Senior Pharmacovigilance Specialist -EAC
at Abbott Laboratories
Johannesburg, Gauteng, South Africa -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 30 Jun, 2024 | Not Specified | 31 Mar, 2024 | 4 year(s) or above | Time Management,Interpersonal Skills,Pharmaceutical Industry,Computer Literacy,Communication Skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
ABOUT ABBOTT
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
REQUIRED QUALIFICATIONS
- Pharmacy or related health science degree
PREFERRED QUALIFICATIONS
- At a minimum 4 years PV experience in pharmaceutical industry or PH Health authority. .
- Profound understanding of local PV regulation
- Ability to give attention to the detail.
- Computer literacy (Windows, MS Office)
- Good English language skills
- Good communication skills with internal and external stakeholders
- Excellent time management, organizational and planning skills.
- The ability to work independently and as a part of a team.
- Independent thinker with the ability to challenge the status quo with outstanding interpersonal skills.
Responsibilities:
- Acts as a local QPPV on a 24/7/365 basis in EAC Affiliate.
- Maintenance of the Affiliate PV System Country Chapter and additional local PV procedures, forms, and templates
- PV business continuity planning and notification of any business interruptions that pose a threat locally or globally to pharmacovigilance processes or endanger regulatory compliance
- Receipt, recording, and reconciliation of safety information
- Safety surveillance including literature and health authority website screening and preparation of local periodic safety reports and Risk Management Plans
- Regulatory submission of safety information
- Basic PV training of local EPD staff
- PV record retention and archiving
- Implementation of out-of-office coverage for receiving and recording safety-relevant information
- Maintenance of local PV product list
- Ensure PV matters in local interventional studies and local non-interventional organized data collection schemes.
- Negotiation and implementation of local commercial pharmacovigilance agreements and local pharmacovigilance service agreements
- Due Diligence for product acquisition or in-licensing negotiated by an Affiliate organization.
- Provision of local PV Compliance metrics and management of non-compliances
- Coordination/management of PV audits and inspections at the Affiliate level
- Ensure vigilance compliant to local legislation for Abbott EPD products beyond medicinal products such as medical devices and food supplements.
- Contribution to benefit-risk assessment of the Abbott EPD products portfolio;
- Act as the key expert for any PV-relevant topics and ensures proactive communication as appropriate;
- Leading regional PV projects and contribution to global PV projects.
REQUIREMENT SUMMARY
Min:4.0Max:9.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Proficient
1
Johannesburg, Gauteng, South Africa