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