QC Micro Analyst - Cork

Pe Global

Cork

PE Global is currently recruiting for a QC Micro Analyst for a client site in Cork: QC Micro Analyst - BC2 - 18 month contract - 2 cycle shift @ 20% POSITION SUMMARY: This position is responsible for carrying out tasks and projects related to raw material, utility, in process, release and stability testing of biotechnology products as required by Good Manufacturing Practice (GMP. GENERAL SCOPE OF RESPONSIBILITIES: • Achieves a high level of competency in laboratory methods and procedures to support raw material, utility, in process, release and stability testing of biotechnology products. • Performs routine and non-routine Microbiological and or Biochemical/Chemical testing activities as required. • Ensures that all testing is completed, reviewed and approved within agreed turnaround times. • Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards. • Trains other QC analysts and Manufacturing personnel in laboratory methods and procedures when required. • Writes/updates and reviews TMs, SOPs and WIs as required. • Writes and reviews invalid assays, non-conformances and deviations as required. • Initiates and drives change controls to completion to implement process improvements. • Actively participates in lean initiatives such as Kaizen, 5S and Gemba. • Is an active member of the QC group and provide assistance with other group activities as required. • Communicates relevant issues to the QC Team Leader promptly. SPECIFIC TESTING EXPERIENCE REQUIRED. • Initiation and Maintenance of Mammalian Cell Lines. • Cell Culture Based Bioactivity Testing. • ELIZA Testing. • qPCR Testing. • Bioburden. • Endotoxin. • Environmental Monitoring. • Microbial Identification. OTHER RESPONSIBILITIES / DETAILED DUTIES MAY APPLY: • Deputises for the QC Team Leader as appropriate. • Maintains and develops knowledge of analytical technology as well as cGMP standards. • Partners with other departments to ensure that all QC testing activities are completed in a compliant and efficient manner. KEY COMPETENCIES REQUIRED: • Excellent interpersonal skills. • Ability to operate as part of a team is critical. • Excellent communication skills both written and verbal. • Good knowledge of LIMS, Track wise and Electronic documentations systems. • Good knowledge of Microsoft Office applications such as word, excel, PowerPoint. • Experience working in a high throughput laboratory environment. • Excellent technical writing skills. • Customer focus. • Attention to detail. • Good problem solving skills. • Results and performance driven. • Adaptable and flexible. QUALIFICATIONS AND EXPERIENCE: • BSc (Honors) in a scientific/technical discipline. • A minimum of 2 years’ experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry. • Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory. Interested candidates should send their CV to Audrey.mccarthy@peglobal.net or call 0214297900. Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. This job originally appeared on RecruitIreland.com.

1924 days ago