Connecting...

W1siziisijiwmtyvmduvmtmvmdivmzivmtyvnzuzl3zvbhquanbnil0swyjwiiwidgh1bwiilciyntywedewmfx1mdazyyjdxq

GMP Documentation Technician

Job Title: GMP Documentation Technician
Contract Type: Temporary
Location: Leicestershire
Industry:
Salary: £9.00 - £10.00 per hour
Start Date: March 2017
Reference: 68993-PHARM-JHY_1489575489
Contact Name: James Harvey
Contact Email: James.Harvey@volt.eu.com
Job Published: March 15, 2017 10:58

Job Description

Job title: GMP Documentation Technician
Job type: 6 month contract + potential extensions
Location: Leicestershire, UK
Salary / rate: £9 - £10/hour

SUMMARY

- My client is a highly-regarded pharmaceutical company renowned for applying
science in collaborative ways to improve lives daily. With $30 billion in sales
and 90,000 employees connecting with customers all around the world
- I am currently recruiting for them a GMP Documentation Technician to join their
Laboratory team based in Leicestershire
- Applicants for this position should have some previous experience in the
Pharmaceutical industry, ideally having worked with GLP / GMP specifications
and procedures

MAIN PURPOSE AND KEY RESPONSIBILITIES

- Management of documentation within the Document Assurance department, including
preparing and scanning, compiling documentation packages and reviewing archived
documents
- Working in a safe manner whilst taking responsibility for personal safety and
the safety of others
- Actively raise APRs, DOs and MIs as required

*ALWAYS FOLLOW THE 10 RULES OF GMP*

- Work to appropriate laboratory systems, standards and procedures, e.g. data
recording, labelling, investigation and calibration procedures
- Complete analytical documentation including the input of results onto the LIMS
system
- Maintain good laboratory housekeeping at all times
- Maintain the documentation required for their role, including training record
- Provide training as required in analytical techniques, processes and systems
- Review and issue GMP documentation
- Understand the site documentation and change control systems
- Work positively as part of a team and communicate effectively with Group and
peers
- Develop a basic understanding of the role of other functions within own value
stream
- Support continuous improvement activities within own group
- Understand how to communicate with auditors and general employee expectations
during an audit

PERSON PROFILE

Education:

- Educated to at least A-Level standard in a scientific discipline or,
- BTEC National Diploma or,
- Advanced GNVQ or,
- NVQ Level 2/3 with some relevant experience

Experience:

- Some prior experience within the Pharmaceutical Industry ideally within GLP,
GMP, Specifications and Procedures

Knowledge:

- Knowledge of pharmaceutical testing requirements, testing equipment and
current Analytical techniques