Work Schedule

Flex Shifts 40 hrs/wk

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Position Summary:

Included in the daily responsibility, is supporting the implementation and maintenance of quality systems and ensuring that FBS NL adheres to all site applicable EU GMP, IGJ and other identified applicable regulations! Working a rotating 7 day a week shift pattern, you will be responsible for ensuring compliance as per the requirements as per the Quality Management System and to provide support to the Quality Manager.

Key Responsibilities:

SOP Management, including Document Control as Coordinator on eDMSQuality Reviewing and as required, approving Trackwise QRsReviewing and where appropriate approving draft operational documentationPerforming Quality review of change controlsResponsible for status control of products/materialManages items and content on SFLMSPerforming Supplier assessmentEnsures compliance to company QMS and any other applicable regulations/standardsAssures compliance to EU GMP and IGJ regulations to ensure retention of site licensesPerforms required duties as an approved ArchivistPerforms verification as part of Quality.Supports Client audits and Internal Audit Programs where requiredProvides training and conducts proficiency assessments for other QA staffChecking completed operational documentation for ALCOA+ and adherence to Good Documentation Practices, where appropriate Quality approving documentation.Performs QA related tasks as assigned by the site Head of Quality.Performs QC functions as per required daily activities.Travel might be required.May be required to perform off site work in line with work requirements.

Minimum Requirements/Qualifications:  

Educated to degree level / equivalent in relevant subjects and/or has at least 1 years GMP experience

Required Skills/Experience:

A high degree of accuracy and attention to detailAbility to read and interpret general procedures and government regulationsGood problem solving skillsAbility to efficiently present information and respond to questions from groups of managers, clients and inspectorsAbility to calculate figures and amounts such as proportions, percentages, area and volumeGood computer knowledge, proficient in MS Office (Word, Excel, and PowerPoint) and ability to acquire knowledge and master all clinical trial database systemsGood verbal and written communicationBuilds good working teamworks with site employees and external individuals.Able to operate under pressure and to support others within the teamEmployment is subject to 10 year history screening for criminal records, qualifications, previous employment and credit history – Thermo Fisher Scientific have the right not to employ people failing to meet the standards requiredThis position functions in a repository environment, which may include working with dry ice, liquid nitrogen cryogenics, hazardous and infectious agents as well as marked changes in temperatureProficient in English

Although not required, the following would be preferable:

Valid driver’s license and a good driving recordLive no more than 30 minutes driving time from the facility