Validation Specialist

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Validation Specialist Wanted for Permanent role in the Hertfordshire Area! £35k-£45k! Apply Now!My client is a leading pharmaceutical organisation based in the Herfordshire area and they are looking for experienced validation engineer or specialists to join them on a permanent basis. If you have experience in the pharmaceutical industry and are looking for a new challenge please apply now via the website or call Joseph Tiffin on 0161 868 2214 for more information.Key responsibilities;* Responsible for key aspects of the day-to-day validation planning and qualification testing within Validation Compliance Unit as outlined in the duties below. * The co-ordination and execution of process / equipment / system verification/qualification.* Result reporting associated with plans, protocols and regulatory requirements defined by validation management.* Co-ordination of validation test equipment, resources and support staff / contractors to ensure validation / verification / qualification is correctly controlled in respect to secure storage, annual service and renewals, accuracy checks.* Performing testing and qualification in accordance with Site Validation Master Plan and associated procedures.* Ensure up to date authorised documentation is generated in a timely manner for all validation exercises and projects for which the post holder is responsible.* Ensure testing schedules and execution status are clearly planned and presented to stakeholders and validation management.* Ensure validation testing is performed at necessary times with agreed stakeholders including peak and off peak operating periods (which may include shift cover and weekend testing)* Determine and write procedures associated with validation exercises and projects according to cGMP and Regulatory (MHRA and FDA) requirements.* Investigate, develop and implement new and improved validation procedures to support validation deliverables and execution.* Liaise with project stakeholders to ensure necessary training and awareness is provided to ensure correct GMP and compliant operation.* Liaise and co-operate with other departments to carry out Validation activities and changes as necessary to meet cGMP and regulatory requirements* Supervise and train others in areas where the post holder has specialist knowledge.* Advise on validation requirements necessary in area of expertise to maintain compliance with current GMP and regulatory requirements, within the post holder's area of technical specialty.* Use of validation equipment and computer software for data collection, collation and analysis of validation / qualification processes and equipment (e.g. Kaye Dataloggers, MS Excel, Yokogawa).* Ensure validation deliverables, execution and equipment are in compliance with Health and Safety and Environmental requirements.* Ensure validation equipment is maintained and calibrated in a timely manner, to agreed standards. * Ensure process equipment and areas are correctly handed back into to productive use and process / equipment owner responsibilities.If you believe you meet the above criteria and would like to apply for the role of validation specialist please apply now via the SRG website or call Joseph Tiffin for more information on 0161 868 2214.

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.