Environmental Monitoring Analyst I - Midnight Shift Apply
Location: United States - Michigan - Rochester
Time Type: Full time
Posted on: Posted 2 Days Ago
Job Requisition ID: 4923410
Why Patients Need You Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer-oriented. Your contribution will directly impact patients.
What You Will Achieve You will be a team member who is relied upon to have a good understanding of procedures, techniques, tools, materials, and equipment. Your decision-making will help you prioritize workflows based on the available resources. You will follow standard procedures to complete tasks, contributing to the team's success by sharing your previously acquired knowledge.
How You Will Achieve It Perform environmental monitoring in a safe, compliant, and efficient manner. Responsibilities include performing environmental monitoring in the Aseptic Manufacturing Environment to ensure that our products meet the highest standards of quality.
Key Tasks: 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 accurately 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.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. Work Practices and Processes: Maintain a neat and tidy workspace.Adhere to company, site, and laboratory safety rules and raise any safety observations, concerns, or suggestions.Follow company, site, and global procedures at all times adopting cGMP, cGDP practices.Follow management direction at all times.Able to function independently while asking questions when needed.Accept dynamic work sequences and schedule changes.This position requires schedule flexibility including weekends when required by the manufacturing schedule. Planning, Communication, Teamwork, Initiative, and Performance Expectations: Actively participate in daily and weekly planning discussions among teammates and Management.Consistently communicate work sequence status in a timely manner.Participate in discussions to identify opportunities for correction and improvement.Engage in helping to achieve QC Team, individual, and site goals.Offer suggestions for improvements when faced with roadblocks or issues.Maintain a positive influence on the QC Team, supporting and assisting teammates across different shifts as necessary. Qualifications Must-Have: High School/GED and one year experience, or equivalent combination of education and experience.Willing to learn and develop a career in the pharmaceutical manufacturing industry.Capable of reading, understanding, and executing instructions in basic site procedures. Nice-to-Have: Experience in a GMP environment.Environmental monitoring experience within the pharmaceutical industry.Strong documentation and communication skills.Strong organizational skills and the ability to multi-task across various projects and activities.Good written and verbal communication skills.Ability to follow written and verbal instructions.Ability to obtain and 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 needs dictate. PHYSICAL/MENTAL REQUIREMENTS: Must not have Penicillin allergy.
Minimal travel for training/seminars.
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS: Midnight shift hours from ******** . Aseptic gowning required for the role.
Work Location Assignment: On Premise
Last Day to Apply: November 18, 2024
No relocation support available.
The salary for this position ranges from $18.62 to $31.03 per hour. This position offers eligibility for overtime, weekend, holiday, and other pay premiums depending on the work schedule and the Company's policies. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments.
EEO & Employment Eligibility: Pfizer is committed to equal opportunity in employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or expression, national origin, disability, or veteran status. Pfizer also complies with all applicable national, state, and local laws governing nondiscrimination in employment.
About Us 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.
#J-18808-Ljbffr