proven experience in handling direct reports
- An Extensive knowledge of Regulatory Affairs within the medical device industry
- Has participated in post and pre market submissions
- CE Marking experience
Requirements
- Must be a clear communicator
- Efficient in time management to be able to handle multiple projects at one time
- A positive attitude to ensure effective collaboration within the team
- Ideally degree educated with vast experience working with medical devices
How to Apply
Interested and qualified candidate should send their CV’s to:gileadpharm@gmail.com
Note: Only shortlisted applicants will be contacted
Deadline:
24th April, 2016.
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