Pharmacovigilance Specialist
Job title: Pharmacovigilance Specialist
Company: On Q Recruitment
Job description: Since its establishment nearly 100 years ago this organisation has expanded significantly with close to 3000 employees worldwide and ranked in the top 3 in their field of expertise. This has been achieved due to continually discovering innovations and acquisitions in the field of medical imaging technologies and the contrast media associated with them. Recent advancement has seen them progress to digital technologies and artificial intelligence improving the productivity of the Specialists who utilise the products, in addition to assisting in the improved guidance of treatments to patients.As the Pharmacovigilance Specialist you will be part of a multinational organisation with a boutique-type feel enabling faster workflows and agile decision-making processes that drive business growth.Benefits on offer
- development for high-performers
- working days (hybrid role)
- annual leave for Christmas
- leave and birthday payment
- On-site parking
About the roleAn opening for a Pharmacovigilance Specialist has arisen which offers the exceptional opportunity to work not only in Pharmacovigilance but to support and develop skills in Regulatory Affairs and Quality Assurance.PharmacovigilanceReporting to the Regulatory Affairs Manager, you will be the pharmacovigilance expert managing ADR case reporting in line with local requirements and timelines. Looking after the compliance and robustness of the pharmacovigilance system will be a key component in addition to conducting regular training for relevant stakeholders. Additionally, you will serve as the central point of contact for pharmacovigilance activities and have the opportunity to participate in global pharmacovigilance projects.Quality Assurance /Regulatory AffairsGiven the nature of a smaller organisation, you will be given the opportunity to expand your skills to other disciples. The responsibility of the Quality Management System (QMS) and quality release activities will also sit within the remit of this role, in addition to some Regulatory Affairs activities. QA/RA experience is not a mandatory requirement to be successful in this role, as training will be provided.To be a successful candidate:
- A pharmacist or Nurse background is preferable.
- Minimum 2-3 years of experience in PV/Drug Safety in a Pharmaceutical organisation.
- Quality Assurance and Regulatory Affairs experience is advantageous but not essential.
- Strong attention to detail.
- Ability to multitask and take on responsibilities outside of the Position Description to be adaptable to the requirements of a smaller company environment and goals.
- Willingness to grow, learn, and assimilate information quickly, present data clearly, and concisely, and discuss relevance in line with development strategy whilst having the confidence to take calculated risks.
- Proactive and flexible with the ability to collaborate with cross-functional teams.
- Proficient in MS Office, including Excel, Word, and PowerPoint
For a confidential discussion, contact Edessa Tanafranca at 02 7253 3090 or via email at etanafranca@onqrecruitment.com.auAt On Recruitment, we’re always interested in hearing from talented and engaging people.Interested in this job?Save JobShare this JobCreate AlertSimilar JobsConsultant Name: Consultant Email: Social AccountsSCHEMA MARKUP ( This text will only show on the editor. )Welcome to On Q Recruitment, a specialist Sydney based Life Sciences and Government recruitment agency.
Expected salary:
Location: Sydney, NSW
Job date: Tue, 09 Apr 2024 23:25:26 GMT
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