Environmental Monitoring Assistant

1 week ago

London, United Kingdom Guy's and St Thomas' NHS Foundation Trust Full time

This is an ideal opportunity for a recent graduate in a biology / microbiology / biomedical sciences field or an aseptic / production operator who has previously successfully undertaking monitoring activities in a cleanroom / laboratory environment.

Training on gowning procedures and sampling techniques will be provided.

**Note**: this post operates across both Guys (London Bridge) and St Thomas' (Waterloo) sites

If you are looking for a new challenge then this could be the opportunity for you.

To undertake the physical and environmental monitoring of aseptic, production, radiopharmacy and other trust manufacturing units. Supervision of media incubation and reading/recording of results of microbiological recoveries and accurately imputing data onto Quality Management Systems in accordance with GMP and current departmental procedures.

Department Information

The Pharmacy Quality Assurance department at Guy’s and St Thomas NHS Foundation Trust is an independent department within Pharmacy which provides support and guidance to clinical pharmacists and in-patient pharmacy dispensaries at Guys and St Thomas’ Hospital plus alongside the on-site Quality Control department provide a full Quality Assurance manufacturing and product release service to aseptic, sterile and non-sterile manufacturing. There is a new classical manufacturing facility on the Guy’s site, a new Parenteral Nutrition Unit on the St Thomas site and a new chemotherapy pharmacy in the Guy’s Cancer Centre

The manufacturing units undertake a wide range of manufacturing and dispensed activities to provide medicines to meet the special clinical needs of patients which are not commercially available. Each unit has a full complement of Pharmacists, Technicians and Assistants and prepare a wide range of products.

Pharmacy Quality Assurance - Micro-team SATO
1. To carry out routine physical and microbiological environmental monitoring of pharmaceutical production areas following Standard Operating Procedures and schedules.
2. To use environmental monitoring and other QA equipment correctly by following the procedures for use, cleaning and monitoring of such equipment.
3. To ensure that all required documentation is filled in correctly, processed and filed in the correct manner according to GMP principles.
4. To maintain and update accurate record logs of environmental monitoring undertaken and subsequent results.
5. To assist in the arrangements for QA equipment calibrations.
6. To accept delivery of materials for the Pharmacy QA micro-team.
7. To book in raw materials and containers on receipt from external suppliers according to Standard Operating Procedures.
8. To assist in the stock control of media used in the microbiological monitoring service.
9. To actively assist senior staff in the maintenance of the Quality Management System.
10. To contribute to the development of GMP documentation such as standard operating procedures and worksheets.
11. To contact Manufacturers and Suppliers to obtain appropriate Certificate of Analysis or Certificates of Conformity for received raw materials and containers.
12. To ensure that working procedures at all times conform with standards of Good Laboratory Practice, The Health and Safety at Work Act, Control of Substances Hazardous to Health Regulations and other relevant legal and professional directives.

**General**:
1. To undertake other duties as required in order to maintain the safe, efficient and effective provision of Pharmaceutical services.
2. To contact appropriate supervisor for assistance as required when undertaking the activities of this job description.
3. To attend courses and undertake training to develop expertise in appropriate skills, where training needs are identified.

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