Connecting...

W1siziisimnvbxbpbgvkx3rozw1lx2fzc2v0cy9uzxh0lxboyxnllxjly3j1axrtzw50l2pwzy9iyw5uzxitzgvmyxvsdc5qcgcixv0

CSV Manager - Pharmaceutical

CSV Manager - Pharmaceutical

Job Title: CSV Manager - Pharmaceutical
Contract Type: Contract
Location: Sandwich
Industry:
Salary: Up to £300 per day
Start Date: ASAP
Reference: 15749a AP
Contact Name: Adrienn Prezenszki
Contact Email: adrienn.prezenszki@nextphaserecruitment.com
Job Published: April 24, 2018 16:54

Job Description

Do you have strong experience in Computer Systems Validation practices? Are you familiar with FDA regulations and do you have a deep knowledge of Quality processes and Data Integrity?

We have an URGENT requirement for an experienced CSV professional to join a global pharmaceutical business, working in state of the art facilities in Sandwich, Kent. This is a varied, multi-disciplinary role in which you will look after computer system processes across different global sites. The company if offering a competitive rate and the contract is for 6 months initially, though with a strong chance of extension beyond this.

The Role

You will be responsible for supporting the operations and deployment of Business Technology supported Pharmaceutical Sciences Computer Systems. You will need to make sure that the company’s System LifeCycle documents meet regulatory and the company’s compliance requirements across different sites. You will receive the Validation Plan to be able to perform investigations to identify computer issues, carry out root cause analyses and come up with resolution. The roles involve support Data Integrity assessment activities through guidance and review as well as perform jobs responsibilities in compliance with cGMP and all other regulatory requirements.

This is a varied and engaging role, with a CV-enhancing company, initially for a contract for 6 months but with a strong possibility of extension well beyond this.

Experience

The successful candidate will ideally be a graduate with strong experience in computer systems validation practices and regulatory requirements as well as data integrity, preferable gained within a Pharma company. You need to have experience with documentation management systems like Trackwise, Empower and IQ systems and good understanding of IT systems (applications and infrastructure) and systems governance. You need to be able to work autonomously in a matrix model and in a team environment and be someone who goes beyond the obvious and seeks novel approaches to complex situations.

Full details will be provided on application.
 

Get similar jobs like these by email

By submitting your details you agree to our T&C's