Bioprocess Technician IV (3rd Shift)

Pfizer • Sanford, NC

132d • $25 - $42

About The Position

In this role, you will execute manufacturing operations on the production floor for buffer/media make-up tanks, glass washers, autoclaves, bioreactors/fermentors, filtration equipment, inoculum preparation, chromatography skids and/or UF/DF skids with varying levels of automation. You will follow SOPs and batch records for unit operations, support the operation of manufacturing equipment, and resolve issues associated with process equipment commissioning, qualification, and validation. You will drive troubleshooting, technical support/analysis, and resolution of equipment, automation, and process issues on the manufacturing floor. Your efforts will ensure that patients and physicians have timely access to the medicines they need.

Requirements

• High School Diploma or GED.
• 4+ years of experience in a pharmaceutical or cGMP environment.
• Effective verbal and written communication skills.
• 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.

Nice To Haves

• 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.

Responsibilities

• Executes manufacturing operations on the production floor for various equipment.
• Follows SOPs and batch records for unit operations.
• Supports operation of manufacturing equipment and issue resolution.
• Drives troubleshooting and technical support for equipment and process issues.
• Ensures timely review of daily documentation and completes data entry.
• Identifies and communicates process and compliance concerns in real time.
• Supports audits and observation improvements.
• Collaborates with Subject Matter Experts for QTS investigations and CAPA implementations.
• Implements Lean Manufacturing, Sustainability, and Operational Excellence initiatives.
• Generates work requests for facility/manufacturing equipment issues.
• Maintains facility in a safe and GMP compliant manner.

Benefits

• 401(k) plan with Pfizer Matching Contributions.
• Paid vacation, holiday, and personal days.
• Paid caregiver/parental and medical leave.
• Health benefits including medical, prescription drug, dental, and vision coverage.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Industry: Chemical Manufacturing
• Education Level: High school or GED