What You Will Achieve
In this role, you will:
Work in a structured environment using established procedures and seek guidance from colleagues.
Ensure work is regularly reviewed for technical judgment, completeness, and accuracy.
Maintain compliance with current Good Manufacturing Practices (cGMP) by following site procedures.
Identify and implement improvements in efficiency, safety, quality, and cost for equipment and processes.
Develop metrics and action plans to meet customer and business needs, promoting compliance with cGMP.
Use project management skills to lead and participate in cross-functional teams, supervising inspection, reconciliation, dispensing, and receivals of components.
Here Is What You Need (Minimum Requirements):
BA/BS degree with any years of experience, or Associate's degree with 4+ years of experience, or high school diploma (or equivalent) with 6+ years of relevant experience
Effective verbal and written communication skills
Proficiency in MS Office programs
Strong organizational skills
Basic understanding of manufacturing processes
Bonus Points If You Have (Preferred Requirements):
Pharmaceutical experience in Operations Engineering
Experience in a highly regulated environment
Knowledge of cGMP and regulatory standards
Strong problem-solving skills
Ability to identify and implement cost-effective solutions
Experience in optimizing production workflows
Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Physical/Mental Requirements
Job will include standing, walking, and sitting. Occasional lifting may be required.
Non-Standard Work Schedule, Travel, or Environment Requirements
Job is posted as 1st shift. However, off shift and weekend coverage is occasionally required to meet the project objectives.
Other Job Details:
The annual base salary for this position ranges from $68,600.00 to $114,300.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Candidates must be authorized to be employed in the U.S. by any employer.
U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.
Manufacturing
