About the role
Why Patients Need You
Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need when they need them.
What You Will Achieve
The Bioprocess Technician IV leads the execution of Commercial, Clinical, and/or Development production according to Standard Operating Procedures and Production Schedule for mAb products. You will work on interdisciplinary teams, to own and implement process improvements, and lead/participate in process troubleshooting.
How You Will Achieve It
- Serve as a key resource and potentially lead lower levels within your area of expertise.
- Manage personal time and professional development, taking accountability for results and prioritizing workflow.
- Contribute to project and department tasks, providing direction and training to team members, and may act as a lead worker.
- Be recognized as a "LEAD" or "Subject Matter Expert" within your field.
- Proactively identify and resolve potential problems, considering wider implications beyond immediate issues.
- Complete assignments independently, selecting appropriate methods and ensuring team assignments are completed.
- Review non-standard work for technical soundness and may review the work of others.
- Adhere to Pfizer standards, guidelines, and values, influencing teams and contributing to the development of departmental standards and guidelines.
- Leverage knowledge of process equipment, systems, manufacturing operations, and automation control to plan and execute activities.
- Ensure compliance with Company policies, standard operating procedures, and global regulatory and environmental guidelines, adapting methods and procedures as necessary.
Qualifications
Must-Have
- High School Diploma or GED
- 6+ years of experience
- Experience within the biopharmaceutical industry, including knowledge and experience with relevant biopharmaceutical unit operations and/or laboratory operations
- Understanding of continuous improvement processes
- Proficiency in process equipment, systems, manufacturing operations, and automation control
Bonus Points If You Have (Preferred Requirements):
- Advanced knowledge of biopharmaceutical manufacturing processes
- Proficiency in project management
- Familiarity with global regulatory and environmental guidelines
- Ability to adapt to changing priorities and work effectively under pressure
Physical/Mental Requirements
- Lifting, sitting, standing, walking, bending, requires the moving of heavy equipment and the ability to lift ~40 pounds.
- Ability to perform mathematical calculations and ability to perform complex data analysis.
- Strong problem-solving skills with the ability to identify and resolve potential issues
- Strong communication and interpersonal skills
Non-Standard Work Schedule, Travel, or Environment Requirements
Work schedule is shift 3 on 2/2/3 schedule. Nightshift 6pm-6am
Other Job Details:
- Last day to Apply: May 7th, 2025
- Eligible for Relocation Assistance: NO
- Work Location Assignment: On Premise
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
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