Microbiology Coordinator?

Job Description

Microbiology Coordinator? page is loadedMicrobiology Coordinator?Microbiology Coordinator?locationsSaudi Arabia - KAEC PGS Plant time typeFull time posted onPosted Yesterday job requisition id4844966*ROLE SUMMARY* *Perform all the microbiology required analysis and all related tasks.*Performing all relevant documentation and tasks.*ROLE RESPONSIBILITIES* * Perform all microbiological required analysis ?Raw materials, Stability, Finished Good and Validation analysis? as microbial count test.* Responsible for the fulfillment of GLP, EHS requirements and PQS requirements.* Controlling microbiology lab. GMP documents.* Requesting and contacting the vendors of all the equipment, reagents, media, and instruments required for the microbiology lab.* Prepare the environmental monitoring programs of the Nonsterile area, record and trend the environmental monitoring data.* Prepare the water monitoring program of the Plant and Record and trend Water data.* Responsible for microbiology instrument maintenance and contacting their vendors.* Review the Microbiology consumables and contact with suppliers if required.* Participate in the microbiological laboratory investigation in case of out of specifications test results.* Preparing SOPs and participate in method validation protocols necessary for the microbiological laboratory activities and ensuring that these procedures are strictly followed during laboratory practices.* Participate in Troubleshooting for microbiology section problems.*How You Will Achieve It* * Manage own time, professional development and be accountable for own results.* Prioritize own workflow, allocate work of others and assist in establishing their priorities, pushing self and others to exceed goals.* Responsible for providing input to performance assessment on team members.* Ensure compliant and timely documentation and resolution of events.* Develop working process to enhance Good Manufacturing Practices {also cGMP} standards for the team.* Maintain a high level of personal safety and housekeeping considerations.* Identify Continuous Improvement opportunities and participates in Continuous Improvement projects.* Author /review QC (Quality Control) documentation and document all results in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements.* Responsible for the endorsement of Good Laboratory Practices {part of GxP} Environment, Health & Safety requirements and Pfizer Quality Standards (PQS) requirements.* Ensure compliance with all policies and procedures in accordance with the Company Handbook.* Provide an efficient customer focused service by representing the area at designated meetings, and by ensuring laboratory processes, equipment and services are maintained in an operational state.* Provide training for team members and perform peer reviews of data and logbooks.*Qualifications****Must-Have* * University degree of relevant section.* Minimum 1-3 years relevant experience in Quality Control.* Ability to read English and interpret documents such as cGMP/ FDA regulations, standard operating procedures, and Pfizer corporate policy manuals.* Strong interpersonal and technical writing skills and the ability to interact across divisional boundaries.* Ability to report results clearly and concisely. Sound reasoning and ability to quickly analyze and solve.* Good command of English both written and spoken.* Excellent attention to detail and time management skills.* Ability to work independently and with work teams* Ability to manage multiple tasks and projects simultaneously, and to prioritize work, goals and tasks per the divisional and corporate objectives.* PC literate with the following applications: MS Excel, Word, PowerPoint*Nice-to-Have* * Quality certificate is a plus.PHYSICAL/MENTAL REQUIREMENTS-Good command of English both written and spoken. ? Knowledgeable with interpersonal learning. ? Communication, teaching and coaching skills. ? Logic way of thinking ? Management and decision making skills ? High analytical skills ? Professional in reports writing. ? Has the ability to work under stress ? PC literate with the following applications: MS Excel, Word, PowerPoint Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control#LI-PFE Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We?re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.

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