REGULATORY AND PHARMACOVIGILANCE PRODUCT jobs in UNITED KINGDOM, United Kingdom

that ensures what we do, we do well. Responsibilities As the Senior Manager – Pharmacovigilance, you will be responsible... department initiatives and to advance your management skills as part of the Pharmacovigilance FSP leadership team Manages...

.com and follow @JazzPharma on Twitter. Brief Description: To lead Jazz's Pharmacovigilance QA (GvP) function to assure regulatory... therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage...

strategies to maximize regulatory and pharmacovigilance success. · Sound knowledge of requirements of MA Transfer in EU... activities are carried out in Regulatory and Pharmacovigilance. · Drive all pre-submission meetings including inputting...

and service providers. · Management mentoring and training of all regulatory staff. · Management of all pharmacovigilance...Reference Number: JO-2402-529333 Regulatory Affairs Lead/Head of Department Rate: Negotiable Job Type: Permanent...

local and global submissions Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA...SRG are partnered with a pharmaceutical organisation who are seeking a Product Surveillance Reporting Analyst...

Partners with pharmacovigilance, regulatory affairs, in-country teams, and device QA for submissions and escalates requests...Product Surveillance Reporting Analyst 12 months £17.96 p/h Marlow - hybrid (3 days on site) SRG are partnered...

submissions, responses to regulatory agency inquiries, pharmacovigilance (PV) processes and projects, and PV or other audits... into product development and lifecycle management as well as perform or oversee other advanced MSS activities...

and Product Technical Complaints. Key Responsibilities: Effectively Navigate Pharmacovigilance Activities: Assess when adverse... events and product technical complaints are reported within one business day, maintaining compliance with regulatory...

of experience in the Regulatory Affairs & Pharmacovigilance · Proficiency in the use of MS Office suite (Excel, PowerPoint...Job Title: Pharmacovigilance Co-ordinator Employment Type: Permanent Position Salary: £35,000 per annum Location...

Brands req? No Keywords Medicine, Regulatory, Manager Latitude,longitude 1 52.927182,-1.183948 Function Product...Job Description Medicine Regulatory Manager Vacancy closing date: 22nd May 2024 Recruitment Partner: Laura Taylor...

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...

and GLP standards and global regulations. As an integral member of the team tasked with product development, the position... with global program teams to ensure protocol, procedural, GCP / regulatory compliance and inspection readiness throughout...

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...

with complaints management within the organization, like affiliate CQA, Medical Information, Regulatory Affairs and Pharmacovigilance... · Supports more complex complaints that are escalated. · Serve as a Subject Matter Expert for a designated product...

of senior management key pharmacovigilance findings Provides global medical leadership for product-focused safety activities... and initiatives based on deep understanding of good pharmacovigilance practices (GVP) and other regulatory guidance Participates in...

oversight, per Good Clinical Practice, of sponsored studies in alignment with the Target Product Profile​. In this role, the..., and regulatory submission documents, among other study related documents. Effectively collaborate and communicate with study...