What are the responsibilities and job description for the PCI Pharma Services Pharmaceutical Career Fair - Madison, WI - Friday August 7, 2026 position at PCI Pharma Services?
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
PCI is hosting an onsite career 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.
Manufacturing Technician I/II/III: 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.
Manufacturing Technician IV : 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.
Material Handler I/II/III: Assists in the day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. The main responsibility of this position is to assist with all aspects of logistics such as receiving, shipping, data entry, inventory control, labeling and maintaining all associated cGMP documentation as needed.
QA Associate I – Operations: Provides real-time QA support on the floor for GMP Manufacturing of drug product. The work scope includes floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed.
QA Specialist I – Aseptic Core Monitoring: 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.
QA Specialist I – Operations: 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.
QC Microbiology Technician I: 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.
QC Microbiologist I: 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.
QC Sample Coordinator: Supports daily operations within the QC Sample Management group. The work scope includes executing material control procedures and reviewing specification documents, performing raw material sampling and inspection, coordinating testing activities with internal and external laboratories, and collecting data and material certificates for QA reviews.
Supervisor, Quality: Leads the QA Associates, who provide QA support in the manufacturing of clinical and commercial drug products, to ensure compliance with the principles and guidelines of cGMP. Assists in maintaining quality systems, management of investigations, material management, and providing QA support in real time for manufacturing, to ensure control of the manufacturing process.
Visual Inspection Technician I: 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.
Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future
Equal Employment Opportunity (EEO) Statement
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, 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.
We are PCI.
Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.
PCI is hosting an onsite career 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.
- PCI Pharma Services Pharmaceutical Career Fair
- Friday, August 7th, 2026
- 1:00 PM–3:00 PM
- 5501 Research Park Blvd. Madison, WI
Manufacturing Technician I/II/III: 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.
Manufacturing Technician IV : 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.
Material Handler I/II/III: Assists in the day-to-day activities relating to inventory control functions supporting pharmaceutical fill/finish operations. The main responsibility of this position is to assist with all aspects of logistics such as receiving, shipping, data entry, inventory control, labeling and maintaining all associated cGMP documentation as needed.
QA Associate I – Operations: Provides real-time QA support on the floor for GMP Manufacturing of drug product. The work scope includes floor oversight of manufacturing including observing critical processes and performing AQL visual inspection, executed GMP documentation review and supporting other QA functions as needed.
QA Specialist I – Aseptic Core Monitoring: 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.
QA Specialist I – Operations: 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.
QC Microbiology Technician I: 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.
QC Microbiologist I: 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.
QC Sample Coordinator: Supports daily operations within the QC Sample Management group. The work scope includes executing material control procedures and reviewing specification documents, performing raw material sampling and inspection, coordinating testing activities with internal and external laboratories, and collecting data and material certificates for QA reviews.
Supervisor, Quality: Leads the QA Associates, who provide QA support in the manufacturing of clinical and commercial drug products, to ensure compliance with the principles and guidelines of cGMP. Assists in maintaining quality systems, management of investigations, material management, and providing QA support in real time for manufacturing, to ensure control of the manufacturing process.
Visual Inspection Technician I: 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.
Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future
Equal Employment Opportunity (EEO) Statement
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.
At PCI, 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.