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

PCI Pharma Services•Madison, WI

9d•Onsite

About The Position

PCI Pharma Services is hosting an onsite job fair for multiple positions in Madison, WI. PCI provides a comprehensive range of pharmaceutical services from early development through commercial launch and ongoing supply, with a focus on quality, operational excellence, and customer experience. The company is committed to building teams to pioneer and shape the future of PCI, emphasizing that their people drive progress and create a better tomorrow. They foster a culture of purposeful work, intentional learning, and competitive rewards, aiming to be an interesting and fulfilling place for talented individuals to grow their careers.

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.
Resolves non‑routine issues using advanced technical expertise.
Reviews and updates MPRs and SOPs.
Supervises operations such as equipment preparation, filling, and lyophilization.
Manages staff performance.
Supports operational goals.
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.
Provides 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.
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.

Nice To Haves

Mentors others
Trains less experienced staff
Models Guardian values
Leads others in complex manufacturing tasks
Trains less experienced staff
Models Guardian values
Manages staff performance
Supports operational goals
Maintains consistent oversight of team activities and behaviors.
Provides 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.
Leads others in complex manufacturing tasks while ensuring compliance with GMP/ISO and PCI safety standards.
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.
Provides 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.
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.