QC Raw Materials Sampling Scientist_UK

Description:

Please ensure you use the Lonza coversheet.


Please note, heavy lifting will be required for this role.


Working Pattern:
Monday to Tuesday 9 am to 5:30pm
Wednesday to Friday 11am to 6:30pm


6 month position, fully onsite.


Skills: Aseptic skills, Flexible to work in a clean room environment. Able to work as a team


Job summary:


Main role is to work effectively in a clean room environment, accurately dispensing required weights and volumes of raw materials whilst maintaining a high standard of GMP. However, they will also be responsible for the area, maintaining calibration dates working with other departments, maintaining schedules, logbooks, the training and support of other members of the team. They will be based within the warehouse and must be able to work with several electronic and paper based GMP systems to accurately record the sampling they have performed. They must be able to maintain the clean room environment, ensuring they have appropriate inventory


Job Description:


Sampling of raw materials which includes, but not limited to the following requirements: - Generation of sampling labels - Transfer of raw materials on GMP electronic systems - Transfer of raw material containers into sampling clean room environment - Opening and Sampling of Raw Material containers following appropriate GMP procedures - GMP documentation of transfer and sampling in logbooks and GMP documents - Returning of raw material containers to original stock location - Transfer of sampled raw materials to QC laboratory - Maintaining ambient raw material retention sample storage area -Assist with the disposal of Raw Material retention samples - Coordinates with Warehouse, Supply Chain and Procurement to solve problems and raise issues. Be the responsible person for the sampling area Be aware and ensure calibration dates for the room and equipment are maintained Work with engineering and validation to plan and schedule maintenance activities Be the responsible supervisor for cleaning and usage logbooks, ensuring they are maintained to a high standard and are routinely signed Delivering training and support to junior members / Scientist Analyst of the team Raise EWRP paper bases / electronic system Testing of samples and reporting of all results according to the relevant procedures in accordance with the expectations of GMP Lead or assist with creation and completion of quality records including; Deviations, Change Controls, OOS / OOT, CAPA s Tasks Own document updates and be able to control timelines for successful implementation of changes.


Housekeeping and maintaining the clean room environment Maintaining sampling rooms inventory. Assist with internal, customer or regulatory audits and complete any actions assigned. Maintaining training profile at 95% or above and attending all required training sessions within the required time.


Degree (required)* A-Level Education or relative experience Field of Study Chemistry


Degree (preferred) BSc Field of Study Chemistry


Skills required:
GMP


Working in a laboratory environment


Chemical / Biochemical techniques and methods


Reporting of Data


Quality records

No