Role overview
About this role
<img src="http://counter.adcourier.com/bmlraXRhc2hlbGxhcmQuNDI2MzcuNDI0QGVsYW5pdC5hcGxpdHJhay5jb20.gif" /><br />MAIN DUTIES AND RESPONSIBILITIES: <br />· Understand and comply with the requirements of Good Manufacturing Practices (GMP) or Good <br />· Laboratory Practices (GLP) while carrying out all tasks. <br />Comply with EHS and Quality regulations and policies. Maintain the working environment in safe and tidy conditions based on the defined standard rules and schedules (such as carrying out daily <br />· Health and Safety Checks) <br />Ensuring all tasks assigned on daily scheduling are completed on time. <br />- Carryout water and product bio burden testing following documented procedures and in accordance <br />· with the stipulated deadline. <br />Carryout routine microbial monitoring plate reading and total particle monitoring calculations <br /> following documented procedures meeting deadlines. Be able to identify microbial isolates <br /> found on monitoring plates. <br />· Ensure good documentation practices while recording results and maintaining records. Generating QC Microbiology monitoring batch files and preparing test pieces for testing. <br />· Carryout routine temperature & pressure checks and air velocities in the controlled QC Microbiology clean room. <br />· Maintain and monitor stock levels of consumables to include tracking of deliveries, and coordinate purchasing requirements. <br />· Assist the team with non routine analyses, investigations and audit preparation when required. <br /> <br />Qualifications and Requirements: <br />· <br />Candidate should be educated to HND or degree level in Microbiology or related life science <br />· qualification. <br />· Experience in relevant field is desirable. <br />· Computer knowledge in MS Office and Excel. <br />· Good communication and interpersonal skills. <br />· Microbiological knowledge for better understanding of testing procedures. <br />· Be able to work as a team, manual dexterity and the ability to adhere to tight deadlines whilst not compromising GMP. <br /> <br />Desired Qualities: <br /> <br />The successful candidate must be able to work as a team in supporting goals and objectives of the department, complying with Good Manufacturing Practices, Good Laboratory Practices and meeting Service Level Agreements. <br /> <br />If you believe you possess the above skill and attributes please apply through this site. <br />