Vacancy posted: Wednesday, 17 Oct 2012
You will be responsible for working in multi-disciplinary teams across site to ensure that both existing and new equipment, processes and site systems are fully compliant with internal policy and procedures, as well as with EC Directives and Code of Federal Regulations. Ensuring all processes and equipment are validated in line with regulatory and company requirements. Ensuring correct operation of change control for procedures and systems where there may be an impact on their validated state. Providing consistent validation advice and inform validation working party members on changes in GMP, compliance or other regulatory expectations relating to validation of production equipment and processes. Chairing of validation working parties, provision of validation documentation for projects and validation reviews and the presentation of validation documents at audits.
The successful applicant will be experienced in a similar role and will have good planning, organisational and time management skills along with an ability to make decisions, solve problems, negotiate, influence and communicate effectively with others. Knowledge of pharmaceutical manufacturing equipment and processes or alternatively knowledge of controls and IT systems is essential.
Please apply online or contact Helen on 0141 332 9060 for further information
The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.
SRG, winners of the Recruitment Professional Awards 2011 'Best Company to work for' and 'Best People Development Business' awards, and the only "highly commended" company in the Annual Recruiter Awards for Excellence 2011, for 'Best Small Recruitment Agency to Work For'.
Job Reference: 27725
Closing Date: 19-Oct-2012