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MSAT Technician
Job Posted: 24 minutes ago
Salary: £ 20 - 20 / Hour
Job Type: Contract
Location: Cambridgeshire
Expire in: a month
Job Description
MSAT Technician - Pharmaceutical - Cambridge - Contract
Our client is a leading pharmaceutical manufacturer. At present, they are seeking an MSAT Technician on a temporary contract basis for 4 months at their facility in Cambridge.
Overview:
* Day to day activities in a sterile manufacturing facility, filling of sterile products, autoclaving and washing of components.
* Maintaining the facility to GMP standards of cleanliness and environmental standards.
* Ensuring all paperwork is completed to GMP standards and non-conformity documentation and investigation
Key Responsibilities:
* Ensure compliance with all regulatory requirements and maintain excellent GMP, quality control and safety.
* Excellent attention to detail and accuracy, all paperwork to be completed accurately and in a timely manner compliant with cGMP.
* Support the sterile Team Leader at weekly meeting, KPI’s, planning and deviation investigations
* Experienced in working in a sterile environment, an isolator or RABS unit (Grade A).
* Work with single use sterile technologies, and closed systems
* Demonstrate ability to build bonds and work with other departments QA, QC, Validation etc.
* Prepare autoclave and washer loads in accordance to procedure
* Write and review new SOP’s and Batch records and roll these out to the team
* Have the flexibility to operate in all areas of production, sterile operation, validation equipment, cleaning and autoclaving
* On-going cleaning, environmental monitor and building compliance
* Investigate any deviations and action CAPA’s
* Perform regular cleaning of the cleanroom to ensure it remains within GMP standards.
* Perform stock management tasks within the warehouse.
Candidates will ideally have GMP experience in a production environment with experience of sterile production and demonstrated aseptic techniques.
Additional skills:
* Experience in GMP manufacturing.
* Experienced in Clean Room Grade A environments, Isolators or RABS.
* Should be assessor or qualified in safety systems, i.e. COSHH, risk assessments, manual handling or IOSH Managing Safely.
* Experienced working with Excel and Word.
* Knowledge of lean production or six Sigma.
* Evidence of excellent attention to detail and ability to follow Standard Operating Procedures.
* Experienced in writing SOPs for cleanroom activities.
* Knowledge of validation operations, such as; FATs, SATs and IOQ/PQBefore You Apply
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