Process Tech II

About the position

Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on 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 strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. The Biological Operations Tech II / Biologic Operations Sr. Tech I-II role is responsible for processing and formulation of ATGAM Purified Drug Substance and Coral Snake Anti-Venin as well as other biological operations steps. The role may also take on stroma processing when necessary or any other aspect of the biological operation area unit operations. Work is performed in strict compliance with manufacturing standards (SOPs) and following all regulatory requirements (i.e., GMPs & OSHA).

Responsibilities

• Performing all unit operations in the biological processing area with a variety of different equipment types (tanks, pumps, centrifuges, scales, filters, freeze dryers, etc.)
• Washing, sanitizing and cleaning facilities and equipment
• Handling, Charging and packaging materials
• Monitoring process parameters and batch end reports for quality or equipment concerns
• Utilizing computer skills to interact with multiple complex PLC and SCADA systems
• Collaborating with maintenance and engineers to troubleshoot equipment and perform TPM tasks
• Supporting development and execution of capital projects, corrective actions, and continuous improvement ideas
• Demonstrating growth mindset to share best practices & utilize downtime effectively
• Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation
• Completing and maintaining all required training on time
• Demonstrating ownership and accountability of the production schedule and product quality
• Executing in-process quality inspections
• Other duties as assigned by the supervisor

Requirements

• High school diploma / general education degree (GED) plus an associate degree, OR Veteran/Military experience, OR one year of relevant work experience in a manufacturing or GMP facility
• Mechanical experience/aptitude
• Experience handling biologic substances, APIs, or drug products

Nice-to-haves

• Previous experience in cGMPs (current Good Manufacturing Practices) environment
• Proficiency in using manufacturing software and tools
• Ability to adapt to changing priorities and work in a fast-paced environment
• Demonstrated leadership skills and ability to mentor team members

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