On-site Job Fair - PCI Pharma Services Madison, WI

PCI Pharma Services • Madison, WI

6d • Onsite

About The Position

PCI Pharma Services is hosting an onsite job fair for multiple positions. At PCI Pharma Services, we provide a comprehensive range of pharmaceutical services from the earliest stages of development through to commercial launch and ongoing supply. We have an uncompromising focus on providing quality and operational excellence and providing the industry with leading customer experience. The job fair is for various roles including Formulation Technician, Manufacturing Technician, Supervisor, Manufacturing, QA Specialist, QC Microbiology Technician, and Visual Inspection Technician. PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer committed to cultivating an inclusive workplace.

Requirements

• Mentors others and performs complex formulation tasks under general guidance and in compliance with GMP/ISO and PCI safety standards.
• Advanced technical knowledge.
• Works with MPRs and SOPs.
• Trains less experienced staff.
• Models Guardian values.
• Learn and perform a variety of tasks in accordance with the manufacturing GMP/ISO requirement and standards.
• Performs routine and critical manufacturing operations.
• Leads others in complex manufacturing tasks while ensuring compliance with GMP/ISO and PCI safety standards.
• Advanced technical expertise.
• Supervises operations such as equipment preparation, filling, and lyophilization, ensuring production plans are executed across multiple shifts.
• Manages staff performance, supports operational goals, and maintains consistent oversight of team activities and behaviors.
• Provides real‑time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
• Ensures product quality and compliance with internal procedures and external standards.
• Core responsibilities include Batch Record Review, Lot Disposition, and Quality System oversight.
• May also evaluate deviations, determine escalation needs, review and approve investigations, and manage associated CAPAs.
• Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures.
• Performs Lab work and other tasks as assigned by management.
• Conducts environmental and clean‑utility sampling and testing in accordance with approved procedures.
• Performs laboratory analyses and supports additional microbiology tasks as assigned by management.
• Performing visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives.

Nice To Haves

• Mentors others.
• Trains less experienced staff.
• Leads others in complex manufacturing tasks.
• Supervises operations.
• Manages staff performance.
• Supports operational goals.
• Maintains consistent oversight of team activities and behaviors.
• Provides real‑time monitoring of aseptic behaviors.
• May also evaluate deviations, determine escalation needs, review and approve investigations, and manage associated CAPAs.
• This role provides the opportunity to strengthen GxP programs by delivering QA expertise for clinical and commercial manufacturing.

Responsibilities

• Executes all formulation operations, including equipment prep, dispensing, dissolution, formulation, purification, and aseptic compounding.
• Addresses non‑routine issues using advanced technical knowledge and escalates matters as needed.
• Works with MPRs and SOPs, monitors team behaviors, and trains less experienced staff while modeling Guardian values.
• Learn and perform a variety of tasks in accordance with the manufacturing GMP/ISO requirement and standards.
• Performs routine and critical manufacturing operations, including but not limited to work functions in equipment prep, formulation, aseptic compounding, and filling activities for biopharma and medical device products.
• Performs and oversees all operations, including equipment prep, dispensing, dissolution, formulation, purification, aseptic compounding, filling, and packaging.
• Resolves non‑routine issues using advanced technical expertise and escalates matters as needed.
• Reviews and updates MPRs and SOPs, monitors team behaviors, trains less experienced staff, and models Guardian values.
• Leads an aseptic manufacturing team in compliance with FDA and other regulatory requirements while following all PCI safety standards.
• Supervises operations such as equipment preparation, filling, and lyophilization, ensuring production plans are executed across multiple shifts.
• Manages staff performance, supports operational goals, and maintains consistent oversight of team activities and behaviors.
• Provides real‑time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/6 areas.
• Supports PCI’s commitment to aseptic integrity, product quality, and patient safety.
• Ensures product quality and compliance with internal procedures and external standards.
• Core responsibilities include Batch Record Review, Lot Disposition, and Quality System oversight.
• May also evaluate deviations, determine escalation needs, review and approve investigations, and manage associated CAPAs.
• This role provides the opportunity to strengthen GxP programs by delivering QA expertise for clinical and commercial manufacturing.
• Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures.
• Performs Lab work and other tasks as assigned by management.
• Conducts environmental and clean‑utility sampling and testing in accordance with approved procedures.
• Performs laboratory analyses and supports additional microbiology tasks as assigned by management.
• Performing visual inspection of sterile filled containers (vials) in accordance with all applicable procedures, regulations, and safety directives.
• The primary job function will be to ensure finished drug product vials manufactured by PCI are free of visible defects which are culled through the visual inspection process to support patient safety and product quality.

Benefits

• Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies.
• We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level.
• We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed