Country QRVI Director M/F
Sydney, Australia
Job description
Position description
Job profile
QRVI (Quality, Regulatory, Vigilance, Medical information) - Country QRVI Director
Job title
Country QRVI Director M/F
Contract
Permanent contract
Activity Rate
Full time
Mission
QRVI Team Management
Management of the local QRVI team: direct coordination and supervision of all local Q/R/V/I activities, organizational improvements, people's skills and expertise development
Regulatory Affairs
• Take responsibility for all regulatory activities for PFM & PFDC of PFA in accordance with local legislation in force
• Supports the business in NZ in providing regulatory assistance to the local partner(s) and regulatory input/expertise to Corporate projects
• Manages Regulatory intelligence for all types of products: anticipates, assess and communicate any legislative changes in Australia/NZ that may affect our products to reduce the business impact
Quality Management
• Develop, implement and manage a Quality Management System according GxP's and Corporate requirements for all activities for PFM and PFDC of PFA in accordance with the Australian legislation in force
• Ensure that the Quality Management System (QMS) is in use for all local quality processes
Medical Information
• Supervises and /or takes over the responsibility of local medical and scientific information (LMSI) activities of all PFM, PFD, and PFDC marketed products (including compassionate/name patient basis uses), according to the Corporate guidelines/SOPs and local SOPs, and in coordination with local Medical Director for PFM.
Pharmaco / Cosmeto Vigilance
• Coordinates and organizes, at the national/area level and in liaison with the Corporate Vigilances Direction (CVD), all activities in relation with the oversight on the safety profile of the portfolio
• Management of Vigilances Cases whatever the status of the product and the sources
• Oversight of Risk Management Plan (RMP) Implementation (medicinal products only)
• Ensures that safety queries, other significant safety issues and, if applicable, local/global crisis management are performed according to Corporate processes and local regulatory authority requirements
• Maintains oversight of any safety communication to Healthcare Professionals or consumers as applicable
• Ensures appropriate safety reporting processes are in place at affiliate level and, if applicable, described in relevant local documents, for global and local interventional clinical trials, Non-Interventional Studies (NISs), Non-Interventional Programs (NIPs) and Compassionate Use in accordance with Corporate processes and local regulatory authority requirements
• Provides safety related information to global teams for the preparation of Aggregate Reports, when necessary
• Ensures local signal detection activities and communicate to Corporate any potential local safety signal detected during the routine vigilance activities
• Ensures the implementation and maintenance of a Vigilances Quality System in the affiliate in accordance with Corporate processes and local regulatory authority requirements
• Participates to the negotiation and writing of local vigilance agreement with local partners or services
Profile
• Degree in Medicine, Pharmacy or life science
• Successful previous job experience (7-10 years) in QRVI in pharmaceutical and/or cosmetic industry
• Significant experience in Safety (especially, operational PV) + qualification per training and Over 2 (two) years' experience in Pharmacovigilance
• Demonstrated success in defining and implementing SOP at a local level are mandatory:
• Training or previous successful experience in risk management or equivalent is mandatory
Competencies
• Leadership and management skills
• Organization and planning skills
• Communication skills
• Fluent English language knowledge, written and verbal
• Influencing skills
• Proven ability to interact well in a multifunctional team setting
• Drug Safety knowledge
• Medical terminology in English – verbal and written
Behavioural skills
• Rigour, analysis and synthesis capabilities
• Adaptability, anticipation
• Personal assertion, management skills
• Open-mindedness, team spirit, communication with corporate entities
• Sense of result
• Quality and compliance oriented
Position location
Job location
Oceania, Australia
Location
Sydney NSW
Candidate criteria
Minimum level of education required
Postgraduate
Qualification
3-Associate/Foundation degr./BTEC HNC/HND/Bachelor
Minimum level of experience required
8 years and more
Languages
English (4 - Fluent)
Requester
Expected date of arrival
18/07/2022
Ces offres pourraient vous intéresser
Chargé(e) de contrôle qualité H/F - CDI
Réf. : 2022-10406 | 04/08/2022 16:31:57 | GIEN (45)
Chargé(e) affaires pharmaceutiques - STAGE H/F - Stage
Réf. : 2021-9125 | 04/11/2021 10:42:30 | Castres (81)
Responsable unité qualité H/F - CDI
Réf. : 2022-10362 | 25/07/2022 15:08:07 | Soual (81)
· Mentions légales Aller en haut
Desired profile
Profile
• Degree in Medicine, Pharmacy or life science
• Successful previous job experience (7-10 years) in QRVI in pharmaceutical and/or cosmetic industry
• Significant experience in Safety (especially, operational PV) + qualification per training and Over 2 (two) years' experience in Pharmacovigilance
• Demonstrated success in defining and implementing SOP at a local level are mandatory:
• Training or previous successful experience in risk management or equivalent is mandatory
Competencies
• Leadership and management skills
• Organization and planning skills
• Communication skills
• Fluent English language knowledge, written and verbal
• Influencing skills
• Proven ability to interact well in a multifunctional team setting
• Drug Safety knowledge
• Medical terminology in English – verbal and written
Behavioural skills
• Rigour, analysis and synthesis capabilities
• Adaptability, anticipation
• Personal assertion, management skills
• Open-mindedness, team spirit, communication with corporate entities
• Sense of result
• Quality and compliance oriented
Position location
Job location
Oceania, Australia
Location
Sydney NSW
Candidate criteria
Minimum level of education required
Postgraduate
Qualification
3-Associate/Foundation degr./BTEC HNC/HND/Bachelor
Minimum level of experience required
8 years and more
Languages
English (4 - Fluent)
Requester
Expected date of arrival
18/07/2022
Ces offres pourraient vous intéresser
Chargé(e) de contrôle qualité H/F - CDI
Réf. : 2022-10406 | 04/08/2022 16:31:57 | GIEN (45)
Chargé(e) affaires pharmaceutiques - STAGE H/F - Stage
Réf. : 2021-9125 | 04/11/2021 10:42:30 | Castres (81)
Responsable unité qualité H/F - CDI
Réf. : 2022-10362 | 25/07/2022 15:08:07 | Soual (81)
· Mentions légales Aller en haut