Bioprocess Technician IV (2nd shift)
PfizerAbout the role
Use Your Power for Purpose
Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.
What You Will Achieve
In this role, you will:
Operate, service, adjust, clean, and sterilize production-related equipment in compliance with cGMPs and safety regulations.
Maintain a clean room environment and complete work instructions to meet regulatory requirements.
Ensure equipment functionality, report or correct malfunctions, and assist in complex setup or repair operations.
Manage time effectively, focus on professional development, and take accountability for results.
Prioritize workflow, assist less-experienced colleagues, and adhere to quality standards and best practices.
Maintain accurate documentation, including training records, batch records, check sheets, and log books.
Support audits, help close audit observations, and utilize automated and enterprise systems to perform tasks.
Communicate cross-functionally with technology transfer teams, lab scientists, supply chain, quality, and engineering.
Take responsibility for individual contributions to team deliverables, represent the work group, and foster a positive team environment.
Complete assignments based on established procedures, identify process improvements, troubleshoot issues, and provide direction and training to team members.
Here Is What You Need (Minimum Requirements)
High School Diploma or GED
4+ years of experience, particularly in a pharmaceutical or other cGMP (Current Good Manufacturing Practices) environment
Effective verbal and written communication
Proficiency in operating and troubleshooting production equipment
Strong understanding of cGMP and safety regulations
Ability to maintain accurate documentation and records
Experience in a clean room environment
Competence in using automated and enterprise systems
Effective cross-functional communication skills
Bonus Points If You Have (Preferred Requirements)
Basic mechanical knowledge and hands-on experience using various hand tools
Experience in a pharmaceutical manufacturing environment
Knowledge of process improvement methodologies
Ability to train and mentor less-experienced colleagues
Ability to work independently and as part of a team
Attention to detail and commitment to quality
Adaptability and flexibility in a dynamic work environment
Physcial / Mental requirements
Requires the moving of heavy equipment and the ability to lift ~40 pounds.
Moderate repetitive standing, sitting, bending, and ladder climbing on a daily basis.
The incumbent needs to take the necessary safety precautions when working with pressurized systems, steam, and corrosive chemicals.
The incumbent is required to attain knowledge of the operational equipment.
The incumbent will be required to assist in solving problems regarding site assessment, specific units used in Biopharmaceutical manufacturing.
The incumbent must be able to follow SOPs, MBRs and be able to use a multitude of enterprise systems including SAP, Delta-V, etc.
Non-Standard work schedule, travel or environment requirements
Supports a 24/7 facility.
Schedule: M-F 2nd Shift 2:00PM-10:30PM.
Ability to work 1st shift until GMP operations start.
Ability to support operations and training in other shifts when needed.
Ability to work weekends when needed.
Other job details
Last day to apply: november 3rd, 2025
Work Location Assignment: On Premise
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