Environmental Monitoring Analyst I at Pfizer · United…

Summary: Pfizer is a leading pharmaceutical company committed to quality and patient safety. The Environmental Monitoring Analyst I will perform environmental monitoring in the Aseptic Manufacturing Environment to ensure product quality and compliance with standards. Responsibilities: - Perform environmental monitoring in a safe, compliant, and efficient manner - Gain an understanding of cGMPs, GLPs EHS and site/ department policies and environmental monitoring concepts - Perform all routine weekly/monthly sampling activities at the site including viable, non-viable, water, ISO and batch process environmental monitoring - Enter and verify environmental monitoring data into various databases/computerized systems and review associated documentation in an accurate and in a timely manner - Author and review monthly/annual data reports - Ensure environmental monitoring supplies are ready and available within the Aseptic Processing Area (APA) and in the QC Laboratory. Support of production/manufacturing team members as business partners working in the APA - Become qualified on aseptic gowning and participate in a successful media filling operation - Consistently demonstrate proper documentation practices - Perform and document aseptic observations and coaching of Manufacturing Operators per the site aseptic practices program - Must maintain and neat and tidy workspace - Consistently adheres to company, site and laboratory safety rules and immediately raises any safety observations, concerns or suggestions - Follow company, site and global procedures at all times adopting cGMP, cGDP practices - Follows management direction at all times - Able to function independently while asking questions without hesitation when needed or unsure - Accepts dynamic work sequences and schedule changes - Actively participates in daily and weekly planning discussions among teammates and Management (as needed) offering suggestions to improve RFT and Manufacturing Schedule support as needed - Consistently communicates work sequence status in a timely manner - Where work was not achieved, actively participates in discussions to identify opportunities for correction and improvement - Demonstrates engagement in helping to achieve EM Team, individual, as well as site goals - When faced with roadblocks or issues, routinely offers suggestions for improvements - Maintains a positive influence on the EM Team, often going out of their way to support and assist teammates across different shifts as necessary Required Qualifications: - Entry Level Position, High School/GED and one year experience, and or training; or equivalent combination of education and experience - Willing to learn and develop a career in the pharmaceutical manufacturing industry - Capable to read, understand and execute instructions in basic site procedures - Must be able to lift a minimum of 30lbs - Must not have Penicillin allergy - Must be able to work 3rd shift (2300-0730) Preferred Qualifications: - Strong documentation and communication skills - Strong Organizational skills and the ability to multi-task across various projects and activities - Must have good written and verbal communication skills - Follow written and verbal instructions - Must be able to obtain and to maintain multiple technique proficiencies (as dictated by site and business needs) - Complete all training, written exams and certifications - Flexible to work on any shift temporarily as business need dictate Required Skills: Environmental monitoring, cGMP, GLP, Aseptic gowning, Data entry, Media filling operation, Documentation practices Benefits: 401(k) plan with Pfizer Matching Contributions, Additional Pfizer Retirement Savings Contribution, Paid vacation, Holiday and personal days, Paid caregiver/parental and medical leave, Health benefits to include medical, prescription drug, dental and vision coverage