Purpose:
This role will support manufacturing operations on a 24/7 shift pattern and may include extended hours.
Responsibilites
:****
* Environmental Monitoring of Grade 8/9 Cleanrooms
* Environmental Monitoring of Grade 5/7 Cleanrooms & Isolators
* Reading of Environmental Monitoring Plates
* Bioburden testing of water & disinfectants
* Writing technical reports
* Water sampling
* Testing of In Process samples such as Density & pH
Requirements
* Bachelors degree in a science discipline
* Biopharmaceutical QC experience in a microbiology lab
* Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products
Preferred Qualifications
* Experience working in an aseptic cleanroom performing Environmental Monitoring
* Proficient in the use of LIMS & LMES
Competencies
* Technically strong background in microbiology and aseptic manufacturing
* Experience in LIMS, Change Control, Trackwise, SAP and CDOCS an advantage
* Flexibility - the EM role often encounters changing priorities on a daily basis
* Problem solving skills
* Experience with Regulatory inspectors and interacting with inspectors desirable
* Demonstrated ability to work independently and deliver right first time results
* Works under minimal direction
* Work is guided by objectives of the department or assignment
* Follows procedures
* Refers to technical standards, principles, theories and precedents as needed
* May set project timeframes and priorities based on project objectives and ongoing assignments.
* Recognizes and escalates problems
* Demonstrated leadership and communication skills
* Auditing documentation and operation process
* Demonstrated ability to interact with regulatory agencies
* Shift Patterns
: This role will support manufacturing operations on a 24/7 shift pattern and may include extended hours.
* Two shift patterns
: Two days followed by Two nights - from 07:00 to 19:00 & 19:00 to 07:00.